Elective irradiation of pelvic lymph nodes during postprostatectomy salvage radiotherapy

被引:45
|
作者
Moghanaki, Drew [1 ,2 ]
Koontz, Bridget F. [3 ]
Karlin, Jeremy D. [1 ]
Wan, Wen [4 ]
Mukhopadhay, Nitai [4 ]
Hagan, Michael P. [1 ,2 ,5 ]
Anscher, Mitchell S. [1 ]
机构
[1] Virginia Commonwealth Univ, Dept Radiat Oncol, Richmond, VA 23291 USA
[2] Hunter Holmes McGuire Vet Affairs Med Ctr, Radiat Oncol Serv, Richmond, VA USA
[3] Duke Univ, Med Ctr, Dept Radiat Oncol, Durham, NC USA
[4] Virginia Commonwealth Univ, Dept Biostat, Richmond, VA 23291 USA
[5] US Dept Vet Affairs, Natl Radiat Oncol Program, Richmond, VA USA
关键词
prostate cancer; radiotherapy; lymph nodes; salvage radiotherapy; elective lymph node; whole pelvis; pelvic lymph nodes; prostatectomy; postprostatectomy; biochemical relapse; CONFORMAL RADIATION-THERAPY; PROSTATE-SPECIFIC ANTIGEN; RELAPSE-FREE SURVIVAL; BIOCHEMICAL RECURRENCE; PATHOLOGICAL STAGE; CANCER; RISK; ADENOCARCINOMA; FAILURE; SCORE;
D O I
10.1002/cncr.27712
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Success rates with salvage radiotherapy (SRT) in men who have a postprostatectomy biochemical relapse are suboptimal. One treatment-intensification strategy includes elective irradiation of the pelvic lymph nodes with whole pelvis radiotherapy (WPRT). METHODS: An inter-institutional retrospective cohort study compared outcomes for patients who received SRT at 2 separate academic institutions with disparate treatment paradigms: almost exclusively favoring WPRT (n = 112) versus limiting treatment to the prostate bed (PBRT) (n = 135). Patients were excluded if they had lymph node involvement or if they received androgen-deprivation therapy. The Cox proportional hazards model was used to adjust for potential confounders. RESULTS: In total, 247 patients were analyzed with a median follow-up of 4 years. The pre-SRT prostate-specific antigen (PSA) level (adjusted hazard ratio [HR], 1.58; P < .0001) and a Gleason score of 8 to 10 (adjusted HR, 3.21; P < .0001) were identified as independent predictors of increased risk of biochemical PSA progression after SRT. However, WPRT was not independently associated with biochemical progression-free survival in the multivariate model (adjusted HR, 0.79; P = .20). Neither low-risk patients nor high-risk patients (defined a priori by a preoperative PSA level =20 ng/mL, a pathologic Gleason score between 8 and 10, or pathologic T3 tumor classification) benefited from WPRT. Overall survival was similar between treatment groups. When restricting the analysis to patients with pre-SRT PSA levels =0.4 ng/mL (n = 139), WPRT was independently associated with a 53% reduction in the risk of biochemical progression (adjusted HR, 0.47; P = .031). CONCLUSIONS: WPRT did not improve outcomes among the entire group but was independently associated with improved biochemical control among patients with pre-SRT PSA levels =0.4 ng/mL. Cancer 2013. (c) 2012 American Cancer Society.
引用
收藏
页码:52 / 60
页数:9
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