Multiple-drug chemotherapy for acute leukemia.The TRAMPCOL regimen: Results in 86 patients
Autor: | JohnM. Goldman, Christine Costello, A.S.D. Spiers, David A. G. Galton, N. A. Buskard, Daniel Catovsky |
---|---|
Rok vydání: | 1977 |
Předmět: |
Cancer Research
medicine.medical_specialty Acute leukemia Vincristine Cyclophosphamide business.industry Myeloid leukemia medicine.disease Gastroenterology Surgery Leukemia Regimen Oncology hemic and lymphatic diseases Internal medicine Acute lymphocytic leukemia medicine Cytarabine business medicine.drug |
Zdroj: | Cancer. 40:20-29 |
ISSN: | 1097-0142 0008-543X |
DOI: | 10.1002/1097-0142(197707)40:1<20::aid-cncr2820400106>3.0.co;2-w |
Popis: | A combination of eight cytotoxic drugs, administered simultaneously, has been used in 86 cases of acute leukemia. The regimen, designated TRAMPCOL, incorporated thioguanine, rubidomycin, (daunorubicin), cytosine arabinoside, methotrexate, prednisolone, cyclophosphamide, vincristine, and usually L-asparaginase. Treatment was administered in five-day pulses with treatment-free intervals varying from nine to 23 days. Subjective and objective toxic effects were not more severe than those seen with two- and four-drug regimens previously employed. Substantial clinical and hematologic improvement occurred in 8/19 patients with chronic granulocytic leukemia (CGL) in acute transformation. Complete clinical and hematologic remission (CR) was achieved in 3/7 patients with untreated acute myeloid leukemia (AML), 5/19 patients with AML who had failed to achieve CR with other therapy, and 4/18 patients with AML in relapse after CR obtained with regimens other than TRAMPCOL. CR occurred in 15/17 patients with acute lymphocytic leukemia (ALL), most of whom had had multiple previous relapses. CR was not achieved in four patients with AML superimposed on pre-existing myeloproliferative disorders. The TRAMPCOL regimen merits further evaluation in CGL after acute transformation, as a primary treatment for AML, and as therapy for ALL 1) in relapse, 2) in adults, 3) in children with adverse prognostic features, and 4) in T-cell ALL. |
Databáze: | OpenAIRE |
Externí odkaz: |