Clarification

Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on print

Clarification

A guest editorial in The Cancer Letter stated that “work has halted on ECOG-ACRIN Cancer Research Group’s landmark Tomosynthesis Mammographic Imaging Screening Trial.” (The Cancer Letter, April 10, 2020) The TMIST breast cancer screening trial is not suspended. TMIST formally remains an ongoing study under the NCI and Cancer Trials Support Unit. Active participation at this time is at the discretion of individual sites. Sites are making critical local operational decisions to help manage any potential influx of COVID-19 patients and maintain the safety of patients and staff. As a result, some sites have suspended non-urgent health care services, such as screening mammography, and research operations.

Correction

A COVID-19 Update on April 24 reported that The Association of American Cancer Institutes annual meeting has moved to a virtual format (The Cancer Letter, April 24, 2020). The Association of American Cancer Institutes’ Clinical Research Innovation (CRI) program has moved its July 7-8 annual meeting to a virtual format. The AACI annual meeting, which takes place Oct. 11-13 in Kansas City, MO, is still scheduled as an in-person meeting at this time.

Table of Contents

YOU MAY BE INTERESTED IN

Recently, HHS Secretary Robert F. Kennedy Jr. posted a video montage featuring himself shirtless in jeans, working out with Kid Rock. The duo is in a blue-lit grotto with a cold plunge and sauna. Set to Kid Rock’s “Bawitdaba” and intercut with a selection of patriotic imagery, the video ends with the two men in a hot tub, chugging what appears to be milk.
In January, FDA released a draft guidance entitled “Minimal Residual Disease and Complete Response in Multiple Myeloma: Use as Endpoints to Support Accelerated Approval.” This release came roughly 20 months after the Oncologic Drugs Advisory Committee (ODAC) voted unanimously that minimal residual disease (MRD) negativity, in combination with complete response (CR), is an acceptable primary endpoint to support accelerated approval for multiple myeloma (MM) therapies. 

Never miss an issue!

Get alerts for our award-winning coverage in your inbox.

Login