Hormonal and Reproductive Factors and Risk of Myeloproliferative Neoplasms in Postmenopausal Women

Menée aux Etats-Unis à partir des données de la base Medicare, cette étude de cohorte évalue l'association entre des facteurs hormonaux et reproductifs et le risque de tumeurs myéloprolifératives après la ménopause (durée de suivi supérieure à 250 000 personnes-années)

Cancer Epidemiology Biomarkers & Prevention, sous presse, 2015, résumé

Résumé en anglais

Background: Hormonal and reproductive history has been associated with risk of some hematologic malignancies, but their role in myeloproliferative neoplasms (MPN) is largely unknown.

Methods: Using a population-based cohort study, we evaluated the association of these factors with risk of MPN overall, and for essential thrombocythemia (ET) and polycythemia vera (PV) specifically. Incident MPN cases from 1993-2004 were identified via linkage to Medicare. Relative risks (RR) and 95% confidence intervals (CI) were estimated utilizing Cox proportional hazard regression.

Results: After >250,000 person-years of follow-up, 257 cases of MPN were identified (172 ET, 64 PV). Ever use of hormone therapy (HT) was associated with an increased risk of ET (RR=1.63; 95%CI 1.19-2.23) but a decreased risk of PV (RR=0.58; 95%CI 0.34-0.98). There were no statistically significant associations of oral contraceptives or reproductive factors with MPN risk overall, or by MPN subtype. Bilateral oophorectomy was associated with increased risk of ET (RR=1.58; 95%CI 1.11-2.25) and decreased risk of PV (RR=0.32; 95%CI 0.12-0.88). There was no association of ovulatory years with ET risk, however there was increased risk of PV (RR=1.68 for >36.8 compared to ≤27.6 years; p-trend=0.045). Adjustment for potential confounding factors did not alter these associations.

Conclusions: HT use and bilateral oophorectomy had opposite associations for ET and PV. Except for ovulatory years and PV risk, reproductive history did not appear to play a role in the etiology of MPN.

Impact: This study suggests different mechanistic impacts of estrogen, and perhaps distinct etiologies, for the two major MPN subtypes.