Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Clin Cancer Res. 2020 Jul 1;26(13):3211-3219. doi: 10.1158/1078-0432.CCR-19-3977. Epub 2020 Apr 8.
In oropharyngeal squamous cell carcinoma (OPC), high CD8 tumor-infiltrating lymphocyte (CD8TIL) density confers improved prognosis. We compared neoadjuvant durvalumab (PD-L1 inhibitor) with durvalumab + tremelimumab (CTLA-4 inhibitor) in terms of impact on CD8TIL density, safety, and efficacy in patients with OPC.
Patients with newly diagnosed stage II-IVA OPC or locoregionally recurrent OPC amenable to resection were included. Patients were randomized to two cycles of durvalumab or durvalumab + tremelimumab before surgery. The primary endpoint was change between baseline and resection specimen in CD8TIL density between arms. Secondary endpoints included safety, response rate per RECIST, major pathologic response (MPR; ≤10% viable tumor cells) rate, and patient-reported outcomes.
Of 28 eligible patients (14/arm), 20 (71%) had newly diagnosed OPC, and 24 (86%) were p16-positive. The posttreatment to pretreatment median CD8TIL density ratio was 1.31 for durvalumab and 1.15 for combination treatment ( = 0.97; 95% CI: -1.07-2.28). In each group, 6 patients (43%, 95% CI: 17.66-71.14) had a response. Eight patients (29%) had a MPR at the primary tumor and/or nodal metastases. Neither baseline CD8TIL density nor PD-L1 expression level correlated with overall response, but a trend toward greater CD8TIL change in patients with a MPR was seen ( = 0.059; 95% CI: -0.33-3.46). Four patients (14%) had grade ≥3 adverse events. At median follow-up time of 15.79 months, all patients were alive, and one had an additional recurrence.
Durvalumab + tremelimumab did not increase CD8TIL density more than durvalumab alone did. The observed safety and activity support further investigation of neoadjuvant checkpoint inhibitor for OPC.
在口咽鳞状细胞癌(OPC)中,高肿瘤浸润 CD8 淋巴细胞(CD8TIL)密度预示着更好的预后。我们比较了新辅助度伐利尤单抗(PD-L1 抑制剂)和度伐利尤单抗联合 Tremelimumab(CTLA-4 抑制剂)对 OPC 患者 CD8TIL 密度、安全性和疗效的影响。
纳入新诊断为 II-IVA 期 OPC 或局部复发性 OPC 且可切除的患者。患者随机分为两组,分别接受两周期的度伐利尤单抗或度伐利尤单抗联合 Tremelimumab 治疗,然后手术。主要终点是两组之间基线和切除标本之间 CD8TIL 密度的变化。次要终点包括安全性、RECIST 缓解率、主要病理缓解(MPR;≤10%存活肿瘤细胞)率和患者报告的结果。
28 例符合条件的患者(每组 14 例)中,20 例(71%)为新诊断的 OPC,24 例(86%)为 p16 阳性。度伐利尤单抗组和联合治疗组的治疗后与治疗前的 CD8TIL 密度比值中位数分别为 1.31 和 1.15(=0.97;95%CI:-1.07-2.28)。每组有 6 例患者(43%,95%CI:17.66-71.14)有反应。8 例患者(29%)在原发肿瘤和/或淋巴结转移部位有 MPR。基线 CD8TIL 密度和 PD-L1 表达水平均与总反应无关,但 MPR 患者的 CD8TIL 变化趋势更大(=0.059;95%CI:-0.33-3.46)。4 例患者(14%)发生 3 级及以上不良事件。中位随访时间为 15.79 个月,所有患者均存活,1 例患者出现额外复发。
度伐利尤单抗联合 Tremelimumab 并未增加 CD8TIL 密度,超过了度伐利尤单抗单药治疗的效果。观察到的安全性和疗效支持进一步研究新辅助检查点抑制剂治疗 OPC。