Data from Clinical and Genome-Wide Analysis of Serum Platinum Levels after Cisplatin-Based Chemotherapy

Abstract

<div>AbstractPurpose:<p>Serum platinum is measurable for years after completion of cisplatin-based chemotherapy (CBC). We report the largest investigation of serum platinum levels to date of 1,010 testicular cancer survivors (TCS) assessed 1–35 years after CBC and evaluate genetic contributions to these levels.</p>Experimental Design:<p>Eligible TCS given 300 or 400 (±15) mg/m<sup>2</sup> cisplatin underwent extensive audiometric testing, clinical examination, completed questionnaires, and had crude serum platinum levels measured. Associations between serum platinum and various risk factors and toxicities were assessed after fitting a biexponential model adjusted for follow-up time and cumulative cisplatin dose. A genome-wide association study (GWAS) was performed using the serum platinum residuals of the dose and time-adjusted model.</p>Results:<p>Serum platinum levels exceeded the reference range for approximately 31 years, with a strong inverse relationship with creatinine clearance at follow-up (age-adjusted <i>P</i> = 2.13 × 10<sup>−3</sup>). We observed a significant, positive association between residual platinum values and luteinizing hormone (age-adjusted <i>P</i> = 6.58 × 10<sup>−3</sup>). Patients with high residual platinum levels experienced greater Raynaud phenomenon than those with medium or low levels (age-adjusted OR<sub>high/low</sub> = 1.46; <i>P</i> = 0.04), as well as a higher likelihood of developing tinnitus (age-adjusted OR<sub>high/low</sub> = 1.68, <i>P</i> = 0.07). GWAS identified one single-nucleotide polymorphism (SNP) meeting genome-wide significance, rs1377817 (<i>P</i> = 4.6 × 10<sup>−8</sup>, a SNP intronic to <i>MYH14</i>).</p>Conclusions:<p>This study indicates that residual platinum values are correlated with several cisplatin-related toxicities. One genetic variant is associated with these levels.</p></div>