Division of Hematology/Oncology, University of Cincinnati, Cincinnati, Ohio.
University of Cincinnati Cancer Center, Cincinnati, Ohio.
Clin Cancer Res. 2022 Apr 1;28(7):1345-1352. doi: 10.1158/1078-0432.CCR-21-3351.
Patients with resected, local-regionally advanced, head and neck squamous cell carcinoma (HNSCC) have a one-year disease-free survival (DFS) rate of 65%-69% despite adjuvant (chemo)radiotherapy. Neoadjuvant PD-1 immune-checkpoint blockade (ICB) has demonstrated clinical activity, but biomarkers of response and effect on survival remain unclear.
Eligible patients had resectable squamous cell carcinoma of the oral cavity, larynx, hypopharynx, or oropharynx (p16-negative) and clinical stage T3-T4 and/or two or more nodal metastases or clinical extracapsular nodal extension (ENE). Patients received neoadjuvant pembrolizumab 200 mg 1-3 weeks prior to surgery, were stratified by absence (intermediate-risk) or presence (high-risk) of positive margins and/or ENE, and received adjuvant radiotherapy (60-66 Gy) and concurrent pembrolizumab (every 3 weeks × 6 doses). Patients with high-risk HNSCC also received weekly, concurrent cisplatin (40 mg/m2). Primary outcome was one-year DFS. Secondary endpoints were one-year overall survival (OS) and pathologic response (PR). Safety was evaluated with CTCAE v5.0.
From February 2016 to October 2020, 92 patients enrolled. The median age was 59 years (range, 27-80), 30% were female, 86% had stage T3-T4, and 69% had ≥N2. At a median follow-up of 28 months, one-year DFS was 97% (95% CI, 71%-90%) in the intermediate-risk group and 66% (95% CI, 55%-84%) in the high-risk group. Patients with a PR had significantly improved one-year DFS relative to patients without response (93% vs. 72%, hazard ratio 0.29; 95% CI, 11%-77%). No new safety signals were identified.
Neoadjuvant and adjuvant pembrolizumab increased one-year DFS rate in intermediate-risk, but not high-risk, HNSCC relative to historical control. PR to neoadjuvant ICB is a promising surrogate for DFS.
尽管接受了辅助(化疗)放疗,局部区域晚期切除的头颈部鳞状细胞癌(HNSCC)患者的一年无病生存率(DFS)仍为 65%-69%。新辅助 PD-1 免疫检查点阻断(ICB)已显示出临床活性,但反应的生物标志物和对生存的影响仍不清楚。
符合条件的患者为可切除的口腔、喉、下咽或口咽鳞状细胞癌(p16 阴性),临床分期为 T3-T4 和/或两个或更多淋巴结转移或临床包膜外淋巴结扩展(ENE)。患者在术前 1-3 周接受新辅助 pembrolizumab 200mg,根据有无阳性切缘和/或 ENE(中危)或存在(高危)进行分层,并接受辅助放疗(60-66Gy)和同期 pembrolizumab(每 3 周×6 剂)。高危 HNSCC 患者还接受每周一次、同期顺铂(40mg/m2)。主要终点为一年 DFS。次要终点为一年总生存率(OS)和病理反应(PR)。采用 CTCAE v5.0 评估安全性。
从 2016 年 2 月至 2020 年 10 月,共有 92 例患者入组。中位年龄为 59 岁(范围 27-80),30%为女性,86%为 T3-T4 期,69%有≥N2。在中位随访 28 个月时,中危组的一年 DFS 为 97%(95%CI,71%-90%),高危组为 66%(95%CI,55%-84%)。与无反应者相比,PR 患者的一年 DFS 显著提高(93%比 72%,危险比 0.29;95%CI,11%-77%)。未发现新的安全信号。
与历史对照相比,新辅助和辅助 pembrolizumab 增加了中危 HNSCC 的一年 DFS 率,但对高危 HNSCC 无效。新辅助 ICB 的 PR 是 DFS 的一个很有前途的替代指标。