Literature DB >> 7397630

A new effective four-drug combination of CCNU (1-[2-chloroethyl]-3-cyclohexyl-1-nitrosourea) (NSC-79038), vinblastine, prednisone, and procarbazine for the treatment of advanced Hodgkin's disease.

M R Cooper, T F Pajak, N I Nissen, L Stutzman, K Brunner, J Cuttner, G Falkson, H Grunwald, A Bank, L Leone, B R Seligman, R T Silver, R B Weiss, F Haurani, J Blom, C L Spurr, O J Glidewell, A J Gottlieb, J F Holland.   

Abstract

Five hundred and sixty-six patients with either Stage III or IV Hodgkin's disease were prospectively randomized to test whether CCNU and/or vinblastine are more effective than mechlorethamine and/or vincristine with procarbazine and prednisone. The combination of CCNU, vinblastine, procarbazine, and prednisone (CVPP) was shown to be a highly effective program with a complete response frequency of 69%. The use of CCNU as part of the induction program was also shown to be the most significant determinant of prolonged remissions (P = .025). Reduced vomiting and neurotoxicity, as well as the oral administration, were the chief advantages of the CVPP as compared with MOPP. These factors resulted in improved patient and physician compliance. The MVPP regimen was also shown to be a highly effective regimen with a complete response frequency of 73% in patients without prior exposure to chemotherapy. However, the induction regimens containing vinblastine were associated with a significantly higher frequency of fatal hematopoietic toxicities than the induction regimens containing vincristine (P = .05). This higher frequency was almost exclusively seen in the elderly or in patients previously treated with both chemotherapy and radiotherapy. At this time, the remission durations maintained by vinblastine with periodic reinforcement are longer when compared with vinblastine maintenance alone (P = .06), but there is no corresponding increase in survival.

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Year:  1980        PMID: 7397630     DOI: 10.1002/1097-0142(19800815)46:4<654::aid-cncr2820460405>3.0.co;2-a

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  7 in total

1.  Prognostic value of response after three MOPP cycles in Hodgkin's disease--stage III and IV.

Authors:  M Monconduit; H Tilly; J F Menard; R Le Fur; A Barbot; H Piguet
Journal:  Blut       Date:  1987-03

Review 2.  Current management of Hodgkin's disease.

Authors:  B C Behrens; R C Young; V T DeVita
Journal:  Drugs       Date:  1985-10       Impact factor: 9.546

3.  VIM-D salvage chemotherapy in Hodgkin's disease.

Authors:  J K Phillips; R L Spearing; J M Davies; C R Hay; H Parry; J R Nash; J C Cawley
Journal:  Cancer Chemother Pharmacol       Date:  1990       Impact factor: 3.333

4.  [Stage IIIB and IVB Hodgkin's disease. Response to chemotherapy, relapses, survival rates (author's transl)].

Authors:  R Kuse; A Calavrezos; A Hinrichs; K Hausmann
Journal:  Klin Wochenschr       Date:  1981-07-01

5.  Prognostic factors in COPP-treated patients with Hodgkin's disease.

Authors:  W Gassmann; L Perenyi; N Schmitz; W Kayser; H Pralle; H Löffler
Journal:  Blut       Date:  1982-06

6.  CCNU in combination chemotherapy for advanced histologically unfavorable non-Hodgkin's lymphoma.

Authors:  D V Jackson; H B Muss; F Richards; D R White; C L Spurr; M R Cooper; R M Christian; T F Trahey; L D Case; H B Wells
Journal:  Cancer Chemother Pharmacol       Date:  1983       Impact factor: 3.333

7.  The cyclophosphamide equivalent dose as an approach for quantifying alkylating agent exposure: a report from the Childhood Cancer Survivor Study.

Authors:  Daniel M Green; Vikki G Nolan; Pamela J Goodman; John A Whitton; DeoKumar Srivastava; Wendy M Leisenring; Joseph P Neglia; Charles A Sklar; Sue C Kaste; Melissa M Hudson; Lisa R Diller; Marilyn Stovall; Sarah S Donaldson; Leslie L Robison
Journal:  Pediatr Blood Cancer       Date:  2013-08-12       Impact factor: 3.167

  7 in total

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