Incidence of late rectal and urinary toxicities after three-dimensional conformal radiotherapy and intensity-modulated radiotherapy for localized prostate cancer

被引:585
作者
Zelefsky, Michael J. [1 ]
Levin, Emily J. [1 ]
Hunt, Margie [2 ]
Yamada, Yoshiya [1 ]
Shippy, Alison M. [1 ]
Jackson, Andrew [2 ]
Amols, Howard I. [2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Med Phys, New York, NY 10065 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2008年 / 70卷 / 04期
关键词
prostate cancer; radiotherapy; toxicity; IMRT; dose escalation;
D O I
10.1016/j.ijrobp.2007.11.044
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To report the incidence and predictors of treatment-related toxicity at 10 years after three-dimensional conformal radiotherapy (3D-CRT) and intensity-modulated radiotherapy (IMRT) for localized prostate cancer. Methods and Materials: Between 1988 and 2000,1571 patients with stages T1 - T3 prostate cancer were treated with 3D-CRT/IMRT with doses ranging from 66 to 81 Gy. The median follow-up was 10 years. Posttreatment toxicities were all graded according to the National Cancer Institute's Common Terminology Criteria for Adverse Events. Results: The actuarial likelihood at 10 years for the development of Grade >= 2 GI toxicities was 9%. The use of IMRT significantly reduced the risk of gastrointestinal (GI) toxicities compared with patients treated with conventional 3D-CRT (13% to 5%; p < 0.001). Among patients who experienced acute symptoms the 10-year incidence of late toxicity was 42%, compared with 9% for those who did not experience acute symptoms (p < 0.0001). The 10-year incidence of late Grade >= 2 genitourinary (GU) toxicity was 15%. Patients treated with 81 Gy (IMRT) had a 20% incidence of GU symptoms at 10 years, compared with a 12% for patient treated to lower doses (p=0.01). Among patients who had developed acute symptoms during treatment, the incidence of late toxicity at 10 years was 35%, compared with 12% (p < 0.001). The incidence of Grade 3 GI and GU toxicities was 1% and 3%, respectively. Conclusions: Serious late toxicity was unusual despite the delivery of high radiation dose levels in these patients. Higher doses were associated with increased GI and GU Grade 2 toxicities, but the risk of proctitis was significantly reduced with IMRT. Acute symptoms were a precursor of late toxicities in these patients. (c) 2008 Elsevier Inc.
引用
收藏
页码:1124 / 1129
页数:6
相关论文
共 21 条
[1]   Planning, delivery, and quality assurance of intensity-modulated radiotherapy using dynamic multileaf collimator: A strategy for large-scale implementation for the treatment of carcinoma of the prostate [J].
Burman, C ;
Chui, CS ;
Kutcher, G ;
Leibel, S ;
Zelefsky, M ;
LoSasso, T ;
Spirou, S ;
Wu, QW ;
Yang, J ;
Stein, J ;
Mohan, R ;
Fuks, Z ;
Ling, CC .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1997, 39 (04) :863-873
[2]   Escalated-dose versus standard-dose conformal radiotherapy in prostate cancer: first results from the MRC RT01 randomised controlled trial [J].
Dearnaley, David P. ;
Sydes, Matthew R. ;
Graham, John D. ;
Aird, Edwin G. ;
Bottomley, David ;
Cowan, Richard A. ;
Huddart, Robert A. ;
Jose, Chakiath C. ;
Matthews, John H. L. ;
Millar, Jeremy ;
Moore, A. Rollo ;
Morgan, Rachel C. ;
Russell, J. Martin ;
Scrase, Christopher D. ;
Stephens, Richard J. ;
Syndikus, Isabel ;
Parmar, Mahesh K. B. .
LANCET ONCOLOGY, 2007, 8 (06) :475-487
[3]  
DENHAM JW, 1995, RADIOTHER ONCOL, V32, P643
[4]   Late normal tissue sequelae in the second decade after high dose radiation therapy with combined photons and conformal protons for locally advanced prostate cancer [J].
Gardner, BG ;
Zietman, AL ;
Shipley, WU ;
Skowronski, UE ;
McManus, P .
JOURNAL OF UROLOGY, 2002, 167 (01) :123-126
[5]   Dose escalation with 3D conformal treatment: Five year outcomes, treatment optimization, and future directions [J].
Hanks, GE ;
Hanlon, AL ;
Schultheiss, TE ;
Pinover, WH ;
Movsas, B ;
Epstein, BE ;
Hunt, MA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1998, 41 (03) :501-510
[6]   Gastrointestinal toxicity and its relation to dose distributions in the anorectal region of prostate cancer patients treated with radiotherapy [J].
Heemsbergen, WD ;
Hoogeman, MS ;
Hart, GAM ;
Lebesque, JV ;
Koper, PCM .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2005, 61 (04) :1011-1018
[7]   Acute and late gastrointestinal toxicity after radiotherapy in prostate cancer patients: Consequential late damage [J].
Heemsbergen, Wilma D. ;
Peeters, Stephanie T. H. ;
Koper, Peter C. M. ;
Hoogeman, Mischa S. ;
Lebesque, Joos V. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 66 (01) :3-10
[8]   The relationship of increasing radiotherapy dose to reduced distant metastases and mortality in men with prostate cancer [J].
Jacob, R ;
Hanlon, AL ;
Horwitz, EM ;
Movsas, B ;
Uzzo, RG ;
Pollack, A .
CANCER, 2004, 100 (03) :538-543
[9]   Acute symptoms, not rectally administered sucralfate, predict for late radiation proctitis: Longer term follow-up of a phase III Trial-Trans-Tasman Radiation Oncology Group [J].
O'Brien, PC ;
Franklin, CI ;
Poulsen, MG ;
Joseph, DJ ;
Spry, NS ;
Denham, JW .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2002, 54 (02) :442-449
[10]   Dose-response in radiotherapy for localized prostate cancer: Results of the Dutch multicenter randomized phase III trial comparing 68 Gy of radiotherapy with 78 Gy [J].
Peeters, STH ;
Heemsbergen, WD ;
Koper, PCM ;
van Putten, WLJ ;
Slot, A ;
Dielwart, MFH ;
Bonfrer, JMG ;
Incrocci, L ;
Lebesque, AV .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (13) :1990-1996