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

被引:26
作者
Gobbi, PG
Pieresca, C
Frassoldati, A
Carotenuto, M
DiRenzo, N
LaSala, A
Berte, R
Avanzini, P
Federico, M
Silingardi, V
Ascari, E
机构
[1] UNIV MODENA, CATTEDRA ONCOL, I-41100 MODENA, ITALY
[2] IST RICOVERO & CURA CARRATTERE SCI CASA SOLLIEVO, FOGGIA, ITALY
[3] OSPED S MARIA NUOVA, DIV MED 1, REGGIO EMILIA, ITALY
关键词
D O I
10.1200/JCO.1996.14.2.527
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (C) 1996 by American Society of Clinical Oncology.
引用
收藏
页码:527 / 533
页数:7
相关论文
共 23 条
[1]  
ARMITAGE P, 1987, STATISTICAL METHODS, P296
[2]   EFFICACY AND TOXICITY OF VINBLASTINE, BLEOMYCIN, AND METHOTREXATE WITH INVOLVED-FIELD RADIOTHERAPY IN CLINICAL STAGE IA AND IIA HODGKINS-DISEASE - A BRITISH NATIONAL LYMPHOMA INVESTIGATION PILOT-STUDY [J].
BOTES, NP ;
WILLIAMS, MV ;
BESSELL, EM ;
HUDSON, GV ;
HUDSON, BV .
JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (02) :288-296
[3]  
CARBONE PP, 1968, CANCER RES, V28, P811
[4]  
Comis R L, 1992, Semin Oncol, V19, P64
[5]  
DEVITA VT, 1987, CANCER RES, V47, P5810
[6]  
ECKHARDT S, 1974, 1 LINFORMI MALIGNI, P377
[7]  
GOBBI PG, 1994, HAEMATOLOGICA, V79, P241
[8]  
HENRYAMAR M, 1990, COLLOQ INSE, V196, P355
[9]  
HORNING S J, 1986, Proceedings American Society of Clinical Oncology Annual Meeting, V5, P198
[10]   VINBLASTINE, BLEOMYCIN, AND METHOTREXATE - AN EFFECTIVE ADJUVANT IN FAVORABLE HODGKINS-DISEASE [J].
HORNING, SJ ;
HOPPE, RT ;
HANCOCK, SL ;
ROSENBERG, SA .
JOURNAL OF CLINICAL ONCOLOGY, 1988, 6 (12) :1822-1831