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Cyclophosphamide, doxorubicin, vincristine, and low‐dose continuous infusion bleomycin in non‐Hodgkin's lymphoma: Cancer and leukemia group B study #7804
Author(s) -
Ginsberg Sandra J.,
Crooke Stanley T.,
Bloomfield Clara D.,
Peterson Bruce,
Kennedy B. J.,
Blom Johannes,
Ellison Rose Ruth,
Pajak Thomas F.,
Gottlieb Arlan J.
Publication year - 1982
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(19820401)49:7<1346::aid-cncr2820490706>3.0.co;2-#
Subject(s) - medicine , bleomycin , vincristine , cyclophosphamide , pulmonary toxicity , chemotherapy , doxorubicin , bolus (digestion) , vinblastine , lymphoma , prednisone , gastroenterology , toxicity , pharmacology
Fifty‐eight evaluable patients with non‐Hodgkin's lymphoma were treated with a low dose, 120‐hour continuous intravenous infusion of bleomycin in combination with cyclophosphamide, doxorubicin, vincristine, and prednisone. Pharmacokinetic data, obtained in six patients, confirm that steady‐state plasma concentrations of bleomycin can be attained even with the administration of 2 units/day of the drug. Neither clinical pulmonary toxicity nor subclinical pulmonary changes, as determined by serial measurement of the single breath carbon monoxide‐diffusing capacity, were observed. Compared to similar chemotherapeutic programs utilizing bolus administration of bleomycin, pulmonary toxicity may be reduced. Response frequencies among 37 previously untreated patients were similar to those obtained using the same chemotherapeutic agents but with intravenous bolus administration of bleomycin. In addition, 18 of 21 patients who had received prior chemotherapy responded. Low dose, continuous intravenous infusion of bleomycin may improve the therapeutic index of combination chemotherapy programs for non‐Hodgkin's lymphoma.