http://www.curetoday.com/articles/expert-provides-update-on-immunotherapy-research-in-sarcoma
Expert Provides Update on Immunotherapy Research in Sarcoma

Laura Panjwani

While immunotherapy is proving to be promising in many other fields, it is still too early to get excited over its potential use in treating sarcoma, says Katherine Thornton, M.D., co-clinical director, Center for Sarcoma and Bone Oncology at Dana-Farber Cancer Institute.

“Immunotherapy isn’t quite the ‘magic bullet’ for sarcoma that it has been in melanoma, lung cancer, and other various diseases—but we are still learning a lot,” she added. “The jury is still out on whether we are going to have immunotherapy be the ‘holy grail’ for our tumors. Right now, I don’t see it happening.”

There has been some limited success of immunotherapy in sarcoma.

Keytruda (pembrolizumab) was investigated in seven different subtypes of previously treated sarcoma in the phase 2 SARC-028 trial.

In this study, the best response rate was seen among patients with undifferentiated pleomorphic sarcoma. Of the nine evaluable patients in that subgroup, four had a partial response (PR) and three experienced stable disease (SD). Among patients with liposarcoma (nine patients), two had a PR and four had SD. In the synovial sarcoma cohort (nine patients), one patient had a PR and two had SD. In leiomyosarcoma (10 patients), no patients experienced a PR and six had stable disease.

However, many questions still remain regarding this and other immunotherapy trials for sarcoma, said Thornton. In an interview with CURE, the expert discusses the potential that immunotherapy agents could have, as well as the role of genomic profiling in understanding the patients who may benefit from select treatments.

Where are we right now with immunotherapy in sarcoma?

There were two larger trials that were presented in June at the 2016 American Society of Clinical Oncology (ASCO) Annual Meeting. One was a specific anti–PD-1 therapy in uterine leiomyosarcoma, and the other one was an all-comer sarcoma trial looking at Keytruda.

Unfortunately, in my mind, they were both really resounding thuds on the floor. There were no responders in the uterine leiomyosarcoma trial and only a handful of responders in the all-comers trial. They did report out the negative study, which I was really appreciative of because it is important to hear about the negative studies as well as the positive studies.

They made a lot of ado about the few responders who were in the larger Keytruda study—trying to stir up some excitement. There are a lot of questions that remain. The biggest question for me is, “Why did those patients respond when the vast majority of patients did not?”

That is what we are trying to figure out right now. There are certainly a lot of trials that are still speculating, and I do have patients coming to my clinic requesting immunotherapy. However, off of a clinical trial, I am very hesitant to use them with patients.

In what area is the immunotherapy research happening?

Synovial sarcoma is one of the sarcomas that has traditionally responded to immunotherapy-type treatments in the past, and there are a fair amount of trials right now looking at synovial sarcoma as well as looking at myxoid liposarcoma. Those are some areas that are a little bit more exciting in the immunotherapy realm, but a lot is still unknown. The correlative studies that go along with the clinical portion are really going to tell us more information as we go forward.

What role does genomic testing play in the treatment of sarcoma?

There have been some opinions on whether it is helpful or not. It is something that can open up some opportunities. There is such a diverse tumor panel in sarcoma; there are so many diverse diseases within this sarcoma label, that the more we sequence these tumors and the more we learn about the nuances of all of them, the more it will help guide treatment.

We are in the infancy of the field right now and the more we learn, the more we will be able to forge forward. Hopefully, we will find a target and a drug will be developed. The only way we are going to learn is by doing.



 
 
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