Published April 1, 2008 | Version v1
Journal article

3D Radiotherapy Can Be Safely Combined With Sandwich Systemic Gemcitabine Chemotherapy in the Management of Pancreatic Cancer: Factors Influencing Outcome

  • 1. Department of Radiation Oncology, Sir Charles Gairdner Hospital, Nedlands, WA (Australia)
  • 2. Department of Radiation Oncology, Princess Alexandra Hospital, Woolloongabba, Queensland (Australia)
  • 3. Department of Radiation Oncology, Murray Valley Private Hospital, Wodonga, Victoria (Australia)
  • 4. Adelaide Radiotherapy Centre, Adelaide, SA (Australia)
  • 5. Division of Radiation Oncology, Peter MacCallum Cancer Centre, East Melbourne, Victoria (Australia)
  • 6. Department of Radiation Oncology, The Alfred, Prahran, Victoria (Australia)
  • 7. Department of Radiation Oncology, St. George Hospital, Kogarah, NSW (Australia)
  • 8. Department of Radiation Oncology, Royal Perth Hospital, Perth, WA (Australia)
  • 9. Cancer Therapy Centre, Liverpool Hospital, Liverpool, NSW (Australia)
  • 10. Department of Radiation Oncology, Prince of Wales Hospital, Randwick, NSW (Australia)
  • 11. Eli Lilly Australia, West Ryde, NSW (Australia)
  • 12. School of Surgery and Pathology, University of Western Australia, Nedlands, WA (Australia)
  • 13. Department of Medical Oncology, Prince of Wales Hospital, Randwick, NSW (Australia)

Description

Purpose: The aim of this Phase II study was to examine whether concurrent continuous infusion 5-fluorouracil (CI 5FU) plus three-dimensional conformal planning radiotherapy sandwiched between gemcitabine chemotherapy is effective, tolerable, and safe in the management of pancreatic cancer. Methods and Materials: Patients were enrolled in two strata: (1) resected pancreatic cancer at high risk of local relapse (postsurgery arm, n = 22) or (2) inoperable pancreatic cancer in head or body without metastases (locally advanced arm, n = 41). Gemcitabine was given at 1,000 mg/m2 weekly for 3 weeks followed by 1 week rest then 5-6 weeks of radiotherapy and concurrent CI 5FU (200 mg/m2/day). After 4 weeks' rest, gemcitabine treatment was reinitiated for 12 weeks. Results: For the two arms combined, treatment-related Grade 3 and 4 toxicities were reported by 25 (39.7%) and 7 (11.1%) patients, respectively. No significant late renal or hepatic toxicity was observed. In the postsurgery arm (R1 54.5%), median time to progressive disease from surgery was 11.0 months, median time to failure of local control was 32.9 months, and median survival time was 15.6 months. The 1- and 2-year survival rates were 63.6% and 31.8%. No significant associations between outcome and mutations in K-ras or TP53 or microsatellite instability were identified. Post hoc investigation of cancer antigen 19-9 levels found baseline levels and increases postbaseline were associated with shorter survival (p = 0.0061 and p < 0.0001, respectively). Conclusions: This three-dimensional chemoradiotherapy regimen is safe and promising, with encouraging local control for a substantial proportion of patients, and merits testing in a randomized trial

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2007.08.070

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2007.08.070;
PII
S0360-3016(07)04234-4;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
70
Journal Issue
5
Journal Page Range
p. 1438-1446
ISSN
0360-3016
CODEN
IOBPD3

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
40006854
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
CARCINOMAS; CHEMOTHERAPY; COMBINED THERAPY; KIDNEYS; LIVER; PANCREAS; RADIOTHERAPY
Descriptors DEC
BODY; DIGESTIVE SYSTEM; DISEASES; ENDOCRINE GLANDS; GLANDS; MEDICINE; NEOPLASMS; NUCLEAR MEDICINE; ORGANS; RADIOLOGY; THERAPY

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.