cris.boxmetadata.label.title
Intermittent continuous iv infusion of high-dose cyclophosphamide for remission induction in acute lymphocytic leukemia
cris.boxmetadata.label.dateissued
29 browse.startsWith.months.august 1981
cris.boxmetadata.label.accesslevel
metadata only access
cris.boxmetadata.label.resourcetype
journal article
cris.boxmetadata.label.publisher
U.S. National Cancer Institute
cris.boxmetadata.label.abstract
Cyclophosphamide was administered to 42 patients with acute lymphocytic leukemia (ALL) as a daily continuous iv infusion at a dose of 400 mg/m 2/day x 5 days; the courses of treatment were repeated every 3 weeks. Of the 42 patients entered, 21 achieved a complete response, 2 achieved a partial response, 12 failed to respond, and 7 were considered to have early deaths. The response rate was 69.5% if only patients who received adequate trials are considered; mean duration of response was 18.5 weeks and mean survival time was 24.2 weeks. Twenty-three patients had relapsed after previous chemotherapy, and 19 patients were untreated for advanced high-risk cases of ALL; no difference was found in the response rates, durations of response, and survival times between these groups. No significant genitourinary toxicity occurred. Myelosuppression became the dose-limiting toxic effect. Continuous infusion of cyclophosphamide is a clinically effective method of ALL treatment and may have a role in the initial combination regimens for this hematologic malignancy.
cris.boxmetadata.label.citationstartpage
213
cris.boxmetadata.label.citationendpage
218
cris.boxmetadata.label.volume
65
cris.boxmetadata.label.issue
browse.startsWith.months.april 3
cris.boxmetadata.label.language
English
cris.boxmetadata.label.ocdeknowledgeArea
Hematología Oncología
cris.boxmetadata.label.scopusidentifier
2-s2.0-0019412545
cris.boxmetadata.label.pubmedidentifier
cris.boxmetadata.label.source
Cancer Treatment Reports
cris.boxmetadata.label.containerissn
03615960
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