Alliance A022104/NRG-GI010: The Janus Rectal Cancer Trial: a randomized phase II/III trial testing the efficacy of triplet versus doublet chemotherapy regarding clinical complete response and disease-free survival in patients with locally advanced rectal cancer

医学 外科肿瘤学 肿瘤科 随机对照试验 内科学 临床试验 结直肠癌 癌症 疾病 化疗
作者
Janet Alvarez,Qian Shi,Arvind Dasari,Julio García‐Aguilar,Hanna Sanoff,Thomas J. George,Theodore S. Hong,Greg Yothers,Philip Philip,Garth D. Nelson,Tareq Al Baghdadi,Olatunji B. Alese,Wini Zambare,Dana M. Omer,Floris S. Verheij,Aron Bercz,Min Jung Kim,James J. Buckley,Hannah Williams,Manju George,Reese Garcia,Phuong Gallagher,Eileen M. O’Reilly,Jeffrey A. Meyerhardt,Jamie Crawley,Ardaman Shergill,Natally Horvat,Paul B. Romesser,William A. Hall,J. Joshua Smith
出处
期刊:BMC Cancer [Springer Nature]
卷期号:24 (1) 被引量:1
标识
DOI:10.1186/s12885-024-12529-7
摘要

Recent data have demonstrated that in locally advanced rectal cancer (LARC), a total neoadjuvant therapy (TNT) approach improves compliance with chemotherapy and increases rates of tumor response compared to neoadjuvant chemoradiation (CRT) alone. They further indicate that the optimal sequencing of TNT involves consolidation (rather than induction) chemotherapy to optimize complete response rates. Data, largely from retrospective studies, have also shown that patients with clinical complete response (cCR) after TNT may be managed safely with the watch and wait approach (WW) instead of preemptive total mesorectal resection (TME). However, the optimal consolidation chemotherapy regimen to achieve cCR has not been established, and a randomized clinical trial has not robustly evaluated cCR as a primary endpoint. Collaborating with a multidisciplinary oncology team and patient groups, we designed this NCI-sponsored study of chemotherapy intensification to address these issues and to drive up cCR rates, to provide opportunity for organ preservation, improve quality of life for patients and improve survival outcomes.

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