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Survival and patient-reported outcomes of real-world high-risk stage II and stage III colon cancer patients after reduction of adjuvant CAPOX duration from 6 to 3 months.
Franken, Ingrid A; van der Baan, Frederieke H; Vink, Geraldine R; May, Anne M; van Grevenstein, Wilhelmina M U; Koopman, Miriam; Roodhart, Jeanine M L.
Afiliação
  • Franken IA; Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • van der Baan FH; Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • Vink GR; Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands; Department of Research and Development, Netherlands Comprehensive Cancer Organisation (IKNL), Utrecht, the Netherlands.
  • May AM; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • van Grevenstein WMU; Department of Surgical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • Koopman M; Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • Roodhart JML; Department of Medical Oncology, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands. Electronic address: j.roodhart@umcutrecht.nl.
Eur J Cancer ; 208: 114207, 2024 Sep.
Article em En | MEDLINE | ID: mdl-39024724
ABSTRACT

AIM:

Adjuvant chemotherapy has been advised for high-risk stage II and III colon cancer since 2004. After the IDEA study showed no clinically relevant difference in outcome, reduction of adjuvant CAPOX duration from 6 to 3 months was rapidly adopted in the Dutch treatment guideline in 2017. This study investigates the real-world impact of the guideline change on overall survival (OS) and patient-reported outcomes (PROs).

METHODS:

Patients with high-risk stage II (pT4 +) and III (pN+) colon cancer were selected from the Netherlands Cancer Registry, based on surgical resection and adjuvant CAPOX before (2015-2016) versus after (2018-2019) the guideline change. Both groups were compared on OS, using multivariable Cox regression, and on PROs.

RESULTS:

Patients treated before (n = 2330) and after (n = 2108) the guideline change showed similar OS (HR 1.02; 95 %CI [0.89-1.16]), also in high-risk stage III (pT4/N2, HR 1.06 [0.89-1.26]). After the guideline change, 90 % of patients were treated for 3 months with no inferior OS to those still receiving 6 months (HR 0.89 [0.66-1.20]). PROs 2 years after CAPOX completion, available for a subset of patients, suggest a lower neuropathy (n = 366; 26.2 [21.3-31.1] to 16.5 [14.4-18.6]) and better quality of life (n = 396; 80.9 [78.6-83.2] to 83.9 [82.8-84.9]), but no significant difference in workability (n = 120; 31.5 [27.9-35.1]) to 35.3 [33.8-36.7]), with reduction from 6 to 3 months of CAPOX.

CONCLUSION:

This real-world study confirmed that shorter adjuvant CAPOX did not compromise OS and may improve PROs, complementing the IDEA study and supporting 3 months of adjuvant CAPOX in daily clinical practice.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Medidas de Resultados Relatados pelo Paciente / Estadiamento de Neoplasias País/Região como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Medidas de Resultados Relatados pelo Paciente / Estadiamento de Neoplasias País/Região como assunto: Europa Idioma: En Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda