Male breast cancer after childhood cancer: Systematic review and analyses in the PanCareSurFup cohort
: Wang Yuehan, Reulen Raoul C., Kremer Leontien C.M., de Vathaire Florent, Haupt Riccardo, Zadravec Zaletel Lorna, Bagnasco Francesca, Demoor-Goldschmidt Charlotte, van Dorp Willem J., Haddy Nadia, Hjorth Lars, Jakab Zsuzsanna, Kuehni Claudia E., Lähteenmäki Päivi M, van der Pal Helena J.H., Sacerdote Carlotta, Skinner Roderick, Terenziani Monica, Wesenberg Finn, Winther Jeanette.F., van Leeuwen Flora E., Hawkins Mike M., Teepen Jop C., van Dalen Elvira C., Ronckers Cécile M.
Publisher: Elsevier Ltd
: 2022
: European Journal of Cancer
: European Journal of Cancer
: 165
: 27
: 47
: 1879-0852
DOI: https://doi.org/10.1016/j.ejca.2022.01.001
: https://doi.org/10.1016/j.ejca.2022.01.001
Background
Breast cancer is a well-recognised late adverse effect in female childhood cancer survivors (CCSs), especially after chest radiotherapy; information on subsequent male breast cancer (SMBC) is limited. We summarised the existing evidence on SMBC after childhood cancer in a systematic review and investigated the risk of SMBC among males in a Pan-European cohort.
Methods
We searched Medline/PubMed for cohort studies and case reports/series that assessed SMBC after childhood cancer (≤21 years). Furthermore, we analysed data on SMBC in the PanCareSurFup cohort, reporting standardised incidence ratios (SIRs), absolute excess risks (AERs), and 5- and 10-year survival rates.
Results
The systematic review included 38 of 7080 potentially eligible articles. Cohort-specific SMBC frequencies were 0–0.40% (31 studies). SMBC occurred after a follow-up ranging from 24.0 to 42.0 years. Nine case reports/series described 11 SMBC cases, occurring 11.0–42.5 years after primary childhood cancer. In the PanCareSurFup cohort (16 SMBC/37,738 males; 0.04%), we observed a 22.3-fold increased risk of SMBC relative to the general male population (95% CI 12.7–36.2; absolute excess risk/100,000 person-years: 2.3, 95% CI 1.3–3.7). The five- and ten-year survival rates after SMBC diagnosis were 60.3% (95% CI 35.6%–85.0%) and 43.0% (95% CI 16.1%–69.9%), respectively. Clear evidence of risk factors did not emerge from these comprehensive efforts.
Conclusions
Compared to the general population, male CCSs have an elevated risk of developing subsequent breast cancer, although the absolute risk is low. Health care providers should be aware of this rare yet serious late effect; male CCSs with symptoms potentially related to SMBC warrant careful examination.