Dosimetry and preliminary acute toxicity in the first 100 men treated for prostate cancer on a randomized hypofractionation dose escalation trial

被引:210
作者
Pollack, A
Hanlon, AL
Horwitz, EM
Feigenberg, SJ
Konski, AA
Movsas, B
Greenberg, RE
Uzzo, RG
Ma, CMC
McNeeley, SW
Buyyounouski, MK
Price, RA
机构
[1] Fox Chase Canc Ctr, Dept Radiat Oncol, Philadelphia, PA 19111 USA
[2] Fox Chase Canc Ctr, Dept Urol, Philadelphia, PA 19111 USA
[3] Fox Chase Canc Ctr, Dept Radiat Phys, Philadelphia, PA 19111 USA
[4] Henry Ford Hosp, Dept Radiat Oncol, Detroit, MI 48202 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2006年 / 64卷 / 02期
关键词
IMRT; dosimetry; hypofractionation; toxicity;
D O I
10.1016/j.ijrobp.2005.07.970
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The alpha/beta ratio for prostate cancer is postulated to be between 1 and 3, giving rise to the hypothesis that there may be a therapeutic advantage to hypofractionation. The dosimetry and acute toxicity are described in the first 100 men enrolled in a randomized trial. Patients and Methods: The trial compares 76 Gy in 38 fractions (Arm 1) to 70.2 Gy in 26 fractions (Arm II) using intensity modulated radiotherapy. The planning target volume (PTV) margins in Arms I and 11 were 5 mm and 3 mm posteriorly and 8 mm and 7 mm in all other dimensions. The PTV D95% was at least the prescription dose. Results: The mean PTV doses for Arms I and II were 81.1 and 73.8 Gy. There were no differences in overall maximum acute gastrointestinal (GI) or genitourinary (GU) toxicity acutely. However, there was a slight but significant increase in Arm II GI toxicity during Weeks 2, 3, and 4. In multivariate analyses, only the combined rectal DVH parameter of V65 Gy/V50 Gy was significant for GI toxicity and the bladder volume for GU toxicity. Conclusion: Hypofractionation at 2.7 Gy per fraction to 70.2 Gy was well tolerated acutely using the planning conditions described. (C) 2006 Elsevier Inc.
引用
收藏
页码:518 / 526
页数:9
相关论文
共 54 条
[1]   THE AMERICAN-UROLOGICAL-ASSOCIATION SYMPTOM INDEX FOR BENIGN PROSTATIC HYPERPLASIA [J].
BARRY, MJ ;
FOWLER, FJ ;
OLEARY, MP ;
BRUSKEWITZ, RC ;
HOLTGREWE, HL ;
MEBUST, WK ;
COCKETT, ATK ;
BLAIVAS, JG ;
WEIN, AJ .
JOURNAL OF UROLOGY, 1992, 148 (05) :1549-1557
[2]   The getug 70 GY vs. 80 GY randomized trial for localized prostate cancer:: Feasibility and acute toxicity [J].
Beckendorf, V ;
Guérif, S ;
Le Prisé, E ;
Cosset, JM ;
Lefloch, O ;
Chauvet, B ;
Salem, N ;
Chapet, O ;
Bourdin, S ;
Bachaud, JM ;
Maingon, P ;
Lagrange, JL ;
Malissard, L ;
Simon, JM ;
Pommier, P ;
Hay, MH ;
Dubray, B ;
Luporsi, E ;
Bey, P .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 60 (04) :1056-1065
[3]   Fractionation and late rectal toxicity [J].
Brenner, DJ .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 60 (04) :1013-1015
[4]  
Brenner DJ, 2002, INT J RADIAT ONCOL, V52, P6
[5]   Fractionation and protraction for radiotherapy of prostate carcinoma [J].
Brenner, DJ ;
Hall, EJ .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1999, 43 (05) :1095-1101
[6]  
BUYYOUNOUSKI MK, 2005, IN PRESS IMRT HDB CO
[7]   Comparison of α/β estimates from homogeneous (individual) and heterogeneous (population) tumor control models for early stage prostate cancer [J].
Carlone, M ;
Wilkins, D ;
Nyiri, B ;
Raaphorst, P .
MEDICAL PHYSICS, 2003, 30 (10) :2832-2848
[8]  
Catton C. N., 2002, International Journal of Radiation Oncology Biology Physics, V54, P188, DOI 10.1016/S0360-3016(02)03382-5
[9]   Acute toxicity of three-dimensional conformal radiotherapy in prostate cancer patients eligible for implant monotherapy [J].
Chou, RH ;
Wilder, RB ;
Ji, M ;
Ryu, JK ;
Leigh, BR ;
Earle, JD ;
Doggett, RLS ;
Kubo, HD ;
Roach, M ;
White, RWD .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2000, 47 (01) :115-119
[10]  
Collins C D, 1991, Clin Oncol (R Coll Radiol), V3, P127, DOI 10.1016/S0936-6555(05)81183-5