ONCAlert | Upfront Therapy for mRCC

Experts Discuss Treatment Sequencing Strategies in CRPC

Published Online: Apr 20,2016
As the treatment landscape for patients with metastatic castration-resistant prostate cancer (CRPC) continues to evolve, optimal strategies are becoming more apparent on how to best sequence the multitude of novel therapies that have been approved in the past decade.

To gain insight into current best practices and strategies that are on the horizon, Targeted Oncology spoke with two of the leading experts in the field: E. David Crawford, MD, endowed chair in Urologic Oncology at the University of Colorado, and Leonard G. Gomella, MD, senior director for Clinical Affairs at Jefferson Kimmel Cancer Center.

TARGETED ONCOLOGY: What factors guide your selection of frontline therapy for men with CRPC?

CRAWFORD: We are entering an era of castration-resistant prostate cancer where we are trying to really personalize it to the patient, and not just throw out a big net and say, “everybody fits into this one.” You look at how fast they got there, how they got there, what prior treatments they received—many other things like that.

The good thing is, we have a whole bunch of things to treat patients with. In general, they are not for patients who are sort of “circling the drain,” but for the minimally symptomatic patient.

What I normally would do is think about things I really want to get into the patient—things like immunotherapy or sipuleucel-T. I sort of consider that a platform you really build on. The question is, “Do you start with an androgen biosynthesis inhibitor? Do you start out with radium-223? Do you start out with things like anti-androgens, such as enzalutamide? Do you put combinations together?” Those are all conversations you need to have with the patient.

Right now, people are doing things like sequencing. I think we need to start thinking beyond that. We need to think about the fact that, in most cancers that we cure, it’s not sequencing “A, B, C, and D,” it’s putting “A, B, C, D” together and treating the patient. It may not be for a lifetime; it may be a short time. 

That is certainly the case for certain lymphomas, leukemias, and testicular cancers, and I think the same thing really applies to prostate cancer.

Currently, I think people tend to start out with the bettertolerated agents and then move to the drugs that have more significant side effects. That means that chemotherapy has been pushed to the end of the line again. But, in newly diagnosed patients, that’s different.

GOMELLA: When we look at managing patients with castration-resistant prostate cancer, we have many options available to us right now. We are learning, as time goes on, that certain agents are best used early in the course of the disease; meanwhile, other agents may be used early but may be optimally used later. A classic example of that is using sipuleucel-T very early in the course of CRPC, when patients are minimally symptomatic or asymptomatic. It is probably not a good idea to use it later when people have a lot of pain or other symptoms.

In general, we like to use agents such as immunotherapy with sipuleucel-T early in the disease. Other agents are certainly valid to use. The androgen receptor-pathway blockers enzalutamide and abiraterone are certainly fair to use early in the course of the disease. More recently, for patients with metastatic castration-resistant prostate cancer, there tends to be use of chemotherapy a little bit later in the course of the disease. However, that is variable depending on local practice patterns and how the medical oncologists really feel about the use of chemotherapy.

Radium-223 is out there, also. The difference with radium-233 is it can be used across the spectrum of the disease, but it tends not to be used early in current practice. It tends to be used a little bit later. However, using it early is something that is under investigation, as well.

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Experts Discuss Treatment Sequencing Strategies in CRPC
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