PMID- 18395362 OWN - NLM STAT- MEDLINE DCOM- 20081231 LR - 20221207 IS - 1879-355X (Electronic) IS - 0360-3016 (Linking) VI - 72 IP - 3 DP - 2008 Nov 1 TI - Gemcitabine chemotherapy and single-fraction stereotactic body radiotherapy for locally advanced pancreatic cancer. PG - 678-86 LID - 10.1016/j.ijrobp.2008.01.051 [doi] AB - PURPOSE: Fractionated radiotherapy and chemotherapy for locally advanced pancreatic cancer achieves only modest local control. This prospective trial evaluated the efficacy of a single fraction of 25 Gy stereotactic body radiotherapy (SBRT) delivered between Cycle 1 and 2 of gemcitabine chemotherapy. METHODS AND MATERIALS: A total of 16 patients with locally advanced, nonmetastatic, pancreatic adenocarcinoma received gemcitabine with SBRT delivered 2 weeks after completion of the first cycle. Gemcitabine was resumed 2 weeks after SBRT and was continued until progression or dose-limiting toxicity. The gross tumor volume, with a 2-3-mm margin, was treated in a single 25-Gy fraction by Cyberknife. Patients were evaluated at 4-6 weeks, 10-12 weeks, and every 3 months after SBRT. RESULTS: All 16 patients completed SBRT. A median of four cycles (range one to nine) of chemotherapy was delivered. Three patients (19%) developed local disease progression at 14, 16, and 21 months after SBRT. The median survival was 11.4 months, with 50% of patients alive at 1 year. Patients with normal carbohydrate antigen (CA)19-9 levels either at diagnosis or after Cyberknife SBRT had longer survival (p <0.01). Acute gastrointestinal toxicity was mild, with 2 cases of Grade 2 (13%) and 1 of Grade 3 (6%) toxicity. Late gastrointestinal toxicity was more common, with five ulcers (Grade 2), one duodenal stenosis (Grade 3), and one duodenal perforation (Grade 4). A trend toward increased duodenal volumes radiated was observed in those experiencing late effects (p = 0.13). CONCLUSION: SBRT with gemcitabine resulted in comparable survival to conventional chemoradiotherapy and good local control. However, the rate of duodenal ulcer development was significant. FAU - Schellenberg, Devin AU - Schellenberg D AD - Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, USA. FAU - Goodman, Karyn A AU - Goodman KA FAU - Lee, Florence AU - Lee F FAU - Chang, Stephanie AU - Chang S FAU - Kuo, Timothy AU - Kuo T FAU - Ford, James M AU - Ford JM FAU - Fisher, George A AU - Fisher GA FAU - Quon, Andrew AU - Quon A FAU - Desser, Terry S AU - Desser TS FAU - Norton, Jeffrey AU - Norton J FAU - Greco, Ralph AU - Greco R FAU - Yang, George P AU - Yang GP FAU - Koong, Albert C AU - Koong AC LA - eng PT - Clinical Trial, Phase II PT - Journal Article DEP - 20080418 PL - United States TA - Int J Radiat Oncol Biol Phys JT - International journal of radiation oncology, biology, physics JID - 7603616 RN - 0 (Antineoplastic Agents) RN - 0W860991D6 (Deoxycytidine) RN - 0 (Gemcitabine) SB - IM MH - Adenocarcinoma/diagnostic imaging/*drug therapy/mortality/radiotherapy/surgery MH - Aged MH - Aged, 80 and over MH - Antineoplastic Agents/*therapeutic use/toxicity MH - Combined Modality Therapy MH - Deoxycytidine/*analogs & derivatives/therapeutic use/toxicity MH - Disease Progression MH - Female MH - Gastrointestinal Diseases/chemically induced MH - Humans MH - Male MH - Middle Aged MH - Pancreatic Neoplasms/diagnostic imaging/*drug therapy/mortality/radiotherapy/surgery MH - Radiography MH - *Radiosurgery MH - Radiotherapy Dosage MH - Survival Analysis MH - Survivors MH - Gemcitabine EDAT- 2008/04/09 09:00 MHDA- 2009/01/01 09:00 CRDT- 2008/04/09 09:00 PHST- 2007/10/11 00:00 [received] PHST- 2007/12/12 00:00 [revised] PHST- 2008/01/21 00:00 [accepted] PHST- 2008/04/09 09:00 [pubmed] PHST- 2009/01/01 09:00 [medline] PHST- 2008/04/09 09:00 [entrez] AID - S0360-3016(08)00227-7 [pii] AID - 10.1016/j.ijrobp.2008.01.051 [doi] PST - ppublish SO - Int J Radiat Oncol Biol Phys. 2008 Nov 1;72(3):678-86. doi: 10.1016/j.ijrobp.2008.01.051. Epub 2008 Apr 18.