Literature DB >> 6722721

Treatment of advanced non-Hodgkin's lymphoma with vincristine infusion.

D V Jackson, E H Paschold, C L Spurr, H B Muss, F Richards, M R Cooper, D R White, J J Stuart, J O Hopkins, R Rich.   

Abstract

Twenty-five patients with a variety of histologic types of advanced non-Hodgkin's lymphoma refractory to previous chemotherapy were entered into a trial of vincristine infusion. Patients received 5-day courses of vincristine 0.25 mg/m2/day by continuous intravenous infusion after an initial 0.5 mg intravenous bolus injection. Courses were repeated every 3 weeks. Objective responses were observed in nine patients (36%), all of whom had previously received vincristine given by conventional bolus injection. A complete response occurred in a patient with diffuse mixed histiocytic lymphocytic lymphoma, and partial responses were observed in eight patients with the following histologic types: diffuse poorly differentiated lymphocytic (4); nodular poorly differentiated lymphocytic (2); diffuse mixed histiocytic lymphocytic (1); and diffuse histiocytic (1). Duration of response lasted from 1.2 to 16.2 months (mean, 4.4 months). The principal complication of therapy was mild-to-moderate neurotoxicity; this occurred in 12 patients (48%) who received a total of 54 courses of vincristine infusion. Hematologic toxicity was minimal and nausea/vomiting did not occur. Vincristine infusion may afford palliation for patients with advanced non-Hodgkin's lymphomas who have become refractory to standard chemotherapeutic regimens even if they have received prior vincristine by conventional bolus injection. These data suggest the possibility of enhancing the therapeutic efficacy of vincristine in the treatment of non-Hodgkin's lymphoma by use of an infusion technique.

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Year:  1984        PMID: 6722721     DOI: 10.1002/1097-0142(19840615)53:12<2601::aid-cncr2820531205>3.0.co;2-d

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


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3.  Hepatic intra-arterial infusion of vincristine.

Authors:  D V Jackson; F Richards; C L Spurr; T R Long; D A Rardin; D A Albertson; J M Sterchi
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4.  Continuous vincristine infusion as part of a high dose chemoradiotherapy regimen: drug kinetics and toxicity.

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Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

5.  Identification of vesicle properties that enhance the antitumour activity of liposomal vincristine against murine L1210 leukemia.

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6.  Phase I study of 21 days continuous infusion with vindesine.

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  6 in total

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