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

医学 伊立替康 奥沙利铂 内科学 氟尿嘧啶 卡培他滨 临床研究阶段 临床终点 结直肠癌 化疗 胃肠病学 放化疗 新辅助治疗 外科 肿瘤科 癌症 临床试验 乳腺癌
作者
Cesar Gregorio Muñoz,Manuel Martı́nez,Lisardo Ugidos,Pilar García‐Alfonso,Rafael Álvarez-Gallego,Paloma Peinado,Carmen Toledano,Luka Mihic-Góngora,Justo Gabriel Ortega Anselmi,Enrique Sanz Garcia,Emilio Vicente,Yolanda Quijano,Hipólito Durán,Eduardo M. Diaz,Valentina Ferri,Carmen Rubio,Ovidio Hernando-Requejo,Mercedes López González,Susana Prados,Ulpiano López
出处
期刊:American Journal of Clinical Oncology [Lippincott Williams & Wilkins]
卷期号:48 (3): 142-147
标识
DOI:10.1097/coc.0000000000001157
摘要

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.
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