Department of Radiation Oncology, Virginia Commonwealth University, Richmond, USA.
Cancer. 2013 Jan 1;119(1):52-60. doi: 10.1002/cncr.27712. Epub 2012 Jun 26.
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).
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.
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).
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.
在前列腺癌根治术后生化复发的患者中,挽救性放疗(SRT)的成功率并不理想。一种治疗强化策略包括对骨盆淋巴结进行选择性照射,使用全骨盆放疗(WPRT)。
一项机构间回顾性队列研究比较了在 2 家学术机构接受 SRT 的患者的结果,这 2 家机构的治疗模式截然不同:几乎完全赞成 WPRT(n=112)与限制治疗于前列腺床(PBRT)(n=135)。如果患者有淋巴结受累或接受雄激素剥夺治疗,则将其排除在外。使用 Cox 比例风险模型调整潜在混杂因素。
共分析了 247 例患者,中位随访时间为 4 年。在 SRT 前前列腺特异性抗原(PSA)水平(调整后的风险比[HR],1.58;P<0.0001)和 Gleason 评分 8 至 10 分(调整后的 HR,3.21;P<0.0001)被确定为 SRT 后生化 PSA 进展风险增加的独立预测因素。然而,在多变量模型中,WPRT 与生化无进展生存率无独立相关性(调整后的 HR,0.79;P=0.20)。无论是低危患者还是高危患者(术前 PSA 水平≥20ng/mL、病理 Gleason 评分 8 至 10 分或病理 T3 肿瘤分类)都没有从 WPRT 中获益。两组患者的总生存率相似。当将分析限制在 SRT 前 PSA 水平≥0.4ng/mL 的患者(n=139)时,WPRT 与生化进展风险降低 53%独立相关(调整后的 HR,0.47;P=0.031)。
WPRT 并没有改善整个组的结果,但与 SRT 前 PSA 水平≥0.4ng/mL 的患者的生化控制改善独立相关。