Treating Renal Cell Carcinoma in 2013: An Interview With Sumanta Kumar Pal, MD
Published Online: Tuesday, November 19, 2013
Sumanta Kumar Pal, MD
OncLive.com: What is the role of adjuvant therapy in RCC?
Pal: This is a frequent consultation at my clinic from urologists. They’ll often times see a patient with high-risk disease, perhaps pathologic T2 or T3 disease with sarcomatoid features and aggressive tumor grade and the question will be, “would you or would you not put this patient immediately on some of the targeted agents that are used in the metastatic setting?” I would argue right now, in 2013, the answer to that question is no.
What are some of the key trials for adjuvant therapy?
First and foremost, I would suggest that at this point in time adjuvant therapy is really not a standard of care for localized RCC. However, there are several studies that are potentially going to put these agents into that disease space.
So, for instance, in the category of VEGF-directed therapies, I can think of five trials that have been completed to date that assess targeted therapies directed at VEGF. Just as one example, the ASSURE trial, which was completed about two years ago now, compares sunitinib, sorafenib and placebo in a large pool of patients—close to 2,000 patients. That study will hopefully report out within the next two or three years.
We had a couple of important lessons learned from studies like the ASSURE trial. First and foremost, patients in the adjuvant setting may not tolerate the same doses that they might in the metastatic setting. For instance, in the ASSURE trial, doses had to be reduced with sunitinib and sorafenib. Patients, as opposed to starting out with the standard 50 mg/day of sunitinib or 800 mg total per day of sorafenib, received just 37.5 mg of sunitinib and literally half the dose of sorafenib therapy. So these might be important lessons moving forward.
We do have one trial in the adjuvant setting that looks at mTOR inhibition using the agent everolimus. This is the so-called EVEREST trial and this trial compares everolimus versus placebo at a total pool of about 1,100 patients. That study is about halfway accrued.
The only assessment of a targeted therapy that has been completed to date, that is outside of the VEGF and mTOR directed categories, is for one of the nontraditional agents called girentuximab. This is an agent that targets CA9. These data were just reported at ASCO this past year, and girentuximab was not noted to have any significant impact on disease-free survival or overall survival—two of the critical endpoints in that study.
In the metastatic setting, is there an optimal treatment sequence?
Sequencing therapies in RCC is an incredibly complex issue. There are relatively firm guidelines set forth by groups like the NCCN that really informs us on how to utilize these agents. For instance, if you run into a patient with what’s categorized as poor risk disease, you might want to start with the mTOR inhibitor temsirolimus. On the other hand, if you have a patient with good or intermediate risk disease, I would typically start with a VEGF-directed agent—your options in that category are sunitinib, pazopanib or bevacizumab. And we actually do have a good level of evidence for all three of those agents in that specific setting. There was a phase III data set pitting sunitinib and pazopanib head-to-head against one another and that data set I thought was somewhat equivocal so I still tend to use sunitinib as my preferred first-line agent.
What are some of the challenges of treating patients with RCC?
People look at metastatic RCC as a disease in which there’s been massive progress, and I wouldn’t disagree with that. If we look at the trajectory of drug approvals in RCC between 1992 and 2005, they literally had one drug approval and that was for interleukin-2. From that point forward, we’ve actually had seven drug approvals. So incredibly promising for patients and their families.
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