Phase III trial of long-term adjuvant androgen deprivation after neoadjuvant hormonal cytoreduction and radiotherapy in locally advanced carcinoma of the prostate: The Radiation Therapy Oncology Group Protocol 92-02

被引:553
作者
Hanks, GE
Pajak, TF
Porter, A
Grignon, D
Brereton, H
Venkatesan, V
Horwitz, EM
Lawton, C
Rosenthal, SA
Sandler, HM
Shipley, WU
机构
[1] Radiat Therapy Oncol Grp, Dept Stat, Philadelphia, PA 19107 USA
[2] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[3] Mercy Hosp, Scranton, PA USA
[4] Wayne State Univ, Harper Hosp, Detroit, MI 48202 USA
[5] Univ Western Ontario, London, ON, Canada
[6] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[7] Radiol Associates Sacramento, Sacramento, CA USA
[8] Univ Michigan, Sch Med, Ann Arbor, MI 48109 USA
[9] Massachusetts Gen Hosp, Boston, MA 02114 USA
关键词
D O I
10.1200/JCO.2003.11.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
(Purpose) under bar: Radiation Therapy Ontology Group (RTOG) Protocol 92-02 was a randomized trial testing long-term (LT) adjuvant androgen deprivation (AD) after initial AD with external-beam radiotherapy (RT) in patients with locally advanced prostate cancer (PC; T2c-4) and with prostate-specific antigen level less than 150 ng/mL. (Patients and Methods) under bar: Patients received a total of 4 months of goserelin and flutamide, 2 months before and 2 months during FIT. A radiation dose of 65 to 70 Gy was given to the prostate and a dose of 44 to 50 Gy to the pelvic lymph nodes. Patients were randomly assigned to receive no additional therapy (short-term [ST]AD-RT) or 24 months of goserelin (LTAD-RT),- 1,554 patients were entered onto the study. (Results) under bar: The LTAD-RT arm showed significant improvement in all efficacy end points except overall survival (OS, 80.0% v 78.5% at 5 years, P = .73), compared with the STAD-RT arm. In a subset of patients not part of the original study design, with tumors assigned Gleason scares of 8 to 10 by the contributing institutions, the LTAD-RT arm had significantly better OS (81.0% v 70.7%, P = .044). There was a small but significant increase in the frequency of late radiation grades 3, 4, and 5 gastrointestinal toxicity ascribed to the LTAD-RT arm (2.6% v 1.2% at 5 years, P = .037), the cause of which is not clear. (Conclusion) under bar: The RTOG 92-02 trial supports the addition of LT adjuvant AD to STAD with RT for T2c-4 PC. In the exploratory subset analysis of patients with Gleason scares 8 to 10, LT adjuvant AD resulted in a survival advantage. (C) 2003 by American Society of Clinical Oncology.
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收藏
页码:3972 / 3978
页数:7
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