Studies show immunotherapy drugs improve outcomes in Hodgkin lymphoma patients
In recent years, a number of scientific breakthroughs have led to the development of drugs that unleash the power of the immune system to recognize and attack cancer. Studies presented at the 56th Annual Meeting of the American Society of Hematology (ASH) highlight the enormous potential these novel treatments have for patients with a variety of hematologic disorders. For Classical Hodgkin lymphoma (cHL) patients, two phase I studies are already demonstrating dramatic results. A study led by Craig H. Moskowitz, MD, Clinical Director of the Division of Hematologic Oncology at Memorial Sloan Kettering Cancer Center (MSK), showed that 66 percent of cHL patients had a complete or partial response after receiving the immunotherapy drug pembrolizumab.
"These results are quite extraordinary given the dire circumstances these patients were facing," said Dr. Moskowitz. "Pembrolizumab has already been approved for patients with advanced melanoma and we're excited that the drug is producing responses in other cancer types."
Pembrolizumab is an inhibitor of PD-1, a protein on the surface of T cells that normally regulates the immune system by stopping T cell activation. Some cancers have developed ways of exploiting this shutdown mechanism by interacting with PD-1, enabling the cancer to escape T cell attack. Pembrolizumab blocks PD-1 from stopping T cell activation, allowing the T cells to keep fighting.
MSK physicians played a major role in the clinical trials that led to pembrolizumab's approval and are continuing to conduct trials using the therapy in melanoma, lymphoma, and other cancers.
Dr. Moskowitz's study examined pembrolizumab in 29 patients with cHL who had failed to respond to treatment with brentuximab vedotin. Twenty patients had also relapsed after autologous stem cell transplantation. "Phase I studies are designed for patients who have few, if any, treatment options left," added Dr. Moskowitz.
After twelve weeks, six patients (21 percent) achieved a complete response and thirteen patients (45 percent) went into partial remission. No serious adverse events were reported, and only one patient discontinued therapy because of a moderate side effect.
"Using the immune system as a weapon against cancer is just now beginning to gain momentum," said Dr. Moskowitz. "The results of this study are encouraging as we gather evidence that immunotherapies have the potential to work in many different types of cancer."
A second study presented at the ASH Annual Meeting and simultaneously published in the New England Journal of Medicine showed similarly positive results in cHL patients when using the immunotherapy drug nivolumab, another PD-1 inhibitor.
Twenty-three cHL patients who had failed prior treatment -- 18 of whom had also relapsed after autologous stem cell transplantation -- were given nivolumab. After 24 weeks, four patients (17 percent) achieved a complete response and sixteen patients (70 percent) went into partial remission. Only three serious adverse events were reported.
"These data are the first to be reported for a completed study of a PD-1 inhibitor in Classical Hodgkin lymphoma," said Alexander M. Lesokhin, MD, a medical oncologist at MSK who co-led the study. "This is good news for Hodgkin lymphoma patients and for the advancement of immunotherapies. It's an exciting time to be an oncologist."
Based on these results, the U.S. Food and Drug Administration granted nivolumab Breakthrough Therapy Designation in relapsed cHL. A large phase II trial of this therapy is underway at MSK and other institutions.
Source: Memorial Sloan Kettering Cancer Center
Other sources
- Immunotherapy drugs improve outcomes in Hodgkin lymphoma patients, study showsfrom Science DailyMon, 8 Dec 2014, 21:01:19 UTC
- Positive data from pivotal phase III study could improve standard of care for Hodgkin lymphoma patientsfrom Science DailyMon, 8 Dec 2014, 21:01:18 UTC
- Immunotherapy achieves breakthrough result in patients with Hodgkin lymphomafrom Science DailyMon, 8 Dec 2014, 21:01:11 UTC