Organ Preservation in Patients With Rectal Adenocarcinoma Treated With Total Neoadjuvant Therapy

Julio García‐Aguilar(Memorial Sloan Kettering Cancer Center), Sujata Patil(Memorial Sloan Kettering Cancer Center), Marc J. Gollub(Memorial Sloan Kettering Cancer Center), Jin K. Kim(Memorial Sloan Kettering Cancer Center), Jonathan B. Yuval(Memorial Sloan Kettering Cancer Center), Hannah M. Thompson(Memorial Sloan Kettering Cancer Center), Floris S. Verheij(Memorial Sloan Kettering Cancer Center), Dana M. Omer(Memorial Sloan Kettering Cancer Center), Meghan Lee(Memorial Sloan Kettering Cancer Center), Richard F. Dunne(University of Rochester Medical Center), Jorge Marcet(University of South Florida), Peter A. Cataldo(University of Vermont), Blasé N. Polite(University of Chicago), Daniel O. Herzig(Oregon Health & Science University), David Liska(Cleveland Clinic), Samuel Oommen(John Muir Health), Charles M. Friel(University of Virginia), Charles A. Ternent(Mercy Medical Center), Andrew L. Coveler(University of Washington), Steven R. Hunt(Washington University in St. Louis), Anita Gregory(St. Joseph Hospital), Madhulika G. Varma(University of California, San Francisco), Brian L. Bello(MedStar Washington Hospital Center), Joseph C. Carmichael(University of California, Irvine), John C. Krauss(University of Michigan), Ana Gleisner(University of Colorado Denver), Philip B. Paty(Memorial Sloan Kettering Cancer Center), Martin R. Weiser(Memorial Sloan Kettering Cancer Center), Garrett M. Nash(Memorial Sloan Kettering Cancer Center), Emmanouil P. Pappou(Memorial Sloan Kettering Cancer Center), José G. Guillem(University of North Carolina at Chapel Hill), Larissa K. Temple(University of Rochester Medical Center), Iris H. Wei(Memorial Sloan Kettering Cancer Center), Maria Widmar(Memorial Sloan Kettering Cancer Center), Sabrina T. Lin(Memorial Sloan Kettering Cancer Center), Neil H. Segal(Memorial Sloan Kettering Cancer Center), Andrea Cercek(Memorial Sloan Kettering Cancer Center), Rona Yaeger(Memorial Sloan Kettering Cancer Center), J. Joshua Smith(Memorial Sloan Kettering Cancer Center), Karyn A. Goodman(Icahn School of Medicine at Mount Sinai), Abraham J. Wu(Memorial Sloan Kettering Cancer Center), Leonard B. Saltz(Memorial Sloan Kettering Cancer Center)
Journal of Clinical Oncology
April 28, 2022
Cited by 885Open Access
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Abstract

PURPOSE: Prospective data on the efficacy of a watch-and-wait strategy to achieve organ preservation in patients with locally advanced rectal cancer treated with total neoadjuvant therapy are limited. METHODS: In this prospective, randomized phase II trial, we assessed the outcomes of 324 patients with stage II or III rectal adenocarcinoma treated with induction chemotherapy followed by chemoradiotherapy (INCT-CRT) or chemoradiotherapy followed by consolidation chemotherapy (CRT-CNCT) and either total mesorectal excision (TME) or watch-and-wait on the basis of tumor response. Patients in both groups received 4 months of infusional fluorouracil-leucovorin-oxaliplatin or capecitabine-oxaliplatin and 5,000 to 5,600 cGy of radiation combined with either continuous infusion fluorouracil or capecitabine during radiotherapy. The trial was designed as two stand-alone studies with disease-free survival (DFS) as the primary end point for both groups, with a comparison to a null hypothesis on the basis of historical data. The secondary end point was TME-free survival. RESULTS: Median follow-up was 3 years. Three-year DFS was 76% (95% CI, 69 to 84) for the INCT-CRT group and 76% (95% CI, 69 to 83) for the CRT-CNCT group, in line with the 3-year DFS rate (75%) observed historically. Three-year TME-free survival was 41% (95% CI, 33 to 50) in the INCT-CRT group and 53% (95% CI, 45 to 62) in the CRT-CNCT group. No differences were found between groups in local recurrence-free survival, distant metastasis-free survival, or overall survival. Patients who underwent TME after restaging and patients who underwent TME after regrowth had similar DFS rates. CONCLUSION: Organ preservation is achievable in half of the patients with rectal cancer treated with total neoadjuvant therapy, without an apparent detriment in survival, compared with historical controls treated with chemoradiotherapy, TME, and postoperative chemotherapy.


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