Long-term sexual functioning in germ-cell tumor survivors

BMC Cancer. 2020 Aug 20;20(1):779. doi: 10.1186/s12885-020-07301-6.

Abstract

Background: Survivors of germ-cell tumors (GCT) may suffer from long-term adverse consequences. Our study was conducted to assess a long-term sexual functioning in GCT survivors.

Methods: GCT survivors (N = 170) from the National Cancer Institute in Slovakia completed a Sexual Function Questionnaire that was modified from PROMIS Sexual Function and Satisfaction Questionnaire 9-year median follow up (range 5-32) as a primary exploratory aim. Study groups consisted of 17 survivors (10%) who had active surveillance (AS, controls), and 153 (90%) survivors who received treatment beyond orchiectomy (Tx), including cisplatin-based chemotherapy (CT, N = 132; 78%), radiotherapy to the retroperitoneal lymph nodes (RT, N = 12; 7%) or both (CTRT, N = 9; 5%).

Results: In univariate analysis, treatment of any type resulted in difficulty to maintain erection during sexual intercourse compared to patients treated with AS (P = 0.04). Survivors who received CTRT had lower ability to achieve orgasm during sexual activities (P = 0.04) and they reported disappointment with their overall quality of sex life (P = 0.002). The number of attempts to initiate sexual intercourse did not differ. Sexual relationships caused none or mild anxiety and the desire to be sexually active was higher after CTRT (P = 0.05). Multivariable analysis confirmed that orgasmic dysfunction after ≥400 mg/m2 of cisplatin and issues in maintaining erection after Tx were independent of retroperitoneal lymph-node dissection (P = 0.03 and P = 0.04, respectively). Survivors were disappointed with the quality of sex life and had stronger desire to be sexually active independent of age, (P = 0.01 and P = 0.05, respectively).

Conclusions: This study identified an impairment in sexual function may represent an issue for long-term GCT survivors. Treatment with chemotherapy plus radiotherapy were associated with disappointment and stronger sexual desire, while a higher cumulative dose of cisplatin may be responsible for orgasmic dysfunction.

Keywords: Chemotherapy; Germ cell tumors; Long-term toxicity; Radiotherapy; Sexual impairment.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Cancer Survivors / psychology
  • Cancer Survivors / statistics & numerical data*
  • Chemoradiotherapy, Adjuvant / adverse effects
  • Cisplatin / adverse effects
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Middle Aged
  • Neoplasms, Germ Cell and Embryonal / complications
  • Neoplasms, Germ Cell and Embryonal / mortality
  • Neoplasms, Germ Cell and Embryonal / therapy*
  • Orchiectomy / adverse effects
  • Orgasm / drug effects
  • Orgasm / radiation effects
  • Penile Erection / drug effects
  • Penile Erection / radiation effects
  • Prospective Studies
  • Quality of Life
  • Self Report / statistics & numerical data
  • Sexual Behavior / drug effects
  • Sexual Behavior / radiation effects
  • Sexual Dysfunction, Physiological / diagnosis
  • Sexual Dysfunction, Physiological / epidemiology*
  • Sexual Dysfunction, Physiological / etiology
  • Slovakia / epidemiology
  • Testicular Neoplasms / complications
  • Testicular Neoplasms / mortality
  • Testicular Neoplasms / therapy*
  • Time Factors
  • Young Adult

Substances

  • Cisplatin