CStone’s anti-PD-L1 antibody demonstrates promising antitumor activity with a complete response rate of 33.3% and a good safety profile in patients with relapsed or refractory extranodal natural killer/T-cell lymphoma

On December 9, 2019 CStone Pharmaceuticals ("CStone" or the "Company", HKEX: 2616) reported that results from the CS1001-201 trial in a poster presentation at the 2019 American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting (Press release, CStone Pharmaceauticals, DEC 9, 2019, View Source [SID1234552151]).

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CS1001-201 trial is a single-arm, multicenter Phase II clinical study designed to evaluate CS1001 monotherapy in relapsed or refractory extranodal natural killer (NK)/T-cell lymphoma (rr-ENKTL).

ENKTL is a subtype of mature T cell and NK cell lymphoma. It has a higher incidence in Asia than in Europe or North America. ENKTL is characterized by its rapid progression and poor prognosis. Currently, patients with rr-ENKTL lack effective treatment after failing an L-asparaginase-based combination chemotherapy regimen and targeted monotherapy only produces a complete response (CR) rate of below 10%.

"ENKTL accounts for approximately 6% of all lymphoma incidences, and there are vast unmet medical needs in this patient population that has failed the first-line treatment," said Dr. Frank Jiang, Chief Executive Officer and Chairman of CStone. "The CS1001-201 trial is the first clinical study of an anti-PD-L1 antibody in ENKTL worldwide. Our latest data have shown CS1001 to be well-tolerated with preliminary antitumor efficacy and survival benefit in rr-ENKTL patients. We will continue to advance this development program and hope that CS1001 will soon become a new treatment option for rr-ENKTL patients."

"CR is a critical outcome measure for the treatment of ENKTL. Studies have shown that ENKTL patients who achieved CR prior to autologous transplantations have a significantly better prognosis and longer survival than those who achieved partial response," said Dr. Jason Yang, Chief Medical Officer of CStone. "These latest results of CS1001 demonstrated a CR rate of 33.3% with durable response, an objective response rate of 43.3%, and a 1-year overall survival rate of 72.4%. These results represent a major breakthrough compared to current treatment options and support CS1001 as a potential conditioning regimen for hematopoietic stem cell transplantations."

Overview of the CS1001-201 trial

CS1001-201 is a single-arm, multicenter Phase II clinical study designed to evaluate CS1001 monotherapy in relapsed or refractory extranodal natural killer (NK)/T-cell lymphoma (rr-ENKTL).

The primary endpoint of the trial is ORR assessed by an independent radiological review committee (IRRC);
Secondary endpoints include investigator-assessed ORR; IRRC-assessed CR and PR rates, time to response, duration of response, progression-free survival; overall survival, and safety.
Results reported in the poster at the 2019 ASH (Free ASH Whitepaper) Annual Meeting

As of October 8, 2019, 32 patients were enrolled in the study. Among them, 24 patients (75.0%) had Stage IV ENKTL at screening, 9 patients (28.1%) received 2 lines of prior treatments, and 7 patients (21.9%) received 3 or more lines of prior treatments. All patients received 1200 mg CS1001 intravenously every 3 weeks for up to 2 years, until disease progression, intolerance, etc. The median duration of follow-up was 6.54 months (range, 0.72-15.64).

13 (40.6%) of the 32 enrolled patients remained on treatment, and 19 (59.4%) had discontinued from the study treatment.
Reasons for discontinuations included radiographic disease progression (12 patients), adverse events (AEs, 4 patients), and non-radiographic symptomatic progression (3 patients).
No deaths due to treatment-related AEs (TRAEs).
Preliminary efficacy data

CS1001 demonstrated promising antitumor activity and a favorable CR rate with durable response and survival benefit in rr-ENKTL patients.

Among the 30 efficacy-evaluable patients, the investigator-assessed ORR was 43.3%.
10 patients (33.3%) achieved CR and were still in remission.
3 patients (10.0%) achieved partial response (PR), and 1 additional patient achieved PR after pseudo-progression. The median duration of response (DoR) was not reached, and the maximum DoR was 10.9+ months.
The 1-year overall survival (OS) was 72.4% (95% CI: 52.0%-85.2%).
The IRRC assessments were not available at the time of data cut-off.
Safety data

CS1001 was well tolerated in patients with rr-ENKTL

The median duration of treatment was 12.6 weeks (range, 3.0-69.1).
30 patients (93.8%) reported treatment-emergent AEs (TEAEs).
24 patients (75.0%) reported TRAEs, of which 3 (9.4%) had Grade >3 TRAEs.
Grade 5 AEs were reported in 3 patients (9.4%), and none was assessed as related to CS1001.
7 patients (21.9%) reported serious AEs (SAEs). 1 case of Grade 4 sinus node dysfunction and 1 case of Grade 1 myositis were assessed as related to CS1001 by the investigator. Both patients later recovered from the SAEs.
Immune-related AEs (irAEs) were reported in 5 patients (15.6%). Except for 1 Grade 3 rash, all irAEs were Grade 1 in severity.
TEAEs that led to permanent treatment discontinuation occurred in 4 patients (12.5%).
No deaths due to AEs were assessed as related to CS1001.
About CS1001

CS1001 is an investigational monoclonal antibody directed against PD-L1 being developed by CStone. Authorized by the U.S. based Ligand Corporation, CS1001 is developed by the OMT transgenic animal platform, which can generate fully human antibodies in one step. As a fully human, full-length anti-PD-L1 monoclonal antibody, CS1001 is similar to natural G-type immune globulin 4 (IgG4) human antibody, which can reduce the risk of immunogenicity and potential toxicities, potentially representing a unique advantage over similar drugs.

CS1001 has completed a Phase I dose-escalation study in China, in which CS1001 showed good tolerability and produced sustained clinical benefits during the Phase Ia study.

CS1001 is being investigated in a number of ongoing clinical trials, including one Phase I bridging study in the U.S. In China, its clinical program includes one multi-arm Phase Ib study, two pivotal Phase II studies, and three Phase III studies for several tumor types.

Amphivena Reports Data on Phase 1 Study of AMV564 at Ash Annual Meeting

On December 9, 2019 Amphivena Therapeutics, Inc., a private clinical stage immuno-oncology company developing T cell engager therapeutics for cancer, reported at the American Society of Hematology (ASH) (Free ASH Whitepaper) annual meeting data from a Phase 1 study of its bivalent T cell engager clinical candidate, AMV564 (Press release, Amphivena Therapeutics, DEC 9, 2019, View Source [SID1234552150]). In an oral presentation, Dr. Jorge E. Cortes, of the Georgia Cancer Center, Augusta University, Augusta, Georgia, said that the data provide early evidence of safety and clinical activity with evidence of T cell activation, increases in bone marrow T cells, and anti-leukemic blast activity. Of the 38 patients for whom response data was reported, five had Complete or Partial Responses as defined by the European LeukemiaNet (ELN) criteria.

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"AMV564 was shown to be safe and well-tolerated, with no dose-limiting toxicities and no Grade 3+ Cytokine Release Syndrome (CRS), at doses up to 450 mcg/day in heavily pre-treated relapsed/refractory AML patients when administered by continuous IV infusion with a 14-day dosing regimen," said Dr. Cortes. "These findings provide a differentiated product profile that we believe should be further advanced in clinical development."

"We are pleased with the early signs of efficacy and safety in this First in Human clinical trial, and we are exploring subcutaneous and chronic dosing of AMV564 in other clinical trials," said Curtis Ruegg, Ph.D., President and CEO of Amphivena. "AMV564’s excellent safety profile supports conduct of combination trials of AMV564 with other agents as we look ahead into the AMV564 development program."

As of the data cutoff, 41 patients had been dosed with AMV564 and 11 dose cohorts were explored in a 14-day continuous IV dosing regimen. The primary objectives of the Phase 1 dose escalation study are to characterize the safety of AMV564 as well as identify a maximum tolerated dose and a recommended Phase 2 dose.

The presentation was made at 5:45 PM EST in the Chapin Theater (W320), Orange County Convention Center, Orlando, FL.

About AMV564

AMV564 is a bivalent, bispecific (2:2) T cell engager that binds CD33 and CD3. To date, over 50 patients have received AMV564 in two Phase 1 clinical trials for acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS). It is currently being evaluated in a First-in-Human Phase 1 trial in patients with relapsed/refractory AML at Washington University School of Medicine, MD Anderson Cancer Center, New York-Presbyterian/Weill Cornell Medical Center and Weill Cornell Medicine, Fred Hutchinson Cancer Research Center, The Ohio State University Wexner Medical Center, University of Pennsylvania Medical Center, Northwestern Memorial Hospital, and The Johns Hopkins Hospital.

The safety, efficacy and selectivity of AMV564 was highlighted most recently at the Society for Immunotherapy in Cancer (SITC) (Free SITC Whitepaper) Annual Meeting on November 7 where it was reported that AMV564 selectively reduces MDSC in the bone marrow and periphery in acute myeloid leukemia and myelodysplastic syndrome patients. The company also observed at SITC (Free SITC Whitepaper) that T cell activation on therapy can lead to rapid increases in MDSC that can be modulated by AMV564 due to avid binding of activated CD33 on MDSC. Amphivena also presented data at the 24th European Hematology Association (EHA) (Free EHA Whitepaper) meeting in Amsterdam (Abstract S877). Amphivena believes that AMV564 has demonstrated novel clinical activity by rapidly and selectively eliminating leukemic blasts and rare immature, granulocytic and monocytic MDSCs while sparing normal CD33-expressing cells, including neutrophils and monocytes.

Darzalex®▼ (daratumumab) Shows Overall Survival Benefit and Continued Improvement in Progression-Free Survival in Patients with Newly Diagnosed Multiple Myeloma Who are Ineligible for Transplant

On December 9, 2019 The Janssen Pharmaceutical Companies of Johnson & Johnson reported overall survival (OS) results from the Phase 3 ALCYONE study, which showed the addition of Darzalex (daratumumab) to bortezomib, melphalan and prednisone (D-VMP) improved OS in patients with newly diagnosed, transplant-ineligible multiple myeloma, with a 40 percent reduction in the risk of death compared to VMP alone (Press release, Janssen Pharmaceuticals, DEC 9, 2019, View Source [SID1234552149]).1 These updated data from the ALCYONE study also demonstrated that the addition of daratumumab to VMP resulted in higher rates of minimal residual disease (MRD) negativity.1 These data are the first OS results from the ALCYONE study and are being featured during an oral session (Abstract #859) at the 2019 American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting in Orlando. The data were simultaneously published in The Lancet.

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"As a physician treating patients with multiple myeloma, I want to achieve the deepest response in the frontline setting to hopefully provide long-term benefit," said Maria-Victoria Mateos, M.D., Ph.D., Director of the Myeloma Unit at University Hospital of Salamanca-IBSAL, Salamanca, Spain, and a study investigator. "This longer follow-up from the ALCYONE study is encouraging because we see that adding daratumumab to VMP in the frontline setting can provide an important overall survival advantage compared with a current standard of care."

Results of a pre-specified interim analysis, after a median duration of follow-up of more than three years, showed an estimated 42-month OS rate of 75 percent for daratumumab-VMP versus 62 percent for VMP, with a statistically significant improvement in OS observed for daratumumab-VMP versus VMP alone (hazard ratio [HR]=0.60; 95 percent confidence interval [CI], 0.46-0.80; p=0.0003).1 Of note, median OS was not reached in either group and follow-up is ongoing. In addition, daratumumab-VMP resulted in a median progression-free survival (PFS) of 36.4 months versus 19.3 months with VMP alone after a median follow-up of 40.1 months (HR=0.42; 95 percent CI, 0.34-0.51; p<0.0001).1 The results also demonstrated that daratumumab-VMP achieved significantly higher rates of MRD-negativity compared to VMP alone (28 percent vs. 7 percent respectively), at a threshold of one tumour cell per 10-5 white cells.1

The most common Grade 3/4 treatment-emergent adverse events (TEAEs) occurring in ≥3 percent for daratumumab-VMP compared to the VMP arm were neutropenia (40.2 percent vs. 39 percent), thrombocytopenia (34.7 percent vs. 37.9 percent), anaemia (17.3 percent vs. 19.8 percent) and pneumonia (13 percent vs. 4.2 percent).1 Grade 5 TEAEs were 6.9 percent in the daratumumab-VMP treatment arm compared with 5.6 percent in the VMP arm and discontinuation due to TEAEs was 6.9 percent vs. 9.3 percent.1 The rate of invasive second primary malignancy was 4.9 percent in the daratumumab-VMP treatment arm compared with 4.5 percent in the VMP arm.1 No new safety concerns were identified.1

Additional data from longer follow-up (median of 36.4 months) from the Phase 3 MAIA study (Abstract #1875) presented at ASH (Free ASH Whitepaper) 2019 demonstrated daratumumab in combination with lenalidomide and dexamethasone (D-Rd) continued to significantly reduce the risk of disease progression or death by ≥44 percent in patients with newly diagnosed multiple myeloma who are transplant ineligible, compared to treatment with Rd alone (HR=0.56; 95 percent CI: 0.44-0.71; p<0.0001), with no new safety concerns after three years of follow-up with daratumumab-Rd.2 Additionally, time from randomisation to progression on next-line treatment or death (PFS2) favoured the daratumumab arm (HR=0.69; 95 percent CI, 0.53-0.91; p=0.0079).2

"Transplant ineligible represents the largest group of newly diagnosed patients with multiple myeloma, and they have the highest unmet need. Accordingly, the advances presented at ASH (Free ASH Whitepaper) on the ALCYONE and MAIA studies for this population are very significant," said Dr Patrick Laroche, Haematology Therapy Area Lead, Europe, Middle East and Africa (EMEA), Janssen-Cilag. "The results show the benefit of adding daratumumab on OS and PFS in the frontline setting – an improvement which could open the door to helping even more patients with multiple myeloma live longer."

The most common Grade 3/4 TEAEs (≥10 percent) for patients in the daratumumab-Rd compared to the Rd arm were neutropenia (51 percent vs. 35 percent), lymphopenia (15 percent vs. 11 percent), pneumonia (15 percent vs. 9 percent), anaemia (14 percent vs. 21 percent), leukopenia (11 percent vs. 6 percent) and hypokalaemia (10 percent vs. 10 percent).2 The most common serious TEAE was pneumonia (14 percent vs. 9 percent) in the daratumumab-Rd arm compared to the Rd arm.2 The most common Grade 3/4 infection rates were 36 percent in the daratumumab-Rd treatment arm compared with 27 percent in the Rd arm.2

#ENDS#

In Europe, daratumumab is indicated:3

in combination with lenalidomide and dexamethasone or bortezomib, melphalan and prednisone for the treatment of adult patients with newly diagnosed multiple myeloma who are ineligible for autologous stem cell transplant
in combination with lenalidomide and dexamethasone, or bortezomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy
as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, whose prior therapy included a proteasome inhibitor and an immunomodulatory agent and who have demonstrated disease progression on the last therapy
About the ALCYONE study (NCT02195479)4

The randomised, open-label, multicentre Phase 3 ALCYONE (MMY3007) study enrolled 706 newly diagnosed patients with multiple myeloma who were ineligible for high-dose chemotherapy with autologous stem cell transplant. The median age was 71 years (range: 40-93).1 Patients were randomised to receive up to nine cycles of either daratumumab-VMP or VMP alone. In the daratumumab-VMP arm, patients received 16 mg/kg of daratumumab once weekly for the first six weeks (Cycle 1), followed by once every three weeks for the next 48 weeks (Cycles 2-9). Following the nine cycles, patients in the daratumumab-VMP arm continued to receive 16 mg/kg of daratumumab once every four weeks until disease progression.

About the MAIA study (NCT02252172)5

In this open-label, multicentre Phase 3 study 737 patients were randomised to receive either daratumumab-Rd or Rd alone in 28-day Cycles. The median age was 73 years (range: 45-90).2 In the daratumumab-Rd treatment arm, patients received daratumumab 16 (mg/kg) IV weekly for Cycles 1 – 2, every two weeks for Cycles 3 – 6 and every 4 weeks for Cycle 7 and thereafter. The primary endpoint was progression-free survival, defined as the time from date of randomisation to either progressive disease, or death, whichever occurred first. Patients in the daratumumab-Rd and Rd treatment arm received 25 mg of lenalidomide on Days 1 – 21 of each 28-day Cycle, and dexamethasone at 40 mg once a week for each Cycle. Patients in both treatment arms continued until disease progression or unacceptable toxicity.

About daratumumab

Daratumumab is a first-in-class6 biologic targeting CD38, a surface protein that is highly expressed across multiple myeloma cells, regardless of disease stage.7 Daratumumab is believed to induce tumour cell death through multiple immune-mediated mechanisms of action, including complement-dependent cytotoxicity (CDC), antibody-dependent cell-mediated cytotoxicity (ADCC) and antibody-dependent cellular phagocytosis (ADCP), as well as through apoptosis, in which a series of molecular steps in a cell lead to its death.3 A subset of myeloid derived suppressor cells (CD38+ MDSCs), CD38+ regulatory T cells (Tregs) and CD38+ B cells (Bregs) were decreased by daratumumab.3

Since launch, daratumumab has been used to treat more than 100,000 patients worldwide.8 Daratumumab is being evaluated in a comprehensive clinical development programme across a range of treatment settings in multiple myeloma, such as in frontline and relapsed settings.9,10,11,12,13,14,15,16 Additional studies are ongoing or planned to assess its potential in other malignant and pre-malignant haematologic diseases in which CD38 is expressed, such as smouldering myeloma.17,18 For more information, please see www.clinicaltrials.gov.

For further information on daratumumab, please see the Summary of Product Characteristics at View Source

In August 2012, Janssen Biotech, Inc. and Genmab A/S entered a worldwide agreement, which granted Janssen an exclusive licence to develop, manufacture and commercialise daratumumab.19

About Multiple Myeloma

Multiple myeloma (MM) is an incurable blood cancer that starts in the bone marrow and is characterised by an excessive proliferation of plasma cells.20 In Europe, more than 48,200 people were diagnosed with MM in 2018, and more than 30,800 patients died.21 Almost 60 percent of patients with MM do not survive more than five years after diagnosis.22

Although treatment may result in remission, unfortunately, patients will most likely relapse as there is currently no cure.23 Refractory multiple myeloma is when a patient’s disease progresses within 60 days of their last therapy.24,25 Relapsed cancer is when the disease has returned after a period of initial, partial or complete remission.26 While some patients with MM have no symptoms at all, most patients are diagnosed due to symptoms that can include bone problems, low blood counts, calcium elevation, kidney problems or infections.27 Patients who relapse after treatment with standard therapies, including PIs and immunomodulatory agents, have poor prognoses and few treatment options available.28

City of Hope Doctors Present Research on New Immunotherapies at American Society of Hematology Conference

On December 9, 2019 City of Hope physicians and researchers at the American Society of Hematology (ASH) (Free ASH Whitepaper) meeting in Orlando reported that research on novel chimeric antigen receptor (CAR) T therapy and other potential new therapies for blood cancers, as well as a comprehensive report on long-term health problems bone marrow transplant (BMT) survivors face and prevention efforts that can be taken (Press release, City of Hope, DEC 9, 2019, View Source [SID1234552148]).

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"City of Hope continues to be at the forefront of finding new treatments and pursuing innovative research for blood cancers and other hematological malignancies," said Eileen Smith, M.D., chair of City of Hope’s Department of Hematology & Hematopoietic Cell Transplantation and the Francis & Kathleen McNamara Distinguished Chair in Hematology and Hematopoietic Cell Transplantation. "Our clinical and laboratory researchers are dedicated to finding more effective CAR T cell therapies and other immunotherapies, and our survivorship studies on BMT patients seek to improve long-term health outcomes for these survivors."

City of Hope physicians and scientists discussed clinical trials that provide the foundation for new treatments for patients with leukemia, lymphoma and multiple myeloma. They also discussed preclinical studies on a new target for acute myeloid leukemia.

Study on long-term health complications for acute myeloid leukemia BMT survivors

There are currently 200,000 BMT survivors and that number is expected to increase to exceed half a million over the next decade. BMTs can cure blood cancer patients but there are short-term and long-term health complications that patients and their health care providers need to be aware of so they can also try to prevent these complications.

"Many of our BMT patients will live for many decades after their transplant so our goal is to understand what happens to them, educate them about potential short-term and long-term risks and what can be done to prevent some of these health conditions," said Saro Armenian, D.O., M.P.H., City of Hope associate professor in the departments of Pediatrics and Population Sciences and director of the Center for Survivorship and Outcomes within the Hematologic Malignancies Research Institute. "Some of these conditions are preventable. For instance, there are early screenings for some cancers. If someone is at a high risk of developing cardiovascular disease, that is a condition you can pick up early and help prevent before it becomes a life-threatening condition."

Led by Armenian, a first-of-its-kind study took a closer look at this issue. The study examined long-term health outcomes for nearly 1,200 acute myeloid leukemia BMT survivors (the majority were allogenic transplants) compared with nearly 1,200 siblings over a 40-year span. The patients had received transplants at City of Hope, University of Alabama, Birmingham and University of Minnesota.

Approximately 66% of survivors (compared with 30% of their siblings) developed a severe or life-threatening chronic condition 20 years after BMT. The most common conditions were different types of cancers, diabetes, blood clots, cataracts and major joint replacement.

Overall, survivors had a three-fold increased risk of developing a severe health condition compared with their siblings. They were 10 times more likely to develop a different type of cancer such as skin, breast, colon and prostate; these are cancers that are amenable to early screening and prevention. Furthermore, BMT survivors were five times more likely to develop diabetes, and four times more likely to develop a life-threatening blood clot, compared to their siblings.

"It is important to recognize that the benefit of the transplant in terms of curing a patient far outweighs the potential harms that are down the line," Armenian said. "It’s our moral imperative to not only get them through the transplant but to care for them well beyond that into old age."

"What we tell our BMT patients is you’ve made it through the transplant and now it’s time for you to take ownership over your own health and well-being," Armenian said. "That may be an optimal time when patients are actually engaged to think about the next chapter of their lives and how they’re going to optimize their health."

Bispecific antibody for patients with relapsed/refractory non-Hodgkin lymphoma

More effective treatments with fewer side effects are needed for patients with relapsed/refractory non-Hodgkin lymphoma (NHL). Options are particularly limited for those with B cell NHL or who have relapsed or not responded after CAR T cell therapies.

For those reasons, researchers at City of Hope and other institutions are looking for new options and one might be immunotherapy. Mosunetuzumab is a bispecific antibody targeting both CD3 (a protein found on the surface on T cells) and CD20 on the surface of B cells. The therapy redirects T cells to engage and eliminate malignant B cells.

Previous studies have demonstrated that mosunetuzumab had promising efficacy and favorable tolerability. An expanded Phase 1 multicenter trial examined dose escalation of mosunetuzumab.

Elizabeth Budde, M.D., Ph.D., assistant professor in City of Hope’s Department of Hematology & Hematopoietic Cell Transplantation, was the study’s senior. The study reveals results from Group B, in which mosunetuzumab was administered with increased dosing on the first, eighth and 15th day of the first cycle and then as a fixed dose on the first day of each subsequent 21-day cycle.

Approximately 270 patients in Group B were part of the trial. Among efficacy-evaluable patients across all dose levels, overall response rates (ORR) and complete response (CR) rates were 62.7% (42/67) and 43.3% (29/67) in indolent NHL patients, 37.4% ORR (46/124) and nearly 19.5% (24/124) of aggressive NHL patients.

CRs also appeared durable with 82.8% (24/29) of indolent NHL patients in remission after 26 months, and 70.8% (17/24) of aggressive NHL patients were in CR after nearly 16 months.

Side effects were minimal. They included cytokine release syndrome, which occurred in 29% of patients and was mostly low grade (27.9%) with only 1.1% grade 3. Neurological complications occurred in 43.7% of patients: 40% had low-grade problems such as headache, insomnia and dizziness and 3.7% had grade 3. Researchers noted that the frequency of cytokine release syndrome and neurological complications did not correlate with mosunetuzumab exposure, likely due to step-up dosing, which effectively mitigated acute toxicities and allows administration of higher doses.

Researchers concluded that mosunetuzumab had favorable tolerability and durable efficacy in patients with heavily pre-treated relapsed/refractory B cell NHL and achieved complete responses in patients whose disease progressed after CAR T therapies.

"As clinicians, we are always in search of new treatments for patients who have few therapeutic options," Budde said. "Mosunetuzumab, which has also demonstrated few serious side effects and encouraging durable therapeutic efficacy, could be a step in that direction."

A potential new CAR T cell therapy for patients with chronic lymphocytic leukemia works well with few side effects

Oral targeted therapies have improved treatment outcomes for patients with chronic lymphocytic leukemia, an incurable cancer. But some patients may not respond to those drugs, and they are in need of other treatment options.

Lisocabatagene Maraleucel (liso-cel), a Juno CAR T therapy, may be the answer. Updated results from a phase 1 clinical trial of liso-cel for patients who had taken ibrutinib unsuccessfully and had failed two or three lines of therapy for chronic lymphocytic leukemia were presented at ASH (Free ASH Whitepaper) by Tanya Siddiqi, M.D., director of City of Hope’s Chronic Lymphocytic Leukemia Program. A number of these patients had progressed after both ibrutinib and venetoclax therapy.

Of 23 patients evaluated for the therapy’s safety, very few had high grade serious toxicities such as cytokine release syndrome and neurotoxicity.

"Specifically, when you talk about CAR T therapy, you talk about these toxicities being the most common but so far, two had grade 3 cytokine release syndrome and nobody had grade 4 or 5," Siddiqi said. "As far as neurotoxicity is concerned, five patients had grade 3 or 4 neurotoxicity and none had grade 5."

More common side effects included low grade cytokine release syndrome (fever and chills) that is easily manageable.

As early as 30 days after receiving liso-cel, about 75% of 20 patients evaluated for the therapy’s efficacy had undetectable minimal residual disease (MRD) in the blood and 65% in the marrow, that is no detectable traces of cancer in a patient’s blood or bone marrow,

Majority of patients achieved an early objective response (cancer diminished or disappeared) to liso-cel at the 30 day response assessment. Over time, liso-cel has also demonstrated deep and durable remissions in most patients, or a remission that endures over time.

"It’s been almost two years since the first few patients received liso-cel on this trial and at least three or four of them are still in excellent remission with no recurrent MRD, while later patients are still in follow-up at under two years" Siddiqi said. "The results for this trial are very encouraging as liso-cel has so far demonstrated to be highly effective with few serious side effects in patients with fairly refractory CLL."

Liso-cel is now being tested in the phase 2 portion of this trial, which is a continuation of this trial and is also taking place at City of Hope.

Trial examined PET-adapted nivolumab or nivolumab plus chemotherapy as a bridge to transplant in relapsed/refractory Hodgkin lymphoma

The standard treatment for patients with relapsed/refractory Hodgkin lymphoma is second-line chemotherapy followed by a stem cell autologous transplant. A multicenter trial, led by City of Hope’s Alex Herrera, M.D., instead used a sequential immunotherapy first-line approach to treat the cancer. The immunotherapy used was nivolumab, which works by blocking the PD-1 immune checkpoint pathway that tumors often hijack to evade the immune system.

In previous trials also led by Herrera, assistant professor in City of Hope’s Department of Hematology & Hematopoietic Cell Transplantation, nivolumab and brentuximab vedotin — an antibody-based treatment that targets delivery of chemotherapy only to Hodgkin lymphoma cells — have been effective against relapsed/refractory Hodgkin lymphoma. This trial evaluates whether nivolumab alone can be powerful enough to get a patient into remission without the need for chemotherapy prior to a transplant.

For the trial, 43 patients received nivolumab every two weeks for up to six cycles. A PET-CT scan was performed on patients after the third and sixth cycle to assess whether the cancer had responded to treatment. Patients who were not in remission after six cycles of nivolumab then received nivolumab/ICE (NICE), a standard chemotherapy regime for these patients.

For patients who received nivolumab alone, the overall response rate (ORR, or cancer diminished or disappeared) was 78% and the complete response rate (CR, or cancer disappeared) was 70%. Seven patients treated with NICE had a 100% response rate. Among 35 evaluable patients, the ORR was 94% and CR was 91%.

A year after starting the trial, 79% of all patients remained in remission. Twenty-seven patients were also able to receive an autologous transplant directly after the trial.

Nivolumab’s side effects were mild. They included fatigue (28%), rash (18%), and fever (15%). Patients who also received NICE experienced nausea (71%), vomiting (57%), anemia (43%) and fatigue (43%).

The study concluded that PET-adapted nivolumab/NICE in patients was found to be well-tolerated and effective as a second-line therapy. Using nivolumab alone was also an effective bridge to transplant in a majority of patients, sparring them the toxicity of traditional high-dose chemotherapy. Patients who did not achieve CR with nivolumab alone responded to nivolumab/NICE.

"The results of the study are really exciting," Herrera said. "We demonstrated you can use immunotherapy alone to safely and effectively treat relapsed/refractory Hodgkin lymphoma and is also a bridge to transplant. We can spare patients from receiving chemotherapy. In the future, we’ll continue to evaluate immunotherapy approaches to treat relapsed/refractory Hodgkin lymphoma."

Next steps include a trial to establish the role of immunotherapy as a second-line therapy prior to transplant.

Matthew Mei, M.D., assistant clinical professor with City of Hope’s Department of Hematology & Hematopoietic Cell Transplantation, presented this study at the ASH (Free ASH Whitepaper) conference.

Monoclonal antibody TAK-079 as an injection effective against relapsed/refractory multiple myeloma

Multiple myeloma patients whose disease has returned, or is no longer responding to current therapies, are in need of new treatments that are effective and cause few serious side effects. TAK-079, a Takeda immunotherapy drug that is delivered as a subcutaneous injection and targets the CD38 protein expressed by myeloma cells, could be such a therapy.

For the multicenter trial led by Amrita Krishnan, M.D., director of City of Hope’s Judy and Bernard Briskin Center for Multiple Myeloma Research and professor in its Department of Hematology & Hematopoietic Cell Transplantation, 31 patients, who had received at least three other therapies and previous exposure to other specific treatment, were enrolled in four-dose cohorts. They received an initial dose of 135 milligrams and are currently receiving 1,200 milligrams.

After the four-dose levels were tested, 43% of 28 patients (for which data is available) had an objective response rate (cancer had diminished or disappeared) and experienced few side effects. Only 4% of patients had drug-related infections and 11% had drug-related anemia.

"TAK-079 is well-tolerated by patients and they have been able to stay on it," Krishnan said. "Because TAK-079 is so easy to administer as an injection, there is also a potential for patients to use this at home."

Preclinical research on FTO protein in acute myeloid leukemia

Fat mass and obesity-associated (FTO) protein is highly expressed on acute myeloid leukemia (AML) cells, making it a promising target in leukemia treatment. But currently, there are few drugs targeting the FTO protein in treating leukemia.

Under supervision of Jianjun Chen, Ph.D., of the Simms/Mann Family Foundation Chair in Systems Biology, Rui Su, Ph.D., and her colleagues have identified two small-molecule compounds (CS1 and CS2) targeting FTO protein specifically and effectively with measurements showing a high potency of the compounds. Via RNA sequencing, researchers found that CS1 and CS2 exert their anti-leukemic effects through the FTO-associated signaling pathway.

Through bioluminescence imaging, researchers also found that treatment with either CS1 or CS2 suppressed leukemia progression and prolonged survival in ‘human-in-mouse’ xenograft and patient-derived AML PDX models.

Next steps for the research include starting a clinical trial for patients using the CS1 and CS2 compounds to target the FTO protein.

Research uncovers different role for CD25 in some acute lymphoblastic lymphomas and presents a novel target for therapies

A team of researchers led by City of Hope’s Jaewoong Lee, Ph.D., assistant research professor in the Department of Systems Biology, recently sought to understand why, when reviewing data from nearly 140 clinical trials for cancer patients, they saw that a protein called CD25 appears to be one of the strongest predictors of poor clinical outcome in patients with B cell malignancies like lymphoma, but not in other cancer types. It was particularly curious because CD25 is part of a receptor (IL2) that typically promotes the growth of T cells, used by the body to fight infections.

The team’s experiments using genetic mouse models and engineered patient-derived B cell leukemia and lymphoma tissue grafts revealed a surprising function of CD25 that is independent of IL2 in B cells and B cell derived leukemia and lymphoma.

"We were able to identify that CD25 plays a role as a previously unrecognized feedback regulator of tumor-causing B cell receptor signaling, which provides a proliferative advantage to malignant B cells and also acts as a biomarker and predictor of poor clinical outcomes," Lee said.

For adults with a rare subtype of the most common childhood cancer, acute lymphoblastic leukemia (ALL), called Ph-Positive ALL, as well as children with a similar subtype called Ph-like ALL who have high CD25 expression at the time of diagnosis, the findings provide a rationale for the therapeutic targeting of CD25 in such cancers.

To test that rationale, Lee and the team used patient-derived tissue graft models of drug-resistant B cell malignancies and treated them with a with a CD25-specific antibody drug-conjugate (ADCT-301).

"As a strategy to destroy CD25-expressing B cell malignancies, treatment with ADCT-301 either extended the survival of transplant recipients or eradicated disease," said Lee of the successful outcome.

Next, the team would like to figure out how CD25 provides a growth advantage for malignant B cells.

"We found several novel partner proteins working with CD25," Lee added. "So, we will likely test if we can also target novel partner proteins together with CD25 to eliminate malignant B cells."

Kite and the CIBMTR® Present Positive Findings From Real-World Use of Yescarta® (Axicabtagene Ciloleucel) in Relapsed or Refractory Large B-Cell Lymphoma

On December 9, 2019 Kite, a Gilead Company (Nasdaq: GILD), and the CIBMTR (Center for International Blood and Marrow Transplant Research), the research collaboration between the National Marrow Donor Program (NMDP)/Be The Match and the Medical College of Wisconsin (MCW), reported findings from an ongoing post-marketing study evaluating the safety and efficacy of Yescarta (axicabtagene ciloleucel) in adult patients with relapsed or refractory large B-cell lymphoma (Press release, Kite Pharma, DEC 9, 2019, View Source [SID1234552147]). In this analysis, efficacy and safety of Yescarta were comparable to that observed in the ZUMA-1 trial, despite a larger proportion of older, more difficult-to-treat patients in the real-world setting. The findings were presented today at the 61st American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting & Exposition, held in Orlando from December 7–10, 2019.

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"The similar efficacy and safety results seen across this post-approval analysis and the ZUMA-1 registrational trial are extremely encouraging for appropriate patients with relapsed or refractory large B-cell lymphoma who may benefit from Yescarta," said Marcelo Pasquini, MD, MS, co-lead investigator and Senior Scientific Director of the CIBMTR; Cellular Therapy Registry Director; and Associate Professor of Medicine, Division of Hematology / Oncology at the Medical College of Wisconsin. "The comparable early outcomes, including side effects, support the potential of Yescarta in older, higher risk and more difficult-to-treat patients that physicians often see in the clinic."

In October 2017, Yescarta became the first CAR T cell therapy to be approved by the U.S. Food and Drug Administration (FDA) for the treatment of adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy, including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, primary mediastinal large B-cell lymphoma (PMBCL), high grade B-cell lymphoma and DLBCL arising from follicular lymphoma. Yescarta is not indicated for the treatment of patients with primary central nervous system lymphoma. The U.S. Prescribing Information for Yescarta contains a Boxed Warning regarding the risk of cytokine release syndrome (CRS) and neurological toxicities; see below for Important Safety Information.

The post-approval study population (n=533) included a larger proportion of older patients (≥65 years; 37 percent versus 25 percent) and more patients with double and triple hit lymphoma (36 percent versus 11 percent) compared to ZUMA-1.

At follow-up of at least six months after a single infusion of Yescarta, the best objective response via investigator assessment among the 326 patients evaluable for efficacy showed an objective response rate (ORR) of 84 percent, with 66 percent of patients having achieved a complete response (CR). ORR was similar among older and younger patients (92 percent in patients ≥65 years versus 80 percent in patients <65 years). Patients ≥65 years (n=108) achieved a CR rate of 72 percent versus 62 percent in patients <65 years (n=218).

Among all patients evaluable for safety (n=533), those 65 years or older had comparable rates of CRS (Any Grade: 84 percent vs. 80 percent; Grade ≥3: 10 percent vs. 8 percent) and neurologic toxicity (Any grade: 64 percent vs. 55 percent; Grade ≥3: 22 percent vs. 19 percent) as those under 65 years. Four patients died due to CRS, four patients died from neurologic toxicity and one patient died from both CRS and neurologic toxicity. This Grade 5 AE rate of approximately 1 percent for CRS and neurologic toxicity each is comparable to ZUMA-1.

"With more than 85 centers authorized to treat patients with Yescarta, these post-approval results reinforce its potentially transformative role in third line or later relapsed or refractory large B-cell lymphoma," said Christi Shaw, Chief Executive Officer of Kite. "The demonstrated efficacy and safety of Yescarta in the real-world setting, coupled with our industry-leading manufacturing that has delivered for thousands of patients so far, means physicians have a real opportunity to bring the potential benefits of CAR T to their patients in need."

U.S. Important Safety Information for Yescarta

BOXED WARNING: CYTOKINE RELEASE SYNDROME AND NEUROLOGIC TOXICITIES

Cytokine Release Syndrome (CRS), including fatal or life-threatening reactions, occurred in patients receiving Yescarta. Do not administer Yescarta to patients with active infection or inflammatory disorders. Treat severe or life-threatening CRS with tocilizumab or tocilizumab and corticosteroids.
Neurologic toxicities, including fatal or life-threatening reactions, occurred in patients receiving Yescarta, including concurrently with CRS or after CRS resolution. Monitor for neurologic toxicities after treatment with Yescarta. Provide supportive care and/or corticosteroids as needed.
Yescarta is available only through a restricted program under a Risk Evaluation and Mitigation Strategy (REMS) called the Yescarta REMS.
CYTOKINE RELEASE SYNDROME (CRS): CRS occurred in 94% of patients, including 13% with ≥ Grade 3. Among patients who died after receiving Yescarta, 4 had ongoing CRS at death. The median time to onset was 2 days (range: 1-12 days) and median duration was 7 days (range: 2-58 days). Key manifestations include fever (78%), hypotension (41%), tachycardia (28%), hypoxia (22%), and chills (20%). Serious events that may be associated with CRS include cardiac arrhythmias (including atrial fibrillation and ventricular tachycardia), cardiac arrest, cardiac failure, renal insufficiency, capillary leak syndrome, hypotension, hypoxia, and hemophagocytic lymphohistiocytosis/macrophage activation syndrome. Ensure that 2 doses of tocilizumab are available prior to infusion of Yescarta. Monitor patients at least daily for 7 days at the certified healthcare facility following infusion for signs and symptoms of CRS. Monitor patients for signs or symptoms of CRS for 4 weeks after infusion. Counsel patients to seek immediate medical attention should signs or symptoms of CRS occur at any time. At the first sign of CRS, institute treatment with supportive care, tocilizumab or tocilizumab and corticosteroids as indicated.

NEUROLOGIC TOXICITIES: Neurologic toxicities occurred in 87% of patients. Ninety-eight percent of all neurologic toxicities occurred within the first 8 weeks, with a median time to onset of 4 days (range: 1-43 days) and a median duration of 17 days. Grade 3 or higher occurred in 31% of patients. The most common neurologic toxicities included encephalopathy (57%), headache (44%), tremor (31%), dizziness (21%), aphasia (18%), delirium (17%), insomnia (9%) and anxiety (9%). Prolonged encephalopathy lasting up to 173 days was noted. Serious events including leukoencephalopathy and seizures occurred with Yescarta. Fatal and serious cases of cerebral edema have occurred in patients treated with Yescarta. Monitor patients at least daily for 7 days at the certified healthcare facility following infusion for signs and symptoms of neurologic toxicities. Monitor patients for signs or symptoms of neurologic toxicities for 4 weeks after infusion and treat promptly.

YESCARTA REMS: Because of the risk of CRS and neurologic toxicities, Yescarta is available only through a restricted program under a Risk Evaluation and Mitigation Strategy (REMS) called the Yescarta REMS. The required components of the Yescarta REMS are: Healthcare facilities that dispense and administer Yescarta must be enrolled and comply with the REMS requirements. Certified healthcare facilities must have on-site, immediate access to tocilizumab, and ensure that a minimum of 2 doses of tocilizumab are available for each patient for infusion within 2 hours after Yescarta infusion, if needed for treatment of CRS. Certified healthcare facilities must ensure that healthcare providers who prescribe, dispense or administer Yescarta are trained about the management of CRS and neurologic toxicities. Further information is available at www.YESCARTAREMS.com or 1-844-454-KITE (5483).

HYPERSENSITIVITY REACTIONS: Allergic reactions may occur. Serious hypersensitivity reactions including anaphylaxis may be due to dimethyl sulfoxide (DMSO) or residual gentamicin in Yescarta.

SERIOUS INFECTIONS: Severe or life-threatening infections occurred. Infections (all grades) occurred in 38% of patients, and in 23% with ≥ Grade 3. Grade 3 or higher infections with an unspecified pathogen occurred in 16% of patients, bacterial infections in 9%, and viral infections in 4%. Yescarta should not be administered to patients with clinically significant active systemic infections. Monitor patients for signs and symptoms of infection before and after Yescarta infusion and treat appropriately. Administer prophylactic anti-microbials according to local guidelines. Febrile neutropenia was observed in 36% of patients and may be concurrent with CRS. In the event of febrile neutropenia, evaluate for infection and manage with broad spectrum antibiotics, fluids and other supportive care as medically indicated. Hepatitis B virus (HBV) reactivation, in some cases resulting in fulminant hepatitis, hepatic failure and death, can occur in patients treated with drugs directed against B cells. Perform screening for HBV, HCV, and HIV in accordance with clinical guidelines before collection of cells for manufacturing.

PROLONGED CYTOPENIAS: Patients may exhibit cytopenias for several weeks following lymphodepleting chemotherapy and Yescarta infusion. Grade 3 or higher cytopenias not resolved by Day 30 following Yescarta infusion occurred in 28% of patients and included thrombocytopenia (18%), neutropenia (15%), and anemia (3%). Monitor blood counts after Yescarta infusion.

HYPOGAMMAGLOBULINEMIA: B-cell aplasia and hypogammaglobulinemia can occur. Hypogammaglobulinemia occurred in 15% of patients. Monitor immunoglobulin levels after treatment and manage using infection precautions, antibiotic prophylaxis and immunoglobulin replacement. The safety of immunization with live viral vaccines during or following Yescarta treatment has not been studied. Vaccination with live virus vaccines is not recommended for at least 6 weeks prior to the start of lymphodepleting chemotherapy, during Yescarta treatment, and until immune recovery following treatment.

SECONDARY MALIGNANCIES: Patients may develop secondary malignancies. Monitor life-long for secondary malignancies. In the event that a secondary malignancy occurs, contact Kite at 1-844-454-KITE (5483) to obtain instructions on patient samples to collect for testing.

EFFECTS ON ABILITY TO DRIVE AND USE MACHINES: Due to the potential for neurologic events, including altered mental status or seizures, patients are at risk for altered or decreased consciousness or coordination in the 8 weeks following Yescarta infusion. Advise patients to refrain from driving and engaging in hazardous occupations or activities, such as operating heavy or potentially dangerous machinery, during this initial period.

ADVERSE REACTIONS: The most common adverse reactions (incidence ≥ 20%) include CRS, fever, hypotension, encephalopathy, tachycardia, fatigue, headache, decreased appetite, chills, diarrhea, febrile neutropenia, infections-pathogen unspecified, nausea, hypoxia, tremor, cough, vomiting, dizziness, constipation, and cardiac arrhythmias.