Review
Oncologic and Reproductive outcomes with progestin therapy in women with
endometrial hyperplasia and grade 1 Adenocarcinoma: A systematic review
Camille C. Gunderson
a,
⁎, Amanda Nickles Fader
a, b
, Kathryn A. Carson
c
, Robert E. Bristow
d
a
Johns Hopkins Medical Institutions, Baltimore, MD, USA
b
Greater Baltimore Medical Center, Baltimore, MD, USA
c
Johns Hopkins School of Public Health, Baltimore, MD, USA
d
University of California Irvine Medical Center, Orange, CA, USA
abstract article info
Article history:
Received 30 November 2011
Accepted 4 January 2012
Available online 11 January 2012
Keywords:
Endometrial hyperplasia
Endometrial carcinoma
Progestin therapy
Disease persistence
Reproductive outcomes
Objective. The objective of this review was to analyze published contemporary oncologic and reproductive
outcomes in women with endometrial hyperplasia or cancer undergoing medical management with proges-
tin therapy.
Methods. A systematic review of oncologic and pregnancy outcomes in women with complex atypical hy-
perplasia or grade 1 adenocarcinoma was performed using a comprehensive search of the MEDLINE litera-
ture. English language studies published from 2004 to 2011 which utilized hormonal therapy were
identified using key words endometrial hyperplasia, endometrial cancer, fertility preservation, hormone
and progestin therapy. Fisher's exact test was used to calculate statistical differences.
Results. Forty-five studies with 391 study subjects were identified. The median age was 31.7 years. Ther-
apies included medroxyprogesterone (49%), megestrol acetate (25%), levonorgestrel intrauterine device
(19%), hydroxyprogesterone caproate (0.8%), and unspecified/miscellaneous progestins (13.5%). Overall,
344 women (77.7%) demonstrated a response to hormonal therapy. After a median follow up period of
39 months, a durable complete response was noted in 53.2%. The complete response rate was significantly
higher for those with hyperplasia than for women with carcinoma (65.8% vs. 48.2%, p = .002). The median
time to complete response was 6 months (range, 1–18 months). Recurrence after an initial response was
noted in 23.2% with hyperplasia and 35.4% with carcinoma during the study periods (p = .03). Persistent dis-
ease was observed in 14.4% of women with hyperplasia and 25.4% of women with carcinoma (p = .02). Dur-
ing the respective study periods, 41.2% of those with hyperplasia and 34.8% with a history of carcinoma
became pregnant (p = .39), with 117 live births reported.
Conclusion. Based on this systematic review of the contemporary literature, endometrial hyperplasia has a
significantly higher likelihood of response (66%) to hormonal therapy than grade 1 endometrial carcinoma
(48%). Disease persistence is more common in women with carcinoma (25%) compared to hyperplasia
(14%). Reproductive outcomes do not seem to differ between the cohorts.
© 2012 Elsevier Inc. All rights reserved.
Contents
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 478
Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 478
Results . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 478
Discussion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 479
Conflict of interest statement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 481
Acknowledgment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 481
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 481
Gynecologic Oncology 125 (2012) 477–482
⁎ Corresponding author at: Johns Hopkins Hospital, Department of Gynecology and Obstetrics, 600 North Wolfe Street, Phipps 279, Baltimore, MD 21287, USA. Fax: +1 410
502 6683.
E-mail address: ccgunder@gmail.com (C.C. Gunderson).
0090-8258/$ – see front matter © 2012 Elsevier Inc. All rights reserved.
doi:10.1016/j.ygyno.2012.01.003
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Gynecologic Oncology
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