VINBLASTINE, BLEOMYCIN, AND METHOTREXATE CHEMOTHERAPY PLUS EXTENDED-FIELD RADIOTHERAPY IN EARLY, FAVORABLY PRESENTING, CLINICALLY STAGED HODGKINS PATIENTS - THE GRUPPO-ITALIANO-PER-LO-STUDIO-DEI-LINFOMI EXPERIENCE
Pg. Gobbi et al., VINBLASTINE, BLEOMYCIN, AND METHOTREXATE CHEMOTHERAPY PLUS EXTENDED-FIELD RADIOTHERAPY IN EARLY, FAVORABLY PRESENTING, CLINICALLY STAGED HODGKINS PATIENTS - THE GRUPPO-ITALIANO-PER-LO-STUDIO-DEI-LINFOMI EXPERIENCE, Journal of clinical oncology, 14(2), 1996, pp. 527-533
Purpose: To ascertain whether vinblastine, bleomycin, and methotrexate
(VBM) (CT) combined with extended-field radiotherapy (EF RT) is effec
tive enough to spare laparotomy in early, favorably presenting Hodgkin
's disease (HD) patients. Patients and Methods: Fifty patients with cl
inical stage IA or IIAHD with favorable or masses entered a prospectiv
e multicenter study started in January 1988. The median follow-vp time
was 38 months. Results: All patients achieved a complete remission (C
R). Five relapsed after 3 to 40 months and underwent successful salvag
e therapy. The actuarial remission rate wets 0.89% at 3 years and 0.82
% at 5 years. Two patients died in CR: one of severe pulmonary toxicit
y, the other of a second neoplasia (adenocarcinoma of the lung), 2 and
43 months after the end of therapy, respectively. The hematologic tox
icity recorded during VBM CT was mild on the whole, Major toxicity was
represented by pulmonary side effects and neurologic symptoms. Multip
le regression analysis demonstrated that pulmonary toxicity was signif
icantly related only to the amount of RT delivered to the mediastinum
and not to the relative dose of bleomycin, to the dose-intensities of
the three drugs in the regimen, or to patient age or sex, The same sta
tistical technique showed that the only clinical factor related to gra
de of neurotoxicity was vinblastine dosage. Conclusion: VBM CT combine
d with EF RT is an effective treatment early, clinically staged, favor
able HD patients, However, the toxicity of this combination suggests t
hat certain modifications should be evaluated. (C) 1996 by American So
ciety of Clinical Oncology.