News from the FDA/CDC

Pembrolizumab SCLC indication withdrawn in U.S.


 

Merck & Co. is withdrawing the U.S. indication for pembrolizumab (Keytruda) for metastatic small cell lung cancer (SCLC) in patients with disease progression on or after platinum-based chemotherapy and at least one other prior line of therapy, according to a company statement.

The move does not affect any of the drug’s other indications. The immunotherapy is used in the treatment of many different types of cancer.

The SCLC indication had been granted an accelerated approval by the Food and Drug Administration in 2019 based on tumor response rate and durability of response data from patient cohorts in two trials. However, the anti-PD-1 therapy failed to demonstrate statistically significant improved overall survival in a confirmatory trial, which is mandated after an accelerated approval.

The FDA is conducting “an industry-wide evaluation of indications based on accelerated approvals that have not yet met their postmarketing requirements,” said Merck.

In February of 2021, an indication for durvalumab (Imfinzi) was withdrawn by AstraZeneca in concert with the FDA after the drug failed to improve overall survival in unresectable metastatic bladder cancer in a confirmatory trial, as reported by Medscape Medical News.

“We will continue to rigorously evaluate the benefits of [pembrolizumab] in small cell lung cancer and other types of cancer, in pursuit of Merck’s mission to save and improve lives,” Roy Baynes, MD, chief medical officer, Merck Research Laboratories, said in the company statement

Dr. Baynes also championed the value of accelerated approvals.

“The accelerated pathways created by the FDA have been integral to the remarkable progress in oncology care over the past 5 years and have helped many cancer patients with advanced disease, including small cell lung cancer, access new treatments,” he said.

However, in the past, the FDA has been criticized for approving new cancer drugs based on surrogate markers such as response rates because, in many cases, subsequent studies often show that the drug fails to improve overall survival.

For example, a 2015 study found that 36 (67%) of 54 cancer drug approvals from 2008 to 2012 were made on the basis of surrogate markers – either tumor response rate or progression-free survival. Over a median follow-up period of 4.4 years, only 5 of those 36 drugs were shown in randomized studies to improve overall survival, as reported by Medscape Medical News.

The FDA says that it instituted the accelerated approval program to “allow for earlier approval of drugs that treat serious conditions, and that fill an unmet medical need based on a surrogate endpoint.” The program was started in 1992, in the midst of the HIV/AIDS epidemic.

In 2020, the nonprofit Friends of Cancer Research issued a white paper calling for reform in the accelerated approval process, which included a proposal to add risk assessment to surrogate endpoints that would factor in variables such as toxicity.

A version of this article first appeared on Medscape.com.

Recommended Reading

CXR-Net: An AI-based diagnostic tool for COVID-19
MDedge Hematology and Oncology
Customized chemotherapy did not improve survival in early NSCLC
MDedge Hematology and Oncology
Model could reduce some disparities in lung cancer screening
MDedge Hematology and Oncology
‘Unprecedented’ long-term survival after immunotherapy in pretreated NSCLC
MDedge Hematology and Oncology
FDA approves first drug that protects against chemo-induced myelosuppression
MDedge Hematology and Oncology
X-ray vision: Using AI to maximize the value of radiographic images
MDedge Hematology and Oncology
How has the pandemic affected rural and urban cancer patients?
MDedge Hematology and Oncology
FDA approves cemiplimab-rwlc for NSCLC with PD-L1 expression
MDedge Hematology and Oncology
Researchers identify four small cell lung cancer subtypes and their best therapies
MDedge Hematology and Oncology
Study: Shared decision-making in lung cancer screening needs work
MDedge Hematology and Oncology