STEREOTACTIC BODY RADIOTHERAPY AND GEMCITABINE FOR LOCALLY ADVANCED PANCREATIC CANCER

被引:175
作者
Mahadevan, Anand [1 ]
Jain, Sanjay [2 ]
Goldstein, Michael [2 ]
Miksad, Rebecca [2 ]
Pleskow, Douglas [3 ]
Sawhney, Mandeep [3 ]
Brennan, Darren [4 ]
Callery, Mark [5 ]
Vollmer, Charles [5 ]
机构
[1] Beth Israel Deaconess Med Ctr, Dept Radiat Oncol, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Dept Med Oncol, Boston, MA 02215 USA
[3] Beth Israel Deaconess Med Ctr, Dept Gastroenterol, Boston, MA 02215 USA
[4] Beth Israel Deaconess Med Ctr, Dept Intervent Radiol, Boston, MA 02215 USA
[5] Beth Israel Deaconess Med Ctr, Dept Surg, Boston, MA 02215 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2010年 / 78卷 / 03期
基金
美国国家卫生研究院;
关键词
Hypofractionated stereotactic body radiotherapy; Locally advanced pancreatic cancer; Gemcitabine; Chemotherapy; PHASE-II TRIAL; RADIATION-THERAPY; 5-FLUOROURACIL; CONCURRENT; ADENOCARCINOMA; LIVER; CHEMOTHERAPY; INFUSION; GERCOR; CHEMORADIOTHERAPY;
D O I
10.1016/j.ijrobp.2009.08.046
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Patients with nonmetastatic locally advanced unresectable pancreatic cancer have a dismal prognosis. Conventional concurrent chemoradiotherapy requires 6 weeks of daily treatment and can be arduous. We explored the safety and effectiveness of a 3-day course of hypofractionated stereotactic body radiotherapy (SBRT) followed by gemcitabine in this population. Patients and Methods: A total of 36 patients with nonmetastatic, locally advanced, unresectable pancreatic cancer with >= 12 months of follow-up were included. They received three fractions of 8, 10, or 12 Gy (total dose, 24-36 Gy) of SBRT according to the tumor location in relation to the stomach and duodenum, using fiducial-based respiratory motion tracking on a robotic radiosurgery system. The patients were then offered gemcitabine for 6 months or until tolerance or disease progression. Results: With an overall median follow-up of 24 months (range, 12-33), the local control rate was 78%, the median overall survival time was 14.3 months, the median carbohydrate antigen 19-9-determined progression-free survival time was 7.9 months, and the median computed tomography-determined progression-free survival time was 9.6 months. Of the 36 patients, 28 (78%) eventually developed distant metastases. Six patients (17%) were free of progression at the last follow-up visit (range, 13-30 months) as determined by normalized tumor markers with stable computed tomography findings. Nine Grade 2 (25%) and five Grade 3 (14%) toxicities attributable to SBRT occurred. Conclusion: Hypofractionated SBRT can be delivered quickly and effectively in patients with nonmetastatic, locally advanced, unresectable pancreatic cancer with acceptable side effects and minimal interference with gemcitabine chemotherapy. (C) 2010 Elsevier Inc.
引用
收藏
页码:735 / 742
页数:8
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