Zurita A J, Pisters L L, Wang X, Troncoso P, Dieringer P, Ward J F, Davis J W, Pettaway C A, Logothetis C J, Pagliaro L C
Department of Genitourinary Medical Oncology, MD Anderson Cancer Center, The University of Texas, Houston, TX, USA.
Department of Urology, MD Anderson Cancer Center, The University of Texas, Houston, TX, USA.
Prostate Cancer Prostatic Dis. 2015 Sep;18(3):276-80. doi: 10.1038/pcan.2015.23. Epub 2015 May 26.
Prostate cancer persisting in the primary site after systemic therapy may contribute to emergence of resistance and progression. We previously demonstrated molecular characteristics of lethal cancer in the prostatectomy specimens of patients presenting with lymph node metastasis after chemohormonal treatment. Here we report the post-treatment outcomes of these patients and assess whether a link exists between surgery and treatment-free/cancer-free survival.
Patients with either clinically detected lymph node metastasis or primaries at high risk for nodal dissemination were treated with androgen ablation and docetaxel. Those responding with PSA concentration <1 ng ml(-1) were recommended surgery 1 year from enrollment. ADT was withheld postoperatively. The rate of survival without biochemical progression 1 year after surgery was measured to screen for efficacy.
Forty patients were enrolled and 39 were evaluable. Three patients (7.7%) declined surgery. Of the remaining 36, 4 patients experienced disease progression during treatment and 4 more did not reach PSA <1. Twenty-six patients (67%) completed surgery, and 13 (33%) were also progression-free 1 year postoperatively (8 with undetectable PSA). With a median follow-up of 61 months, time to treatment failure was 27 months in the patients undergoing surgery. The most frequent patterns of first disease recurrence were biochemical (10 patients) and systemic (5).
Half of the patients undergoing surgery were off treatment and progression-free 1 year following completion of all therapy. These results suggest that integration of surgery is feasible and may be superior to systemic therapy alone for selected prostate cancer patients presenting with nodal metastasis.
全身治疗后原发部位持续存在的前列腺癌可能导致耐药和疾病进展。我们之前在接受化疗和激素治疗后出现淋巴结转移的患者的前列腺切除标本中,展示了致命性癌症的分子特征。在此,我们报告这些患者的治疗后结局,并评估手术与无治疗/无癌生存之间是否存在关联。
对临床检测到有淋巴结转移或原发灶有高淋巴结转移风险的患者,采用雄激素剥夺和多西他赛治疗。那些前列腺特异性抗原(PSA)浓度<1 ng/ml的有反应者,自入组起1年后建议进行手术。术后停用雄激素剥夺治疗(ADT)。测量术后1年无生化进展的生存率以筛查疗效。
入组40例患者,39例可评估。3例患者(7.7%)拒绝手术。其余36例中,4例患者在治疗期间出现疾病进展,另有4例未达到PSA<1。26例患者(67%)完成手术,13例(33%)术后1年也无进展(8例PSA检测不到)。中位随访61个月,接受手术的患者至治疗失败时间为27个月。首次疾病复发最常见的类型是生化复发(10例患者)和全身复发(5例)。
所有治疗完成后1年,接受手术的患者中有一半停止治疗且无进展。这些结果表明,对于选定的出现淋巴结转移的前列腺癌患者,手术结合治疗是可行的,可能优于单纯的全身治疗。