Author/Authors :
Del Mastro، نويسنده , , Lucia and Ceppi، نويسنده , , Marcello and Poggio، نويسنده , , Francesca and Bighin، نويسنده , , Claudia and Peccatori، نويسنده , , Fedro and Demeestere، نويسنده , , Isabelle and Levaggi، نويسنده , , Alessia and Giraudi، نويسنده , , Sara and Lambertini، نويسنده , , Matteo and D’Alonzo، نويسنده , , Alessia and Canavese، نويسنده , , Giuseppe and Pronzato، نويسنده , , Paolo an، نويسنده ,
Abstract :
AbstractBackground
le of temporary ovarian suppression with gonadotropin-releasing hormone analogues (GnRHa) in the prevention of chemotherapy-induced premature ovarian failure (POF) is still controversial. We conducted a systematic review and meta-analysis of randomized trials evaluating the efficacy of GnRHa, given before and during chemotherapy, in the prevention of POF in premenopausal cancer patients.
s
s were retrieved by searching PubMed, Web of Knowledge database and the proceedings of major conferences. We calculated Odds Ratios (OR) and 95% confidence intervals (CIs) for POF from each trial and obtained pooled estimates through the random effects model as suggested by DerSimonian and Laird.
s
tudies were included in the meta-analysis with 225 events of POF occurring in 765 analyzed patients. The pooled OR estimate indicates a highly significant reduction in the risk of POF (OR = 0.43; 95% CI: 0.22–0.84; p = 0.013) in patients receiving GnRHa. There was statistically significant heterogeneity among studies (I2 = 55.8%; p = 0.012). There was no evidence of publication bias. Subgroups analyses showed that the protective effect of GnRHa against POF was similar in subgroups of patients defined by age and timing of POF assessment, while it was present in breast cancer but unclear in ovarian cancer and lymphoma patients.
sions
oled analysis of randomized studies shows that the temporary ovarian suppression induced by GnRHa significantly reduces the risk of chemotherapy-induced POF in young cancer patients.
Keywords :
Fertility preservation , GnRH analogues , META-ANALYSIS , breast cancer , Chemotherapy-induced ovarian failure , Lymphoma