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. 2020 May 19;10:779. doi: 10.3389/fonc.2020.00779

Table 1.

Platinum derived drugs.

Electrolyte disorder Drug Incidence (%) Type of study Mechanism(s)
Hyponatremia Cisplatin
Carboplatin
43-59 (B) (29, 30)
20 (C) (31)
SIADH;
RSWS, DNA damage of the gene encoding the thiazide-sensitive chloride channel (29, 3234)
Hypernatremia Platinum-drugs n.a. Acquired NDI (32)
Hypokalemia Cisplatin
Carboplatin
27 (D,B) (31, 35) Renal potassium wasting due to hypomagnesemia;
Decreased intestinal absorption due to enterocyte cytoxicity (35, 36)
Hypomagnesemia Cisplatin
Carboplatin
56-90 (B, D) (22, 23, 37)
7-29 (D) (3840)
Calcium-sensing receptor impairment;
TRPM6/EGF pathway downregulation
(18, 22, 41)
Gitelman-like syndrome (42)
Hypocalcemia Cisplatin
Carboplatin
6-20 (B, D) (43)
16-31 (B, D) (43)
Impaired PTH release due to hypomagnesemia (24, 44, 45)
Altered bone metabolism due to hypomagnesemia; Low vitamin D due to decreased 1-alpha-OHase activity
(24, 43, 46)
Hypophosphatemia Cisplatin alone
(combined with Cyclophosphamide)
10-77 (D) (47, 48) Partial proximal tubular damage;
Acquired FS (47, 49)

Incidence and type of study column: the letter after the percentage indicates the type of evidence available: A isolated case; B case series; C pharmacovigilance notifications or registry; D observational study, clinical trial, metanalysis of clinical trials. n.a. not available. References in bracket square. FS = Fanconi Syndrome; NDI, Nephrogenic Diabetes Insipidus; PTH, Parathyroid hormone; RSWS = Renal Salt Wasting Syndrome; SIADH, Syndrome of inappropriate antidiuretic hormone secretion; TRPM6, Transient Receptor Potential Cation Channel, subfamily M, member 6/EGF = Epidermal Growth Factor.