Kauffman Eric C, Lee Min-Jung, Alarcon Sylvia V, Lee Sunmin, Hoang Anthony N, Walton Diaz Annerleim, Chelluri Raju, Vourganti Srinivas, Trepel Jane B, Pinto Peter A
Urologic Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; Departments of Urology and Cancer Genetics, Roswell Park Cancer Institute, Buffalo.
Developmental Therapeutics Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
J Urol. 2016 Apr;195(4 Pt 1):1136-42. doi: 10.1016/j.juro.2015.11.013. Epub 2015 Nov 12.
While the significance of circulating tumor cells in clinically localized cancer remains controversial, it has been reported that surgical tumor manipulation can increase circulating tumor cells, including during open prostatectomy. To our knowledge it is unknown whether this cell shedding also occurs during minimally invasive prostatectomy, which minimizes tumor palpation and uses earlier vascular control. We tested the impact of robotic assisted laparoscopic radical prostatectomy on intraoperative circulating tumor cell levels.
Circulating tumor cell counts were compared in peripheral blood specimens from 25 patients treated with robotic assisted laparoscopic radical prostatectomy preoperatively vs intraoperatively after prostate excision, in addition to 11 healthy blood donors. Circulating tumor cell detection was performed using EpCAM immunomagnetic enrichment and multiparametric flow cytometry quantification of viable EpCAM positive/prostate specific membrane antigen positive/CD45 negative cells. Intraoperative cell counts and increases were tested in univariable analyses for associations with perioperative variables, histopathology and postoperative progression.
Circulating tumor cells were detected in 0% of healthy controls compared to 48% and 52% of prostatectomy cases preoperatively and intraoperatively, respectively (range 1 to 8 cells). There was no difference in the incidence or mean number of circulating tumor cells preoperatively vs intraoperatively. Of the patients 60% had no intraoperative change from preoperative levels. Intraoperative cell increases vs decreases were equally infrequent (each 20%) with no intraoperative increase greater than 1 circulating tumor cell. Intraoperative circulating tumor cell detection was not significantly associated with prostatectomy operative characteristics, histopathology or early postoperative progression at a median 21-month followup.
Robotic assisted laparoscopic radical prostatectomy does not cause significant intraoperative increases in circulating tumor cells in contrast to historical reports of open prostatectomy. These findings may aid urologists in counseling candidates for robotic assisted laparoscopic radical prostatectomy regarding the possibility of intraoperative tumor cell shedding.
虽然循环肿瘤细胞在临床局限性癌症中的意义仍存在争议,但据报道手术操作肿瘤可增加循环肿瘤细胞,包括在开放性前列腺切除术中。据我们所知,尚不清楚这种细胞脱落是否也发生在微创前列腺切除术中,因为微创前列腺切除术可尽量减少肿瘤触诊并更早控制血管。我们测试了机器人辅助腹腔镜根治性前列腺切除术对术中循环肿瘤细胞水平的影响。
除了11名健康献血者外,对25例行机器人辅助腹腔镜根治性前列腺切除术患者术前及前列腺切除术后术中的外周血标本中的循环肿瘤细胞计数进行了比较。使用EpCAM免疫磁珠富集和对存活的EpCAM阳性/前列腺特异性膜抗原阳性/CD45阴性细胞进行多参数流式细胞术定量检测循环肿瘤细胞。在单变量分析中测试术中细胞计数及增加情况与围手术期变量、组织病理学和术后进展的相关性。
健康对照组中0%检测到循环肿瘤细胞,而前列腺切除术病例术前和术中分别为48%和52%(范围为1至8个细胞)。术前和术中循环肿瘤细胞的发生率或平均数量无差异。60%的患者术中循环肿瘤细胞水平与术前无变化。术中细胞增加与减少的情况同样少见(各占20%),术中增加的循环肿瘤细胞数均未超过1个。在中位随访21个月时,术中循环肿瘤细胞检测与前列腺切除术的手术特征、组织病理学或术后早期进展无显著相关性。
与开放性前列腺切除术的既往报道相比,机器人辅助腹腔镜根治性前列腺切除术不会导致术中循环肿瘤细胞显著增加。这些发现可能有助于泌尿外科医生在为机器人辅助腹腔镜根治性前列腺切除术的候选者提供咨询时,告知其术中肿瘤细胞脱落的可能性。