Department of Colorectal surgery, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Department of Hepatobiliary and Pancreatic Surgery, Yunnan Cancer Hospital, The Third Affiliated Hospital of Kunming Medical University, Kunming, China.
Front Immunol. 2022 Jul 25;13:913483. doi: 10.3389/fimmu.2022.913483. eCollection 2022.
To explore the efficacy and safety of single-agent programmed cell death protein-1 (PD-1) inhibitor in the neoadjuvant treatment of patients with mismatch repair-deficient (dMMR) or microsatellite instability-high (MSI-H) locally advanced colorectal cancer (LACRC) through single-center large⁃sample analysis based on real⁃world data in China.
This study was a retrospective, single-center, case series study. 33 colorectal cancer (CRC) patients with clinical stage of T34N02M0 treated in Yunnan Cancer Hospital from June 2019 to June 2021 were analyzed retrospectively. Among them, 32 patients were dMMR or MSI-H or both dMMR and MSI-H, and one patient was both dMMR and microsatellite stability (MSS) (excluded in the final analysis). All 32 patients received neoadjuvant immunotherapy (nIT) with single-agent PD⁃1 inhibitor.
Among the 32 patients, 8 (25%) were locally advanced rectal cancer (LARC) and 24 (75%) were locally advanced colon cancer (LACC); 4 (12.55%) were stage II and 28 (87.5%) were stage III. The median number of cycles of 32 patients with dMMR/MSI-H LACRC receiving nIT with single-agent PD-1 blockade was 6 (410), and the median number of cycles to achieve partial response (PR) was 3 (24). Among them, three LARC patients achieved clinical complete response (cCR) and adopted the watch-and-wait (W&W) strategy. The objective response rate (ORR) of the other 29 patients with radical surgery was 100% (29/29), the pathological response rate was 100% (29/29), the rate of major pathological response (MPR) was 86.2% (25/29), and the rate of pathological complete response (pCR) was 75.9% (22/29). The incidence of immune-related adverse events (irAEs) in 32 patients during nIT was 37.5% (12/32), while the incidence of irAEs in 22 patients with operation during adjuvant immunotherapy was 27.3% (6/22), all of which were grade 12. No grade 3 or above irAEs were occured. The median time from the last nIT to surgery was 27 (1642) days. There were no delayed radical resection due to irAEs in these patients. All 29 patients achieved R0 resection. The incidence of surgical-related adverse events (srAEs) in perioperative period was 10.3% (3/29).
Neoadjuvant monoimmunotherapy with PD-1 inhibitor has favorable ORR and pCR rate, and relatively low incidences of irAEs and srAEs for patients with dMMR/MSI-H LACRC, suggesting that this nIT regimen of single-agent PD-1 inhibitor is significantly effective and sufficiently safe.
通过在中国基于真实世界数据的单中心大样本分析,探讨单药程序性死亡蛋白-1(PD-1)抑制剂在错配修复缺陷(dMMR)或微卫星不稳定高(MSI-H)局部晚期结直肠癌(LACRC)新辅助治疗中的疗效和安全性。
这是一项回顾性、单中心、病例系列研究。分析了 2019 年 6 月至 2021 年 6 月在云南省肿瘤医院接受治疗的 33 例临床分期为 T34N02M0 的结直肠癌(CRC)患者。其中,32 例为 dMMR 或 MSI-H 或 dMMR 和 MSI-H 均阳性,1 例为 dMMR 和微卫星稳定性(MSS)均阳性(排除在最终分析之外)。所有 32 例患者均接受了单药 PD-1 抑制剂的新辅助免疫治疗(nIT)。
在 32 例患者中,8 例(25%)为局部晚期直肠肿瘤(LARC),24 例(75%)为局部晚期结肠肿瘤(LACC);4 例(12.55%)为 II 期,28 例(87.5%)为 III 期。32 例 dMMR/MSI-H LACRC 患者接受单药 PD-1 阻断 nIT 的中位周期数为 6(410),达到部分缓解(PR)的中位周期数为 3(24)。其中,3 例 LARC 患者达到临床完全缓解(cCR)并采用观察等待(W&W)策略。其他 29 例接受根治性手术的患者的客观缓解率(ORR)为 100%(29/29),病理缓解率为 100%(29/29),主要病理缓解率(MPR)为 86.2%(25/29),病理完全缓解率(pCR)为 75.9%(22/29)。32 例患者在 nIT 期间发生免疫相关不良事件(irAEs)的发生率为 37.5%(12/32),而在 22 例接受辅助免疫治疗的手术患者中,irAEs 的发生率为 27.3%(6/22),均为 12 级。无 3 级或以上的 irAEs 发生。从最后一次 nIT 到手术的中位时间为 27(1642)天。这些患者中没有因 irAEs 而延迟根治性切除。所有 29 例患者均达到 R0 切除。围手术期手术相关不良事件(srAEs)的发生率为 10.3%(3/29)。
单药 PD-1 抑制剂新辅助 monoimmunotherapy 对 dMMR/MSI-H LACRC 患者具有良好的 ORR 和 pCR 率,以及相对较低的 irAEs 和 srAEs 发生率,提示该单药 PD-1 抑制剂 nIT 方案具有显著的有效性和足够的安全性。