Paclitaxel-Based Chemoradiotherapy in the Treatment of Patients With Operable Esophageal Cancer
Creators
- 1. Department of Radiation Oncology, Duke University Medical Center, Durham, NC (United States)
- 2. Department of Internal Medicine, Division of Medical Oncology and Transplantation, Duke University Medical Center, Durham, NC (United States)
- 3. Department of General Surgery, Duke University Medical Center, Durham, NC (United States)
Description
Purpose: To compare a neoadjuvant regimen of cisplatin/5-fluorouracil (5-FU) and concurrent radiation therapy (RT) with paclitaxel-based regimens and RT in the management of operable esophageal (EC)/gastroesophageal junction (GEJ) cancer. Methods and Materials: All patients receiving neoadjuvant chemotherapy (CT) and RT for EC/GEJ cancer at Duke University between January 1995 and December 2004 were included. Clinical end points were compared for patients receiving paclitaxel-based regimens (TAX) vs. alternative regimens (non-TAX). Local control (LC), disease-free survival (DFS), and overall survival (OS) were estimated using the Kaplan-Meier method. Chi-square analysis was performed to test the effect of TAX on pathologic complete response (pCR) rates and toxicity. Results: A total of 109 patients received CT-RT followed by esophagectomy (95 M; 14 F). Median RT dose was 45 Gy (range, 36-66 Gy). The TAX and non-TAX groups comprised 47% and 53% of patients, respectively. Most (83%) TAX patients received three drug regimens including platinum and a fluoropyrimidine. In the non-TAX group, 89% of the patients received cisplatin and 5-FU. The remainder received 5-FU or capecitabine alone. Grade 3-4 toxicity occurred in 41% of patients receiving TAX vs. 24% of those receiving non-TAX (p = 0.19). Overall pCR rate was 39% (39% with TAX vs. 40% with non-TAX, p = 0.9). Overall LC, DFS, and OS at 3 years were 80%, 34%, and 37%, respectively. At 3 years, there were no differences in LC (75% vs. 85%, p = 0.33) or OS (37% vs. 37%, p = 0.32) between TAX and non-TAX groups. Conclusions: In this large experience, paclitaxel-containing regimens did not improve pCR rates or clinical end points compared to non-paclitaxel-containing regimens
Availability note (English)
Available from http://dx.doi.org/10.1016/j.ijrobp.2007.03.035Additional details
Identifiers
- DOI
- 10.1016/j.ijrobp.2007.03.035;
- PII
- S0360-3016(07)00557-3;
Publishing Information
- Journal Title
- International Journal of Radiation Oncology, Biology and Physics
- Journal Volume
- 69
- Journal Issue
- 3
- Journal Page Range
- p. 770-776
- ISSN
- 0360-3016
- CODEN
- IOBPD3
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 39059580
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CHEMOTHERAPY; COMBINED THERAPY; DRUGS; NEOPLASMS; PATIENTS; PLATINUM; POLYMERASE CHAIN REACTION; RADIATION DOSES; RADIOTHERAPY; TOXICITY; URACILS
- Descriptors DEC
- AZINES; DISEASES; DOSES; ELEMENTS; GENE AMPLIFICATION; HETEROCYCLIC COMPOUNDS; HYDROXY COMPOUNDS; MEDICINE; METALS; NUCLEAR MEDICINE; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; PLATINUM METALS; PYRIMIDINES; RADIOLOGY; THERAPY; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2007 Elsevier Science B.V., Amsterdam, Netherlands, All rights reserved.