CLINICAL TOXICITIES AND DOSIMETRIC PARAMETERS AFTER WHOLE-PELVIS VERSUS PROSTATE-ONLY INTENSITY-MODULATED RADIATION THERAPY FOR PROSTATE CANCER

被引:32
作者
Deville, Curtiland [1 ]
Both, Stefan [1 ]
Hwang, Wei-Ting [2 ]
Tochner, Zelig [1 ]
Vapiwala, Neha [1 ]
机构
[1] Hosp Univ Penn, Dept Radiat Oncol, Philadelphia, PA 19104 USA
[2] Hosp Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2010年 / 78卷 / 03期
关键词
Pelvic nodal irradiation; Whole pelvis; IMRT; Toxicity; Prostate cancer; PHASE-III TRIAL; EXTERNAL-BEAM RADIOTHERAPY; DOSE-VOLUME CONSTRAINTS; LATE RECTAL TOXICITY; ANDROGEN SUPPRESSION; GASTROINTESTINAL TOXICITY; CONFORMAL RADIOTHERAPY; ONCOLOGY GROUP-9413; RANDOMIZED-TRIAL; NEOADJUVANT;
D O I
10.1016/j.ijrobp.2009.08.043
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess whether whole-pelvis (WP) intensity-modulated radiation therapy (IMRT) is associated with increased toxicity compared with prostate-only (PO) IMRT. Methods and Materials: We retrospectively analyzed all patients with prostate cancer undergoing definitive IMRT to 79.2 Gy with concurrent androgen deprivation at our institution from November 2005 to May 2007 with a minimum follow-up of 12 months. Thirty patients received initial WP IMRT to 45 Gy in 1.8-Gy fractions, and thirty patients received PO IMRT. Study patients underwent computed tomography simulation and treatment planning by use of predefined dose constraints. Bladder and rectal dose volume histograms, maximum genitourinary (GU) and gastrointestinal (GI) Radiation Therapy Oncology Group toxicity grade, and late Grade 2 or greater toxicity-free survival curves were compared between the two groups by use of the Student t test, Fisher exact test, and Kaplan-Meier curve, respectively. Results: Bladder minimum dose, mean dose, median dose, volume receiving 5 Gy, volume receiving 20 Gy, volume receiving 40 Gy, and volume receiving 45 Gy and rectal minimum dose, median dose, and volume receiving 20 Gy were significantly increased in the WP group (all p values < 0.01). Maximum acute GI toxicity was limited to Grade 2 and was significantly increased in the WP group at 50% vs. 13% the PO group (p = 0.006). With a median follow-up of 24 months (range, 12-35 months), there was no difference in late GI toxicity (p = 0.884) or in acute or late GU toxicity. Conclusions: Despite dosimetric differences in the volume of bowel, bladder, and rectum irradiated in the low-dose and median-dose regions, WP IMRT results only in a clinically significant increase in acute GI toxicity, in comparison to PO IMRT, with no difference in GU or late GI toxicity. (C) 2010 Elsevier Inc.
引用
收藏
页码:763 / 772
页数:10
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