Some Head and Neck Cancer Patients Benefit From Continued Checkpoint Inhibitor Treatment After Tumor Growth

Findings argue against stopping treatment prematurely for some patients

Article ID: 672352

Released: 3-Apr-2017 1:05 PM EDT

Source Newsroom: Dana-Farber Cancer Institute

  • Credit: DFCI

    Dana-Farber Cancer Institute

Some head and neck cancer patients benefit from continued checkpoint inhibitor treatment after tumor growth

• Findings argue against stopping treatment prematurely for some patients

Newswise — WASHINGTON –– New research suggests that some patients with head and neck cancers can benefit by continuing treatment with an immunotherapy drug after their tumors show signs of enlargement according to investigators at Dana-Farber Cancer Institute and other organizations.

The researchers will report the findings at a poster session from 1:00 p.m. to 5:00 p.m. in Section 33 at the American Association for Cancer Research (AACR) Annual Meeting on Monday, April 3, 2017 at 10:30 a.m., in Washington DC.

The findings, from CheckMate 141, a phase 3 clinical trial, represent the first time that continued use of an immune checkpoint inhibiting drug has been shown to extend survival in patients whose head and neck tumors have grown during initial treatment with the drug.

The trial involved 139 patients with recurrent or metastatic squamous cell cancer of the head and neck that had progressed after treatment with nivolumab, a Food and Drug Administration-approved drug that works by blocking a molecule that deters immune system T cells from attacking tumor cells. Patients who were doing well clinically and were strong enough to handle further treatment – were given the opportunity to continue taking nivolumab. The others received no further nivolumab.

The 57 patients who continued with nivolumab had a median survival period of 12.7 months, compared to 6.1 months for the 82 patients did not. Almost one quarter of the patients in the first group had their tumors shrink – by more than 30 percent in two cases.

Adverse side effects of the treatment were similar in both groups, although patients who received nivolumab after progression of their disease had higher rates of disorders of the skin or tissue below the skin.

The results underscore that for nivolumab, as for some other immunotherapy drugs, “the benefit is often seen with increased survival, not necessarily tumor shrinkage an response rate,” said study lead author Robert Haddad, MD, leader of the Head and Neck Oncology Program at Dana-Farber. “Our findings suggest that for patients with head and neck cancer who are doing well enough, continuing nivolumab therapy after disease progression can often lengthen survival. For such patients, it can be a mistake to give up on these drugs too early, and clinical judgment should be exercised to determine whether it would be beneficial to continue therapy.”

The senior author of the study is Kevin Harrington of Royal Marsden NHS Foundation Trust/The Institute of Cancer Research, London, United Kingdom. Co-authors are Robert L. Ferris, MD, PhD, of University of Pittsburgh Medical Center Cancer Center; George Blumenschein, Jr., MD, of MD Anderson Cancer Center; Jerome Fayette of Centre Leon Berard, Lyon, France; Joel Guigay of Centre Antoine Lacassagne, FHU Oncoage, Nice, France; Alexander D. Colevas, MD, of Stanford University; Lisa Licitra, MD, of Fondazione IRCCS Istituto Nazionale dei Tumori Milan and University of Milan, Milan, Italy; Stefan Kasper, of West German Cancer Center, University Hospital, Essen, Germany; Everett E. Vokes, MD, of University of Chicago Medical Center; Francis Worden, MD, of the University of Michigan; Nabil F. Saba, MD, of Winship Cancer Institute of Emory University; Makoto Tahara of National Cancer Center, Tokyo, Japan; Manish Monga, MD, Mark Lynch, Jin Zhu, James W. Shaw, PhD, PharmD, MPH, of Bristol-Myers Squibb; and Maura L. Gillison, MD, PhD, of The Ohio State University.

The research (Control Number 17-LB-7877-AACR) will be presented at a poster session on Phase III Clinical Trials and Phase II/III Clinical Trials in Progress.

About Dana-Farber Cancer InstituteFrom achieving the first remissions in childhood cancer with chemotherapy in 1948, to developing the very latest new therapies, Dana-Farber Cancer Institute is one of the world’s leading centers of cancer research and treatment. It is the only center ranked in the top 4 of U.S. News and World Report’s Best Hospitals for both adult and pediatric cancer care. Dana-Farber sits at the center of a wide range of collaborative efforts to reduce the burden of cancer through scientific inquiry, clinical care, education, community engagement, and advocacy. Dana-Farber/Brigham and Women’s Cancer Center provides the latest in cancer care for adults; Dana-Farber/Boston Children's Cancer and Blood Disorders Center for children. The Dana-Farber/Harvard Cancer Center unites the cancer research efforts of five Harvard academic medical centers and two graduate schools, while Dana-Farber Community Cancer Care provides high quality cancer treatment in communities outside Boston’s Longwood Medical Area. Dana-Farber is dedicated to a unique 50/50 balance between cancer research and care, and much of the Institute’s work is dedicated to translating the results of its discovery into new treatments for patients in Boston, and around the world.

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