On January 8, 2020, the Food and Drug Administration approved pembrolizumab (KEYTRUDA®, Merck & Co. Inc.) for the treatment of patients with Bacillus Calmette-Guerin (BCG)-unresponsive, high-risk, non-muscle invasive bladder cancer (NMIBC) with carcinoma in situ (CIS) with or without papillary tumors who are ineligible for or have elected not to undergo cystectomy.
ASCO in Action provides the latest news and analysis related to critical policy issues affecting the cancer community, updates on the Association for Clinical Oncology’s ongoing advocacy efforts, and opportunities for members and others in the cancer care community to take action.
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The Centers for Medicare & Medicaid Services (CMS) announced important updates for 2019 and 2020 Merit-based Incentive Payment System (MIPS) participants, including the 2019 data submission period for MIPS eligible clinicians and how participants can check their 2020 MIPS eligibility.
ASCO recently submitted comments to the House Committee on Ways and Means and the House Rural and Underserved Communities Health Task Force in response to a request for information (RFI) on priority topics that affect the health status and outcomes for rural and underserved communities.
The Food and Drug Administration (FDA) recently issued a ban on flavored e-cigarette pods, except for those that are menthol and tobacco flavored. Despite pressure for a comprehensive ban from the anti-smoking community, the FDA rule, as written, will affect a relatively small portion of the vaping industry. It will only apply to cartridge-based products, leaving larger, tank-style vapes exempt from the ban. Single use and disposable vapes, which are becoming increasingly popular among children, are also exempt.
President Trump recently signed into law a bill that funds the federal government for Fiscal Year (FY) 2020 and raises the purchasing age of tobacco products to 21.
On December 27, 2019, the Food and Drug Administration approved olaparib (LYNPARZA®, AstraZeneca Pharmaceuticals LP) for the maintenance treatment of adult patients with deleterious or suspected deleterious germline BRCA-mutated (gBRCAm) metastatic pancreatic adenocarcinoma, as detected by an FDA-approved test, whose disease has not progressed on at least 16 weeks of a first-line platinum-based chemotherapy regimen.