Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Oct 1;19(10):2999.
doi: 10.3390/ijms19102999.

Impact of Sarcopenia as a Prognostic Biomarker of Bladder Cancer

Affiliations
Review

Impact of Sarcopenia as a Prognostic Biomarker of Bladder Cancer

Hiroshi Fukushima et al. Int J Mol Sci. .

Abstract

Sarcopenia, the degenerative and systemic loss of skeletal muscle mass, indicates patient frailty and impaired physical function. Sarcopenia can be caused by multiple factors, including advanced age, lack of exercise, poor nutritional status, inflammatory diseases, endocrine diseases, and malignancies. In patients with cancer cachexia, anorexia, poor nutrition and systemic inflammation make the metabolic state more catabolic, resulting in sarcopenia. Thus, sarcopenia is considered as one of manifestations of cancer cachexia. Recently, growing evidence has indicated the importance of sarcopenia in the management of patients with various cancers. Sarcopenia is associated with not only higher rates of treatment-related complications but also worse prognosis in cancer-bearing patients. In this article, we summarized metabolic backgrounds of cancer cachexia and sarcopenia and definitions of sarcopenia based on computed tomography (CT) images. We conducted a systematic literature review regarding the significance of sarcopenia as a prognostic biomarker of bladder cancer. We also reviewed recent studies focusing on the prognostic role of changes in skeletal muscle mass during the course of treatment in bladder cancer patients. Lastly, we discussed the impact of nutritional support, medication, and exercise on sarcopenia in cancer-bearing patients.

Keywords: biomarker; bladder cancer; prognosis; sarcopenia; urothelial carcinoma.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Computed tomography (CT) images of typical sarcopenic and non-sarcopenic cases. Skeletal muscle area is shown in red.
Figure 2
Figure 2
Hybrid nature of sarcopenia.
Figure 3
Figure 3
Flow diagram of systematic literature search.

Similar articles

Cited by

References

    1. Antoni S., Ferlay J., Soerjomataram I., Znaor A., Jemal A., Bray F. Bladder Cancer Incidence and Mortality: A Global Overview and Recent Trends. Eur. Urol. 2017;71:96–108. doi: 10.1016/j.eururo.2016.06.010. - DOI - PubMed
    1. Babjuk M., Bohle A., Burger M., Capoun O., Cohen D., Comperat E.M., Hernandez V., Kaasinen E., Palou J., Roupret M., et al. EAU Guidelines on Non-Muscle-invasive Urothelial Carcinoma of the Bladder: Update 2016. Eur. Urol. 2017;71:447–461. doi: 10.1016/j.eururo.2016.05.041. - DOI - PubMed
    1. Witjes J.A., Lebret T., Comperat E.M., Cowan N.C., De Santis M., Bruins H.M., Hernandez V., Espinos E.L., Dunn J., Rouanne M., et al. Updated 2016 EAU Guidelines on Muscle-invasive and Metastatic Bladder Cancer. Eur. Urol. 2017;71:462–475. doi: 10.1016/j.eururo.2016.06.020. - DOI - PubMed
    1. Dalbagni G., Genega E., Hashibe M., Zhang Z.F., Russo P., Herr H., Reuter V. Cystectomy for bladder cancer: A contemporary series. J. Urol. 2001;165:1111–1116. doi: 10.1016/S0022-5347(05)66440-3. - DOI - PubMed
    1. Bellmunt J., von der Maase H., Mead G.M., Skoneczna I., De Santis M., Daugaard G., Boehle A., Chevreau C., Paz-Ares L., Laufman L.R., et al. Randomized phase III study comparing paclitaxel/cisplatin/gemcitabine and gemcitabine/cisplatin in patients with locally advanced or metastatic urothelial cancer without prior systemic therapy: EORTC Intergroup Study 30987. J. Clin. Oncol. 2012;30:1107–1113. doi: 10.1200/JCO.2011.38.6979. - DOI - PMC - PubMed

Substances