Second malignant neoplasms and cause of death in patients with germ cell cancer a danish nationwide cohort study

Maria G. Kier*, Merete K. Hansen, Jakob Lauritsen, Mette S. Mortensen, Mikkel Bandak, Mads Agerbaek, Niels V. Holm, Susanne O. Dalton, Klaus K. Andersen, Christoffer Johansen, Gedske Daugaard

*Corresponding author af dette arbejde

    Publikation: Bidrag til tidsskriftArtikelForskningpeer review


    IMPORTANCE Patients given systemic treatment for testicular germ cell cancer (GCC) are at increased risk for a second malignant neoplasm (SMN). Previous studies on SMN and causes of death lacked information on the exact treatment applied or were based on patients receiving former treatment options. OBJECTIVE To evaluate the treatment-specific risks for SMN and death in a nationwide population-based cohort of patients with GCC treated with current standard regimens. DESIGN, SETTING, AND PARTICIPANTS This study examined a Danish nationwide cohort of 5190 men with GCC who entered the Danish Testicular Cancer database between January 1, 1984, and December 31, 2007. Treatment results were compared with a randomly sampled, age-stratified, population-based control group. Cases of gonadal and extragonadal primary were included in the nationwide cohort. The treatments were surveillance only retroperitoneal radiotherapy (RT) bleomycin, etoposide, and cisplatin (BEP) or more than 1 line of treatment (MTOL). MAIN OUTCOMES AND MEASURES Cumulative incidence and hazard ratios (HRs) for SMN and death calculated by the Cox proportional hazards model were compared with those of age-matched controls. RESULTS The study population comprised 2804 patients with seminoma and 2386 with nonseminoma. The median follow-up was 14.4 years (interquartile range, 8.6-20.5 years). The 20-year cumulative incidence of SMN with death as a competing risk was 7.8%(surveillance), 7.6%(BEP), 13.5%(RT), 9.2%(MTOL), and 7.0% (controls). We found no increased risk for SMN after surveillance, while the HRs were 1.7 (95%CI, 1.4-2.0), 1.8 (95%CI, 1.5-2.3), and 3.7 (95%CI, 2.5-5.5), respectively, after BEP, RT, and MTOL. Mortality owing to non-GCC causes was decreased after surveillance, but increased by 1.3 times after BEP and RT and by 2.6 times after MTOL. Excess mortality due to SMN was found after BEP (HR, 1.6 95%CI, 1.2-2.2), RT (HR, 2.1 95%CI, 1.5-2.9), and MTOL (HR, 5.8 95%CI, 3.6-9.6). CONCLUSIONS AND RELEVANCE We found no increased risk for SMN or death among patients undergoing surveillance only. The risks for SMN and death due to SMN were increased after BEP alone, RT alone, and MTOL. Approaches to define patients who might benefit from less intensive treatment are needed.

    Sider (fra-til)1624-1627
    Antal sider4
    TidsskriftJAMA Oncology
    Udgave nummer12
    StatusUdgivet - dec. 2016


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