DoD Rare Cancers Research Program funding opportunities for FY21

The FY21 RCRP program announcements and General Application Instructions for the FY21 Department of Defense Rare Cancers Research Program to support research of exceptional scientific merit in the area of rare cancers research the following award mechanisms are posted on the Grants.gov website.

More information can be found here.

A pre-application is required and must be submitted through the electronic Biomedical Research Application Portal (eBRAP) at https://eBRAP.org prior to the pre-application deadline. All applications must conform to the final program announcements and General Application Instructions available for electronic downloading from the Grants.gov website.

The application package containing the required forms for each award mechanism will also be found on Grants.gov. A listing of all CDMRP and other USAMRDC extramural funding opportunities can be obtained on the Grants.gov website by performing a basic search using CFDA Number 12.420.

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Table of Contents

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Clinical News Analysis

ACS report trumpets 70% five-year survival for all cancers amid uncertain funding outlook

The American Cancer Society’s 2026 annual statistics report trumpets a symbolic milestone for oncology—for the first time, the five-year relative survival rate for all cancers combined has reached 70% for people diagnosed between 2015 and 2021 in the U.S.

January 16, 2026

Vol.52 No.02

By Jacquelyn Cobb and Paul Goldberg

Clinical Health Equity

New Medicaid work requirements could lead to 1.6 million missed cancer screenings over two years

New Medicaid work requirements included in President Donald Trump’s “One Big Beautiful Bill Act” could result in as many as 1.6 million missed screenings for breast, colon, and lung cancers within the first two years, researchers at the University of Chicago reported in a paper published in JAMA Oncology earlier this month.

When “safe and effective” is not “reasonable and necessary”
We can curb excessive drug dosing and improve the quality of cancer care

By law, the Food and Drug Administration is required to determine whether a drug, device, biologic, or medical device is “safe and effective.” But the FDA determination does not control whether the Centers for Medicare & Medicaid Services will pay for it. To satisfy CMS, medical products and services must be “reasonable and necessary,” meaning...

January 16, 2026

Vol.52 No.02

By Mark J. Ratain and David A. Hyman

Clinical Trials & Tribulations

A radiation oncologist’s perspective: Why we need to accelerate early detection strategies for lung cancers

As a radiation oncologist, I am struck by how often the decisive variable in lung cancer is not the sophistication of our therapy, but the timing of our encounter with the disease. The American Cancer Society projects 618,120 cancer deaths in the United States in 2025, with lung cancer remaining as the single largest contributor,...

January 16, 2026

Vol.52 No.02

By Kevin King

Obituary

Ben Seon, immunologist whose work led to development of lymphoma drug Polivy, dies at 89

Ben K. Seon, a senior faculty member and distinguished immunology scientist at Roswell Park Comprehensive Cancer Center across six decades, died Dec. 17, 2025. He was 89.

January 16, 2026

Vol.52 No.02

By Roswell Park Comprehensive Cancer Center

Cancer Policy

FDA releases 10 guiding principles for AI use in drug development

FDA, in collaboration with the European Medicines Agency, has published 10 principles to help guide pharmaceutical companies using artificial intelligence to develop drug, biological, and medical devices.

January 16, 2026

Vol.52 No.02

By Sara Willa Ernst

DoD Rare Cancers Research Program funding opportunities for FY21

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ACS report trumpets 70% five-year survival for all cancers amid uncertain funding outlook

New Medicaid work requirements could lead to 1.6 million missed cancer screenings over two years

When “safe and effective” is not “reasonable and necessary”
We can curb excessive drug dosing and improve the quality of cancer care

A radiation oncologist’s perspective: Why we need to accelerate early detection strategies for lung cancers

Ben Seon, immunologist whose work led to development of lymphoma drug Polivy, dies at 89

FDA releases 10 guiding principles for AI use in drug development

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DoD Rare Cancers Research Program funding opportunities for FY21

YOU MAY BE INTERESTED IN

ACS report trumpets 70% five-year survival for all cancers amid uncertain funding outlook

New Medicaid work requirements could lead to 1.6 million missed cancer screenings over two years

When “safe and effective” is not “reasonable and necessary”We can curb excessive drug dosing and improve the quality of cancer care

A radiation oncologist’s perspective: Why we need to accelerate early detection strategies for lung cancers

Ben Seon, immunologist whose work led to development of lymphoma drug Polivy, dies at 89

FDA releases 10 guiding principles for AI use in drug development

Never miss an issue!

Login

When “safe and effective” is not “reasonable and necessary”
We can curb excessive drug dosing and improve the quality of cancer care