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2期多中心开放标签非随机研究:脂质体伊立替康联合5-氟尿嘧啶、亚叶酸钙和奥沙利铂用于直肠癌患者新辅助化疗,随后在观察等待方案中进行放化疗

Phase 2, Multicenter, Open-label, Nonrandomized Study of Neoadjuvant Chemotherapy Liposomal Irinotecan With 5-Fluorouracil, Leucovorin, and Oxaliplatin, Followed by Chemoradiotherapy in Patients With Rectal Cancer in a Watch-and-Wait Program.

作者信息

Muñoz César, Riesco Martinez María-C, Ugidos Lisardo, García-Alfonso Pilar, Alvarez-Gallego Rafael, Peinado Paloma, Toledano Carmen, Mihic-Góngora Luka, Ortega Anselmi Justo Gabriel, Sanz Garcia Enrique, Vicente Emilio, Quijano Yolanda, Durán Hipólito J, Díaz Eduardo, Ferri Valentina, Rubio Carmen, HernandoRequejo Ovidio, López González Mercedes, Prados Susana, López Ulpiano, Allona María, PérezDueñas Virginia, Perez-Escutia María Angeles, Cubillo Antonio

机构信息

HM CIOCC MADRID (Centro Integral Oncológico Clara Campal), Hospital Universitario HM Sanchinarro, HM Hospitales.

Hospital Universitario HM Montepríncipe, HM Hospitales.

出版信息

Am J Clin Oncol. 2025 Mar 1;48(3):142-147. doi: 10.1097/COC.0000000000001157. Epub 2024 Nov 29.

Abstract

OBJECTIVE

To evaluate the efficacy of neoadjuvant chemotherapy combination with liposomal irinotecan, 5-fluorouracil, leucovorin, and oxaliplatin in patients with locally advanced rectal cancer.

METHODS

This was a phase 2, nonrandomized, multicenter study in adults with stage II or III rectal cancer and an Eastern Cooperative Oncology Group performance status of 0 to 1. Total neoadjuvant therapy (TNT) consisted of neoadjuvant chemotherapy combination with liposomal irinotecan (60 mg/m 2 ), oxaliplatin (60 mg/m 2 ), leucovorin (400 mg/m 2 ), and fluorouracil (2400 mg/m²), followed by chemoradiotherapy [ie, capecitabine (825 mg/m 2 ) and radiotherapy according to the standard of care]. The primary efficacy endpoint was the proportion of patients who achieved clinical complete response (cCR), defined as the normalization of pelvic magnetic resonance imaging, rectoscopy, computed tomography scan, and tumor markers.

RESULTS

The median follow-up was 32.3 months. Of the 30 patients who underwent TNT and were evaluated, 6 (20.0%; 95% CI: 5.2%-34.8%) patients achieved a cCR. There were no deaths. The median disease-free survival (DFS) for patients with cCR was not reached after a follow-up of 32 months; the 1-year DFS rate was 90.0% (95% CI: 71.0%-100%), and the 2-year and 3-year DFS rates were 80.0% (95% CI: 55.0%-100%). No grade ≥4 adverse events (AEs) were observed. Grade 3 AEs occurred in 18 patients (60%), most frequent was diarrhea (n = 9, 30%). Eleven (36.7%) patients experienced serious AEs, with diarrhea being the most frequent (n = 6, 20.0%).

CONCLUSION

TNT with 5-fluorouracil, leucovorin, and oxaliplatin and chemoradiation is a safe and effective therapeutic alternative for the management of locally advanced rectal cancer.

摘要

目的

评估新辅助化疗联合脂质体伊立替康、5-氟尿嘧啶、亚叶酸钙和奥沙利铂治疗局部晚期直肠癌患者的疗效。

方法

这是一项针对II期或III期直肠癌成人患者且东部肿瘤协作组体能状态为0至1的2期非随机多中心研究。新辅助化疗总疗程(TNT)包括新辅助化疗联合脂质体伊立替康(60mg/m²)、奥沙利铂(60mg/m²)、亚叶酸钙(400mg/m²)和氟尿嘧啶(2400mg/m²),随后进行放化疗[即卡培他滨(825mg/m²)并按标准治疗方案进行放疗]。主要疗效终点是达到临床完全缓解(cCR)的患者比例,定义为盆腔磁共振成像、直肠镜检查、计算机断层扫描和肿瘤标志物均恢复正常。

结果

中位随访时间为32.3个月。在接受TNT并接受评估的30例患者中,6例(20.0%;95%CI:5.2%-34.8%)达到cCR。无死亡病例。cCR患者的中位无病生存期(DFS)在随访32个月后未达到;1年DFS率为90.0%(95%CI:71.0%-100%),2年和3年DFS率为80.0%(95%CI:55.0%-100%)。未观察到≥4级不良事件(AE)。18例患者(60%)发生3级AE,最常见的是腹泻(n = 9,30%)。11例(36.7%)患者发生严重AE,腹泻最为常见(n = 6,20.0%)。

结论

5-氟尿嘧啶、亚叶酸钙、奥沙利铂联合放化疗的TNT是治疗局部晚期直肠癌的一种安全有效的治疗选择。

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