Intensive chemotherapy for adult acute lymphoblastic leukaemia given with or without granulocyte-macrophage colony stimulating factor |
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Authors: | D. Papamichael T. Andrews D. Owen M. Carter J. Amess T. A. Lister A. Z. Rohatiner |
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Affiliation: | (1) ICRF Department of Medical Oncology, St. Bartholomew's Hospital, West Smithfield, London EC1A 7BE, England, GB;(2) Department of Haematology, St. Bartholomew's Hospital, London, England, GB |
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Abstract: | ![]() Twenty-six patients with newly diagnosed ALL (age range 15–49 years, median 32 years) received treatment comprising: cycles 1 and 2: adriamycin 30 mg/m2 days 1–3, vincristine: 2 mg days 1, 8, and 15, with prednisolone 40 mg daily, given until complete remission (CR). l-asparaginase 10000 units/m2, days 1–14, was given only with the first cycle. Cycle 3 consisted of 100 mg/m2 etoposide orally, days 1–5, and 1 gm/m2 bd cytosine arabinoside (ara-C) days 1–5. Cycles 1–3 were then repeated. Intrathecal methotrexate (MTX) 12.5 mg was given on day 1 of each treatment cycle. The first 12 consecutive patients received this chemotherapy alone, the subsequent 14 received, in addition, 3 μg/kg GM-CSF subcutaneously, from day 4 of cycles 1, 2, 4, and 5 (and from day 6 of cycles 3 and 6) until the absolute neutrophil count had reached 0.5×109/l. All patients in whom CR was achieved then received prophylactic cranial irradiation. With the exception of those with T-ALL, this was followed by oral maintenance therapy consisting of 6-mercaptopurine, MTX, and cyclophosphamide for 3 years. Patients receiving GM-CSF did not have shorter intercycle times or a lower incidence of documented infections than those who did not receive it. The CR rate was 89% overall - uninfluenced by GM-CSF, but higher than that achieved previously at St Bartholomew's Hospital in an equivalent age-group. Received: 15 April 1996 / Accepted: 2 September 1996 |
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Keywords: | ALL Intensive chemotherapy GM-CSF |
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