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

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...

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Autores principales: Kennecke, Hagen F., O'Callaghan, Chris J., Loree, Jonathan M., Moloo, Hussein, Auer, Rebecca, Jonker, Derek J., Raval, Manoj, Musselman, Reilly, Ma, Grace, Caycedo-Marulanda, Antonio, Simianu, Vlad V., Patel, Sunil, Pitre, Lacey D., Helewa, Ramzi, Gordon, Vallerie L., Neumann, Katerina, Nimeiri, Halla, Sherry, Max, Tu, Dongsheng, Brown, Carl J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9839227/
https://www.ncbi.nlm.nih.gov/pubmed/35981270
http://dx.doi.org/10.1200/JCO.22.00184
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author Kennecke, Hagen F.
O'Callaghan, Chris J.
Loree, Jonathan M.
Moloo, Hussein
Auer, Rebecca
Jonker, Derek J.
Raval, Manoj
Musselman, Reilly
Ma, Grace
Caycedo-Marulanda, Antonio
Simianu, Vlad V.
Patel, Sunil
Pitre, Lacey D.
Helewa, Ramzi
Gordon, Vallerie L.
Neumann, Katerina
Nimeiri, Halla
Sherry, Max
Tu, Dongsheng
Brown, Carl J.
author_facet Kennecke, Hagen F.
O'Callaghan, Chris J.
Loree, Jonathan M.
Moloo, Hussein
Auer, Rebecca
Jonker, Derek J.
Raval, Manoj
Musselman, Reilly
Ma, Grace
Caycedo-Marulanda, Antonio
Simianu, Vlad V.
Patel, Sunil
Pitre, Lacey D.
Helewa, Ramzi
Gordon, Vallerie L.
Neumann, Katerina
Nimeiri, Halla
Sherry, Max
Tu, Dongsheng
Brown, Carl J.
author_sort Kennecke, Hagen F.
collection PubMed
description 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.
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spelling pubmed-98392272023-01-17 Neoadjuvant Chemotherapy, Excision, and Observation for Early Rectal Cancer: The Phase II NEO Trial (CCTG CO.28) Primary End Point Results Kennecke, Hagen F. O'Callaghan, Chris J. Loree, Jonathan M. Moloo, Hussein Auer, Rebecca Jonker, Derek J. Raval, Manoj Musselman, Reilly Ma, Grace Caycedo-Marulanda, Antonio Simianu, Vlad V. Patel, Sunil Pitre, Lacey D. Helewa, Ramzi Gordon, Vallerie L. Neumann, Katerina Nimeiri, Halla Sherry, Max Tu, Dongsheng Brown, Carl J. J Clin Oncol ORIGINAL REPORTS 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. Wolters Kluwer Health 2023-01-10 2022-08-18 /pmc/articles/PMC9839227/ /pubmed/35981270 http://dx.doi.org/10.1200/JCO.22.00184 Text en © 2022 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle ORIGINAL REPORTS
Kennecke, Hagen F.
O'Callaghan, Chris J.
Loree, Jonathan M.
Moloo, Hussein
Auer, Rebecca
Jonker, Derek J.
Raval, Manoj
Musselman, Reilly
Ma, Grace
Caycedo-Marulanda, Antonio
Simianu, Vlad V.
Patel, Sunil
Pitre, Lacey D.
Helewa, Ramzi
Gordon, Vallerie L.
Neumann, Katerina
Nimeiri, Halla
Sherry, Max
Tu, Dongsheng
Brown, Carl J.
Neoadjuvant Chemotherapy, Excision, and Observation for Early Rectal Cancer: The Phase II NEO Trial (CCTG CO.28) Primary End Point Results
title Neoadjuvant Chemotherapy, Excision, and Observation for Early Rectal Cancer: The Phase II NEO Trial (CCTG CO.28) Primary End Point Results
title_full Neoadjuvant Chemotherapy, Excision, and Observation for Early Rectal Cancer: The Phase II NEO Trial (CCTG CO.28) Primary End Point Results
title_fullStr Neoadjuvant Chemotherapy, Excision, and Observation for Early Rectal Cancer: The Phase II NEO Trial (CCTG CO.28) Primary End Point Results
title_full_unstemmed Neoadjuvant Chemotherapy, Excision, and Observation for Early Rectal Cancer: The Phase II NEO Trial (CCTG CO.28) Primary End Point Results
title_short Neoadjuvant Chemotherapy, Excision, and Observation for Early Rectal Cancer: The Phase II NEO Trial (CCTG CO.28) Primary End Point Results
title_sort neoadjuvant chemotherapy, excision, and observation for early rectal cancer: the phase ii neo trial (cctg co.28) primary end point results
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9839227/
https://www.ncbi.nlm.nih.gov/pubmed/35981270
http://dx.doi.org/10.1200/JCO.22.00184
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