McKesson Declares Quarterly Dividend

On January 29, 2020 The Board of Directors of McKesson Corporation (NYSE:MCK) reported that declared a regular dividend of 41 cents per share of common stock (Press release, McKesson, JAN 29, 2020, View Source [SID1234553667]). The dividend will be payable on April 1, 2020, to stockholders of record on March 2, 2020.

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Canady Helios Cold Plasma Scalpel Successfully Used by Chaim Sheba Medical Center Surgeons to Remove Inoperable Retroperitoneal Cancer

On January 29, 2020 A surgical team at The Chaim Sheba Medical Center in Tel HaShomer, Israel, with coordination by US Medical Innovations, LLC (USMI), reported that successfully used the Canady HeliosTM Cold Plasma Scalpel (CHCPS) for a rare advanced reoccurring inoperable retroperitoneal sarcoma (Press release, US Medical Innovations, JAN 29, 2020, View Source [SID1234553666]).

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CHCPS is new cold atmospheric plasma device that specifically eradicates microscopic remnants of cancer cells while sparing normal cells and tissue.

After a one-time pre-market Humanitarian Compassionate-Use Exemption from the Investigational Review Board at Sheba Medical Center, a surgical team successfully used the Canady HeliosTM Cold Plasma Scalpel (CHCPS) for the selective killing of cancerous tissue during the groundbreaking surgery. The surgery was performed on August 20, 2019 on a 33-year-old man with a rare inoperable Retroperitoneal Sarcoma. The patient was first diagnosed at age 20 and the tumor had reoccurred twice prior to this surgery.

Retroperitoneal sarcoma occurs in the retroperitoneum, the area behind the peritoneum. The peritoneum is a thin tissue lining of the abdominal area that covers the abdominal organs. The surgery entailed removing the tumor and its attachment to adjacent tissue in the abdomen. Afterwards, the patient received intra-operative radiation therapy (IORT) at the surgical resected site; cold plasma was subsequently sprayed over the surgical site. The surgery was successful, and the patient returned back to the U.S. in September 2019.

A multidisciplinary group of healthcare professionals and physicians from Sheba Medical Center and research scientists, and engineers from USMI collaborated to achieve this successful outcome. The complex surgery was performed by Aviram Nissum, M.D. Chief of General and Oncological surgery at Sheba Medical Center.

USMI CEO, Chief Science Officer and Surgeon, Jerome Canady, M.D., "USMI and its sister companies are quite excited about the excellent outcome for the patient." We are equally enthusiastic that CHCPS is approved by the FDA for a multi-center phase I clinical trial Investigational Device Exemption (IDE #G190195). Clinical trials will occur at Sheba Medical Center, Tel HaShomer, Israel and Rush University Medical Center, Chicago, Illinois starting February 2020.

American Childhood Cancer Organization Seeks Increased Research Funding Through United States Postal Service Semipostal Stamp

On January 29, 2020 The American Childhood Cancer Organization (ACCO) reported that is launching "Stamp Out Childhood Cancer," a public appeal campaign to demonstrate broad, national support for the creation of a new United States Postal Service (USPS) semipostal stamp to help fund the fight against childhood cancer (Press release, American Childhood Cancer Organization, JAN 29, 2020, View Source [SID1234553665]). The campaign calls on the public to write and send letters of support for the stamp to USPS, the final step in the process of applying for a USPS semipostal stamp.

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The stamp is the latest innovative effort by ACCO to raise much needed resources to combat childhood cancer, the leading cause of death by disease for children in the U.S.

"Every year in the United States approximately 16,000 American children are diagnosed with cancer," said Ruth Hoffman, ACCO CEO. "While we have seen many advancements in adult cancer treatment, the majority of children with cancer continue to be treated with drugs that were approved by the FDA more than 50 years ago. A childhood cancer semipostal stamp would support the research we need to increase survival rates and reduce late effects from toxic treatments. Through ‘Stamp Out Childhood Cancer,’ we are asking all Americans to join ACCO and tell USPS that they want a stamp to benefit children and adolescents fighting cancer."

ACCO has completed the official application for the creation of the childhood cancer stamp including filing a formal proposal with the USPS Office of Stamp Services and securing the required support from an executive agency—the National Institutes of Health—which would collect the monies raised by the stamp and disburse the funds appropriately for research support.

ACCO’s stamp application is now in the final phase, which requires a demonstration of broad, national enthusiasm for the childhood cancer semipostal stamp in the form of supportive letters to USPS. ACCO is calling on the public to write to USPS in one of three ways:

1. Visiting www.acco.org/stamp to customize and sign a letter, which ACCO will print and deliver to USPS.

2. Emailing letters to ACCO at [email protected], which ACCO will print and deliver to USPS.

3. Sending letters of support for the childhood cancer stamp directly to

Office of Stamp Services
Attn: Semipostal Discretionary Program
475 L’Enfant Plaza SW, Room 3300
Washington, DC 20260-3501

The childhood cancer stamp would be the first semipostal devoted to a childhood disease, and would join a small and distinguished group of other cause-based stamps produced and sold at post offices, online, and by phone order.

The first semipostal stamp, a congressionally-mandated Breast Cancer Research (BCR) stamp, was issued in 1998. As of the year 2000, the Semipostal Authorization Act gives USPS the discretionary authority to issue and sell new semipostal fundraising stamps. In recent years, two semipostal stamps have been issued – an Alzheimer’s stamp in 2017 and a Post-Traumatic Stress Disorder stamp in 2019. In two years of circulation, sales of the Alzheimer’s stamp raised over $1 million to fight the disease.

"By contacting USPS, Americans have a unique opportunity to directly demonstrate their support for childhood cancer fighters, survivors and their families," said Jamie Ennis Bloyd, ACCO Director of Government Relations/External Affairs.

Syros Presents New Preclinical Data Highlighting Its Leadership in CDK Inhibition to Discover and Develop New Medicines for Difficult-to-Treat Cancers

On January 29, 2020 Syros Pharmaceuticals (NASDAQ: SYRS), a leader in the development of medicines that control the expression of genes, reported new preclinical data showing that inhibiting cyclin-dependent kinase 7 (CDK7) results in different transcriptional effects than inhibiting cyclin-dependent kinase 12 (CDK12), pointing to distinct therapeutic opportunities to benefit patients with difficult-to-treat cancers (Press release, Syros Pharmaceuticals, JAN 29, 2020, View Source [SID1234553664]). Building on its leadership in gene control, Syros also described new methods for identifying essential genes and transcriptional dependencies in cancer that could serve as potential drug targets. These data were presented at the 2020 Keystone Symposia Cancer Epigenetics: New Mechanisms and Therapeutic Opportunities.

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"Together, these presentations underscore our leadership in CDK inhibition and, more broadly, in the field of gene control," said Eric R. Olson, Ph.D., Syros’ Chief Scientific Officer. "Our understanding of how regulatory regions of the genome control the expression of genes is growing by leaps and bounds, bringing into reach a wide range of diseases that have long eluded effective treatment with other genomics-based approaches. Our platform allows us to elucidate those regulatory regions to pinpoint which genes to control, in which cells, for which patients, and how best to control the expression of those genes using oral molecules to maximize the chances of providing a profound benefit for patients."

CDK7 Inhibition and CDK12 Inhibition as Distinct Therapeutic Approaches
Syros scientists studied the transcriptional effects of selective CDK7 and CDK12 inhibition in an ovarian cancer cell line, marking the first reported direct comparison of these two approaches. CDK7 and CDK12 are members of the CDK family that have emerged as potentially important drug targets in cancer because of their roles in transcription, the process by which genes express proteins. The findings showed that, under the conditions tested, CDK7 and CDK12 inhibition had distinct effects despite decreasing expression of many of the same genes:

CDK7 decreased expression of more genes.
CDK12 inhibition preferentially decreased expression of genes with longer transcripts, a phenomenon that was not observed with CDK7 inhibition.
The DNA double-stranded break repair pathway is enriched for genes with longer transcripts that are preferentially downregulated by CDK12 inhibition.
CDK12 inhibition induced DNA damage, while CDK7 inhibition did not.
The results suggest that a selective CDK12 inhibitor presents distinct therapeutic opportunities from a selective CDK7 inhibitor, such as increasing the susceptibility of cancer to targeted therapies involved in DNA damage repair such as PARP1 inhibitors.

Syros has a highly selective and potent oral CDK7 inhibitor, SY-5609, currently in a Phase 1 trial in patients with advanced breast, colorectal, lung or ovarian cancer, or with solid tumors of any histology that harbor Rb pathway alterations. In addition to decreasing the expression of cancer-driving genes, CDK7 inhibition has also been shown to interfere with cancer’s ability to progress unchecked through the cell cycle. Syros also has a CDK12/13 inhibitor program in preclinical development in cancer.

Building on its Leadership in Gene Control
Syros scientists also presented on two new methods for identifying genes and transcriptional regulators upon which cancer cells are particularly dependent for their survival with the aim of identifying new drug targets.

By analyzing cancer cells with gene copy-number deletions, Syros scientists identified approximately 200 genes that represent dose-dependent transcriptional liabilities across several cancers, including general regulators of transcription that may be attractive drug targets in genetically defined tumor types. Since cancers with copy-number deletions may be more dependent on these regulators than non-cancerous cells, inhibiting them may kill cancer cells while sparing non-cancerous cells. Syros presented preclinical data on one of these transcriptional regulators, INTS11, showing that a glioblastoma cancer cell line with a 1p36-deletion, which is commonly associated with INTS11 copy-number loss, is more sensitive to decreased levels of INTS11 than a cell line without a 1p36-deletion.

In a separate presentation, Syros scientists presented data showing that its new computational model, PETCERF, outperforms earlier-generation models used to score individual enhancers to identify genes critical for a cancer cell’s survival. By integrating multiple variables and inputs related to the enhancer and gene regulatory landscapes into a machine learning model trained using CRISPR knock-out data, PETCERF was shown to identify genes in primary tumor samples that are essential to cancer cells.

Additionally, Dr. Olson will present tomorrow during an oral session on how Syros’ gene control platform has led to a pipeline of small-molecule drug candidates that control the expression of genes with the aim of providing much-needed new medicines for patients with a range of blood cancers and solid tumors.

Bluestar Genomics’ Breakthrough Study Highlights Promising Data for Multi-Cancer Detection From a Single Blood Draw

On January 29, 2020 Bluestar Genomics, a company developing innovative, data-driven, epigenomic approaches to comprehensive disease analysis and diagnostics, reported the publication of a new study demonstrating the efficacy of their 5-hydroxymethylcytosine (5hmC) signal detection technology for its use in breast, lung, pancreatic, and prostate cancer (Press release, Bluestar Genomics, JAN 29, 2020, View Source [SID1234553663]). The study was published online in medRxiv. Results from the study provide further evidence that, using a single blood draw, Bluestar Genomics’ technology can non-invasively detect cancers and help identify the underlying biology of the disease using epigenetic markers.

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Breast, lung, pancreatic, and prostate cancer make up 41% of the cancer incidence in the United States. Early detection and a deep understanding of each cancer remain critical for implementing the highest quality of care. Tissue biopsy is invasive, and screening methods are limited for many forms of cancer and often fall short of capturing the complete genomic landscape. Bluestar Genomics uses liquid biopsy combined with 5hmC profiling to provide a detailed picture of the genomic landscape and identify potential biologic pathways that may be driving tumor progression.

"We have taken significant strides to strengthen our understanding of the underlying biology related to multiple forms of cancer and the tumor microenvironment," said Samuel Levy, Chief Executive Officer and Chief Scientific Officer, Bluestar Genomics. "In addition to early-stage cancer detection capabilities, our knowledge of 5hmC distribution across the genome can potentially yield new candidate biomarkers. With this information, we will create clinical tools that can revolutionize oncology screening and have a significant impact on patient outcomes."

Bluestar Genomics executed the study using multiple cell-free DNA samples to measure 5hmC profiles from patients with breast, lung, pancreatic, and prostate cancer. When used in conjunction with machine learning-based classification methods, their novel enrichment technology exhibited high performance in classifying these samples with Area Under the Curve (AUC) measures of 0.89, 0.84, 0.95 and 0.83, respectively. The majority of the breast and pancreatic cancer samples were stage 1 or stage 2, validating Bluestar Genomics’ potential to aid clinical decision making and detect cancer when treatment is most effective.

"There are significant limitations in screening for various cancers," said Kelly Bethel, MD, Chief Medical Officer, Bluestar Genomics. "Our research data outperforms screening PSA testing, the current standard of care screening blood test for prostate cancer. Detection of small early malignancies is challenging by usual imaging methods, and our platform technology also demonstrates the ability to detect the presence of malignant tumors smaller than 2cm. Overall, these findings suggest a clinical path toward early detection as part of a multi-cancer screening test."

These results were presented by Anna Bergamaschi, Ph.D., Principal Scientist, Bluestar Genomics at the PMWC 2020 Silicon Valley conference on January 23 at the Liquid Biopsy Showcase.