Association between Computed Tomography-Determined Loss of Muscle Mass and Impaired Three-Month Survival in Frail Older Adults with Cancer

Author:

Tolonen Antti12ORCID,Kerminen Hanna234ORCID,Lehtomäki Kaisa25ORCID,Huhtala Heini6,Bärlund Maarit25,Österlund Pia25789ORCID,Arponen Otso12

Affiliation:

1. Department of Radiology, Tampere University Hospital, Kuntokatu 2, 33520 Tampere, Finland

2. Faculty of Medicine and Health Technology, Tampere University, Arvo Ylpön Katu 34, 33520 Tampere, Finland

3. Centre of Geriatrics, Tampere University Hospital, Kuntokatu 2, 33520 Tampere, Finland

4. Gerontology Research Center (GEREC), Tampere University, Arvo Ylpön Katu 34, 33520 Tampere, Finland

5. Department of Oncology, Tays Cancer Centre, Tampere University Hospital, Teiskontie 35, 33520 Tampere, Finland

6. Faculty of Social Sciences, Tampere University, Kalevantie 5, 33014 Tampere, Finland

7. Department of Oncology, Comprehensive Cancer Center, Helsinki University Hospital, University of Helsinki, Haartmaninkatu 4, 00290 Helsinki, Finland

8. Department of Gastrointestinal Oncology, Tema Cancer, Karolinska Universitetssjukhuset, Eugeniavägen 3, 17176 Solna, Sweden

9. Department of Oncology-Pathology, Karolinska Institutet, Solnavägen 1, 17177 Solna, Sweden

Abstract

As patients with solid (non-hematological) cancers and a life expectancy of <3 months rarely benefit from oncological treatment, we examined whether the CT-determined loss of muscle mass is associated with an impaired 3-month overall survival (OS) in frail ≥75-year-old patients with cancer. Frailty was assessed with G8-screening and comprehensive geriatric assessment in older adults at risk of frailty. The L3-level skeletal (SMI) and psoas (PMI) muscle indexes were determined from routine CT scans. Established and optimized SMI and PMI cut-offs were used. In the non-curative treatment group (n = 58), 3-month OS rates for normal and low SMI were 95% and 64% (HR 9.28; 95% CI 1.2–71) and for PMI 88%, and 60%, respectively (HR 4.10; 1.3–13). A Cox multivariable 3-month OS model showed an HR of 10.7 (1.0–110) for low SMI, 2.34 (0.6–9.8) for ECOG performance status 3–4, 2.11 (0.5–8.6) for clinical frailty scale 5–9, and 0.57 (0.1–2.8) for males. The 24-month OS rates in the curative intent group (n = 21) were 91% and 38% for the normal and low SMI groups, respectively. In conclusion, CT-determined low muscle mass is independently associated with an impaired 3-month OS and, alongside geriatric assessment, could aid in oncological versus best supportive care decision-making in frail patients with non-curable cancers.

Funder

Orion Research Foundation

Finnish Medical Association

Tampere University Hospital

Finnish Cancer Foundation

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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