Sysmex Presents Academic Report Related to the Clinical Utility of RAS Gene Mutation Testing for Colorectal Cancer Using Liquid Biopsy(PDF?130KB)

On March 5, 2020 Sysmex Corporation (HQ: Kobe, Japan; Chairman and CEO: Hisashi Ietsugu) reported notice that Dr. Yu Sunakawa, Associate Professor in the Department of Clinical Oncology at the St. Marianna University School of Medicine, presented his research findings at the American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Gastrointestinal Cancers Symposium 2020 (ASCO-GI 2020), held in San Francisco, California, the United States, from January 23 to 25, 2020 (Press release, Sysmex, MAR 5, 2020, View Source [SID1234555193]). This research involved examining the utility of RAS gene1 mutation testing for colorectal cancer with liquid biopsy2 using BEAMing technology3 (OncoBEAMTM RAS CRC Kit) to help guide treatment decisions for the re-challenge of anti-EGFR monoclonal antibody therapy in patients with metastatic colorectal cancer (mCRC).

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This research involved collaborative biomarker studies (JACCRO CC-084 and CC-09AR5) conducted in cooperation with Sysmex and the Japan Clinical Cancer Research Organization (Location: Tokyo, Japan; Director: Dr. Fumimaro Takaku; "JACCRO").

The overexpression of epidermal growth factor receptors (EGFR) on the surface of colorectal cancer cells is known to promote their cellular proliferation. Numerous studies have shown that anti-EGFR monoclonal antibody drugs are effective in preventing the proliferation of these cancer cells; however, this therapy is not effective in patients whose colorectal tumors harbor RAS mutations. Accordingly, decisions on the administration of anti-EGFR monoclonal antibody drugs are usually made by assessing RAS gene mutations using resected tissues.

In recent years, clinical studies have actively investigated re-challenge of mCRC patients with antiEGFR therapy in an effort to improve the prognosis of patients who had previously responded to 1st-line anti-EGFR therapy treatment, but whose disease progressed during subsequent courses of therapy in which anti-EGFR drugs were eliminated. In the process, it was reported that no clinical benefit by the re-challenge of anti-EGFR monoclonal antibody drugs on patients determined to have wild-type RAS genes at the time of initial administration of anti-EGFR monoclonal antibody drugs might be due to the emergence of RAS mutations during anti-EGFR therapy (Source: JAMA Oncol. 2019;5(3):343-350).

Sysmex and JACCRO’s objective of this clinical research (JACCRO CC-08/09AR studies: retrospective6 study), was to examine a possible relationship between clinical outcomes of the antiEGFR re-challenge and the patient’s plasma RAS gene mutation status at the time of rechallenge. This analysis was accomplished via liquid biopsy using OncoBEAMTM RAS CRC Kit to determine the status of RAS gene mutations in circulating tumor DNA of mCRC patients prior to and during anti-EGFR therapy re-challenge. Results showed that the re-challenge of mCRC patients with anti-EGFR monoclonal antibody drugs improved the prognosis (progression-free survival7 and overall survival8) more for RAS wild-type patients than for RAS mutant patients. The results of this research, presented at ASCO (Free ASCO Whitepaper)-GI 2020, indicated the clinical utility of liquid biopsy for RAS gene mutation testing for colorectal cancer when deciding on the re-challenge of anti-EGFR monoclonal antibody drugs.

Since obtaining tumor tissue biopsy samples from metastatic sites place undue physical burden on patients, the liquid biopsy approach to determine RAS mutation status from blood samples is clearly a less invasive approach. Moreover, a liquid biopsy RAS mutation test gives the most timely RAS mutation result at the time of recurrence and anti-EGFR re-challenge, rather than relying on data obtained from testing archival tumor tissue samples. Going forward, progress on prospective6 studies to verify the effectiveness of decisions to re-challenge mCRC patients with anti-EGFR monoclonal antibody drugs informed by OncoBEAMTM RAS CRC Kit for RAS gene mutation testing is expected to contribute to the clinical implementation and utility of this test in the re-challenge treatment of anti-EGFR monoclonal antibody drugs.

By delivering new methods for diagnosing cancer to patients as quickly as possible, Sysmex is taking the lead in the global realization of personalized medicine and contributing to the enhancement of patients’ quality of life and advances in healthcare.

Data Sheet

Presented at: American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Gastrointestinal Cancers Symposium 2020 (ASCO-GI 2020)
Date: January 23–25, 2020
Poster number: 166
Title: RAS status in circulating-tumor DNA (ctDNA) and outcomes during rechallenge treatments with anti-EGFR antibodies in metastatic colorectal cancer (mCRC)

The study was performed on the association between the presence of RAS gene mutations (RAS wild-type patients (10 cases) and RAS mutant patients (6 cases)) and clinical outcome for patients receiving rechallenge with Cetuximab or Panitumumab (16 cases). Prior to re-challenge of antiEGFR monoclonal antibody drugs, OncoBEAMTM RAS CRC Kit was used to measure RAS gene mutations in plasma samples.

The results showed significantly longer survival for RAS wild-type patients than for RAS mutant patients, both for progression-free survival (4.7 months for RAS wild-type patients and 2.3 months for RAS mutant patients) and overall survival (16.0 months for RAS wild-type patients and 3.8 months for RAS mutant patients). These results point to the clinical utility of RAS gene testing using liquid biopsy prior to re-challenge of anti-EGFR monoclonal antibody drugs and are expected to contribute to the determination of more appropriate treatment methods.

Terminology

1 RAS gene: As the likelihood is high that patients with RAS gene (KRAS/NRAS gene) mutations will not benefit (prolongation of life, tumor reduction) from the administration of anti-EGFR drugs, companion diagnostics may be performed to treat the gene mutation first.

2 Liquid biopsy: Similar in performance to a biopsy, which is carried out on a sample taken from tissue such as tumors, but which attempts to reduce the burden on the patient by using blood tests.

3 BEAMing technology: This gene analysis method combines ultrahigh-sensitivity PCR and flow cytometry technologies. BEAMing technology is used to capture individual DNA molecules with magnetic particles in droplets measuring several microns in diameter and then detecting the amplification of the DNA molecules on the magnetic particles. OncoBEAM RAS CRC Kit based on BEAMing technology is an in vitro diagnostic test (in vitro diagnostic medical device registration number: 30100EZX00010000, MHLW-approved on July 19, 2019, Manufactured and supplied by Sysmex) for detecting RAS mutations in ctDNA extracted from the plasma of colorectal cancer patients.

4 JACCRO CC-08AR test: Biomarker research related to a Phase II clinical trial on the re-challenge of Cetuximab for tertiary treatment of KRAS gene wild-type unresectable, advanced, recurrent colorectal cancer to patients with a history of treatment with the anti-EGFR monoclonal antibody drug Cetuximab

5 JACCRO CC-09AR test: Biomarker research related to a Phase II clinical trial on the re-challenge of Panitumumab for tertiary treatment of KRAS gene wild-type unresectable, advanced, recurrent colorectal cancer to patients with a history of treatment with the anti-EGFR monoclonal antibody drug Panitumumab

6 Prospective/retrospective: A prospective (forward-looking) study refers to an epidemiological survey method indicating that information is to be gathered from the start of the survey forward into the future. By contrast, retrospective (backward-looking) studies indicate the gathering of patient information retroactive from the start of the study.

7 Progression-free survival: The period during treatment (following treatment) when cancer is not progressing and the condition is stable.

8 Overall survival: The period of a patient’s survival, beginning with the registration date of a clinical study

Synlogic Announces Fourth Quarter and Full Year 2019 Conference Call and Webcast

On March 5, 2020 Synlogic, Inc. (Nasdaq: SYBX), a clinical stage company applying synthetic biology to beneficial microbes to develop novel, living medicines, reported that the Company will release its fourth quarter and full year 2019 financial results after the market closes on Thursday, March 12, 2020 (Press release, Synlogic, MAR 5, 2020, View Source [SID1234555219]). The press release will be followed by a conference call at 5:00 pm ET, which will be open to the public via telephone and webcast. During the conference call, the Company will review its financial results and provide a corporate update.

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The conference call dial-in numbers are (844) 815-2882 for domestic callers and (213) 660-0926 for international callers. The conference ID number for the call is 4089293. Participants may access the live webcast via a link on the Synlogic website in the Events Calendar of the Investors and Media section. For those unable to participate in the conference call or webcast, a replay will be available for 30 days on the Company’s website.

Castle Biosciences Announces Issuance of First U.S. Patent Covering DecisionDx-Melanoma

On March 5, 2020 Castle Biosciences, Inc. (Nasdaq: CSTL), a skin cancer diagnostics company providing personalized genomic information to improve cancer treatment decisions, reported that the United States Patent and Trademark Office (USPTO) issued the Company its first U.S. patent related to the DecisionDx-Melanoma gene expression profile test for patients with cutaneous melanoma (Press release, Castle Biosciences, MAR 5, 2020, View Source [SID1234555235]).

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Patent No. 10,577,660, issued on March 3, 2020, covers methods of treating cutaneous melanoma in patients having high-risk cutaneous melanoma tumors. The inventors discovered that patients having high-risk cutaneous melanoma tumors can be identified by the gene-expression profile signature of their cutaneous melanoma tumors. The term of the patent extends until September 2034. This brings the total number of issued or allowed patents related to the Company’s DecisionDx-Melanoma test to 10.

"We are pleased to have been issued our first U.S. patent covering DecisionDx-Melanoma," said Derek Maetzold, Castle’s president and chief executive officer. "In the United States, we estimate approximately 130,000 patients are diagnosed with Stage I-III cutaneous melanoma each year. The clinical use of DecisionDx-Melanoma is designed to optimize post-diagnostic treatment decisions, including sentinel lymph node biopsy, frequency of follow-up and the need for imaging, which we believe will lead to improved health outcomes for patients with skin cancer."

Castle Biosciences’ DecisionDx-Melanoma test is a 31-gene expression profile prognostic test for cutaneous melanoma that predicts 5-year risk of metastasis as low risk (Class 1, 1A lowest risk) or high risk (Class 2, 2B highest risk), as well as metastasis to the sentinel lymph node, based on an individual patient’s tumor biology.

About DecisionDx-Melanoma

DecisionDx-Melanoma is a gene expression profile test that uses an individual patient’s tumor biology to predict individual risk of cutaneous melanoma metastasis or recurrence, as well as sentinel lymph node positivity, independent of traditional staging factors, and has been studied in more than 5,700 patient samples. Using tissue from the primary melanoma, the test measures the expression of 31 genes. The test has been validated in four archival risk of recurrence studies of 901 patients and six prospective risk of recurrence studies including more than 1600 patients. Prediction of the likelihood of sentinel lymph node positivity has also been validated in two prospective multicenter studies that included more than 3,000 patients. Impact on patient management plans for one of every two patients tested has been demonstrated in four multicenter and single-center studies including more than 560 patients. The consistent performance and accuracy demonstrated in these studies provides confidence in disease management plans that incorporate DecisionDx-Melanoma test results. Since its commercial launch through December 31, 2019, DecisionDx-Melanoma has been ordered 51,967 times for use in patients with cutaneous melanoma.

More information about the test and disease can be found at www.SkinMelanoma.com.

Kadmon Highlights Recent Progress and Reports Fourth Quarter and Full Year 2019 Financial Results

On March 5, 2020 Kadmon Holdings, Inc. (NYSE: KDMN) reported financial and operational results for the fourth quarter and full year ended December 31, 2019 (Press release, Kadmon, MAR 5, 2020, View Source [SID1234555279]).

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"We achieved significant progress in 2019, led by positive results from the interim analysis of the pivotal trial of KD025 in cGVHD that greatly exceeded the threshold for success, achieving overall response rates of 64% and 67% with KD025 200 mg QD and 200 mg BID, respectively; we also recently presented detailed efficacy and safety data from this trial, further underscoring the therapeutic potential of KD025 in this indication," said Harlan W. Waksal, M.D., President and CEO of Kadmon. "We will meet with the FDA later this month to discuss our planned NDA submission of KD025 and expect to provide an update of that meeting, along with topline results from the primary analysis of the pivotal trial, in the second quarter of 2020. Finally, we raised approximately $123 million and fully paid off our term debt in the fourth quarter of 2019, strengthening our financial position and ability to execute on our anticipated milestones."

2020 Anticipated Key Clinical Milestones:

KD025

Hold pre-New Drug Application (NDA) meeting with the U.S. Food and Drug Administration (FDA) in March 2020 to discuss regulatory pathway for KD025 in chronic graft-versus-host disease (cGVHD); provide an update on the meeting in the second quarter of 2020
Announce topline results from primary analysis of pivotal trial in cGVHD (KD025-213) in the second quarter of 2020
Complete enrollment in ongoing Phase 2 clinical trial in systemic sclerosis (KD025-209)
KD033

Initiate clinical trial of KD033, Kadmon’s anti-PD-L1/IL-15 fusion protein for the treatment of solid tumors, in the second quarter of 2020
KD045

Continue ongoing Investigational New Drug Application (IND)-enabling activities of KD045, Kadmon’s next-generation ROCK inhibitor for the treatment of fibrotic diseases
Q4 2019 Key Business Highlights:

Closed underwritten public offering of 29.9 million shares of common stock for gross proceeds of $101.6 million, including full exercise of the underwriters’ option to purchase additional shares
Divested 1.4 million ordinary shares of MeiraGTx Holdings plc (MGTX), bringing $22 million in net proceeds
Paid off term debt in full; the Company no longer maintains any term debt obligations
Established strategic partnerships to develop KD025 in China and Japan with BioNova Pharmaceuticals Ltd. (BioNova) and Meiji Seika Pharma Co., Ltd., respectively
Financial Results

Fourth Quarter 2019 Results

Loss from operations for the three months ended December 31, 2019 was $18.3 million, compared to $27.8 million for the same period in 2018.

The decrease in loss from operations was primarily due to $4.0 million of license revenue recognized by the Company during the three months ended December 31, 2019 related to the BioNova strategic partnership. The decrease was also driven by a decrease in research and development expense due to timing of direct external costs associated with development of KD025 and compensation for research and development personnel.

Full Year 2019 Results

Loss from operations for the year ended December 31, 2019 was $89.1 million, compared to $85.9 million for the same period in 2018.

The increase in loss from operations was primarily due to an increase in research and development expenses for the year ended December 31, 2019 of $7.5 million, offset by $4.0 million of revenue associated with the BioNova strategic partnership. The increase in research and development expenses was primarily related to direct external costs of KD025 development.

Liquidity and Capital Resources

At December 31, 2019, the Company’s cash and cash equivalents totaled $139.6 million, compared to $94.7 million at December 31, 2018. In addition, as of December 31, 2019, the Company held approximately 2.1 million ordinary shares of MGTX, a publicly traded, clinical-stage gene therapy company.

About KD025

KD025 is a selective oral inhibitor of Rho-associated coiled-coil kinase 2 (ROCK2), a signaling pathway that modulates immune response as well as fibrotic pathways. In addition to the pivotal trial in cGVHD, KD025 is being studied in an ongoing Phase 2 clinical trial in adults with diffuse cutaneous systemic sclerosis (KD025-209). The FDA has granted Breakthrough Therapy Designation to KD025 for the treatment of patients with cGVHD after failure of two or more prior lines of systemic therapy. The FDA has also granted Orphan Drug Designation to KD025 for the treatment of patients with cGVHD.

INmune Bio, Inc. to Present at the 32nd Annual ROTH Conference on March 17

On March 5, 2020 INmune Bio, Inc., an immunology company developing treatments that harness the patient’s innate immune system to fight disease, reported that management will present at the 32nd Annual Roth Conference at 8:30 a.m. (PT) on Tuesday, March 17, 2020 and will conduct one-on-one meetings that day (Press release, INmune Bio, MAR 5, 2020, View Source [SID1234555321]).

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The conference will be held March 15-17, 2020 at The Ritz Carlton, Laguna Niguel in Orange County, CA. The ROTH Conference, with close to 550 participating companies and over 5,100 attendees, will feature presentations from public and private companies in a variety of sectors.

Management will be available for one-on-one meetings. For more information about the conference or to schedule a one-on-one meeting with management, please contact [email protected].