Dosimetric parameters correlate with duodenal histopathologic damage after stereotactic body radiotherapy for pancreatic cancer: Secondary analysis of a prospective clinical trial. Issue 3 (March 2017)

• Record Type: Journal Article
• Authors: Verma, Vivek; Lazenby, Audrey J.; Zheng, Dandan; Bhirud, Abhijeet R.; Ly, Quan P.; Are, Chandrakanth; Sasson, Aaron R.; Lin, Chi
• Is Part Of: Radiotherapy and oncology. Volume 122:Issue 3(2017:Mar.)
• Page Start: 464
• Page End: 469
• Publication Date: 2017-03
• Subjects: Pancreatic cancer -- Stereotactic body radiotherapy -- Duodenum -- Toxicity; Oncology -- Periodicals; Radiotherapy -- Periodicals; Tumors -- Periodicals; Medical Oncology -- Periodicals; Neoplasms -- radiotherapy -- Periodicals; Radiotherapy -- Periodicals; Radiothérapie -- Périodiques; Cancérologie -- Périodiques; Tumeurs -- Périodiques; Electronic journals; 616.9940642
• DOI: 10.1016/j.radonc.2016.12.030
• Languages: English
• ISSNs: 0167-8140

Abstract

Abstract: Purpose: Prospectively assess relationships between dosimetric parameters and histopathologic/clinical duodenal toxicities in patients on a phase I trial for pancreatic cancer. Methods: Forty-six borderline resectable/unresectable patients were enrolled on a prospective trial testing neoadjuvant gemcitabine/5-fluorouracil followed by SBRT (5 daily fractions of 5–8 Gy) and concurrent nelfinavir. Post-SBRT surgery was performed in 13 resectable patients, which constituted the patient population herein. Pathologic duodenal damage was assessed using predetermined criteria: 1, no/minimal; 2, moderate; and 3, marked damage. Clinical toxicities were assessed per the Clinical Terminology Criteria for Adverse Events (CTCAE). Duodenal dosimetric parameters included V5–V40 and mean/maximum doses. Spearman correlation and linear regression evaluated associations between dosimetric parameters and clinical/pathologic duodenal toxicity. Results: The median duodenal mean and maximum doses were 20 and 37 Gy. Median duodenal V5–V40 were 64, 62, 52, 39, 27, 14, 5 and 0 cc, respectively. The median duodenal damage score was 2 (four 1, eight 2, and one 3). Higher duodenal damage scores correlated with higher duodenal mean doses ( r = 0.75, p = 0.003), V35 ( r = 0.61, p = 0.03), V30 ( r = 0.67, p = 0.01), V25 ( r = 0.68, p = 0.01), V20 ( r = 0.56, p = 0.05), and the planning target volume (PTV) mean ( r = 0.59, p = 0.03) and maximum ( r = 0.61, p = 0.03) doses. Clinical toxicities did not correlate with dosimetric parameters or duodenal pathologic damage. Conclusions: Duodenal histologic damage correlates with mean duodenal dose, V20-V35, and PTV mean/maximum doses.