Low body mass index and sarcopenia associated with dose-limiting toxicity of sorafenib in patients with renal cell carcinoma
- PMID: 20089558
- DOI: 10.1093/annonc/mdp605
Low body mass index and sarcopenia associated with dose-limiting toxicity of sorafenib in patients with renal cell carcinoma
Abstract
Background: Patients with severe depletion of skeletal muscle (sarcopenia) are prone to dose-limiting toxicity (DLT) during fluoropyrimidine therapy. We hypothesized that sarcopenia may also predict toxicity of targeted therapy drugs.
Materials and methods: Metastatic renal cell cancer (RCC) patients (n = 55) received sorafenib 400 mg b.i.d. Weight, height and skeletal muscle cross-sectional area at the third lumbar vertebra were measured by computed tomography (CT). Toxicity was assessed.
Results: DLT occurred in 22% of patients overall, of which three-quarters were dose reductions to 400 mg and the remainder entailed termination of treatment. DLT was most common (41%) in sarcopenic patients whose body mass index (BMI) was <25 kg/m(2) and least common (13%) in patients who were not sarcopenic and/or overweight or obese (P = 0.03). Toxicity was especially prevalent in sarcopenic male patients with BMI < 25, with 71% of men with these characteristics being unable to continue treatment at 800 mg/day. By contrast, only 5% of male patients whose muscle index was above the cut-off for sarcopenia and only 11% of male patients whose BMI was >25 experienced a DLT.
Conclusion: BMI < 25 kg/m(2) with diminished muscle mass is a significant predictor of toxicity in metastatic RCC patients treated with sorafenib.
Similar articles
-
Body Composition by Computed Tomography as a Predictor of Toxicity in Patients With Renal Cell Carcinoma Treated With Sunitinib.Am J Clin Oncol. 2017 Feb;40(1):47-52. doi: 10.1097/COC.0000000000000061. Am J Clin Oncol. 2017. PMID: 24685884
-
Sarcopenia predicts early dose-limiting toxicities and pharmacokinetics of sorafenib in patients with hepatocellular carcinoma.PLoS One. 2012;7(5):e37563. doi: 10.1371/journal.pone.0037563. Epub 2012 May 30. PLoS One. 2012. PMID: 22666367 Free PMC article.
-
Sarcopenia and body mass index predict sunitinib-induced early dose-limiting toxicities in renal cancer patients.Br J Cancer. 2013 Mar 19;108(5):1034-41. doi: 10.1038/bjc.2013.58. Epub 2013 Mar 5. Br J Cancer. 2013. PMID: 23462722 Free PMC article.
-
[Myocardial metastasis from renal cell carcinoma treated with sorafenib].Hinyokika Kiyo. 2011 Oct;57(10):555-8. Hinyokika Kiyo. 2011. PMID: 22089153 Review. Japanese.
-
Sorafenib and sunitinib: novel targeted therapies for renal cell cancer.Pharmacotherapy. 2007 Aug;27(8):1125-44. doi: 10.1592/phco.27.8.1125. Pharmacotherapy. 2007. PMID: 17655513 Review.
Cited by
-
Prevalence and prognostic value of baseline sarcopenia in hematologic malignancies: a systematic review.Front Oncol. 2023 Dec 14;13:1308544. doi: 10.3389/fonc.2023.1308544. eCollection 2023. Front Oncol. 2023. PMID: 38162495 Free PMC article.
-
Erlotinib pharmacokinetics: a critical parameter influencing acute toxicity in elderly patients over 75 years-old.Invest New Drugs. 2017 Apr;35(2):242-246. doi: 10.1007/s10637-016-0400-5. Epub 2016 Oct 29. Invest New Drugs. 2017. PMID: 27796680 Clinical Trial.
-
Weight and skeletal muscle loss with cabozantinib in metastatic renal cell carcinoma.J Cachexia Sarcopenia Muscle. 2022 Oct;13(5):2405-2416. doi: 10.1002/jcsm.13021. Epub 2022 Jul 28. J Cachexia Sarcopenia Muscle. 2022. PMID: 35903892 Free PMC article.
-
Exposure-toxicity relationship of sorafenib in Japanese patients with renal cell carcinoma and hepatocellular carcinoma.Clin Pharmacokinet. 2014 Feb;53(2):185-96. doi: 10.1007/s40262-013-0108-z. Clin Pharmacokinet. 2014. PMID: 24135988
-
Is there a genetic cause for cancer cachexia? - a clinical validation study in 1797 patients.Br J Cancer. 2011 Oct 11;105(8):1244-51. doi: 10.1038/bjc.2011.323. Epub 2011 Sep 20. Br J Cancer. 2011. PMID: 21934689 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical