Scalici Jennifer M, Arapovic Sanja, Saks Erin J, Atkins Kristen A, Petroni Gina, Duska Linda R, Slack-Davis Jill K
Department of Obstetrics and Gynecology, University of Virginia, Charlottesville, Virginia.
Department of Pathology, University of Virginia, Charlottesville, Virginia.
Cancer. 2017 May 15;123(6):977-984. doi: 10.1002/cncr.30415. Epub 2016 Nov 7.
Mesothelium vascular cell adhesion molecule-1 (VCAM-1) expression in the metastatic epithelial ovarian cancer (EOC) microenvironment is induced by tumor and mediates tumor cell invasion. VCAM-1 imaging suggests expression during treatment is an indicator of platinum resistance. Here, we assess the potential prognostic significance of mesothelium VCAM-1 expression and prospectively evaluate whether soluble VCAM-1 (sVCAM-1) is a surrogate for mesothelium expression.
A retrospective review of EOC patients was performed to evaluate outcomes with mesothelium VCAM-1 expression determined by immunohistochemistry of peritoneum or omentum specimens. A prospective cohort of EOC patients was identified and followed through primary treatment. Serum for sVCAM-1 evaluation, which was performed via enzyme-linked immunosorbent assay, was collected before surgery or neoadjuvant chemotherapy and at each treatment cycle. Peritoneal specimens were obtained during debulking to assess mesothelial VCAM-1 expression.
A retrospective review identified 54 advanced-stage EOC patients. Patients expressing mesothelium VCAM-1 had shortened overall survival (44 vs 79 months, P = 0.035) and progression-free survival (18 vs 67 months, P = 0.010); the median time to platinum resistance was 36 months for VCAM-1-expressing patients and not yet determined for the VCAM-1-negative group. In our prospective observational cohort, 18 EOC patients completed primary treatment; 3 were negative for mesothelium VCAM-1 expression, and sVCAM-1 did not vary between groups.
Mesothelium VCAM-1 expression is negatively associated with progression-free and overall survival in EOC. This is especially compelling in light of previous data suggesting that persistent VCAM-1 expression during treatment is an indicator of platinum resistance. Our pilot study had insufficient cases to determine whether sVCAM-1 would substitute for mesothelium expression. Cancer 2017;123:977-84. © 2016 American Cancer Society.
间皮血管细胞黏附分子-1(VCAM-1)在转移性上皮性卵巢癌(EOC)微环境中的表达由肿瘤诱导,并介导肿瘤细胞侵袭。VCAM-1成像显示治疗期间的表达是铂耐药的一个指标。在此,我们评估间皮VCAM-1表达的潜在预后意义,并前瞻性评估可溶性VCAM-1(sVCAM-1)是否可替代间皮表达。
对EOC患者进行回顾性分析,以通过腹膜或网膜标本的免疫组织化学确定间皮VCAM-1表达来评估预后。确定了一组EOC患者的前瞻性队列,并对其进行了初始治疗随访。在手术或新辅助化疗前以及每个治疗周期收集血清用于通过酶联免疫吸附测定法评估sVCAM-1。在肿瘤细胞减灭术中获取腹膜标本以评估间皮VCAM-1表达。
回顾性分析确定了54例晚期EOC患者。表达间皮VCAM-1的患者总生存期缩短(44个月对79个月,P = 0.035)和无进展生存期缩短(18个月对67个月,P = 0.010);表达VCAM-1的患者对铂耐药的中位时间为36个月,而VCAM-1阴性组尚未确定。在我们的前瞻性观察队列中,18例EOC患者完成了初始治疗;3例间皮VCAM-1表达为阴性,且各组间sVCAM-1无差异。
间皮VCAM-1表达与EOC的无进展生存期和总生存期呈负相关。鉴于先前的数据表明治疗期间持续的VCAM-1表达是铂耐药的一个指标,这一点尤其引人注目。我们的初步研究病例数不足,无法确定sVCAM-1是否可替代间皮表达。《癌症》2017年;123:977 - 84。©2016美国癌症协会。