Expert Highlights Immunotherapy Potential in Ovarian Cancer

Danielle Bucco
Published Online: Monday, Sep 18, 2017

Dmitriy Zamarin, MD, PhD
Dmitriy Zamarin, MD, PhD
Immunotherapy has been slower to demonstrate progress in gynecologic cancers than in several other solid tumors, experts say.

“We have not increased the number of patients that we have cured of ovarian cancer in the past 20 or 30 years,” states Dmitriy Zamarin, MD, PhD.

Success with these agents may rely on combination approaches, which has shown improvement in responses with other cancer types, such as melanoma. There is an ongoing phase II study investigating the CTLA-4 inhibitor ipilimumab (Yervoy) and the PD-1 inhibitor nivolumab (Opdivo) for patients with recurrent ovarian cancer, primary peritoneal, or fallopian tube cancer, with results expected to readout in the coming months (NCT02498600).

In an interview with OncLive at the 2017 State of the Science SummitTM on Treatment Options in Ovarian Cancer, Zamarin, a medical oncologist at Memorial Sloan Kettering Cancer Center, discusses immunotherapy for patients with ovarian cancer.

OncLive: Please provide an overview of your presentation on immunotherapy in ovarian cancer.

Zamarin: I discussed the different types of treatments that are used, such as vaccines. I mainly focused on immune checkpoint inhibitors, which is the class of agents that has been in the most advanced clinical development—not just in ovarian cancer, but other cancer types, as well.

What have we seen so far regarding vaccines? 

Cancer vaccines are probably one of the older types of immunotherapy. The interest stems from the success of vaccines in the infectious disease setting. The idea was: can we use this in a therapeutic setting in advanced cancers, or even in some of the precancerous conditions?

Unfortunately, in the advanced cancer setting, we have not seen much success from the traditional types of vaccines. By this, I mean peptide vaccines that are representing some of the commonly shared tumor antigens. For example, there are cancer germline antigens, such as NY-ESO-1. Those vaccines have shown some signals of activity, but we have not seen major activity that would cause tumor regressions or, even when used in maintenance, would result in a prolongation of progression-free survival or cures. 

Vaccine is a very broad word. It encompasses many different types of treatment strategies. There is one vaccine that is currently approved for metastatic melanoma that works very well called talimogene laherparepven (T-VEC; Imlygic). This is a vaccine that is an oncolytic herpes virus expressing GM-CSF that is given intralesionally. We don't know if similar strategies will be effective for cancers of gynecologic origin, but they are certainly worthy of investigation. 

This is an in situ vaccine, meaning it targets a patient's own tumor—allowing them to generate immune response against their own cancer. In ovarian cancer, we haven't seen much promise in the advanced confirmatory phase II studies that would suggest that vaccines are effective.

What are the latest data that we have with checkpoint inhibitors in this landscape?

Some checkpoint inhibitors have seen approval in many cancer types, with melanoma being the first one. The main checkpoint inhibitors that we see in clinic are the antibodies that are targeting CTLA-4, PD-1, or PD-L1. All have been tested in ovarian cancer. In the initial studies with antibodies targeting PD-1/PD-L1, the response rates are not as high as what we see in some of these other cancer types. 

In ovarian cancer, the response rates seem to be around 12% to 15%. There is a significant number of patients who do have some disease stabilization with these therapies. This is not to say that the response rate is very low and the drugs are not worth investigation, but durable stable disease is certainly something that we can strive for.

More importantly, what those studies also suggest is that patients with ovarian cancer are obviously different. The biology of the tumor is different than these other cancer types. Perhaps the biomarkers that we have in the other cancers are not the same as what we are going to have for ovarian cancer. 

Most importantly, these drugs are not going to work alone. We need to use them in combination with some of these other drugs—either standard or investigational. 

Are there any combinations going on right now with immunotherapy that you think are interesting?

There are quite a few ongoing combinations in ovarian cancer and in many other cancer types. The only real combination that has been approved so far, at least in metastatic melanoma, is the combination of targeting CTLA-4 and PD-1 with the drugs ipilimumab and nivolumab. There are currently studies that are evaluating the same combination in ovarian cancer. We should probably have the results from these studies coming up within the next few months. 


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