History & Overview Annual Report President's Pages Center News Community Affairs
Make a Gift Cycle for Survival Fred's Team Rock & Run on the River Yankees Universe Fund Thomas Blake Sr. Memorial Research Fund Donating Blood & Platelets Volunteering Thrift Shop Park Avenue Potluck Cookbook
Press Releases In the News Information for Journalists News@MSKCC
Manhattan New Jersey Long Island Westchester
Working at Memorial Sloan-Kettering Work Sites College Recruitment About Nursing Job Fairs & Career Days Job Search & Apply Online
Making an Appointment

A Study of Ofatumumab plus DHAP Chemotherapy in Relapsed or Refractory Aggressive Lymphoma

[Protocol 09-082]


Full Title :
A SINGLE ARM, SAFETY AND EFFICACY STUDY OF OFATUMUMAB IN COMBINATION WITH ICE OR DHAP CHEMOTHERAPY IN RELAPSED OR REFRACTORY AGGRESSIVE LYMPHOMA PRIOR TO AUTOLOGOUS STEM CELL TRANSPLANTATION
Purpose :

The purpose of this study is to evaluate the safety and effectiveness of an investigational drug called ofatumumab when given with chemotherapy in patients with diffuse large B-cell lymphoma or transformed follicular lymphoma that persists or relapses despite prior chemotherapy.

Ofatumumab is an antibody that binds to lymphoma cells and results in lymphoma cell death. Patients in this study will receive ofatumumab plus DHAP (dexamethasone, cytarabine, and cisplatin) chemotherapy. The study will evaluate the effectiveness of this combination therapy both for treating lymphoma and for enabling patients to receive additional treatment with autologous stem cell transplantation.

Eligibility :

To be eligible for this study, patients must meet several criteria, including but not limited to the following:

  • Patients must have CD20-positive diffuse large B-cell lymphoma or transformed follicular lymphoma that persists despite prior chemotherapy which included rituximab and an anthracycline drug.
  • At least 4 weeks must have passed since completion of prior therapy and entry into the study.
  • Patients must be eligible for transplantation.
  • Patients must not be confined to a bed or chair for more than half of their normal waking hours.
  • Patients must be age 18 or older

For more information and to inquire about eligibility for this study, please contact Dr. Matthew Matasar at 212-639-8889.

Bookmark and SharePrintEmail This Page