Journal of Clinical Oncology, Vol 14, 1297-1305, Copyright © 1996 by American Society of Clinical Oncology
Effect of ABVD chemotherapy with and without mantle or mediastinal irradiation on pulmonary function and symptoms in early-stage Hodgkin's disease
A Hirsch, N Vander Els, DJ Straus, EG Gomez, D Leung, CS Portlock and J Yahalom
Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY,USA.
PURPOSE: To evaluate the effect of doxorubicin, bleomycin, vinblastine, and
dacarbazine (ABVD) chemotherapy alone and of ABVD with mantle or
mediastinal irradiation (RT) on the pulmonary function of patients with
early-stage Hodgkin's disease. PATIENTS AND METHODS: Between 1989 and 1993,
60 patients with clinical stage I to IIIA HD enrolled onto randomized
trials at Memorial Sloan-Kettering Cancer Center (MSKCC) underwent
prospective evaluation of pulmonary function. All patients received six
cycles of ABVD, and 30 patients received mantle or mediastinal RT.
Pulmonary function tests (PFTs) and symptom evaluation were conducted
before, during, and after completion of chemotherapy and RT, and at various
intervals thereafter. The median follow-up time was 30 months. RESULTS:
During chemotherapy, symptoms of cough and dyspnea on exertion developed in
32 of 60 patients (53%) and declines in pulmonary function occurred in 22
of 60 patients (37%). Discontinuation of bleomycin was necessary in 14 of
60 patients (23%). Following chemotherapy, there was a significant decline
in median forced vital capacity (FVC) and diffusing capacity of carbon
monoxide (DLCO). In patients who received mantle or mediastinal RT, there
was a further decline in FVC following radiation therapy. At the most
recent follow- up evaluation, five of 29 patients (18%) who received ABVD
alone and nine of 30 (30%) who received ABVD and RT reported persistent
mild pulmonary symptoms (P = .36), which did not significantly affect
normal daily activity. CONCLUSION: ABVD chemotherapy induced acute
pulmonary toxicity that required bleomycin dose modification in a
substantial number of patients. The addition of RT resulted in a further
decrease in FVC; however, this did not significantly affect the functional
status of patients.

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