Neoadjuvant Chemotherapy, Excision, and Observation for Early Rectal Cancer: The Phase II NEO Trial (CCTG CO.28) Primary End Point Results

Author:

Kennecke Hagen F.1ORCID,O'Callaghan Chris J.2,Loree Jonathan M.3ORCID,Moloo Hussein4ORCID,Auer Rebecca4ORCID,Jonker Derek J.4,Raval Manoj5ORCID,Musselman Reilly4,Ma Grace6ORCID,Caycedo-Marulanda Antonio6ORCID,Simianu Vlad V.7,Patel Sunil2,Pitre Lacey D.8ORCID,Helewa Ramzi9,Gordon Vallerie L.10,Neumann Katerina11,Nimeiri Halla12,Sherry Max2,Tu Dongsheng2ORCID,Brown Carl J.5ORCID

Affiliation:

1. Providence Cancer Institute and Earle A Chiles Research Institute, Portland, OR

2. Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada

3. BC Cancer, Vancouver, BC, Canada

4. The Ottawa Hospital Research Institute, Ottawa, ON, Canada

5. Providence-St. Paul's Hospital, Vancouver, BC, Canada

6. Health Sciences North, Sudbury, ON, Canada

7. Virginia Mason Cancer Institute, Seattle, WA

8. Juravinski Cancer Center, Hamilton, ON, Canada

9. University of Manitoba, Winnipeg, MB, Canada

10. CancerCare Manitoba, Winnipeg, MB, Canada

11. Nova Scotia Health, Halifax, NS, Canada

12. Foundation Medicine, Cambridge, MA

Abstract

PURPOSE Organ-sparing therapy for early-stage I/IIA rectal cancer is intended to avoid functional disturbances or a permanent ostomy associated with total mesorectal excision (TME). The objective of this phase II trial was to determine the outcomes and organ-sparing rate of patients with early-stage rectal cancer treated with neoadjuvant chemotherapy followed by transanal excision surgery (TES). METHODS This phase II trial included patients with clinical T1-T3abN0 low- or mid-rectal adenocarcinoma eligible for endoscopic resection who were treated with 3 months of chemotherapy (modified folinic acid–fluorouracil-oxaliplatin 6 or capecitabine-oxaliplatin). Those with evidence of response proceeded to transanal endoscopic surgery 2-6 weeks later. The primary end point was protocol-specified organ preservation rate, defined as the proportion of patients with tumor downstaging to ypT0/T1N0/X and who avoided radical surgery. RESULTS Of 58 patients enrolled, all commenced chemotherapy and 56 proceeded to surgery. A total of 33/58 patients had tumor downstaging to ypT0/1N0/X on the surgery specimen, resulting in an intention-to-treat protocol-specified organ preservation rate of 57% (90% CI, 45 to 68). Of 23 remaining patients recommended for TME surgery on the basis of protocol requirements, 13 declined and elected to proceed directly to observation resulting in 79% (90% CI, 69 to 88) achieving organ preservation. The remaining 10/23 patients proceeded to recommended TME of whom seven had no histopathologic residual disease. The 1-year and 2-year locoregional relapse-free survival was, respectively, 98% (95% CI, 86 to 100) and 90% (95% CI, 58 to 98), and there were no distant recurrences or deaths. Minimal change in quality of life and rectal function scores was observed. CONCLUSION Three months of induction chemotherapy may successfully downstage a significant proportion of patients with early-stage rectal cancer, allowing well-tolerated organ-preserving surgery.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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