Tumor-Induced Osteomalacia in Patients With Malignancy: A Meta-analysis and Systematic Review of Case Reports

Author:

Bouraima Farouk1,Sapin Vincent12ORCID,Kahouadji Samy12,Pickering Marie-Eva3,Pereira Bruno4ORCID,Bouvier Damien12ORCID,Oris Charlotte12

Affiliation:

1. Biochemistry and Molecular Genetics Department, University Hospital , 63000 Clermont-Ferrand , France

2. Clermont Auvergne University, CNRS, INSERM, iGReD , 63000 Clermont-Ferrand , France

3. Rheumatology Department, CHU Clermont-Ferrand , 63000 Clermont-Ferrand , France

4. Biostatistics unit (DRCI) Department, University Hospital , 63000 Clermont-Ferrand , France

Abstract

Abstract Context Tumor-induced osteomalacia (TIO) due to fibroblast growth factor 23 (FGF23) overexpression is becoming recognized in patients with malignancy. The condition may be underdiagnosed, with a scarce medical literature. Objective To perform a meta-analysis of case reports to allow a better understanding of malignant TIO and its clinical implications. Methods Full texts were selected according to strict inclusion criteria. All case reports were included where patients had hypophosphatemia, malignant TIO, and FGF23 blood levels. Thirty-two of 275 eligible studies (n = 34 patients) met inclusion criteria. A list of desired data was extracted and graded for methodological quality. Results Prostate adenocarcinoma (n = 9) were the most tumors reported. Twenty-five of 34 patients had a metastatic disease and a poor clinical outcome was reported for 15 of 28 patients. The median levels of blood phosphate and C-terminal FGF23 (cFGF23) were 0.40 mmol/L and 788.5 RU/mL, respectively. For most of patients, blood PTH was elevated or within range, and calcitriol levels were inappropriately low or normal. Alkaline phosphatase concentrations were increased for 20 of 22 patients. The cFGF23 values were significantly higher for patients with a poor clinical outcome when compared to other patients (1685 vs 357.5 RU/mL). In case of prostate cancer, cFGF23 levels were significantly lower (429.4 RU/mL) than for other malignancies (1007.5 RU/mL). Conclusion We report for the first time a detailed description of the clinical and biological characteristics of malignant TIO. In this context, FGF23 blood measurement would be of value for the diagnostic workup, prognostication, and follow-up of patients.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference57 articles.

1. Tumor-induced osteomalacia;Jan de Beur;JAMA,2005

2. Pleiotropic actions of FGF23;Erben;Toxicol Pathol,2017

3. FGF23 decreases renal NaPi-2a and NaPi-2c expression and induces hypophosphatemia in vivo predominantly via FGF receptor 1;Gattineni;Am J Physiol—Ren Physiol,2009

4. FGF-23 regulates CYP27B1 transcription in the kidney and in extra-renal tissues.;Chanakul;PLoS One,2013

5. Osteomalacia with Looser's nodes (Milkman's syndrome) due to a raised resistance to vitamin D acquired about the age of 15 years;McCance;Q J Med,1947

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