Purpose: To ascertain whether vinblastine, bleomycin, and methotrexate (VBM) (CT) combined with extended-field radiotherapy (EF RT) is effective enough to spare laparotomy in early, favorably presenting Hodgkin´s disease (HD) patients. Patients and Methods: Fifty patients with clinical stage IA or IIAHD with favorable or masses entered a prospective multicenter study started in January 1988. The median follow-vp time was 38 months. Results: All patients achieved a complete remission (CR). Five relapsed after 3 to 40 months and underwent successful salvage 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 toxicity, the other of a second neoplasia (adenocarcinoma of the lung), 2 and 43 months after the end of therapy, respectively. The hematologic toxicity recorded during VBM CT was mild on the whole, Major toxicity was represented by pulmonary side effects and neurologic symptoms. Multiple regression analysis demonstrated that pulmonary toxicity was significantly 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 statistical technique showed that the only clinical factor related to grade of neurotoxicity was vinblastine dosage. Conclusion: VBM CT combined with EF RT is an effective treatment early, clinically staged, favorable HD patients, However, the toxicity of this combination suggests that certain modifications should be evaluated.
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|Data di pubblicazione:||1996|
|Titolo:||Vinblastine, bleomycin, and methotrexate chemotherapy plus extended-field radiotherapy in early, favorably presenting, clinically staged Hodgkin's patients: The Gruppo Italiano per lo Studio dei Linfomi Experience|
|Autori:||PG Gobbi; C. Pieresca; A. Frassoldati; M. Carotenuto; N. DiRenzo; A. LaSala; R. Berte; P. Avanzini; M. Federico; E. Ascari; V. Silingardi|
|Autori interni:||FEDERICO, Massimo |
|Digital Object Identifier (DOI):||10.1200/jco.19126.96.36.1997|
|Rivista:||JOURNAL OF CLINICAL ONCOLOGY|
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