Make your appointment or second opinion with Dana-Farber today to meet with an onsite specialist.

Adult Patients:877-442-3324

Pediatric Patients:888-733-4662

Make Appointment OnlineInternational Patients

Online second opinions

Can’t get to Boston? Explore our Online Second Opinion service to get expert advice from Dana-Farber oncologists.

Request a second opinion

Contact & Directions

Email Dana-Farber

Main Number617-632-3000

Toll-Free Number866-408-DFCI (3324)

Maps & DirectionsContact InformationSend us a Question or Comment

How to Help

Discover the ways to give and how to get involved to support Dana-Farber.

Learn More
Give now
  • Home
  • Newsroom
  • News Releases
  • Some head and neck cancer patients benefit from continued checkpoint inhibitor treatment after tumor growth

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

Robert Haddad, MD - largeRobert Haddad, MD

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.

8/22/2017 1:10:08 AM
  •   Email
  •   Print
  •   Share
  • Media Contacts

    • For all inquiries, call 617-632-4090 and ask to speak to a member of the media team. Please direct emails to
  • Make an Appointment

    • For adults:
      877-442-3324 (877-442-DFCI)

    • Quick access:
      Appointments as soon as the next day for new adult patients

    • For children:
      888-733-4662 (888-PEDI-ONC)

    • Make Appointment Online