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Correspondence

Long-Term Follow-up of Hodgkin's Disease Trial

N Engl J Med 2002; 346:1417-1418May 2, 2002

Article

To the Editor:

In 1992, we reported the results of the prospective, randomized Cancer and Leukemia Group B trial in patients with newly diagnosed, advanced-stage Hodgkin's disease. The study compared three regimens: MOPP (mechlorethamine, vincristine, procarbazine, and prednisone) for 6 to 8 months, the standard treatment at that time; ABVD, a nonalkylating-agent–containing regimen (doxorubicin, bleomycin, vinblastine, and dacarbazine) for 6 to 8 months; and MOPP alternating with ABVD for 12 months.1

Radiation therapy was not administered. ABVD therapy alone for 6 to 8 months resulted in a rate of failure-free survival similar to the rate with a 12-month regimen of MOPP alternating with ABVD, and better than the rate with MOPP alone. ABVD also was not associated with an increased risk of leukemia or a loss of fertility, recognized side effects of alkylating agents contained in the MOPP regimen. These findings led to the widespread use of ABVD as therapy for advanced Hodgkin's disease. The regimen has also been used in early-stage disease with or without radiation therapy.2

We report the results of long-term follow-up of patients enrolled in that study. At a median follow-up of 14.1 years, we tested for equality of the failure-free and overall survival distributions in the three treatment groups using the Cox proportional-hazards model. We found a significant difference in the failure-free survival distributions (score test, P=0.03) but not in the overall survival distributions (score test, P=0.35). Patients who were randomly assigned to ABVD have continued to have a higher rate of failure-free survival than those treated with MOPP alone and a similar rate of failure-free survival to those treated with MOPP alternating with ABVD (Figure 1AFigure 1Failure-free Survival (Panel A) and Overall Survival (Panel B) According to Initial Treatment.). Overall survival is not significantly different among the groups, reflecting the ability of salvage therapy to prolong survival or to cure the disease (Figure 1B).

George P. Canellos, M.D.
Dana–Farber Cancer Institute, Boston, MA 02115

Donna Niedzwiecki, Ph.D.
Duke University Medical Center, Durham, NC 27710

2 References
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