Several immune checkpoint inhibitors (ICIs) are approved for use in patients with metastatic renal cell carcinoma (mRCC), but the efficacy and safety of ICI rechallenge in mRCC is unknown.
To evaluate the safety and efficacy of ICI rechallenge in patients with mRCC.
This multicenter, retrospective cohort study included consecutive patients with mRCC from 9 institutions in the US who received at least 2 separate lines of ICI (ICI-1, ICI-2) between January 2012 and December 2019.
Receipt of an ICI (anticytotoxic T-lymphocyte-associated protein 4, anti-programmed cell death protein 1, or anti-programmed cell death ligand 1), alone or in combination with other therapies, in at least 2 separate lines of therapy for mRCC.
Investigator-assessed best overall response and immune-related adverse events.
A total of 69 patients were included. Median (range) age at diagnosis of mRCC was 61 (36-86) years. Of these, 50 were men and 19 were women. The most common therapies received at ICI-1 were single-agent ICI (n = 27 [39%]) or ICI in combination with targeted therapy (n = 29 [42%]), while at ICI-2, the most common therapies were single-agent ICI (n = 26 [38%]) or dual ICI (n = 22 [32%]). Most patients discontinued ICI-1 owing to disease progression (n = 50 [72%]) or toxic effects (n = 16 [23%]). The overall response rates at ICI-1 and ICI-2 were 37% and 23%, respectively. The likelihood of a response at ICI-2 was greatest among patients who had previously responded to ICI-1 (7 of 24 [29%]), although responses at ICI-2 were seen in those who had progressive disease as their best response following ICI-1 (3 of 14 [21%]) as well as in those who received single-agent ICI at ICI-2 (7 of 23 [30%]). Grade 3 or higher immune-related adverse events were seen in 18 patients (26%) and 11 patients (16%) at ICI-1 and ICI-2, respectively. There were no treatment-related deaths.
The findings of this multicenter cohort study suggest that ICI rechallenge in patients with mRCC may be safe and reasonably efficacious, with an overall response rate of 23%. Data from prospective studies are needed to validate these findings and determine the role of sequential ICI regimens in treatment of mRCC.
JAMA oncology. 2020 May 29 [Epub ahead of print]
Praful Ravi, Charlene Mantia, Christopher Su, Karl Sorenson, Dean Elhag, Nityam Rathi, Ziad Bakouny, Neeraj Agarwal, Yousef Zakharia, Brian A Costello, Rana R McKay, Vivek Narayan, Ajjai Alva, Bradley A McGregor, Xin Gao, David F McDermott, Toni K Choueiri
Dana-Farber Cancer Institute, Boston, Massachusetts., Beth Israel Deaconess Medical Center, Boston, Massachusetts., University of Michigan, Ann Arbor., Mayo Clinic, Rochester, Minnesota., The University of Iowa, Iowa City., Huntsman Cancer Institute, Salt Lake City, Utah., University of California, San Diego., University of Pennsylvania, Philadelphia., Massachusetts General Hospital, Boston.