Long-term Outcomes of Stereotactic Body Radiotherapy for Low-Risk and Intermediate-Risk Prostate Cancer

被引:249
作者
Kishan, Amar U. [1 ,2 ]
Dang, Audrey [2 ]
Katz, Alan J. [3 ]
Mantz, Constantine A. [4 ]
Collins, Sean P. [5 ]
Aghdam, Nima [5 ]
Chu, Fang-I [2 ]
Kaplan, Irving D. [6 ]
Appelbaum, Limor [6 ]
Fuller, Donald B. [7 ]
Meier, Robert M. [8 ]
Loblaw, D. Andrew [9 ]
Cheung, Patrick [9 ]
Pham, Huong T. [10 ]
Shaverdian, Narek [2 ,11 ]
Jiang, Naomi [2 ]
Yuan, Ye [2 ]
Bagshaw, Hilary [12 ]
Prionas, Nicolas [12 ]
Buyyounouski, Mark K. [12 ]
Spratt, Daniel E. [13 ]
Linson, Patrick W. [14 ]
Hong, Robert L. [15 ]
Nickols, Nicholas G. [2 ]
Steinberg, Michael L. [2 ]
Kupelian, Patrick A. [2 ]
King, Christopher R. [2 ]
机构
[1] Univ Calif Los Angeles, Dept Urol, Los Angeles, CA USA
[2] Univ Calif Los Angeles, Dept Radiat Oncol, 200 Med Plaza,Ste B265, Los Angeles, CA 90095 USA
[3] Flushing Radiat Oncol Serv, Flushing, NY USA
[4] 21st Century Oncol, Ft Myers, FL USA
[5] Georgetown Univ, Dept Radiat Oncol, Washington, DC USA
[6] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[7] CyberKnife Ctr San Diego Inc, Div Genesis Healthcare Partners Inc, San Diego, CA USA
[8] Swedish Radiosurg Ctr, Seattle, WA USA
[9] Sunnybrook Hlth Sci Ctr, Dept Radiat Oncol, Odette Canc Ctr, Toronto, ON, Canada
[10] Virginia Mason Med Ctr, Sect Radiat Oncol, Seattle, WA 98101 USA
[11] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, 1275 York Ave, New York, NY 10021 USA
[12] Stanford Univ, Dept Radiat Oncol, Sch Med, Stanford, CA 94305 USA
[13] Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[14] Scripps Hlth, La Jolla, CA USA
[15] Virginia Hosp Ctr, Arlington, VA USA
关键词
RANDOMIZED-TRIAL; COSTS;
D O I
10.1001/jamanetworkopen.2018.8006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE Stereotactic body radiotherapy harnesses improvements in technology to allow the completion of a course of external beam radiotherapy treatment for prostate cancer in the span of 4 to 5 treatment sessions. Although mounting short-term data support this approach, long-term outcomes have been sparsely reported. OBJECTIVE To assess long-term outcomes after stereotactic body radiotherapy for low-risk and intermediate-risk prostate cancer. DESIGN, SETTING, AND PARTICIPANTS This cohort study analyzed individual patient data from 2142 men enrolled in 10 single-institution phase 2 trials and 2 multi-institutional phase 2 trials of stereotactic body radiotherapy for low-risk and intermediate-risk prostate cancer between January 1, 2000, and December 31, 2012. Statistical analysis was performed based on follow-up from January 1, 2013, to May 1, 2018. MAIN OUTCOMES AND MEASURES The cumulative incidence of biochemical recurrence was estimated using a competing risk framework. Physician-scored genitourinary and gastrointestinal toxic event outcomes were defined per each individual study, generally by Radiation Therapy Oncology Group or Common Terminology Criteria for Adverse Events scoring systems. After central review, cumulative incidences of late grade 3 or higher toxic events were estimated using a Kaplan-Meier method. RESULTS A total of 2142 men (mean [SD] age, 67.9 [9.5] years) were eligible for analysis, of whom 1185 (55.3%) had low-risk disease, 692 (32.3%) had favorable intermediate-risk disease, and 265 (12.4%) had unfavorable intermediate-risk disease. The median follow-up period was 6.9 years (interquartile range, 4.9-8.1 years). Seven-year cumulative rates of biochemical recurrence were 4.5%(95% CI, 3.2%-5.8%) for low-risk disease, 8.6%(95% CI, 6.2%-11.0%) for favorable intermediate-risk disease, 14.9% (95% CI, 9.5%-20.2%) for unfavorable intermediate-risk disease, and 10.2%(95% CI, 8.0%-12.5%) for all intermediate-risk disease. The crude incidence of acute grade 3 or higher genitourinary toxic events was 0.60% (n = 13) and of gastrointestinal toxic events was 0.09% (n = 2), and the 7-year cumulative incidence of late grade 3 or higher genitourinary toxic events was 2.4%(95% CI, 1.8%-3.2%) and of late grade 3 or higher gastrointestinal toxic events was 0.4%(95% CI, 0.2%-0.8%). CONCLUSIONS AND RELEVANCE In this study, stereotactic body radiotherapy for low-risk and intermediate-risk disease was associated with low rates of severe toxic events and high rates of biochemical control. These data suggest that stereotactic body radiotherapy is an appropriate definitive treatment modality for low-risk and intermediate-risk prostate cancer.
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