Phase I trial of outpatient weekly paclitaxel and concurrent radiation therapy for advanced non-small-cell lung cancer

H. Choy, W. Akerley, H. Safran, J. Clark, V. Rege, A. Papa, M. Glantz, Y. Puthawala, C. Soderberg, L. Leone

Research output: Contribution to journalArticle

123 Citations (Scopus)

Abstract

Purpose: To determine the maximum-tolerated dose (MTD) and dose-limiting toxicities of paclitaxel administered weekly on an outpatient basis with concurrent thoracic radiation to patients with advanced non-small-cell lung cancer (NSCLC). Patients and Methods: In this phase I clinical trial, paclitaxel was administered as a 3-hour intravenous (IV) infusion, repeated every week for 6 weeks. The starting dose of paclitaxel was 10 mg/m2. Doses were escalated at 10-mg/m2 increments in successive cohorts of three new patients if tolerated. Unacceptable toxicity was defined as grade 3 nonhematologic toxicity, excluding nausea and vomiting, and grade 4 hematologic toxicity according to Cancer and Leukemia Group B expanded common toxicity criteria. Radiation was administered to the primary tumor and regional lymph nodes (40 Gy) followed by a boost to the tumor (20 Gy). Results: Twenty-seven patients were entered onto this study through seven dose escalations (from 10 mg/m2/wk to 70 mg/m2/wk for 6 weeks). Severe esophagitis occurred at 70 mg/m2 (two patients with grade 4 disease and one patient with grade 2). One of six patients at 60 mg/m2 developed grade 3 esophagitis and three of seven patients had grade 2 esophagitis. One of 27 patients developed a hypersensitivity reaction. One of 27 patients developed grade 3 neutropenia. Conclusion: Esophagitis is the principle dose-limiting toxicity of weekly paclitaxel and thoracic radiation in the outpatient setting. A phase II trial using concurrent radiation and paclitaxel at the MTD of 60 mg/m2/wk is underway.

Original languageEnglish (US)
Pages (from-to)2682-2686
Number of pages5
JournalJournal of Clinical Oncology
Volume12
Issue number12
StatePublished - Dec 1994

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Paclitaxel
Non-Small Cell Lung Carcinoma
Outpatients
Radiotherapy
Esophagitis
Radiation
Maximum Tolerated Dose
Thorax
Neoplasms
Clinical Trials, Phase I
Neutropenia
Intravenous Infusions
Nausea
Vomiting
Hypersensitivity
Leukemia
Lymph Nodes

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Choy, H., Akerley, W., Safran, H., Clark, J., Rege, V., Papa, A., ... Leone, L. (1994). Phase I trial of outpatient weekly paclitaxel and concurrent radiation therapy for advanced non-small-cell lung cancer. Journal of Clinical Oncology, 12(12), 2682-2686.

Phase I trial of outpatient weekly paclitaxel and concurrent radiation therapy for advanced non-small-cell lung cancer. / Choy, H.; Akerley, W.; Safran, H.; Clark, J.; Rege, V.; Papa, A.; Glantz, M.; Puthawala, Y.; Soderberg, C.; Leone, L.

In: Journal of Clinical Oncology, Vol. 12, No. 12, 12.1994, p. 2682-2686.

Research output: Contribution to journalArticle

Choy, H, Akerley, W, Safran, H, Clark, J, Rege, V, Papa, A, Glantz, M, Puthawala, Y, Soderberg, C & Leone, L 1994, 'Phase I trial of outpatient weekly paclitaxel and concurrent radiation therapy for advanced non-small-cell lung cancer', Journal of Clinical Oncology, vol. 12, no. 12, pp. 2682-2686.
Choy, H. ; Akerley, W. ; Safran, H. ; Clark, J. ; Rege, V. ; Papa, A. ; Glantz, M. ; Puthawala, Y. ; Soderberg, C. ; Leone, L. / Phase I trial of outpatient weekly paclitaxel and concurrent radiation therapy for advanced non-small-cell lung cancer. In: Journal of Clinical Oncology. 1994 ; Vol. 12, No. 12. pp. 2682-2686.
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