J Gynecol Oncol.  2017 Nov;28(6):e71. 10.3802/jgo.2017.28.e71.

Could fertility-sparing surgery be considered for women with early stage ovarian clear cell carcinoma?

Affiliations
  • 1Department of Obstetrics and Gynecology, Weill Cornell Medicine, New York, NY, USA. din2004@med.cornell.edu, dnasioudis@gmail.com

Abstract


OBJECTIVE
The aim of the present retrospective population-based study was to investigate the oncologic impact of uterine and ovarian preservation (OP) in premenopausal women with stage IA or IC ovarian clear cell carcinoma (OCCC).
METHODS
The National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) database was accessed and a cohort of surgically-staged premenopausal women (age <50 years) diagnosed with unilateral stage IA or IC OCCC was drawn. Based on site-specific surgery codes, women who did not undergo hysterectomy and/or bilateral salpingo-oophorectomy (BSO) were identified. Overall survival (OS) and cancer-specific survival (CSS) rates were calculated following generation of Kaplan-Meier curves; comparisons were made with the log-rank test. Multivariate Cox analysis was performed to control for possible confounders.
RESULTS
A total of 741 premenopausal women who met the inclusion criteria were identified. Based on available information, rate of uterine preservation was 14.5% (96/663) while the rate of OP was 28.1% (71/253). Five-year CSS rates were 90.8% for women who did not undergo hysterectomy compared with 87.7% for those who did (p=0.290). Similarly, 5-year CSS rates in the OP and BSO groups were 92.6% and 85%, respectively (p=0.060). After controlling for disease sub-stage (IA vs. IC), uterine or OP was not associated with a worse overall or cancer-specific mortality.
CONCLUSION
In the present cohort, uterine and OP did not have a negative impact on oncologic outcomes. Selection criteria for fertility-sparing surgery (FSS) could be expanded to include women with stage IA OCCC.

Keyword

Ovarian Neoplasms; Adenocarcinoma, Clear Cell; Fertility; Fertility Preservation

MeSH Terms

Adenocarcinoma, Clear Cell/pathology/*surgery
Adolescent
Adult
Female
Fertility Preservation/*methods
Gynecologic Surgical Procedures/*methods
Humans
Hysterectomy
Middle Aged
Multivariate Analysis
Neoplasm Staging
Organ Sparing Treatments/*methods
Ovarian Neoplasms/pathology/*surgery
Ovariectomy/methods
Proportional Hazards Models
Retrospective Studies
SEER Program
Salpingectomy/methods
Survival Rate
Young Adult

Figure

  • Fig. 1. Patient selection flowchart. CCC, clear cell carcinoma; OCCC, ovarian clear cell carcinoma.

  • Fig. 2. Rate of hysterectomy among premenopausal women with unilateral CCC confined to the ovary per year of diagnosis (final selected model: 0 joinpoints). APC, annual percent charge; CCC, clear cell carcinoma. * The APC is significantly different from zero at alpha=0.05.

  • Fig. 3. CSS of premenopausal women with unilateral CCC confined to the ovary stratified by performance of hysterectomy (n=564 and n=94 in the hysterectomy and uterine preservation groups, respectively; p=0.290 from the log-rank test). CCC, clear cell carcinoma; CSS, cancer-specific survival.

  • Fig. 4. Rate of BSO among premenopausal women with unilateral CCC confined to the ovary per year of diagnosis (final selected model: 0 joinpoints). APC, annual percent charge; BSO, bilateral salpingo-oophorectomy; CCC, clear cell carcinoma. * The APC is significantly different from zero at alpha=0.05.

  • Fig. 5. CSS of premenopausal women with unilateral CCC confined to the ovary stratified by performance of BSO (n=69 and n=181 in the USO and BSO groups, respectively; p=0.060 from the log-rank test). BSO, bilateral salpingo-oophorectomy; CCC, clear cell carcinoma; CSS, cancer-specific survival; USO, unilateral salpingo-oophorectomy.


Cited by  1 articles

Prognostic factors and effects of fertility-sparing surgery in women of reproductive age with ovarian clear-cell carcinoma: a propensity score analysis
Masato Yoshihara, Hiroaki Kajiyama, Satoshi Tamauchi, Shiro Suzuki, Kunihiko Takahashi, Shigeyuki Matsui, Fumitaka Kikkawa
J Gynecol Oncol. 2019;30(6):.    doi: 10.3802/jgo.2019.30.e102.


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