Literature DB >> 3477315

Therapy of lymphoid and undifferentiated chronic myelogenous leukemia in blast crisis with continuous vincristine and adriamycin infusions plus high-dose decadron.

R S Walters1, H M Kantarjian, M J Keating, M Talpaz, C C Childs, K B McCredie, E J Freireich.   

Abstract

Thirty patients with Philadelphia chromosome-positive lymphoid (20 patients) or undifferentiated (ten patients) chronic myelogenous leukemia in blast crisis were treated with 0.4 mg of vincristine by continuous intravenous infusion (CIV) daily for 4 days; (doxorubicin) 12 mg/m2 of Adriamycin (Adria Laboratories, Columbus, OH) by continuous intravenous infusion daily for 4 days; and 40 mg of decadron daily on days 1 through 4, 9 through 12, and 17 through 20 (VAD). Course 2 was given starting on day 24 with the addition of cyclophosphamide 1 g/22. Overall nine patients achieved complete remission (30%) and three attained a partial remission (10%), for an overall response rate of 40%. Four patients expired during induction whereas 14 had resistant disease. Response rate was significantly higher for patients with lymphoid compared to undifferentiated morphology (55% versus 10%; P = 0.05). In lymphoid blast crisis, Calla-positive disease was associated with a higher response rate compared to Calla-negative disease (75% versus 25%; P = 0.08). Eleven patients developed infections, and seven had fever without documented infections. The median overall survival was 29 weeks. Median survival was 43 weeks for patients achieving complete remission and 20 weeks for those with resistant disease. Remission duration was 39 weeks. After primary and salvage therapy, nine patients are alive, six of them in continuous remission for 19+ to 112+ weeks. The authors conclude that VAD chemotherapy is an effective regimen with acceptable toxicity in patients with lymphoid blast crisis especially those with Calla-positive disease. Alternate induction regimens for undifferentiated disease and for maintenance therapy are currently being investigated.

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Year:  1987        PMID: 3477315     DOI: 10.1002/1097-0142(19871015)60:8<1708::aid-cncr2820600803>3.0.co;2-1

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


  3 in total

1.  Improved survival in chronic myeloid leukemia since the introduction of imatinib therapy: a single-institution historical experience.

Authors:  Hagop Kantarjian; Susan O'Brien; Elias Jabbour; Guillermo Garcia-Manero; Alfonso Quintas-Cardama; Jenny Shan; Mary Beth Rios; Farhad Ravandi; Stefan Faderl; Tapan Kadia; Gautam Borthakur; Xuelin Huang; Richard Champlin; Moshe Talpaz; Jorge Cortes
Journal:  Blood       Date:  2012-01-06       Impact factor: 22.113

2.  Non-aggressive therapy for chronic myeloid leukaemia in blastic transformation.

Authors:  R Liang; T K Chan; E Chiu; D Todd
Journal:  Cancer Chemother Pharmacol       Date:  1992       Impact factor: 3.333

3.  Prognostic discrimination for early chronic phase chronic myeloid leukemia in imatinib era: comparison of Sokal, Euro, and EUTOS scores in Korean population.

Authors:  Seung-Ah Yahng; Eun-Jung Jang; Soo-Young Choi; Sung-Eun Lee; Soo-Hyun Kim; Dong-Wook Kim
Journal:  Int J Hematol       Date:  2014-05-31       Impact factor: 2.490

  3 in total

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