Howitt Brooke E, Strickland Kyle C, Sholl Lynette M, Rodig Scott, Ritterhouse Lauren L, Chowdhury Dipanjan, D'Andrea Alan D, Matulonis Ursula A, Konstantinopoulos Panagiotis A
Department of Pathology, Brigham and Women's Hospital, Harvard Medical School , Boston, MA, USA.
Division of Genomic Stability and DNA Repair, Dana Farber Cancer Institute, Harvard Medical School , Boston, MA, USA.
Oncoimmunology. 2017 Jan 6;6(2):e1277308. doi: 10.1080/2162402X.2016.1277308. eCollection 2017.
Clear cell ovarian carcinoma (CCOC) represents a distinct histologic subtype of ovarian cancer associated with significantly worse prognosis across all stages and no effective therapeutic options. Here, we report a rare but clinically important cohort of CCOCs with microsatellite instability (MSI) (MSI-CCOCs), which are highly immunogenic and may thus be very responsive to immune checkpoint blockade. CCOCs with MSI exhibit a significantly higher number of CD8 TILs, higher CD8/CD4 ratio, and higher PD-1 TILs compared with microsatellite stable (MSS) CCOCs and compared with high grade serous ovarian cancers, which are the most common histologic subtype of ovarian cancer. Of note, PD-L1 expression in tumor cells or immune cells was noted in all cases of CCOCs with MSI. These observations open an alternative therapeutic avenue for a fraction of patients with CCOC and argue for the routine testing of CCOCs for MSI, a test that is not currently routinely performed.
透明细胞卵巢癌(CCOC)是卵巢癌的一种独特组织学亚型,在所有分期中预后均显著较差,且没有有效的治疗选择。在此,我们报告了一组罕见但具有临床重要性的微卫星不稳定(MSI)的CCOC(MSI - CCOC),它们具有高度免疫原性,因此可能对免疫检查点阻断非常敏感。与微卫星稳定(MSS)的CCOC以及卵巢癌最常见的组织学亚型高级别浆液性卵巢癌相比,MSI的CCOC表现出显著更多的CD8肿瘤浸润淋巴细胞(TILs)、更高的CD8/CD4比值以及更高的PD - 1 TILs。值得注意的是,在所有MSI的CCOC病例中均观察到肿瘤细胞或免疫细胞中的PD - L1表达。这些观察结果为一部分CCOC患者开辟了另一种治疗途径,并支持对CCOC进行MSI的常规检测,而目前该检测并非常规进行。