ECOG: The Eastern Cooperative Oncology  Group

E1494 ECOG Trial Results Summary


Title
Study of Continuous Infusion, Combination Chemotherapy in Patients with HIV-Associated Non-Hodgkin’s Lymphoma (A Phase II Trial)

Sponsor
Eastern Cooperative Oncology Group through the NCI-sponsored Cancer Cooperative Group Program

Purpose of the Study
To determine the effectiveness of a chemotherapy infusion treatment using a combination of anti-cancer drugs: cyclophosphamide, doxorubicin, and etoposide (CDE) in patients with non-Hodgkin’s lymphoma associated with the human immunodeficiency virus (HIV). The study also evaluated survival rates and the side effects and infections that occurred after this treatment.

Results
Forty-six percent of patients had a complete response to treatment. Forty-nine percent were alive and 38 percent were alive without evidence of lymphoma at two years. During the course of the study in December 1996, highly active antiretroviral therapy (HAART) became standard treatment for patients with HIV infection. Patients treated after this time had improved survival, and were less likely to experience severe or life threatening complications associated with chemotherapy. The study showed that up to one-half of patients with HIV-associated lymphoma may be cured of the lymphoma with infusional chemotherapy. It also showed that the prognosis for HIV-associated lymphoma has significantly improved after HAART became commonly used for the management of HIV infection.

Conclusion
The study showed that up to one-half of patients with HIV-associated lymphoma may be cured of the lymphoma with infusional chemotherapy. It also showed that the prognosis for HIV-associated lymphoma has significantly improved after HAART became commonly used for the management of HIV infection. Additional studies are ongoing evaluating the role of infusional chemotherapy used alone or in conjunction with other lymphoma treatments, such as rituximab.

Start Date
January 1995

Stop Date
June 1999

Number of Participating Patients
113

Eligibility Requirements
Patients were at least 18 years old and had HIV-related non-Hodgkins lymphoma that could be measured or evaluated. They had no previous chemotherapy or radiation therapy and had received a protease inhibitor (which slows growth of virus cells) within one week of the trial. 1

Study Design
Patients received combination anti-cancer chemotherapy by continuous infusion into a blood vessel for four days, every four weeks for up to eight months. In order to give the chemotherapy in this manner, a tube was inserted into a blood vessel and the medication was delivered continuously over the four-day period. Patients also received antiviral medications to slow the growth of the HIV virus and other medications to prevent infections and other complications. Some patients also received additional chemotherapy and radiation therapy to treat or prevent lymphoma in the lining of the brain and in the spinal fluid.

Side Effects
The most frequent side effects were abnormalities in blood counts. Infections, including pneumonia, were experienced by 20 percent of participants, problems with metabolism (how the body processes chemicals to produce energy and support basic body functions) by 17 percent, liver problems and central nervous system problems (14 percent each) and mouth sores (11 percent). Five patients died as a result of complications related to treatment.

References
Sparano JA, Lee S, Chen MG, Nazeer T, Einzig AI, Ambinder RF, Henry DH, Manalo J, Li T, Von Roenn JH. Phase II Trial of Infusional Cyclophosphamide, Doxorubicin, and Etoposide in Patients with HIV-Associated Non-Hodgkin's Lymphoma: An Eastern Cooperative Oncology Group Trial (E1494). J Clin Oncol 2004 Apr 15;22(8):1491-1500. (E1494) [Manuscript published 4/15/2004]

National Cancer Institute Patient Summary
http://www.cancer.gov/clinical_trials/view_clinicaltrials.aspx?version=patient&cdrid=64791

Reviewed by
Joseph A. Sparano, MD, Montefiore Hospital and Medical Center; Sandra Horning, MD, Stanford Cancer Center; Robert Gray, PhD, ECOG Statistician; Cheryl K. Rutledge, BSN, Indiana University Cancer Center; Mike Katz, ECOG Patient Representative

Released February 16, 2005 (Revised July 18, 2006)

1   Source: NCI PDQ patient version (return)