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Plasma camptothecin (NSC-100880) levels during a 5-day course of treatment: relation to dose and toxicity.

Creaven Pj, +2 more
- 01 Oct 1972 - 
- Vol. 56, Iss: 5, pp 573
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This article is published in Cancer chemotherapy reports.The article was published on 1972-10-01 and is currently open access. It has received 68 citations till now. The article focuses on the topics: Camptothecin & Toxicity.

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CPT-11: a new derivative of camptothecin for the treatment of refractory or relapsed small-cell lung cancer.

TL;DR: CPT-11 is an active agent against refractory or relapsed SCLC and deserves to be studied more closely as both a single agent and in combination with other drugs to treat patients with SclC.
Journal ArticleDOI

A phase II study of CPT-11, a new derivative of camptothecin, for previously untreated non-small-cell lung cancer.

TL;DR: CPT-11 is a very active agent for NSCLC with acceptable toxicities and further trials in combination with other agents for this disease are warranted.
Journal ArticleDOI

Phase I and pharmacologic study of topotecan: a novel topoisomerase I inhibitor.

TL;DR: Neutropenia is the dose-limiting toxicity, and 1.5 mg/m2 is the recommended starting dose of topotecan for both minimally and heavily pretreated patients in future phase II trials, with escalation to 2.0 mg/ m2 if treatment is well tolerated.
Journal ArticleDOI

Phase I and pharmacologic studies of the camptothecin analog irinotecan administered every 3 weeks in cancer patients.

TL;DR: The MTD of CPT-11 administered as a 30-minute IV infusion every 3 weeks is 600 mg/m2, with granulocytopenia being dose-limiting, and the activity of this agent in 5-FU-refractory colorectal carcinoma makes it unique and mandates expedited phase II testing.
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