Hypofractionated Conformal Radiotherapy with Concurrent Full-Dose Gemcitabine Versus Standard Fractionation Radiotherapy with Concurrent Fluorouracil for Unresectable Pancreatic Cancer: a Multi-Institution Experience

被引:6
|
作者
Rakhra S. [1 ]
Strauss J.B. [1 ]
Robertson J. [2 ]
McGinn C.J. [3 ]
Kim T. [1 ]
Huang J. [2 ,4 ]
Blake A. [3 ]
Helenowski I. [5 ]
Hayes J.P. [1 ]
Mulcahy M. [6 ]
Small W., Jr. [7 ]
机构
[1] Department of Radiation Oncology, The Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL
[2] Department of Radiation Oncology, Beaumont Health System, Royal Oak, MI
[3] Department of Radiation Oncology, Maine Medical Center, Portland, ME
[4] Department of Radiation Oncology, Washington University School of Medicine, St. Louis, MO
[5] Northwestern University Cancer Biostatistics Core, Chicago, IL
[6] Division of Hematology/Oncology, The Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL
[7] Department of Radiation Oncology, Cardinal Bernardin Cancer Center, Stritch School of Medicine, Loyola University Chicago, 2160 S 1st Ave Maguire Center, Rm 2932, Maywood, 60153, IL
关键词
GEM/RT versus 5-FU/RT; Locally advanced pancreatic cancer;
D O I
10.1007/s12029-016-9821-9
中图分类号
学科分类号
摘要
Purpose/Objective(s): The purpose of this study was to compare oncologic outcomes and toxicity profile of hypofractionated conformal radiotherapy (RT) with concurrent full-dose gemcitabine versus standard fractionation RT with concurrent 5-fluorouracil (5-FU) in the treatment of unresectable non-metastatic pancreatic cancer. Materials/Methods: Patients with unresectable non-metastatic adenocarcinoma of the pancreas treated at three institutions were included. All patients were treated with chemoradiotherapy (CRT) consisting of either hypofractionated RT to the gross disease concurrent with a full-dose gemcitabine-based regimen versus standard fractionation RT to the tumor and elective nodes concurrent with 5-FU. End points included rates of gastrointestinal (GI) toxicities, overall survival (OS), and distant metastasis free survival (DMFS). Results: From January 1999 to December 2009, 170 patients were identified (118 RT/gemcitabine, 52 RT/5-FU). There were no differences in demographic or clinical factors. Acute GI toxicities (grades <3 versus ≥3) were 82.2 and 17.8 %, respectively, for patients treated with RT/gemcitabine and 78.9 and 21.2 % for those treated with RT/5-FU (p = 0.67). Late GI toxicities (grades <3 versus ≥3) were 88.1 and 11.9 %, respectively, for RT/gemcitabine and 80.8 and 19.2 % for RT/5-FU (p = 0.23). OS for RT/gemcitabine and RT/5-FU were 52 versus 36 % at 1 year and 14 versus 6 % at 2 years favoring the RT/gemcitabine group (p = 0.02). DMFS at 1 and 2 years for RT/gemcitabine were 41 and 11 % versus 24 and 4 % for RT/5-FU (p = 0.02). Conclusions: RT/gemcitabine was equivalent in toxicity to RT/5-FU but was associated with superior OS and DMFS. When RT is used in the treatment of unresectable pancreatic cancer, hypofractionated conformal RT with concurrent full-dose gemcitabine may be the preferred approach. © 2016, Springer Science+Business Media New York.
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页码:196 / 201
页数:5
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