Published August 1, 2012 | Version v1
Journal article

High-dose Helical Tomotherapy With Concurrent Full-dose Chemotherapy for Locally Advanced Pancreatic Cancer

  • 1. Department of Radiation Oncology, Yonsei University College of Medicine, Seoul (Korea, Republic of)
  • 2. Department of Radiation Oncology, National Cancer Centre (Singapore)
  • 3. Department of Internal Medicine, Yonsei University College of Medicine, Seoul (Korea, Republic of)

Description

Purpose: To improve poor therapeutic outcome of current practice of chemoradiotherapy (CRT), high-dose helical tomotherapy (HT) with concurrent full-dose chemotherapy has been performed on patients with locally advanced pancreatic cancer (LAPC), and the results were analyzed. Methods and Materials: We retrospectively reviewed 39 patients with LAPC treated with radiotherapy using HT (median, 58.4 Gy; range, 50.8–59.9 Gy) and concomitant chemotherapy between 2006 and 2009. Radiotherapy was directed to the primary tumor with a 0.5-cm margin without prophylactic nodal coverage. Twenty-nine patients (79%) received full-dose (1000 mg/m2) gemcitabine-based chemotherapy during HT. After completion of CRT, maintenance chemotherapy was administered to 37 patients (95%). Results: The median follow-up was 15.5 months (range, 3.4–43.9) for the entire cohort, and 22.5 months (range, 12.0–43.9) for the surviving patients. The 1- and 2-year local progression-free survival rates were 82.1% and 77.3%, respectively. Eight patients (21%) were converted to resectable status, including 1 with a pathological complete response. The median overall survival and progression-free survival were 21.2 and 14.0 months, respectively. Acute toxicities were acceptable with no gastrointestinal (GI) toxicity higher than Grade 3. Severe late GI toxicity (≥Grade 3) occurred in 10 patients (26%); 1 treatment-related death from GI bleeding was observed. Conclusion: High-dose helical tomotherapy with concurrent full-dose chemotherapy resulted in improved local control and long-term survival in patients with LAPC. Future studies are needed to widen the therapeutic window by minimizing late GI toxicity.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2011.10.050

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2011.10.050;
PII
S0360-3016(11)03458-4;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
83
Journal Issue
5
Journal Page Range
p. 1448-1454
ISSN
0360-3016
CODEN
IOBPD3

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.