Evaluation of the efficacy of the VEEP regimen in adult Hodgkin's disease with assessment of gonadal and cardiac toxicity.

PURPOSE The aim of this phase II study was to investigate the potential of the vincristine, epirubicin, etoposide, and prednisolone (VEEP) regimen to reduce the risks of long-term sequelae of chemotherapy such as sterility, cardiopulmonary damage, and second malignancies, while maintaining efficacy in terms of response and survival. PATIENTS AND METHODS Eighty-five adult patients with newly diagnosed and previously untreated stage II to IV Hodgkin's disease (HD) were entered and monitored for a minimum of 1 year. Patients were treated to maximum response plus two further courses, and if they had not attained a complete response (CR) or CR-unconfirmed/uncertain [CR(u)] were changed to second-line chemotherapy. Adjuvant radiotherapy was administered to patients with bulky disease and those with postchemotherapy residual masses. Measurements of left ventricular ejection fraction (LVEF), gonadotropins in females, and sperm count in males were taken both before and after treatment with VEEP. RESULTS The maximum rates of response were as follows: CR, 32%; CR(u), 47%; and PR, 21% [CR + CR(u), 79%]. The median follow-up duration is 45 months, with a 5-year overall survival (OS) rate of 89% and failure-free survival (FFS) rate of 62%. Patients in CR at the end of chemotherapy had a higher FFS at 5 years compared with patients in CR(u) (88% v 56%). Acute toxicity was mild, with no pulmonary toxicity or treatment-related deaths. The median LVEF was 62% before VEEP and 57% after VEEP. Gonadal function tests following treatment were normal in 92% of males and 100% of females. No second malignancies have been observed. CONCLUSION VEEP is an active combination with tolerable acute toxicity that preserves fertility and cardiopulmonary function. The efficacy of VEEP is comparable to that of established regimens, but a definitive evaluation of its potential to reduce second malignancies will require a longer follow-up duration.

[1]  M. Williams,et al.  Efficacy and toxicity of vinblastine, bleomycin, and methotrexate with involved-field radiotherapy in clinical stage IA and IIA Hodgkin's disease: a British National Lymphoma Investigation pilot study. , 1994, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[2]  A. Hagenbeek,et al.  Second cancer risk following Hodgkin's disease: a 20-year follow-up study. , 1994, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[3]  S. Rosenberg,et al.  The treatment of Hodgkin's disease. , 1966, The Medical clinics of North America.

[4]  A. Hagenbeek,et al.  Clinical staging versus laparotomy and combined modality with MOPP versus ABVD in early-stage Hodgkin's disease: the H6 twin randomized trials from the European Organization for Research and Treatment of Cancer Lymphoma Cooperative Group. , 1993, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[5]  T. Hickish,et al.  Role of magnetic resonance imaging in predicting relapse in residual masses after treatment of lymphoma. , 1993, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[6]  L. Kumar Epipodophyllotoxins and secondary leukaemia , 1993, The Lancet.

[7]  R. Demicheli,et al.  Drugs ten years later: epirubicin. , 1993, Annals of oncology : official journal of the European Society for Medical Oncology.

[8]  N R Schneider,et al.  Secondary acute myeloid leukemia in children with acute lymphoblastic leukemia treated with etoposide. , 1993, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[9]  S. Zimmerman,et al.  Hodgkin's disease: study of treatment intensities and incidences of second malignancies. , 1993, Annals of oncology : official journal of the European Society for Medical Oncology.

[10]  S. Kvaløy,et al.  Second malignancies after treatment of Hodgkin's disease: the influence of treatment, follow-up time, and age. , 1993, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[11]  G. Bonadonna,et al.  Hodgkin's disease and second malignancies. , 1993, Annals of Oncology.

[12]  D. Longo Editorial is anything better than MOPP? , 1993 .

[13]  K. Propert,et al.  Chemotherapy of advanced Hodgkin's disease with MOPP, ABVD, or MOPP alternating with ABVD. , 1992, The New England journal of medicine.

[14]  H. Kreisman,et al.  Pulmonary toxicity of antineoplastic therapy. , 1992, Seminars in oncology.

[15]  O. Dapunt,et al.  Secondary leukaemias after etoposide , 1992, The Lancet.

[16]  K. Maclennan,et al.  LOPP alternating with EVAP is superior to LOPP alone in the initial treatment of advanced Hodgkin's disease: results of a British National Lymphoma Investigation trial. , 1992, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[17]  K. Maclennan,et al.  Risk of second primary cancers after Hodgkin's disease by type of treatment: analysis of 2846 patients in the British National Lymphoma Investigation. , 1992, BMJ.

[18]  G. Bonadonna,et al.  ABVD in the treatment of Hodgkin's disease. , 1992, Seminars in oncology.

[19]  M. Ro̸rth,et al.  Increased risk of myelodysplasia and leukaemia after etoposide, cisplatin, and bleomycin for germ-cell tumours , 1991, The Lancet.

[20]  C. Gisselbrecht,et al.  Cardiopulmonary toxicity after three courses of ABVD and mediastinal irradiation in favorable Hodgkin's disease. , 1991, Annals of oncology : official journal of the European Society for Medical Oncology.

[21]  M. Gore,et al.  Ch1vpp Combination Chemotherapy for Hodgkin's Disease: Long Term Results , 2022 .

[22]  M Tubiana,et al.  Report of a committee convened to discuss the evaluation and staging of patients with Hodgkin's disease: Cotswolds meeting. , 1989, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[23]  J. Caillaud,et al.  Male gonadal function after chemotherapy for solid tumors in childhood. , 1989, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[24]  D Crowther,et al.  The significance of residual mediastinal abnormality on the chest radiograph following treatment for Hodgkin's disease. , 1988, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[25]  M. Tucker,et al.  Risk of second cancers after treatment for Hodgkin's disease. , 1988, The New England journal of medicine.

[26]  M. Ratain,et al.  Acute nonlymphocytic leukemia following etoposide and cisplatin combination chemotherapy for advanced non-small-cell carcinoma of the lung. , 1987, Blood.

[27]  B. Hancock Randomised study of MOPP (mustine, Oncovin, procarbazine, prednisone) against LOPP (Leukeran substituted for mustine) in advanced Hodgkin's disease. British National Lymphoma Investigation. , 1986, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[28]  G. Rosner,et al.  BCVPP chemotherapy for advanced Hodgkin's disease: evidence for greater duration of complete remission, greater survival, and less toxicity than with a MOPP regimen. Results of the Eastern Cooperative Oncology Group study. , 1984, Annals of internal medicine.

[29]  A. Barrett,et al.  Five years' experience with ChlVPP: effective low-toxicity combination chemotherapy for Hodgkin's disease. , 1982, British Journal of Cancer.

[30]  D. Crowther,et al.  The effects of Hodgkin's disease and combination chemotherapy on gonadal function in the adult male , 1982, Cancer.

[31]  T. Lister,et al.  MVPP chemotherapy regimen for advanced Hodgkin's disease , 1978, British medical journal.

[32]  G. Bonadonna,et al.  Combination chemotherapy of Hodgkin's disease with adriamycin, bleomycin, vinblastine, and imidazole carboxamide versus MOPP , 1975, Cancer.

[33]  M. A. Douglas,et al.  High temporal resolution ECG-gated scintigraphic angiocardiography. , 1975, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[34]  V. Devita,et al.  Combination chemotherapy in the treatment of advanced Hodgkin's disease. , 1970, Annals of internal medicine.

[35]  H. Kaplan,et al.  The treatment of Hodgkin's disease. , 1994, Annals of oncology : official journal of the European Society for Medical Oncology.

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