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Skeletal muscle loss during chemotherapy and its association with survival and systemic treatment toxicity in metastatic colorectal cancer: An AGEO prospective multicenter study - 11/11/21

Doi : 10.1016/j.clinre.2020.101603 
Claire Gallois a, Camille Bourillon b, Edouard Auclin a, c, Pascal Artru d, Astrid Lièvre e, Thierry Lecomte f, Christophe Locher g, Lysiane Marthey h, Roger Faroux i, Simon Pernot a, Maximilien Barret j, Julien Taieb a,
a Sorbonne Paris Cite, Paris Descartes University, Siric CARPEM, Assistance Publique-Hôpitaux de Paris, Department of Gastroenterology and Digestive Oncology, Hôpital Européen Georges Pompidou, Paris, France 
b Department of Radiology, Groupe Hospitalier Diaconnesses Croix Saint-Simon, Paris, France 
c Methodology and Quality of Life Unit in Oncology, University Hospital of Besançon, Besançon, France 
d Department of Gastroenterology and Digestive Oncology, Hôpital Privé Jean Mermoz, Lyon, France 
e Department of Gastroenterology, Centre Hospitalier Universitaire Pontchaillou, Université Rennes 1, Rennes, France 
f Department of Hepato-Gastroenterology and Digestive Oncology, Centre Hospitalier Régional Universitaire de Tours, Université François Rabelais, Tours, France 
g Department of Hepato-Gastroenterology, Centre Hospitalier de Meaux, Meaux, France 
h Department of Gastroenterology and Digestive Oncology, Hôpital Antoine Béclère, Clamart, France 
i Department of Hepato-Gastroenterology, Hôpital de La Roche-sur-Yon, La Roche-sur-Yon, France 
j Paris Descartes University, Assistance Publique-Hôpitaux de Paris, Department of Gastroenterology, Hôpital Cochin, Paris, France 

Corresponding author at: Department of Gastroenterology and Digestive Oncology, Hôpital Européen Georges Pompidou, 20 Rue Leblanc, 75015 Paris, France.Department of Gastroenterology and Digestive OncologyHôpital Européen Georges Pompidou20 Rue LeblancParis75015France

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Highlights

Pretherapeutic sarcopenia is not associated with poor outcomes in colorectal cancer.
The loss of skeletal muscle mass under treatment is highly prognostic.
The loss of skeletal muscle mass is associated with treatment-related toxicities.

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Abstract

Purpose

We showed in a previous study that the PG-SGA score is associated with survival and chemotherapy-related toxicities in metastatic colorectal cancer (mCRC) patients. The objective was to evaluate the association between pretherapeutic sarcopenia and variation in skeletal muscle index (SMI) during treatment with these outcomes in the same population.

Methods

This prospective, multicenter, observational study enrolled non-pretreated mCRC patients. SMI was measured on routine CT scan at day 0 (D0) and day 60 (D60). Nutritional factors were collected at D0. Progression-free survival (PFS) and overall survival (OS) were calculated from treatment start.

Results

149 patients were included from 7/2013 to 11/2016. Pretherapeutic sarcopenia was not significantly associated with survival or chemotherapy-related toxicities. The decrease in SMI > 14% was significantly associated with shorter PFS (6 vs 9 mo; HR 1.8, 95% CI 1.1−3.1, p = 0.02) and OS (8.5 vs 26 mo; HR 2.6, 95% CI 1.4−4.8, p = 0.002), independently of hypoalbuminemia and malnutrition defined by PG-SGA. Patients with a SMI decrease > 14% had a higher rate of grade ≥ 2 clinical toxicities (40% vs 22%, OR 3.0, 95% CI 1.2−7.7, p = 0.02), but the difference was not statistically significant in multivariable analysis.

Conclusion

To our knowledge, this is the first study to assess prospectively the association of skeletal muscle loss with survival and treatment toxicities in non-pretreated patients with mCRC. Pretherapeutic sarcopenia was not associated with poor outcomes, but the loss of skeletal muscle mass within 60 days from treatment start was highly prognostic, independently of other prognostic and nutritional factors.

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Abbreviations : ALP, CEA, CI, CT, D0, D60, HR, LDH, mCRC, OS, PFS, PG-SGA, PS, SMI

Keywords : Metastatic colorectal cancer, Skeletal muscle index, Sarcopenia, PG-SGA, Prognosis, Chemotherapy toxicity


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Vol 45 - N° 6

Articolo 101603- Novembre 2021 Ritorno al numero
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