作者
Janet Alvarez,Qian Shi,Arvind Dasari,Julio García‐Aguilar,Hanna K. Sanoff,TJ George,T.S. Hong,Greg Yothers,PA Philip,GD Nelson,Tareq Al Baghdadi,Margaret Olutayo Alese,Wini Zambare,D.M. Omer,F.S. Verheij,J. Thomas Buckley,Hannah Williams,Michael H. George,R. García,EM O’Reilly,J. A. Meyerhardt,Ardaman Shergill,Natally Horvat,PB Romesser,W.A. Hall,J. J. Smith
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 neoadjuvant therapy 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.