John Kuruvilla, MD, on the Implications of the Phase III KEYNOTE-204 Study

Article

Results from the study indicated that pembrolizumab (Keytruda) was superior to brentuximab vedotin (Adcetris) in patients with relapsed or refractory classic Hodgkin lymphoma (R/R cHL).

Results from the randomized, open-label phase III KEYNOTE-204 study, presented at the 2020 American Society of Clinical Oncology (ASCO) Virtual Scientific Program, suggested that pembrolizumab (Keytruda) was superior to brentuximab vedotin (Adcetris) in patients with relapsed or refractory classic Hodgkin lymphoma (R/R cHL).

In an interview with CancerNetwork®, John Kuruvilla, MD, of the Princess Margaret Cancer Centre, discussed the implications of the phase III KEYNOTE-204 trial and what these findings represent for this patient population. 

Transcription:

It's been an interesting study to think about because the population is actually both broad and focused in a way, so the real standard in this setting for a long time had been brentuximab vedotin, and that was based on the pivotal trial that had enrolled patients that had had disease progression only following autologous stem cell transplants. And so, clinicians where possible had generalized that data to also include patients that had been ineligible for transplant due to age or comorbidity or the presence of refractory disease. And so, brentuximab was well established in that population. What these data show is in the place where brentuximab had been defined by its pivotal clinical trial, pembrolizumab has more favorable progression-free survival. And similarly, in that population that had not been in the pivotal brentuximab study, but brentuximab had become the standard up until now, pembrolizumab also had superiority in those non-transplanted patients as well.

Recent Videos
relapsed or refractory mantle cell lymphoma, glofitamab, Obinutuzumab, phase 1/2 study, NCT03075696, Tycel J. Phillips, MD
Adverse effects associated with oral azacitidine in low- or intermediate-risk MDS are typically transient, according to Mikkael A. Sekeres, MD, MS.
Ongoing genomic profiling analyses in the ASC4FIRST trial may further determine which patients with CML may benefit from treatment with asciminib.
Gregory W. Roloff, MD, indicates that brexucabtagene autoleucel did not yield significant positive findings in patients with relapsed/refractory B-cell acute lymphoblastic leukemia who were MRD positive.
The education of patients on identifying and reporting adverse effects is a critical part of effective toxicity management.
One role of a physician assistant is to help patients understand their treatment and the results they’re presented with.
Adverse effect management is a concern for clinicians when administering follicular lymphoma treatment, and the use of targeted pathways may help mitigate them.
An expert from Vanderbilt University Medical Center says that patients with relapsed/refractory multiple myeloma may be able to live a normal life following response to salvage treatment with bispecific monoclonal antibodies.
C. Ola Landgren, MD, PhD, discusses progression-free survival findings from the phase 3 DETERMINATION trial, examining lenalidomide, bortezomib, and dexamethasone plus autologous stem cell transplant and lenalidomide maintenance in patients with newly diagnosed multiple myeloma.
Related Content