Prevalence and risk factors for ototoxicity after cisplatin-based chemotherapy

被引:4
|
作者
Sanchez, Victoria A. A. [1 ]
Dinh Jr, Paul C. C. [2 ]
Rooker, Jennessa [3 ]
Monahan, Patrick O. O. [4 ]
Althouse, Sandra K. K. [4 ]
Fung, Chunkit [5 ]
Sesso, Howard D. D. [6 ]
Einhorn, Lawrence H. H. [4 ]
Dolan, M. Eileen [7 ]
Frisina, Robert D. D. [8 ]
Travis, Lois B. B. [4 ]
机构
[1] Univ S Florida, Dept Otolaryngol Head & Neck Surg, 12901 Bruce B Downs Blvd,MDC 73, Tampa, FL 33612 USA
[2] Indiana Univ, Dept Med Oncol, Indianapolis, IN USA
[3] Univ S Florida, Coll Nursing, Tampa, FL USA
[4] Indiana Univ, Dept Biostat & Hlth Data Sci, Indianapolis, IN USA
[5] Univ Rochester, JP Wilmot Canc Inst, Med Ctr, Rochester, NY USA
[6] Brigham & Womens Hosp, Div Prevent Med, Boston, MA USA
[7] Univ Chicago, Dept Med, Chicago, IL USA
[8] Univ S Florida, Dept Med Engn, Tampa, FL USA
关键词
Tinnitus; Hearing loss; Ototoxicity; Cisplatin; Risk factors; Aging; QUALITY-OF-LIFE; TESTICULAR CANCER SURVIVORS; HIGH-FREQUENCY AUDIOMETRY; INDUCED HEARING-LOSS; PLATINUM CHEMOTHERAPY; COGNITIVE FUNCTION; HEALTH OUTCOMES; FAMILY-HISTORY; AID USE; IMPAIRMENT;
D O I
10.1007/s11764-022-01313-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Ototoxicityis a prominent side effect of cisplatin-based chemotherapy. There are few reports, however, estimating its prevalence in well-defined cohorts and associated risk factors. Methods Testicular cancer (TC) survivors given first-line cisplatin-based chemotherapy completed validated questionnaires. Descriptive statistics evaluated the prevalence of ototoxicity, defined as self-reported hearing loss and/or tinnitus. We compared patients with and without tinnitus or hearing loss using Chi-square test, two-sided Fisher's exact test, or two-sided Wilcoxon rank sum test. To evaluate ototoxicity risk factors, a backward selection logistic regression procedure was performed. Results Of 145 TC survivors, 74% reported ototoxicity: 68% tinnitus; 59% hearing loss; and 52% reported both. TC survivors with tinnitus were more likely to indicate hypercholesterolemia (P = 0.008), and difficulty hearing (P < .001). Tinnitus was also significantly related to age at survey completion ( OR = 1.79; P = 0.003) and cumulative cisplatin dose (OR = 5.17; P < 0.001). TC survivors with hearing loss were more likely to report diabetes (P = 0.042), hypertension ( P = 0.007), hypercholesterolemia (P < 0.001), and family history of hearing loss (P = 0.044). Risk factors for hearing loss included age at survey completion (OR = 1.57; P = 0.036), hypercholesterolemia (OR = 3.45; P = 0.007), cumulative cisplatin dose (OR = 1.94; P = 0.049), and family history of hearing loss (OR = 2.87; P = 0.071). Conclusions Ototoxicity risk factors included age, cisplatin dose, cardiovascular risk factors, and family history of hearing loss. Three of four TC survivors report some type of ototoxicity; thus, follow-up of cisplatin-treated survivors should include routine assessment for ototoxicity with provision of indicated treatments. Implications for Cancer Survivors Survivors should be aware of risk factors associated with ototoxicity. Referrals to audiologists before, during, and after cisplatin treatment is recommended.
引用
收藏
页码:27 / 39
页数:13
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