ONCAlert | 2018 Gastrointestinal Cancers Symposium
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Balar Discusses Impact of Pembrolizumab FDA Approval in Urothelial Carcinoma

Danielle Bucco
Published Online:8:17 AM, Wed May 24, 2017

Arjun V. Balar, MD

Patients with metastatic urothelial carcinoma now have yet another immunotherapy option with the recent FDA approval of pembrolizumab (Keytruda) for use in the first- and second-line setting.

The PD-1 inhibitor was specifically approved in the second-line setting for the treatment of patients with locally advanced or metastatic urothelial carcinoma who have disease progression during or following platinum-containing chemotherapy or within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy.

In the frontline setting, the FDA granted an accelerated approval to frontline pembrolizumab for patients with locally advanced or metastatic urothelial carcinoma who are not eligible for cisplatin-containing chemotherapy.

Pembrolizumab joined other approved immunotherapy agents in the urothelial carcinoma armamentarium, including avelumab (Bavencio), durvalumab (Imfinzi), atezolizumab (Tecentriq), and nivolumab (Opdivo).

In an interview with Targeted Oncology, Arjun V. Balar, MD, a lead investigator on pivotal pembrolizumab research in bladder cancer, and an assistant professor, Department of Medicine, and director, Genitourinary Medical Oncology Program, NYU's Perlmutter Cancer Center, discussed the impact of the approval of pembrolizumab and other immunotherapy agents in urothelial carcinoma, as well as the next steps with these treatments.

TARGETED ONCOLOGY:  Can you discuss the significance of the recent FDA approval of pembrolizumab in bladder cancer?

Balar: It comes down to which approval we’re talking about, whether it is the second line or the first line. For the second line, at that point, pembrolizumab becomes the 5th drug approved for the second-line treatment of bladder cancer. From that perspective, it adds to our armamentarium in terms of options that we can provide our patients. It's similar in terms of the class of drug. It’s a PD-1 antibody, allowing it to work on the PD-1 axis, making the response and safety very similar to other agents in its class. 

What's unique about pembrolizumab in the second-line setting is that it was approved on the basis of a randomized phase III trial that definitively demonstrated its improved survival versus standard of care chemotherapy, which no other agent in this class has been able to do. In my opinion, that is probably the strongest level of evidence for any of the drugs. I think that is particularly unique in the second-line setting. 

In terms of the frontline setting, pembrolizumab is now just 1 of 2 drugs that is approved for patients who are ineligible for cisplatin. In this case, these are both accelerated approvals, whereas pembrolizumab’s second-line approval is a full approval. Both accelerated approvals are on the basis of response and durability of responses in the first-line setting. 

What is particularly unique about both atezolizumab and pembrolizumab in the frontline setting is that these are the first FDA-approved drugs for a population of patients who have never had an FDA approved drug. These are the first treatments that have ever been approved for patients who are ineligible for cisplatin. In my opinion, what is particularly unique about these 2 approvals is that about 50% to 70% of our patients with metastatic bladder cancer are cisplatin ineligible. This means that these approvals greatly impact a majority of patients with metastatic bladder cancer, which is quite unique and exciting. 

TARGETED ONCOLOGY:  Now that we have more options for immunotherapy treatments, how do you determine which immunotherapy to use for patients?

Balar: I think that is the main challenge right now. Within 1 year, we’ve had 5 different drugs that have been approved in various settings. It’s been difficult for the research community and the bladder cancer community to parse out the differences between these agents. The response rates, the durability of responses, and the survival rates appear to be very similar. However, again, the caveat is it’s a mix of phase I, phase II, and now a phase III study. In my opinion, I don’t think we can make any comparisons about survival because survival between phase I, II, and III studies can be marginally different for a variety of reasons.  In terms of the response, durability of responses, and the safety of the drugs, I think they are quite comparable and that it probably the most we can say at this point.

TARGETED ONCOLOGY:  What other remaining questions regarding these agents still need to be addressed?

Balar: From these drugs so far, I think what we need to see is in the frontline setting. The major unanswered question is if pembrolizumab and atezolizumab are better than standard of care chemotherapy. We need a randomized phase III trial. There are 2 notable studies that are currently ongoing, the atezolizumab study, which is IMvigor-130, and then the pembrolizumab phase III study where it is compared against chemotherapy, which is KEYNOTE-361. Both of those trials will answer the question of does PD-1 blockade improve survival versus chemotherapy in the frontline setting. 

TARGETED ONCOLOGY:  What do you anticipate for the future of these agents?

Balar: Now that we have these approvals, the challenge is that based on pembrolizumab and atezolizumab, up to 25% of patients are responding to treatment. What that means is the next generation of trials need to improve on that response rate. 

We need to use immunotherapy as a backbone and to develop novel combinations. Perhaps those combinations are with radiation, chemotherapy, targeted therapy, or other immuno-oncology drugs to increase that response rate in terms of immune responses. That is the next generation of trials that we need to focus on. 

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