Association of Low Handgrip Strength with Chemotherapy Toxicity in Digestive Cancer Patients: A Comprehensive Observational Cohort Study (FIGHTDIGOTOX).


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
22 Oct 2022
Historique:
received: 21 09 2022
revised: 17 10 2022
accepted: 20 10 2022
entrez: 11 11 2022
pubmed: 12 11 2022
medline: 15 11 2022
Statut: epublish

Résumé

In the FIGHTDIGO study, digestive cancer patients with dynapenia experienced more chemotherapy-induced neurotoxicities. FIGHTDIGOTOX aimed to evaluate the relationship between pre-therapeutic handgrip strength (HGS) and chemotherapy-induced dose-limiting toxicity (DLT) or all-grade toxicity in digestive cancer patients. HGS measurement was performed with a Jamar dynamometer. Dynapenia was defined according to EWGSOP2 criteria (<27 kg (men); <16 kg (women)). DLT was defined as any toxicity leading to dose reduction, treatment delay, or permanent discontinuation. We also performed an exploratory analysis in patients below the included population’s median HGS. A total of 244 patients were included. According to EWGSOP2 criteria, 23 patients had pre-therapeutic dynapenia (9.4%). With our exploratory median-based threshold (34 kg for men; 22 kg for women), 107 patients were dynapenic (43.8%). For each threshold, dynapenia was not an independent predictive factor of overall DLT and neurotoxicity. Dynapenic patients according to EWGSOP2 definition experienced more hand-foot syndrome (p = 0.007). Low HGS according to our exploratory threshold was associated with more all-grade asthenia (p = 0.014), anemia (p = 0.006), and asthenia with DLT (p = 0.029). Pre-therapeutic dynapenia was not a predictive factor for overall DLT and neurotoxicity in digestive cancer patients but could be a predictive factor of chemotherapy-induced anemia and asthenia. There is a need to better define the threshold of dynapenia in cancer patients.

Identifiants

pubmed: 36364711
pii: nu14214448
doi: 10.3390/nu14214448
pmc: PMC9654937
pii:
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Observational Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Pierre Martin (P)

Department of Medical Oncology, Godinot Cancer Institute, 51100 Reims, France.
Department of Gastroenterology and Digestive Oncology, Université de Reims Champagne-Ardenne, CHU Reims, 51100 Reims, France.

Damien Botsen (D)

Department of Medical Oncology, Godinot Cancer Institute, 51100 Reims, France.
Department of Gastroenterology and Digestive Oncology, Université de Reims Champagne-Ardenne, CHU Reims, 51100 Reims, France.

Mathias Brugel (M)

Department of Gastroenterology and Digestive Oncology, Université de Reims Champagne-Ardenne, CHU Reims, 51100 Reims, France.

Eric Bertin (E)

Department of Nutrition, Endocrinology and Diabetology, CHU Reims, 51100 Reims, France.

Claire Carlier (C)

Department of Medical Oncology, Godinot Cancer Institute, 51100 Reims, France.
Department of Gastroenterology and Digestive Oncology, Université de Reims Champagne-Ardenne, CHU Reims, 51100 Reims, France.

Rachid Mahmoudi (R)

Department of Internal Medicine and Geriatrics, Université de Reims Champagne-Ardenne, VieFra, CHU Reims, 51100 Reims, France.

Florian Slimano (F)

Department of Pharmacy, Université de Reims Champagne-Ardenne, CHU Reims, 51100 Reims, France.

Marine Perrier (M)

Department of Gastroenterology and Digestive Oncology, Université de Reims Champagne-Ardenne, CHU Reims, 51100 Reims, France.

Olivier Bouché (O)

Department of Gastroenterology and Digestive Oncology, Université de Reims Champagne-Ardenne, CHU Reims, 51100 Reims, France.

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