Eisai to Present Abstracts on Lenvatinib at 2021 Gastrointestinal Cancers Symposium

TOKYO, Jan 12, 2021 - (JCN Newswire) - Eisai Co., Ltd. has announced that presentations on a series of abstracts highlighting updates on its in-house discovered lenvatinib mesylate (product name: LENVIMA, the orally available kinase inhibitor, "lenvatinib") will be given at the Gastrointestinal Cancers Symposium Virtual Meeting, from January 15 to 17, 2021.At this symposium, regarding the lenvatinib monotherapy, the real-world effectiveness among unresectable hepatocellular carcinoma (HCC) patients treated in United States clinical practices (Abstract No: 273), as well as the results of a post hoc analysis of patients with unresectable HCC who progressed to the Child-Pugh B stage in the Phase 3 REFLECT study (Abstract No: 298), will be presented.In addition, the data to be presented regarding the combination therapy of lenvatinib plus pembrolizumab (product name: KEYTRUDA), the anti-PD-1 therapy from Merck & Co., Inc., Kenilworth, N.J., U.S.A. (known as MSD outside the United States and Canada), are results from the biliary tract cancer cohort (Abstract No: 321), the colorectal cancer cohort (Abstract No: 94), and the gastric cancer cohort (Abstract No: 230) of the basket-type Phase 2 LEAP-005 clinical study for 6 types of previously treated advanced solid tumors.In March 2018, Eisai and Merck & Co., Inc., Kenilworth, N.J., U.S.A., through an affiliate, entered into a strategic collaboration for the worldwide co-development and co-commercialization of lenvatinib.Eisai positions oncology as a key therapeutic area, and is aiming to discover revolutionary new medicines with the potential to cure cancer. Eisai will continue to create innovation in the development of new drugs based on cutting-edge cancer research, as it seeks to contribute further to addressing the diverse needs of, and increasing the benefits provided to, patients with cancer, their families, and healthcare providers.This release discusses investigational compounds and investigational uses for FDA-approved products. It is not intended to convey conclusions about efficacy and safety. There is no guarantee that any investigational compounds or investigational uses of FDA-approved products will successfully complete clinical development or gain FDA approval.About the Merck & Co., Inc., Kenilworth, N.J., U.S.A. and Eisai Strategic CollaborationIn March 2018, Eisai and Merck & Co., Inc., Kenilworth, N.J., U.S.A., known as MSD outside the United States and Canada, through an affiliate, entered into a strategic collaboration for the worldwide co-development and co-commercialization of LENVIMA. Under the agreement, the companies will jointly develop, manufacture and commercialize LENVIMA, both as monotherapy and in combination with KEYTRUDA, the anti-PD-1 therapy from Merck & Co., Inc., Kenilworth, N.J., U.S.A.In addition to ongoing clinical studies evaluating the KEYTRUDA plus LENVIMA combination across several different tumor types, the companies have jointly initiated new clinical studies through the LEAP (LEnvatinib And Pembrolizumab) clinical program and are evaluating the combination in 13 different tumor types (endometrial carcinoma, hepatocellular carcinoma, melanoma, non-small cell lung cancer, renal cell carcinoma, squamous cell carcinoma of the head and neck, urothelial cancer, biliary tract cancer, colorectal cancer, gastric cancer, glioblastoma, ovarian cancer and triple-negative breast cancer) across 20 clinical trials.Eisai's Focus on CancerEisai focuses on the development of anticancer drugs, targeting the tumor microenvironment (with experience and knowledge from existing in-house discovered compounds) and the driver gene mutation and aberrant splicing (leveraging RNA Splicing Platform) as areas (Ricchi) where real patient needs are still unmet, and where Eisai can aim to become a frontrunner in oncology. Eisai aspires to discover innovative new drugs with new targets and mechanisms of action from these Ricchi, with the aim of contributing to the cure of cancers.Media Inquiries:Public Relations Department,Eisai Co., Ltd.+81-(0)3-3817-5120 Copyright 2021 JCN Newswire. All rights reserved. www.jcnnewswire.com

Blood test for early detection of gastric cancer being evaluated for use in primary healthcare

SINGAPORE - A blood test that can detect gastric cancer in its early stages has been developed and is currently being evaluated for use in hospitals and clinics, said the National University Health System (NUHS) on Friday (Oct 23). In Singapore, gastric cancer is the fifth cause of cancer deaths in men and the sixth in women, claiming around 300 lives yearly. It is the third leading cause of cancer deaths worldwide, as it is often detected at the later stages, making it difficult to treat. Gastric cancer is usually diagnosed through endoscopy, a procedure perceived to be expensive and invasive, as it involves inserting a thin tube with a camera into the patient's mouth and all the way down to the stomach. An endoscopy costs around $200 to $800 with medical subsidy, according to the Ministry of Health's website. On the other hand, using the blood test would be more cost-effective - it would be priced at under $200 at public hospitals. The test is also non-invasive, and can encourage higher uptake among the public for early detection of the cancer and reduce reliance on endoscopy. It would take around three hours to run in a clinical lab and can deliver results to the patient's doctor within a week. The project to develop the new blood test began in 2012. It was led by Professor Jimmy So, head and senior consultant with the National University Hospital's (NUH) division of general surgery (upper gastrointestinal surgery); Professor Yeoh Khay Guan, senior consultant with the NUH's division of gastroenterology and hepatology; and Associate Professor Too Heng-Phon from the National University of Singapore Yong Loo Lin School of Medicine's department of biochemistry. The team also included clinicians and scientists from NUHS; the Bioprocessing Technology Institute (BTI) of the Agency for Science, Technology and Research (A*Star); national platform Diagnostics Development Hub; and MiRXES, a Singapore-headquartered molecular diagnostic company that was spun off from A*Star's BTI.  The blood test can detect 87 per cent of all gastric cancers, including 87.5 per cent of stage one cancers, by looking out for patterns of microRNA - a type of gene in the blood sample. The results were found to be more accurate compared with conventional blood tests for gastric cancer, and were highly sensitive across age groups, genders, ethnicities and tumour stages. More on this topic   Related Story Researchers work to boost treatment of gastric cancer   Related Story Study links gastric cancer to protein level Using a panel of 12 microRNA biomarkers that can differentiate gastric cancer patients from normal patients with an accuracy of more than 92 per cent, an initial test kit was manufactured in 2012. From 2013 to 2018, the test kit was validated among some 5,000 subjects from Singapore, and received approval from the Health Sciences Authority last year. Prof So said: "The majority of gastric cancer patients are diagnosed at advanced stages, for which the five-year survival rate is lower than 5 per cent. Early detecting is thus key to reducing death from gastric cancer. To bring about a meaningful fall in the gastric cancer mortality rate, an effective strategy that would detect gastric cancer early so as to enable prompt intervention is required." He added: "This non-invasive blood test is a breakthrough in gastric cancer diagnosis and it may potentially be used as an effective screening test for the early diagnosis of gastric cancer." As it costs less than endoscopy, the test could potentially be used as part of the national screening programme of gastric cancer in high-risk groups. Patients who have positive 12-microRNA test results will then be recommended to go for endoscopy. More on this topic   Related Story Singapore medical company invents non-invasive cancer screening tests; receives US$20m in funding   Related Story NUS team's 'scorecard' to detect cancer, predict patient survival Prof Too, however, emphasised that the test does not replace endoscopy, and instead provides an option to patients who may not be keen on initial endoscopic screening. Instead, it "adds to the current cancer detection tool armamentarium", and provides the public with access to better healthcare through its convenience and non-invasiveness.