A new approach to the treatment of advanced high-grade non-Hodgkin's lymphoma-intensive two-phase chemotherapy

A new approach to the treatment of advanced high-grade non-Hodgkin's lymphoma-intensive two-phase chemotherapy

A total of 110 patients with high-grade non-Hodgkin's lymphoma (NHL) not previously treated by chemotherapy or by radiotherapy at more than one site of disease underwent a regimen comprising an intensive 6-week initial, induction phase using vincristine, adriamycin, methotrexate, and prednisolo...

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Bibliographic Details
Published in:Cancer chemotherapy and pharmacology Vol. 22; no. 2; pp. 141 - 146
Main Authors: STUART, N. S. A, BLACKLEDGE, G. R. P, MACLENNAN, I. C. M, CULLEN, M. H, BARNARD, D. L, SIMMONS, A. V, CHILD, J. A, FLETCHER, J, PERREN, T. J, O'BRIEN, C. J, JONES, E. L, ELLIS, F. O, KAVANAGH, J. A, KELLY, K. A
Format: Journal Article
Language:English
Published: Berlin Springer 01-08-1988
Subjects:
Adolescent
Adult
Aged
Antineoplastic agents
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Chemotherapy
Cyclophosphamide - administration & dosage
Doxorubicin - administration & dosage
Epirubicin
Female
Humans
Lymphoma, Non-Hodgkin - drug therapy
Male
Medical sciences
Methotrexate - administration & dosage
Methylprednisolone
Middle Aged
Neutropenia - chemically induced
Pharmacology. Drug treatments
Procarbazine - administration & dosage
Vincristine - administration & dosage
Antineoplastic agent
Chemotherapy
Polychemotherapy
Sequential
Malignant lymphoma
Advanced stage
Malignant hemopathy
Non Hodgkin lymphoma
Therapeutic protocol
Prednisolone
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Summary:A total of 110 patients with high-grade non-Hodgkin's lymphoma (NHL) not previously treated by chemotherapy or by radiotherapy at more than one site of disease underwent a regimen comprising an intensive 6-week initial, induction phase using vincristine, adriamycin, methotrexate, and prednisolone (VAMP) followed by the non-cross-resistant combination cyclophosphamide, etoposide, and vindesine (EEE). The median age of patients was 54 years, the majority having stage IV disease. The median follow-up was 34 months and all patients have completed treatment. The overall complete remission (CR) rate for all patients was 68%. The initial phase of treatment produced a CR rate of 49%. The full regimen was completed by 87 patients, and of these, 66 (76%) achieved CR. Of those achieving CR, 72% were relapse-free, on an actuarial basis, at 2 years. Overall 2-year survival was 53%, with a median survival of 31 months. The survival of older patients and those with lymphoblastic histology was comparable to that of other groups. The survival prospects of patients with stage IV disease was not as good as that of other patients, with a significant trend to shorter survival in patients with more advanced disease. Toxicity was predictable and manageable for both phases of the regimen, although it was more severe for the initial phase. Dose-limiting toxicities were neutropenia and mucositis. This regimen is active in the treatment of advanced high-grade NHL with acceptable toxicity. These results have encouraged us to continue the study of weekly chemotherapy, which we will compare with standard cyclical chemotherapy in a prospective, randomized trial.
ISSN:0344-5704
1432-0843
DOI:10.1007/BF00257312