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Cochrane Database of Systematic Reviews

术后激素替代疗法用于上皮性卵巢癌

Information

DOI:
https://doi.org/10.1002/14651858.CD012559.pub2Copy DOI
Database:
  1. Cochrane Database of Systematic Reviews
Version published:
  1. 28 January 2020see what's new
Type:
  1. Intervention
Stage:
  1. Review
Cochrane Editorial Group:
  1. Cochrane Gynaecological, Neuro-oncology and Orphan Cancer Group

Copyright:
  1. Copyright © 2020 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.

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Authors

  • Nungrutai Saeaib

    Correspondence to: Department of Obstetrics and Gynecology, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand

    [email protected]

  • Krantarat Peeyananjarassri

    Department of Obstetrics and Gynecology, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand

  • Tippawan Liabsuetrakul

    Epidemiology Unit, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand

  • Rakchai Buhachat

    Department of Obstetrics and Gynecology, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand

  • Eva Myriokefalitaki

    Gynaecological Oncology, The Christie NHS Foundation Trust, Manchester, UK

Contributions of authors

Protocol development: NS, EM, TL
Selection of studies: NS, RB
Assessing eligibility of studies: NS, RB; third person: TL
Data extraction: NS, KP; third person: RB
Data entry into Review Manager 5: NS, TL; spot‐check: KP
Assessment of risk of bias: NS, RB; third person: EM
Analysing data: NS, TL
Drafting the final review: NS, RB, KP, TL, EM
Updating the review: NS, RB, KP, TL, EM

Sources of support

Internal sources

  • Faculty of Medicine, Prince of Songkla University, Thailand.

External sources

  • Thailand Research Fund (Distinguished Research Professor Award), Thailand.

Declarations of interest

Nungrutai Saeaib: none known
Krantarat Peeyananjarassri: none known
Tippawan Liabsuetrakul: none known
Rakchai Buhachat: none known
Eva Myriokefalitaki: none known

Acknowledgements

We would like to thank Jo Morrison for clinical and editorial advice, Jo Platt for designing and running the searches and Gail Quinn, Clare Jess and Tracey Harrison for their valuable contribution to the editorial process.

This project was supported by the National Institute for Health Research (NIHR), via Cochrane infrastructure funding to the Cochrane Gynaecological, Neuro‐oncology and Orphan Cancers Group. The views and opinions expressed herein are those of the review authors and do not necessarily reflect those of the Systematic Reviews Programme, National Insititute for Health Research (NIHR), National Health Service, or the Department of Health.

We thank the referees for many helpful suggestions and comments; these referees included Fani Kokka, Elly Brockbank, Ruth Payne and Nicolette Biglia.

Version history

Published

Title

Stage

Authors

Version

2020 Jan 28

Hormone replacement therapy after surgery for epithelial ovarian cancer

Review

Nungrutai Saeaib, Krantarat Peeyananjarassri, Tippawan Liabsuetrakul, Rakchai Buhachat, Eva Myriokefalitaki

https://doi.org/10.1002/14651858.CD012559.pub2

2017 Feb 24

Hormone replacement therapy after surgery for epithelial ovarian cancer

Protocol

Nungrutai Saeaib, Krantarat Peeyananjarassri, Tippawan Liabsuetrakul, Rakchai Buhachat, Eva Myriokefalitaki

https://doi.org/10.1002/14651858.CD012559

Differences between protocol and review

We excluded, from further subgroup analysis, women who underwent fertility‐preservation surgery (retention of one ovary). We could not compare regimens and durations of HRT administration because of the small number of participants. Adverse events of pulmonary embolism, deep vein thrombosis and gallstones were not reported in the included studies, however we aim to analyse these results including oestrogen and progesterone receptor status in future updates of this review if appropriate data become available. We added transient ischaemic attack and cerebrovascular accident to the adverse events, and changed the method for estimating the hazard ratio from standard error using methods of Parmar 1998 to using the Observed minus Expected events (O‐E) and the Variance (V) using formula according to Tierney 2007.

Keywords

MeSH

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Study flow diagram.
Figures and Tables -
Figure 1

Study flow diagram.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figures and Tables -
Figure 2

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figures and Tables -
Figure 3

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 1 Overall survival.
Figures and Tables -
Analysis 1.1

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 1 Overall survival.

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 2 Quality of life, general condition.
Figures and Tables -
Analysis 1.2

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 2 Quality of life, general condition.

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 3 Progression‐free survival.
Figures and Tables -
Analysis 1.3

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 3 Progression‐free survival.

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 4 Incidence of breast cancer.
Figures and Tables -
Analysis 1.4

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 4 Incidence of breast cancer.

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 5 Transient ischaemic attack.
Figures and Tables -
Analysis 1.5

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 5 Transient ischaemic attack.

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 6 Cerebrovascular accident.
Figures and Tables -
Analysis 1.6

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 6 Cerebrovascular accident.

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 7 Myocardial infarction.
Figures and Tables -
Analysis 1.7

Comparison 1 Hormone replacement therapy versus no hormone replacement therapy, Outcome 7 Myocardial infarction.

Summary of findings for the main comparison. Hormone replacement therapy (HRT) compared to no HRT for women who have undergone surgery for epithelial ovarian cancer (EOC)

Hormone replacement therapy (HRT) compared to no HRT for epithelial ovarian cancer (EOC)

Patients: women of any age diagnosed with any stage of EOC who had surgical treatment, regardless of chemotherapy treatment
Setting: multiple centres in the United Kingdom, Spain and Hungary, and single institutes in South Africa and China
Intervention: HRT; oestrogen‐alone, and oestrogen combined with progestin, oestrogen agonist/antagonist, testosterone or tibolone in any dose and any route of administration
Comparison: no HRT

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

№ of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Risk with no HRT

Risk with HRT

Overall survival

Study population

HR 0.71
(0.54 to 0.93)

350
(3 RCTs)

⊕⊕⊝⊝
LOW 1, 2

The median follow‐up time in the three included studies was 31.4 months, 90 months and 19.1 years.

795 per 1,000

675 per 1,000
(575 to 771)

Quality of life, general condition

The mean quality of life (general condition) in the no HRT group was 13.84 points.

The mean quality of life (general condition) in the HRT group was 13.67 points higher
(9.26 higher to 18.08 higher)

75
(1 RCT)

⊕⊝⊝⊝
VERY LOW 1, 2, 3

The EORTC‐C30 questionnaire was used to evaluate this outcome; higher values correspond with improvement.

Progression‐free survival

Study population

HR 0.76
(0.57 to 1.01)

275
(2 RCTs)

⊕⊕⊝⊝
LOW 1, 2

The median follow‐up time in the two studies was 90 months and 19.1 years.

773 per 1,000

676 per 1,000
(571 to 776)

Incidence of breast cancer

Study population

RR 2.00
(0.19 to 21.59)

225
(2 RCTs)

⊕⊝⊝⊝
VERY LOW 1, 4

The median follow‐up time in the two studies was 31.41 months and 19.1 years.

8 per 1,000

17 per 1,000
(2 to 181)

Incidence of transient ischaemic attack

Study population

RR 5.00
(0.24 to 102.42)

150
(1 RCT)

⊕⊝⊝⊝
VERY LOW 1, 2, 4

The median follow‐up time in the study was 19.1 years.

7 per 1,000

33 per 1,000
(2 to 683)

Incidence of cerebrovascular accident

Study population

RR 0.67
(0.11 to 3.88)

150
(1 RCT)

⊕⊝⊝⊝
VERY LOW 1, 2, 3

The median follow‐up time in the study was 19.1 years.

40 per 1,000

27 per 1,000
(4 to 155)

Incidence of myocardial infarction

Study population

RR 0.20
(0.01 to 4.10)

150
(1 RCT)

⊕⊝⊝⊝
VERY LOW 1, 2, 3

The median follow‐up time in the study was 19.1 years.

27 per 1,000

5 per 1,000
(0 to 109)

Incidence of gallstones

The incidence of gallstones was not reported in the included studies.

*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: confidence interval; RR: risk ratio; HR: hazard ratio

GRADE Working Group grades of evidence
High‐certainty: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate‐certainty: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low‐certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of the effect
Very low‐certainty: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect

1 Downgraded by one level due to limitations in study design
2 Downgraded by one level due to inconsistency of results
3 Downgraded by one level due to imprecision of results
4 Downgraded by two levels due to imprecision of results

Figures and Tables -
Summary of findings for the main comparison. Hormone replacement therapy (HRT) compared to no HRT for women who have undergone surgery for epithelial ovarian cancer (EOC)
Comparison 1. Hormone replacement therapy versus no hormone replacement therapy

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Overall survival Show forest plot

3

350

Hazard Ratio (95% CI)

0.71 [0.54, 0.93]

2 Quality of life, general condition Show forest plot

1

Mean Difference (IV, Fixed, 95% CI)

Totals not selected

3 Progression‐free survival Show forest plot

2

275

Hazard Ratio (95% CI)

0.76 [0.57, 1.01]

4 Incidence of breast cancer Show forest plot

2

225

Risk Ratio (M‐H, Fixed, 95% CI)

2.0 [0.19, 21.59]

5 Transient ischaemic attack Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

6 Cerebrovascular accident Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

7 Myocardial infarction Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Figures and Tables -
Comparison 1. Hormone replacement therapy versus no hormone replacement therapy