Scognamiglio Theresa, Chen Yao-Tseng
Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, 525 East 68th Street Starr-1005, New York, NY, 10065, USA.
Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, 525 East 68th Street, New York, NY, 10065, USA.
Head Neck Pathol. 2018 Jun;12(2):221-229. doi: 10.1007/s12105-017-0857-3. Epub 2017 Sep 25.
Anti-PD1 antibody has been approved for metastatic squamous cell carcinoma of the head and neck (SCCHN) and objective response rates of approximately 20% have been reported. Defining PD-L1 expression at ≥ 1% tumor cells as positive, PD-L1-positive tumors showed a higher response rate. However, it is unclear whether 1% is the optimal cutoff, and studies on lung cancer suggested 50% cutoff as a stronger predictive biomarker. 96 primary SCCHN from oropharynx and oral cavity and 34 corresponding metastatic lesions were typed for membranous PD-L1 expression. p16 immunohistochemistry was used as a surrogate marker for HPV status in SCCHN from the oropharynx. Fifty-two of 96 (54%) tumors were PD-L1-positive, 72% if PD-L1 expression in tumor-infiltrating immunocytes was also included as positive. Fifteen of 34 primary-metastasis tumor pairs differed in PD-L1 expression, and p16(+) cases more frequently showed PD-L1 expression in immunocytes than p16(-) cases (82 vs. 45%, p < 0.05). PD-L1-positive SCCHN showed two distinct patterns of expression. In the induced pattern of expression, PD-L1-positive tumor cells were limited to the periphery of tumor nests at the tumor-immunocyte interface, comprising < 5% of tumor cells, and were almost always associated with PD-L1-positive immunocytes. In contrast, tumors with constitutive PD-L1 expression had a higher percentage of positive tumor cells, often diffusely distributed throughout the tumor, and often were not accompanied by PD-L1-positive immunocytes. We propose that distinguishing these two biologically distinctive patterns of PD-L1 expression and typing metastatic instead of primary lesions might better predict immunotherapeutic response to anti-PD1/PD-L1 regimens beyond just the percentage of PD-L1-positive tumor cells.
抗PD1抗体已被批准用于治疗转移性头颈部鳞状细胞癌(SCCHN),据报道客观缓解率约为20%。将肿瘤细胞中PD-L1表达≥1%定义为阳性时,PD-L1阳性肿瘤显示出更高的缓解率。然而,尚不清楚1%是否为最佳临界值,而针对肺癌的研究表明,50%的临界值是更强的预测生物标志物。对96例来自口咽和口腔的原发性SCCHN以及34个相应的转移病灶进行膜性PD-L1表达分型。p16免疫组化被用作口咽SCCHN中HPV状态的替代标志物。96例肿瘤中有52例(54%)为PD-L1阳性,若将肿瘤浸润免疫细胞中的PD-L1表达也计为阳性,则为72%。34对原发-转移肿瘤中有15对的PD-L1表达不同,与p16(-)病例相比,p16(+)病例在免疫细胞中更频繁地显示PD-L1表达(82%对45%,p<0.05)。PD-L1阳性的SCCHN表现出两种不同的表达模式。在诱导性表达模式中,PD-L1阳性肿瘤细胞局限于肿瘤巢在肿瘤-免疫细胞界面的周边,占肿瘤细胞的比例<5%,且几乎总是与PD-L1阳性免疫细胞相关。相比之下,具有组成性PD-L1表达的肿瘤中阳性肿瘤细胞的比例更高,通常在整个肿瘤中弥漫分布,且通常不伴有PD-L1阳性免疫细胞。我们提出,区分这两种生物学上不同的PD-L1表达模式并对转移病灶而非原发病灶进行分型,可能比仅依据PD-L1阳性肿瘤细胞的比例能更好地预测对抗PD1/PD-L1方案的免疫治疗反应。