Department of Otolaryngology-Head and Neck Surgery, University of Cincinnati College of Medicine, Cincinnati, Ohio.
Department of Otolaryngology-Head and Neck Surgery, Eastern Virginia Medical School, Norfolk.
JAMA Otolaryngol Head Neck Surg. 2022 Oct 1;148(10):935-939. doi: 10.1001/jamaoto.2022.2291.
Pembrolizumab, a monoclonal antibody targeting programmed cell death 1, is currently approved by the US Food and Drug Administration for recurrent or metastatic head and neck squamous cell carcinoma (HNSCC). The potential neoadjuvant role of programmed cell death 1 inhibitors in primary surgical management of HNSCC and effects on surgical outcomes are poorly understood.
To evaluate the incidence of postoperative adverse events in treatment-naive patients with advanced oral cavity cancer receiving neoadjuvant pembrolizumab when compared with matched controls, as part of a window-of-opportunity multi-institutional clinical trial assessing neoadjuvant pembrolizumab for locally advanced HNSCC.
DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study at a single tertiary academic institution included treatment-naive patients with local regionally advanced oral cavity squamous cell carcinoma (OCSCC) who were undergoing surgical resection.
Patients with local regionally advanced resectable OCSCC who received neoadjuvant pembrolizumab were retrospectively reviewed for postoperative adverse events. Controls were matched by age, race, smoking status, and overall cancer stage based on historical data at the same institution. Matched-cohort analysis was performed using a McNemar test to assess differences between the groups.
Incidence of adverse events following surgical resection of advanced OCSCC within 30 days of surgery and on continued follow-up.
A total of 64 patients (32 as part of the prospective clinical trial and 32 as controls; mean [SD] age, 59.6 [10.3] years; 28 [44%] women) were included in the analysis. Postoperative adverse events in the 32 patients receiving pembrolizumab included lymphedema (n = 20 [63%]), trismus (n = 7 [22%]), return to operating room (n = 7 [22%]), wound infection (n = 7 [22%]), fistula (n = 6 [19%]), wound dehiscence (n = 4 [13%]), flap failure (n = 3 [9%]), and hematoma (n = 2 [6%]). The matched control group demonstrated similar complication rates without considerable differences, except for trismus (n = 16 [50%]), which was greater by a difference of 28.1% (95% CI, 5.6%-50.6%) in the control group.
This cohort study examined surgical complications among patients with local regionally advanced OCSCC treated with neoadjuvant pembrolizumab and found that serious adverse events were similar to those in patients who underwent standard-of-care treatment. This suggests that there is no increased perioperative morbidity in the use of preoperative treatment with immunotherapy. Further prospective studies are needed to validate these findings for oral cavity cancer and other subsites of the head and neck.
帕博利珠单抗是一种针对程序性细胞死亡 1 的单克隆抗体,目前已被美国食品和药物管理局批准用于复发性或转移性头颈部鳞状细胞癌(HNSCC)。程序性细胞死亡 1 抑制剂在 HNSCC 原发性手术治疗中的潜在新辅助作用及其对手术结果的影响尚不清楚。
评估初治晚期口腔癌患者接受新辅助派姆单抗治疗后的术后不良事件发生率,这是一项评估新辅助派姆单抗治疗局部晚期 HNSCC 的机会性多机构临床试验的一部分。
设计、地点和参与者:这是一项在单一三级学术机构进行的回顾性队列研究,纳入了接受手术切除的局部区域晚期口腔鳞状细胞癌(OCSCC)的初治患者。
接受新辅助派姆单抗治疗的局部区域晚期可切除口腔鳞状细胞癌患者接受了术后不良事件的回顾性审查。对照组根据同一机构的历史数据按年龄、种族、吸烟状况和总体癌症分期进行匹配。使用 McNemar 检验对两组之间的差异进行匹配队列分析。
手术切除 30 天内及持续随访期间高级 OCSCC 术后不良事件的发生率。
共纳入 64 例患者(32 例为前瞻性临床试验的一部分,32 例为对照组;平均[标准差]年龄 59.6[10.3]岁;28[44%]为女性)进行分析。接受派姆单抗治疗的 32 例患者的术后不良事件包括淋巴水肿(n=20[63%])、牙关紧闭(n=7[22%])、返回手术室(n=7[22%])、伤口感染(n=7[22%])、瘘管(n=6[19%])、伤口裂开(n=4[13%])、皮瓣失败(n=3[9%])和血肿(n=2[6%])。匹配对照组显示出类似的并发症发生率,没有显著差异,但对照组的牙关紧闭(n=16[50%])明显更高,差异为 28.1%(95%CI,5.6%-50.6%)。
本队列研究检查了接受新辅助派姆单抗治疗的局部区域晚期 OCSCC 患者的手术并发症,发现严重不良事件与接受标准治疗的患者相似。这表明术前使用免疫疗法并没有增加围手术期的发病率。需要进一步的前瞻性研究来验证这些发现是否适用于口腔癌和头颈部的其他部位。