Vinblastine, bleomycin, and methotrexate: an effective adjuvant in favorable Hodgkin's disease.

Sixty-seven patients with favorable pathologic stage (PS) I and IIA or B or IIIA Hodgkin's disease were randomized to receive subtotal or total lymphoid irradiation (STLI/TLI) alone or involved field irradiation (IF) plus six cycles of a novel adjuvant chemotherapy containing vinblastine, bleomycin, and methotrexate (VBM). With a follow-up from 6 to 72 months (median, 37 months), the actuarial freedom-from-progressive disease (FFP) at 5 years is 70% after STLI/TLI and 95% after IF plus VBM. One death has occurred in the irradiation-only treatment group. The data for IF plus VBM are significantly superior to previous actuarial results at 5 years using IF alone (FFP = 35%, P less than .00001) and compare favorably with prior results with IF plus nitrogen mustard, vincristine, procarbazine, +/- prednisone (MOP[P]) chemotherapy (FFP = 80% at 5 years, P = .10). VBM is well tolerated with greater than 90% of calculated doses delivered. As anticipated, VBM has had relatively little adverse effect on male or female fertility. Selected pulmonary functions are reduced early after IF plus VBM to a greater degree than with irradiation of the mediastinum alone, but the differences are modest. Based upon our current numbers and follow-up, we can be 90% confident that VBM as an adjuvant to irradiation in favorable Hodgkin's disease is as effective, or even superior, to MOP(P) chemotherapy. Because of its lesser toxicity, adjuvant VBM may have a broader role in the management of Hodgkin's disease.

[1]  T. Raffin,et al.  Minimal long-term cardiopulmonary dysfunction following treatment for Hodgkin's disease. , 1987, International journal of radiation oncology, biology, physics.

[2]  A. Santoro,et al.  Second acute leukemia and other malignancies following treatment for Hodgkin's disease. , 1986, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[3]  R. Hoppe,et al.  Recovery of spermatogenesis following pelvic irradiation for Hodgkin's disease. , 1986, International journal of radiation oncology, biology, physics.

[4]  A. Santoro,et al.  Gonadal toxicity after combination chemotherapy for Hodgkin's disease. Comparative results of MOPP vs ABVD. , 1985, European journal of cancer & clinical oncology.

[5]  F. Greco,et al.  Lung cancer in Hodgkin's disease: association with previous radiotherapy. , 1985, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[6]  H. Kaplan,et al.  The evolution and summary results of the Stanford randomized clinical trials of the management of Hodgkin's disease: 1962-1984. , 1984, International journal of radiation oncology, biology, physics.

[7]  R. Makuch,et al.  Second malignant neoplasms complicating Hodgkin's disease: the National Cancer Institute experience. , 1984, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[8]  J. Hainsworth,et al.  Testicular function following combination chemotherapy with cis-platin, vinblastine, and bleomycin. , 1984, Medical and pediatric oncology.

[9]  D. Rosenthal,et al.  Pulmonary complications associated with combination chemotherapy programs containing bleomycin. , 1983, The American journal of medicine.

[10]  L. Einhorn,et al.  Fertility after chemotherapy for testicular cancer. , 1983, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[11]  M. Jochelson,et al.  Pulmonary complications of chemotherapy regimens containing bleomycin. , 1982, AJR. American journal of roentgenology.

[12]  C. Coleman Leukemias, non-Hodgkin's lymphomas and solid tumors in patients treated for Hodgkin's disease , 1982 .

[13]  S. Horning,et al.  Female Reproductive Potential after Treatment for Hodgkin's Disease , 1981, The New England journal of medicine.

[14]  R. Hoppe,et al.  Prognostic factors in pathological stage IIIA Hodgkin's disease , 1980, Cancer.

[15]  M. Tubiana,et al.  Long-term results of the E.O.R.T.C. randomized study of irradiation and vinblastine in clinical stages I and II of Hodgkin's disease. , 1979, European journal of cancer.

[16]  C. Edwards,et al.  CYCLICAL COMBINATION CHEMOTHERAPY AND GONADAL FUNCTION Retrospective Study in Males , 1979, The Lancet.

[17]  A. el-Beheiry,et al.  Methotrexate and fertility in men. , 1979, Archives of andrology.

[18]  E. Glatstein,et al.  Initial relapses in previously treated Hodgkin's disease. I. Results of second treatment , 1976, Cancer.

[19]  D. Johnson,et al.  Large-dose bleomycin therapy and pulmonary toxicity. A possible role of prior radiotherapy. , 1976, JAMA.

[20]  R. Adamson,et al.  Toxicity of antineoplastic agents in man, chromosomal aberrations antifertility effects, congenital malformations, and carcinogenic potential. , 1975, Advances in cancer research.

[21]  G. Bonadonna,et al.  Clinical, radiologic, and histopathologic studies on pulmonary toxicity induced by treatment with bleomycin (NSC-125066). , 1972, Cancer chemotherapy reports.

[22]  H. Kaplan,et al.  Oophoropexy: a means of preserving ovarian function following pelvic megavoltage radiotherapy for Hodgkin's disease. , 1970, Radiology.

[23]  E. Frei,et al.  Intensive combination chemotherapy and X-irradiation in Hodgkin's disease. , 2016, Cancer research.

[24]  E. Gehan A GENERALIZED WILCOXON TEST FOR COMPARING ARBITRARILY SINGLY-CENSORED SAMPLES. , 1965, Biometrika.

[25]  D. Rall,et al.  Clinical studies of dichloromethotrexate (NSC 29630) , 1965, Clinical pharmacology and therapeutics.

[26]  E. Kaplan,et al.  Nonparametric Estimation from Incomplete Observations , 1958 .

[27]  C. P. Rhoads,et al.  The effects of the folic acid antagonists and 2,6‐diaminopurine on neoplastic disease. With special reference to acute leukemia , 1951, Cancer.