Prognostic Impact of Early Treatment and Oxaliplatin Discontinuation in Patients With Stage III Colon Cancer: An ACCENT/IDEA Pooled Analysis of 11 Adjuvant Trials.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 02 2023
Historique:
pubmed: 29 10 2022
medline: 1 2 2023
entrez: 28 10 2022
Statut: ppublish

Résumé

Oxaliplatin-based adjuvant chemotherapy in patients with stage III colon cancer (CC) for 6 months remains a standard in high-risk stage III patients. Data are lacking as to whether early discontinuation of all treatment (ETD) or early discontinuation of oxaliplatin (EOD) could worsen the prognosis. We studied the prognostic impact of ETD and EOD in patients with stage III CC from the ACCENT/IDEA databases, where patients were planned to receive 6 months of infusional fluorouracil, leucovorin, and oxaliplatin or capecitabine plus oxaliplatin. ETD was defined as discontinuation of treatment and EOD as discontinuation of oxaliplatin only before patients had received a maximum of 75% of planned cycles. Association between ETD/EOD and overall survival and disease-free survival (DFS) were assessed by Cox models adjusted for established prognostic factors. Analysis of ETD and EOD included 10,447 (20.9% with ETD) and 7,243 (18.8% with EOD) patients, respectively. Compared with patients without ETD or EOD, patients with ETD or EOD were statistically more likely to be women, with Eastern Cooperative Oncology Group performance status ≥ 1, and for ETD, older with a lower body mass index. In multivariable analyses, ETD was associated with a decrease in disease-free survival and overall survival (hazard ratio [HR], 1.61, In patients treated with 6 months of oxaliplatin-based chemotherapy for stage III CC, ETD was associated with poorer oncologic outcomes. However, this was not the case for EOD. These data favor discontinuing oxaliplatin while continuing fluoropyrimidine in individuals with significant neurotoxicity having received > 50% of the planned 6-month chemotherapy.

Identifiants

pubmed: 36306483
doi: 10.1200/JCO.21.02726
doi:

Substances chimiques

Fluorouracil U3P01618RT
Leucovorin Q573I9DVLP
Oxaliplatin 04ZR38536J

Banques de données

ClinicalTrials.gov
['NCT00749450', 'NCT00275210', 'NCT01150045', 'NCT00958737', 'NCT00069121', 'NCT00079274', 'NCT00265811', 'NCT00112918', 'NCT01308086', 'UMIN000008543', 'NCT00646607']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

803-815

Auteurs

Claire Gallois (C)

Paris-Cité University, Department of Gastroenterology and Digestive Oncology, Georges Pompidou European Hospital, SIRIC CARPEM, Paris, France.

Qian Shi (Q)

Department of Health Science Research, Mayo Clinic, Rochester, MN.

Jeffrey P Meyers (JP)

Department of Health Science Research, Mayo Clinic, Rochester, MN.

Timothy Iveson (T)

Department of Medical Oncology, University of Southampton, Southampton, United Kingdom.

Steven R Alberts (SR)

Department of Oncology, Mayo Clinic, Rochester, MN.

Aimery de Gramont (A)

Department of Medical Oncology, Franco-British Institute, Levallois-Perret, France.

Alberto F Sobrero (AF)

Medical Oncology, IRCCS San Martino IST, Genoa, Italy.

Daniel G Haller (DG)

Division of Hematology/Oncology, University of Pennsylvania, Philadelphia, PA.

Eiji Oki (E)

Department of Surgery and Science, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

Anthony Frank Shields (AF)

Karmanos Cancer Institute, Wayne State University, Detroit, MI.

Richard M Goldberg (RM)

West Virginia University Cancer Institute and the Mary Babb Randolph Cancer Center, Morgantown, WV.

Rachel Kerr (R)

Department of Oncology, Oxford University, Oxford, United Kingdom.

Sara Lonardi (S)

Medical Oncology Unit 1, Clinical and Experimental Oncology Department, Veneto Institute of Oncology IRCCS, Padua, Italy.

Greg Yothers (G)

Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA.

Caroline Kelly (C)

Cancer Research UK Clinical Trials Unit, Institute of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.

Ioannis Boukovinas (I)

Bioclinic Thessaloniki Medical Oncology Unit, Thessaloniki, Greece.

Roberto Labianca (R)

Ospdale Papa Giovanni XXIII, Bergamo, Italy.

Frank A Sinicrope (FA)

Department of Oncology, Mayo Clinic, Rochester, MN.

Ioannis Souglakos (I)

Department of Medical Oncology, University Hospital of Heraklion, Heraklion, Greece.

Takayuki Yoshino (T)

Department of Gastrointestinal Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Jeffrey A Meyerhardt (JA)

Dana-Farber Cancer Institute, Boston, MA.

Thierry André (T)

Sorbonne Université, Department of Medical Oncology, Hôpital Saint-Antoine, Paris, France.

Demetris Papamichael (D)

Division of Medical Oncology, Bank Of Cyprus Oncology Centre, Nicosia, Cyprus.

Julien Taieb (J)

Paris-Cité University, Department of Gastroenterology and Digestive Oncology, Georges Pompidou European Hospital, SIRIC CARPEM, Paris, France.

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Classifications MeSH