Gennady Bratslavsky, MD, on Adjuvant Therapy in RCC

Video

Gennady Bratslavsky, MD, spoke about the role of adjuvant therapy in renal cell carcinoma at the 15th Annual Interdisciplinary Prostate Cancer Congress® and Other Genitourinary Malignancies.

During the 15th Annual Interdisciplinary Prostate Cancer Congress® and Other Genitourinary Malignancies, CancerNetwork® spoke with Gennady Bratslavsky, MD, professor and chair of Urology and director of the Prostate Cancer Program at Upstate University Hospital in Syracuse, New York, about the use of adjuvant therapy for treatment of renal cell carcinoma. Bratslavsky mentions numerous trials which are using this strategy, one of which is KEYNOTE-564 (NCT03142334) looking at adjuvant pembrolizumab (Keytruda) after a nephrectomy.

The trial showed a disease-free survival (DFS) rate at 24 months of 77.3% in the pembrolizumab group vs 68.1% in the placebo group (HR, 0.68; 95% CI, 0.53-0.87; P = .002).

Transcript:

The adjuvant [therapy] space is finally having some promise with the recently published KEYNOTE-564 trial. Adjuvant pembrolizumab certainly [provides] an opportunity for us to expect and hope for DFS. Most of the adjuvant trials to date have not been more successful [than KEYNOTE-564]. Even in the S-TRAC (NCT00375674) trial of adjuvant [sunitnib; Sutent] utilization for a year after nephrectomy in patients with the kidney cancer that were found to be high risk, the presence of DFS never translated into overall survival [OS].

While KEYNOTE-564 is yet to mature—to demonstrate whether its use in the adjuvant setting would help with the overall survival is yet to be determined—there is certainly quite a bit of hope that after 2 years of follow up, we’re starting to see a promise and a strong signal that this DFS may translate into OS, although this has yet to be seen. The recently completed PROSPER trial [NCT03055013] is bringing another opportunity for us to evaluate the role of immunotherapy in the neoadjuvant as well as the adjuvant setting for high-risk patients. There are many unanswered questions. Even if we identify an agent that is effective in improving the DFS, we will always question the patients who would have not recurred and still would be subjected to therapy. There is still an ongoing need for better identification of these patients that are most likely to recur beyond our standard clinical variables that have been traditionally used in designing the trials for both neoadjuvant and an adjuvant therapy.

Reference

Choueiri TK, Tomczak P, Park SH, et al. Adjuvant pembrolizumab after nephrectomy in renal-cell carcinoma. N Engl J Med. 2021;385(8):683-694. doi:10.1056/NEJMoa2106391

Recent Videos
Developing odronextamab combinations following CAR T-cell therapy failure may help elicit responses in patients with diffuse large B-cell lymphoma.
An “avalanche of funding” has propelled the kidney cancer field forward, says Jason Muhitch, PhD.
Cytokine release syndrome was primarily low or intermediate in severity, with no grade 5 instances reported among those with diffuse large B-cell lymphoma.
Kidney cancer advocacy efforts have spread the urgency and importance of funding research in the field to members of Congress.
Advocacy efforts have yielded a dramatic increase in kidney cancer research, according to Elizabeth P. Henske, MD.
Safety results from a phase 2 trial show that most toxicities with durvalumab treatment were manageable and low or intermediate in severity.
Updated results from the 1b/2 ELEVATE study elucidate synergizing effects observed with elacestrant plus targeted therapies in ER+/HER2– breast cancer.
Patients with ESR1+, ER+/HER2– breast cancer resistant to chemotherapy may benefit from combination therapy with elacestrant.
Related Content