Gonadotropin-Releasing Hormone Agonists for Ovarian Function Preservation in Premenopausal Women Undergoing Chemotherapy for Early-Stage Breast Cancer A Systematic Review and Meta-analysis
Carregando...
Citações na Scopus
124
Tipo de produção
article
Data de publicação
2016
Editora
AMER MEDICAL ASSOC
Indexadores
Título da Revista
ISSN da Revista
Título do Volume
Autores
SASSE, Andre D.
TRAINA, Tiffany A.
HUDIS, Clifford A.
MARQUES, Ricardo J.
Autor de Grupo de pesquisa
Editores
Coordenadores
Organizadores
Citação
JAMA ONCOLOGY, v.2, n.1, p.65-73, 2016
Resumo
IMPORTANCE Chemotherapy may result in a detrimental effect on ovarian function and fertility in premenopausal women undergoing treatment for early-stage breast cancer (EBC). To minimize risk of harm to ovarian function and fertility for patients in this setting, careful considerations should be made. Gonadotropin-releasing hormone agonists (GnRHa) have been suggested as an alternative to prevent the loss of ovarian function due to exposure to cytotoxic agents, but GnRHa use for ovarian protection in EBC patients is not fully resolved. OBJECTIVE To determine the effectiveness of GnRHa administered concurrently with chemotherapy for ovarian function preservation. DATA SOURCES PubMed, SCOPUS, and Cochrane databases were searched for studies published between January 1975 and March 2015. The abstracts of the American Society of Clinical Oncology Annual Meeting between 1995 and 2014 and the San Antonio Breast Cancer Symposium between 2009 and 2014 were searched as well. STUDY SELECTION Prospective, randomized, clinical trials addressing the role of ovarian suppression with GnRHa in preventing early ovarian dysfunction in premenopausal women undergoing treatment for EBC were selected. DATA EXTRACTION AND SYNTHESIS Data extraction was performed independently by 2 authors. The methodology and the risk of bias were assessment based on the description of randomization method, withdrawals, and blinding process. MAIN OUTCOMES AND MEASURES Rate of resumption of regular menses after a minimal follow-up period of 6 months following chemotherapy was used as a surrogate to assess the incidence of ovarian dysfunction. Additional secondary outcomes included hormone levels and number of pregnancies. Risk ratio estimates were calculated based on the number of evaluable patients. Analyses were conducted using a random effect model. RESULTS Seven studies were included in this analysis, totaling 1047 randomized patients and 856 evaluable patients. The use of GnRHa was associated with a higher rate of recovery of regular menses after 6 months (odds ratio [OR], 2.41; 95% CI, 1.40-4.15; P = .002) and at least 12 months (OR, 1.85; 95% CI, 1.33-2.59; P < .001) following the last chemotherapy cycle. The use of GnRHa was also associated with a higher number of pregnancies (OR, 1.85; 95% CI, 1.02-3.36; P = .04), although this outcome was not uniformly reported and fertility or rate of pregnancy was not the primary outcome in any of the trials. CONCLUSIONS AND RELEVANCE Gonadotropin-releasing hormone agonists given with chemotherapy was associated with increased rates of recovery of regular menses in this meta-analysis. Evidence was insufficient to assess outcomes related to GnRHa and ovarian function and fertility and needs further investigation.
Palavras-chave
Referências
- Anders CK, 2008, J CLIN ONCOL, V26, P3324, DOI 10.1200/JCO.2007.14.2471
- ATAYA K, 1995, BIOL REPROD, V52, P365, DOI 10.1095/biolreprod52.2.365
- ATAYA KM, 1985, CANCER RES, V45, P3651
- Badawy A, 2009, FERTIL STERIL, V91, P694, DOI 10.1016/j.fertnstert.2007.12.044
- Bedaiwy MA, 2011, FERTIL STERIL, V95, P906, DOI 10.1016/j.fertnstert.2010.11.017
- Ben-Aharon I, 2010, BREAST CANCER RES TR, V122, P803, DOI 10.1007/s10549-010-0996-7
- Bines J, 1996, J CLIN ONCOL, V14, P1718
- Blumenfeld Z, 2007, ONCOLOGIST, V12, P1044, DOI 10.1634/theoncologist.12-9-1044
- BOKSER L, 1990, BRIT J CANCER, V61, P861, DOI 10.1038/bjc.1990.192
- Burstein HJ, 2000, NEW ENGL J MED, V343, P1086, DOI 10.1056/NEJM200010123431506
- Chen HX, 2011, COCHRANE DB SYST REV, DOI 10.1002/14651858.CD008018.pub2
- Davis Amy L, 2005, Clin Breast Cancer, V6, P421, DOI 10.3816/CBC.2005.n.046
- Del Mastro L, 2006, ANN ONCOL, V17, P74, DOI 10.1093/annonc/mdj029
- Del Mastro L, 2014, CANCER TREAT REV, V40, P675, DOI 10.1016/j.ctrv.2013.12.001
- Del Mastro L, 2011, JAMA-J AM MED ASSOC, V306, P269, DOI 10.1001/jama.2011.991
- DelMastro L, 1997, BREAST CANCER RES TR, V43, P183, DOI 10.1023/A:1005792830054
- Early Breast Cancer Trialists Collaborative Group, 2005, LANCET, V365, P1687, DOI [DOI 10.1016/S0140-6736(05)66544-0, 10.1016/S0140-6736(05)66544-0]
- Elgindy EA, 2013, OBSTET GYNECOL, V121, P78, DOI [http://10.1097/AOG.0b013e31827374e2, 10.1097/AOG.0b013e31827374e2]
- Falcone T, 2004, FERTIL STERIL, V81, P243, DOI 10.1016/j.fertnstert.2003.06.031
- Fornier MN, 2005, CANCER, V104, P1575, DOI 10.1002/cncr.21385
- Gadducci A, 2007, GYNECOL ENDOCRINOL, V23, P625, DOI 10.1080/09513590701582406
- Ganz PA, 2011, J CLIN ONCOL, V29, P1110, DOI 10.1200/JCO.2010.29.7689
- Gerber B, 2011, J CLIN ONCOL, V29, P2334, DOI 10.1200/JCO.2010.32.5704
- GOLDHIRSCH A, 1990, ANN ONCOL, V1, P183
- Goodwin PJ, 1999, J CLIN ONCOL, V17, P2365
- Han HS, 2009, BREAST CANCER RES TR, V115, P335, DOI 10.1007/s10549-008-0071-9
- Howard-Anderson J, 2012, JNCI-J NATL CANCER I, V104, P386, DOI 10.1093/jnci/djr541
- Jadad AR, 1996, CONTROL CLIN TRIALS, V17, P1, DOI 10.1016/0197-2456(95)00134-4
- Jemal A, 2011, CA-CANCER J CLIN, V61, P69, DOI 10.3322/caac.20107
- Jeruss JS, 2009, NEW ENGL J MED, V360, P902, DOI 10.1056/NEJMra0801454
- Karimi-Zarchi M, 2014, EUR J GYNAECOL ONCOL, V35, P59
- Kil WJ, 2006, BREAST CANCER RES TR, V96, P245, DOI 10.1007/s10549-005-9059-x
- Kim SS, 2010, CLIN OBSTET GYNECOL, V53, P740, DOI 10.1097/GRF.0b013e3181f96cb1
- Lambertini M, 2014, J CLIN ONCOL S, V32, P105
- Lee S, 2009, MENOPAUSE, V16, P98, DOI 10.1097/gme.0b013e3181844877
- Leonard RC, 2010, J CLIN ONCOL S, V28
- Loren AW, 2013, J CLIN ONCOL, V31, P2500, DOI 10.1200/JCO.2013.49.2678
- Moore HCF, 2015, NEW ENGL J MED, V372, P923, DOI 10.1056/NEJMoa1413204
- Munster PN, 2012, J CLIN ONCOL, V30, P533, DOI 10.1200/JCO.2011.34.6890
- Pagani O, 1998, EUR J CANCER, V34, P632, DOI 10.1016/S0959-8049(97)10036-3
- Partridge AH, 2008, CLIN BREAST CANCER, V8, P65, DOI 10.3816/CBC.2008.n.004
- Parulekar WR, 2005, J CLIN ONCOL, V23, P6002, DOI 10.1200/JCO.2005.07.096
- Petrek JA, 2006, J CLIN ONCOL, V24, P1045, DOI 10.1200/JCO.2005.03.3969
- Recchia F, 2006, CANCER, V106, P514, DOI 10.1002/cncr.21646
- Rossi E, 2009, J CLIN ONCOL, V27, P3192, DOI 10.1200/JCO.2008.18.6213
- Schover LR, 2008, J CLIN ONCOL, V26, P753, DOI 10.1200/JCO.2007.14.1655
- Song GP, 2013, MED ONCOL, V30, DOI 10.1007/s12032-013-0667-8
- Stearns V, 2006, NAT REV CANCER, V6, P886, DOI 10.1038/nrc1992
- Sverrisdottir A, 2009, BREAST CANCER RES TR, V117, P561, DOI 10.1007/s10549-009-0313-5
- Swain SM, 2010, NEW ENGL J MED, V362, P2053, DOI 10.1056/NEJMoa0909638
- Tham YL, 2007, AM J CLIN ONCOL-CANC, V30, P126, DOI 10.1097/01.coc.0000251398.57630.4f
- Trivers KF, 2014, ONCOLOGIST, V19, P814, DOI 10.1634/theoncologist.2014-0016
- Urruticoechea A, 2008, BREAST CANCER RES TR, V110, P411, DOI 10.1007/s10549-007-9745-y
- Valagussa P, 1993, Recent Results Cancer Res, V127, P247
- Venturini M, 2005, J NATL CANCER I, V97, P1724, DOI 10.1093/jnci/dji398
- Vitek WS, 2014, FERTIL STERIL, V102, P808, DOI 10.1016/j.fertnstert.2014.06.003
- Wang C, 2013, PLOS ONE, V8, DOI 10.1371/journal.pone.0055587
- Yang B, 2013, BREAST, V22, P150, DOI 10.1016/j.breast.2012.12.008