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Abstract
August 01, 1992

Combined modality therapy of rectal cancer: decreased acute toxicity with the preoperative approach.

Publication: Journal of Clinical Oncology

Abstract

Purpose

We compared the combined radiation therapy (RT) plus chemotherapy segments of two separate parallel phase I trials to determine if combined pelvic RT, fluorouracil (5-FU), and high-dose leucovorin (LV) had less acute toxicity when delivered preoperatively versus postoperatively in patients with rectal cancer.

Patients and Methods

Patients with unresectable disease received preoperative RT plus LV and 5-FU followed by surgery and postoperative LV and 5-FU. Patients with resectable disease received identical doses, techniques, and schedules of RT and LV and 5-FU except all therapy was delivered postoperatively. On day 1, patients received LV and 5-FU times one cycle. RT began on day 8. A second cycle of LV and 5-FU was given concurrently with the fourth week of RT.

Results

Although more patients (75% v 32%; P = .02) received the higher dose level of 5-FU (250 mg/m2), significantly fewer experienced acute grade 3 to 4 toxicity with preoperative versus postoperative therapy (13% v 48%; P = .045). There was no grade 3 to 4 myelosuppression in either group. The two grade 3 toxicities in the preoperative group were gastrointestinal. The grade 3 toxicities in the postoperative group included seven gastrointestinal and two genitourinary; four patients had a grade 4 toxicity.

Conclusion

Given the high incidence of grade 3 to 4 toxicity also reported in the postoperative combined modality adjuvant randomized trials, future adjuvant trials should explore the preoperative approach.

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Information

Published In

Journal of Clinical Oncology
Pages: 1218 - 1224
PubMed: 1634912

History

Published in print: August 01, 1992
Published online: September 21, 2016

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Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021.

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B D Minsky, A M Cohen, N Kemeny, W E Enker, D P Kelsen, B Reichman, L Saltz, E R Sigurdson, J Frankel
Journal of Clinical Oncology 1992 10:8, 1218-1224

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