Journals / Eskisehir Medical Journal / 2026 / Volume: 7 Issue: 2

Longitudinal Temporal Muscle Loss Rate Predicts 90-Day Mortality in Patients with Advanced Solid Cancer

Kamil Konur(RECEP TAYYIP ERDOGAN UNIVERSITY, SCHOOL OF MEDICINE)0000-0002-9666-8085
Mehmet Beyazal(RECEP TAYYIP ERDOGAN UNIVERSITY, SCHOOL OF MEDICINE)0000-0002-4748-4941
Mümin Murat Yazıcı(Recep Tayyip Erdogan University Training and Research Hospital)0000-0003-1957-7283
Hatice Beyazal Polat(RECEP TAYYIP ERDOGAN UNIVERSITY, SCHOOL OF MEDICINE)0000-0002-7947-6874
Pages
—
Publication Date
2026-05-31
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Conclusion: Temporal muscle loss rate may serve as a useful dynamic biomarker for predicting short-term mortality in patients with advanced solid cancer.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Introduction: Early detection of muscle loss and prediction of prognosis in cancer patients are of great importance for clinical management.
📊
Key Findings & Data:This study aimed to investigate the relationship between temporal muscle thickness changes over time and clinical outcomes in patients with advanced solid cancer, and to evaluate the prognostic value of temporal muscle loss rate in predicting 90-day mortality.
💡
Conclusion & Impact:Conclusion: Temporal muscle loss rate may serve as a useful dynamic biomarker for predicting short-term mortality in patients with advanced solid cancer.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Temporal muscle thickness · Sarcopenia · Advanced cancer

Abstract

Introduction: Early detection of muscle loss and prediction of prognosis in cancer patients are of great importance for clinical management. This study aimed to investigate the relationship between temporal muscle thickness changes over time and clinical outcomes in patients with advanced solid cancer, and to evaluate the prognostic value of temporal muscle loss rate in predicting 90-day mortality. Methods: In this retrospective observational study, patients with advanced solid cancer who had at least two cranial computed tomography scans during follow-up were included. Temporal muscle thickness was measured on both the right and left sides at two different time points, and the temporal muscle loss rate (mm/month) was calculated. Demographic data, laboratory parameters, and anthropometric measurements were obtained from patient records. Factors predicting mortality were evaluated using logistic regression analysis, and prognostic performance was assessed by receiver operating characteristic analysis. Results: A total of 57 patients were included in the study. 90-day mortality occurred in 78.9% of patients. Neutrophil levels were significantly higher in the mortality group, while albumin and magnesium levels were significantly lower. Baseline temporal muscle thickness measurements were not associated with mortality; however, right and left temporal muscle loss rates were significantly higher in the mortality group. Multivariable logistic regression analysis identified left temporal muscle loss rate and neutrophil level as independent predictors of mortality. Receiver operating characteristic curve analysis demonstrated good discriminative performance, with the left temporal muscle loss rate exhibiting superior predictive ability. Conclusion: Temporal muscle loss rate may serve as a useful dynamic biomarker for predicting short-term mortality in patients with advanced solid cancer.

🔖

Cite This Article

Konur, K., Beyazal, M., Yazıcı, M. M., Polat, H. B. (2026). Longitudinal Temporal Muscle Loss Rate Predicts 90-Day Mortality in Patients with Advanced Solid Cancer. Eskisehir Medical Journal, Volume: 7 Issue: 2. https://ajindex.com/articles/1614199

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (18)

  1. Bullock AF, Patterson MJ, Paton LW, et al. Malnutrition, sarcopenia and cachexia: exploring prevalence, overlap, and perceptions in older adults with cancer. Eur J Clin Nutr 2024;78:486-93. doi:10.1038/s41430-024-01433-9.
  2. Gökçin Z, Özçelik M, Kulalı F, Emir SN, Uçak Basat S. The relationship of sarcopenia with prognosis in patients diagnosed with metastatic gastric cancer receiving palliative chemotherapy. DAHUDER Med J 2025;5(3):101-8. doi:10.56016/dahudermj.1709426.
  3. Xu H, Song C, Yin L, et al. Extension protocol for the Investigation on Nutrition Status and Clinical Outcome of Patients with Common Cancers in China (INSCOC) study: 2021 update. Precis Nutr 2022;1(2). doi:10.1097/PN9.0000000000000014.
  4. Zhang J, Quan Y, Wang X, et al. Global epidemiological characteristics of malnutrition in cancer patients: a comprehensive meta-analysis and systematic review. BMC Cancer 2025;25(1):1191. doi:10.1186/s12885-025-14558-2.
  5. Song C, Shi H. Diagnosis of malnutrition in cancer patients. Cancer Biol Med 2024;20(12):963-6. doi:10.20892/j.issn.2095-3941.2023.0473.
  6. Liu W, Cao H, Zhou X, et al. From mechanisms to management: a comprehensive review of sarcopenia in gastric cancer. Front Nutr 2026;13:1726256. doi:10.3389/fnut.2026.1726256.
  7. Rakici SY, Aksoy RA, Burakgazi G, et al. Sarcopenia is a bad harbinger of cancer-related survival in rectal cancer. Ann Med 2025;57(1):2603015. doi:10.1080/07853890.2025.2603015.
  8. Anabtawi NM, Pasala MS, Grimshaw AA, et al. Low skeletal muscle mass and treatment outcomes among adults with haematologic malignancies: a systematic review and meta-analysis. J Cachexia Sarcopenia Muscle 2024;15(3):1084-93. doi:10.1002/jcsm.13446.
  9. Mohajerani E, Gümüs M, Dinger TF, et al. Temporal muscle thickness as a feasible sarcopenia marker and outcome predictor after aneurysmal subarachnoid hemorrhage. Acta Neurochir (Wien) 2025;167(1):157. doi:10.1007/s00701-025-06562-z.
  10. Furtner J, Weller M, Weber M, et al. Temporal muscle thickness as a prognostic marker in patients with newly diagnosed glioblastoma: translational imaging analysis of the CENTRIC EORTC 26071-22072 and CORE trials. Clin Cancer Res 2022;28(1):129-36. doi:10.1158/1078-0432.CCR-21-1987.
  11. Tang J, Dong Z, Yang L, et al. The relationship between prognosis and temporal muscle thickness in 102 patients with glioblastoma. Sci Rep 2024;14:13958. doi:10.1038/s41598-024-64947-z.
  12. Lazaridis L, Moenninghoff C, Bumes E, et al. Temporal muscle thickness as a prognostic marker in a real-life cohort of newly diagnosed MGMT promoter methylated glioblastoma: a multicentric imaging analysis. Cancer Med 2025;14(8). doi:10.1002/cam4.70689.
  13. Rafaelian A, Won SY, Behmanesh B, et al. The velocity of temporalis muscle wasting in cerebral metastasis is prognostic for poor survival. Front Oncol 2025;15:1482705. doi:10.3389/fonc.2025.1482705.
  14. Maskos A, Schmidbauer ML, Kunst S, et al. Diagnostic utility of temporal muscle thickness as a monitoring tool for muscle wasting in neurocritical care. Nutrients 2022;14(21):4498. doi:10.3390/nu14214498.
  15. Kanbur B, Unek IT, Uzun M, et al. Association of systemic inflammatory response index and prognostic nutritional index scores with sarcopenia in patients with metastatic gastric cancer. Medicina (Kaunas) 2025;61(5):785. doi:10.3390/medicina61050785.
  16. Pryce BR, Oles A, Talbert EE, et al. Muscle inflammation is regulated by NF-κB from multiple cells to control distinct states of wasting in cancer cachexia. Cell Rep 2024;43(11):114925. doi:10.1016/j.celrep.2024.114925.
  17. Yu Y, Chen B. Association between neutrophil percentage to albumin ratio and sarcopenia among cancer patients: evidence from both the Chinese and American cohorts. Front Nutr 2026;12:1709323. doi:10.3389/fnut.2025.1709323.
  18. Klingenschmid J, Krigers A, Pinggera D, et al. Temporal muscle thickness compared to functional scales as a prognostic parameter in patients with brain metastases. Cancers (Basel) 2024;16(9):1660. doi:10.3390/cancers16091660.