Analysis of acute toxicity with use of transabdominal ultrasonography for prostate positioning during intensity-modulated radiotherapy

被引:10
作者
Jani, AB [1 ]
Gratzle, J [1 ]
Muresan, E [1 ]
Farrey, K [1 ]
Martel, MK [1 ]
机构
[1] Univ Chicago Hosp, Dept Radiat & Cellular Oncol, Chicago, IL 60637 USA
关键词
D O I
10.1016/j.urology.2004.09.062
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives. To analyze the effects of the B-mode ultrasound acquisition and targeting (BAT) system for positioning of patients with prostate cancer receiving intensity-modulated radiotherapy on acute gastrointestinal (GI) and genitourinary (GU) toxicity. Methods. The records of 50 consecutive patients treated using the BAT system were reviewed. Additionally, a comparison (no-BAT) group (ie, a group without a BAT study) treated in a similar manner was identified. The no-BAT group consisted of 49 patients treated immediately before the BAT group. For the two groups, the target definitions and dose prescriptions were identical, the treatment plan acceptance criteria were identical, and intensity-modulated radiotherapy was used for all patients. The daily BAT movements were charted in each of the three principal directions. Acute toxicity was scored for all patients according to the Radiation Therapy Oncology Group GI and GU acute toxicity scales. Results. The GU toxicity rates for the BAT versus no-BAT groups were grade 0 in 20% versus 14%; grade 1 in 38% versus 47%; grade 2 in 38% versus 39%; and grade 3 in 4% versus 0%, respectively (P = 0.284). The corresponding GI toxicity rates were grade 0 in 42% versus 27%; grade 1 in 28% versus 29%; and grade 2 in 30% versus 45% (P = 0.040). The incidence of GU and GI toxicity did not correlate with the directions or size of the BAT moves. Regression analysis revealed that for acute GI toxicity, the only variable reaching statistical significance was BAT use; no variable, including BAT use, reached statistical significance for acute GU toxicity. Conclusions. The use of the BAT system did not change the rate of acute GU toxicity but did reduce the rate of acute GI toxicity. (c) 2005 Elsevier Inc.
引用
收藏
页码:504 / 508
页数:5
相关论文
共 28 条
[1]   3D-ultrasound guided radiation therapy in the post-prostatectomy setting [J].
Chinnaiyan, P ;
Tomé, W ;
Patel, R ;
Chappell, R ;
Ritter, M .
TECHNOLOGY IN CANCER RESEARCH & TREATMENT, 2003, 2 (05) :455-458
[2]  
DAWSONSAUNDERS B, 1990, BASIC CLIN BIOSTATIS
[3]   Conformal radiotherapy for prostate cancer [J].
Hanks, GE .
ANNALS OF MEDICINE, 2000, 32 (01) :57-63
[4]   Intrafraction prostate motion during IMRT for prostate cancer [J].
Huang, E ;
Dong, L ;
Chandra, A ;
Kuban, DA ;
Rosen, II ;
Evans, A ;
Pollack, A .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2002, 53 (02) :261-268
[5]   Early prostate cancer: clinical decision-making [J].
Jani, AB ;
Hellman, S .
LANCET, 2003, 361 (9362) :1045-1053
[6]   Organ motion and IMRT in prostate cancer therapy [J].
Jani, AB .
CANCER JOURNAL, 2003, 9 (04) :244-246
[7]  
Jani Ashesh B, 2003, Clin Prostate Cancer, V2, P98, DOI 10.3816/CGC.2003.n.016
[8]   Cancer statistics, 2004 [J].
Jemal, A ;
Tiwari, RC ;
Murray, T ;
Ghafoor, A ;
Samuels, A ;
Ward, E ;
Feuer, EJ ;
Thun, MJ .
CA-A CANCER JOURNAL FOR CLINICIANS, 2004, 54 (01) :8-29
[9]  
Kupelian PA, 2001, CANCER J, V7, P421
[10]   Short-course intensity-modulated radiotherapy (70 GY at 2.5 GY per fraction) for localized prostate cancer: Preliminary results on late toxicity and quality of life [J].
Kupelian, PA ;
Reddy, CA ;
Klein, EA ;
Willoughby, TR .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2001, 51 (04) :988-993