About this item:

702 Views | 0 Downloads

Author Notes:

Correspondence to: William A. Hall, MD. 1365 Clifton Rd. NE, Atlanta, GA 30322, USA. Email: whall4@emory.edu.

The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

We would like to thank the American College of Surgeons Commission on Cancer for access to the data that enabled this analysis.

Disclosure: The authors declare no conflict of interest.

Subjects:

Research Funding:

Grant support: This work was supported in part by the National Center for Advancing Translational Sciences of the National Institutes of Health under Award Number UL1TR000454 and TL1TR000456.

Research reported in this publication was supported in part by the Biostatistics & Bioinformatics Shared Resource of Winship Cancer Institute of Emory University and NIH/NCI under award number P30CA138292.

Keywords:

  • Radiation dose escalation pancreatic cancer
  • radiation dose escalation in pancreatic adenocarcinoma (PAC)
  • unresectable pancreatic cancer
  • PAC and radiation therapy (RT)
  • RT dose in unresectable pancreatic cancer
  • PAC and intensity modulated radiation therapy (IMRT)
  • dose response pancreatic cancer

The influence of radiation therapy dose escalation on overall survival in unresectable pancreatic adenocarcinoma

Show all authors Show less authors

Tools:

Journal Title:

Journal of Gastrointestinal Oncology

Volume:

Volume 5, Number 2

Publisher:

, Pages 77-85

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Purpose Radiation therapy (RT) dose escalation in unresectable pancreatic adenocarcinoma (PAC) remains investigational. We examined the association between total RT dose and overall survival (OS) in patients with unresectable PAC. Methods and materials National cancer data base (NCDB) data were obtained for patients who underwent definitive chemotherapy and RT (chemo-RT) for unresectable PAC. Univariate (UV) and multivariate (MV) survival analysis were performed along with Kaplan-Meier (KM) estimates for incremental RT dose levels. Results A total of 977 analyzable patients met inclusion criteria. Median tumor size was 4.0 cm (0.3-40 cm) and median RT dose was 45 Gy. Median OS was 10 months (95% CI, 9-10 months). On MV analysis RT dose <30 Gy [HR, 2.38 (95% CI, 1.85-3.07); P<0.001] and RT dose ≥30 to <40 Gy [HR, 1.41 (95% CI, 1.04-1.91); P=0.026] were associated with lower OS when compared with dose ≥55 Gy. Patients receiving RT doses from 40 to <45, 45 to <50, 50 to <55, and ≥55 Gy did not differ in OS. Conclusions Lack of benefit to OS with conventionally delivered RT above 40 Gy is shown. Optimal RT dose escalation methods in unresectable PAC remain an important subject for investigation in prospective clinical trials.

Copyright information:

© 2014 Pioneer Bioscience Publishing Company. All rights reserved.

Export to EndNote