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Meta-Analysis
. 2015 Dec 17;2015(12):CD004706.
doi: 10.1002/14651858.CD004706.pub5.

Adjuvant (post-surgery) chemotherapy for early stage epithelial ovarian cancer

Affiliations
Meta-Analysis

Adjuvant (post-surgery) chemotherapy for early stage epithelial ovarian cancer

Theresa A Lawrie et al. Cochrane Database Syst Rev. .

Abstract

Background: This is the second update of the review first published in the Cochrane Database of Systematic Reviews in 2009, Issue 1. Epithelial ovarian cancer is diagnosed in over 200,000 women worldwide each year. Ten to 20% of women are diagnosed early, when there is still a good possibility of cure. The treatment of early-stage (stage I and IIa) disease involves surgery to remove the disease, often followed by chemotherapy (adjuvant chemotherapy). The largest clinical trials of adjuvant chemotherapy show an overall survival (OS) advantage with platinum-based chemotherapy; however the precise role and type of this treatment in subgroups of women with differing prognoses needs to be defined.

Objectives: To undertake a systematic review of the evidence for adjuvant chemotherapy in early-stage epithelial ovarian cancer to determine whether chemotherapy following surgery offers a survival advantage over the policy of observation following surgery (with chemotherapy reserved for treatment of disease recurrence); and to determine if clinical subgroups of women with differing prognoses, based on histological subtype or completeness of surgical staging, have more or less to gain from adjuvant chemotherapy.

Search methods: We performed an electronic search using the Cochrane Gynaecological Cancer Specialized Register, Cochrane Central Register of Controlled Trials (CENTRAL 2015, Issue 3), MEDLINE (1948 to March week 5, 2015), and EMBASE (1980 to week 14, 2015). We developed the search strategy using free-text and medical subject headings (MeSH). We also searched registers of clinical trials and citation lists of included studies for potentially relevant studies.

Selection criteria: We included randomised clinical trials (RCTs) of women with early stage (I/IIa) epithelial ovarian cancer staged at laparotomy.

Data collection and analysis: Two review authors independently extracted data and assessed study quality of included RCTs. We resolved any disagreements by discussion with a third review author. We used random-effects methods for all meta-analyses, including subgroup analyses.

Main results: The original version of this Cochrane review included five RCTs involving 1277 women. In this 2015 update, no new studies met the inclusion criteria but we included an additional paper with mature data (10-year follow-up) relating to a previously included study (ICON1).We included four studies in the meta-analyses and considered them to be at a low risk of bias. Most study participants (> 95%) had stage I ovarian cancer. Meta-analysis of five-year data from three studies indicated that women who received adjuvant platinum-based chemotherapy had better overall survival (OS) than those who did not (Hazard ratio (HR) 0.71, 95% confidence interval (CI) 0.53 to 0.93; 1008 women; 3 studies; I² statistic = 0%; high quality evidence). Likewise, meta-analysis of five-year data from four studies indicated that women who received adjuvant chemotherapy had better progression-free survival (PFS) than those who did not (HR 0.67, 95% CI 0.53 to 0.84; 1170 women, 4 studies; I² statistic = 0%; high quality evidence). These findings were robust over time, with 10-year HR estimates of 0.72 (95% CI 0.57 to 0.92; 925 women, 2 studies) and 0.67 (95% CI 0.53 to 0.83; 925 women, 2 studies) for OS and PFS, respectively (high quality evidence). The risk of death at 10 years follow-up favoured the adjuvant chemotherapy arm (0.76, 95% CI 0.62 to 0.94; 923 women, 2 studies; I² statistic = 0%), as did the findings for risk of progression at 10 years (RR 0.72, 95% CI 0.60 to 0.87; 925 women, 2 studies; I² statistic = 0%). Low quality evidence suggested that women with high-risk disease may have the most to gain from adjuvant chemotherapy. However, subgroup analyses could neither confirm nor exclude survival benefits in lower risk disease or in optimally staged disease. We found insufficient data to compare adverse events and long term risks between chemotherapy and observation groups.

Authors' conclusions: High-quality evidence indicates that adjuvant platinum-based chemotherapy is effective in prolonging survival in women with early stage (FIGO stage I/IIa) epithelial ovarian cancer. It remains uncertain whether women with low- and intermediate-risk early stage disease will benefit as much from adjuvant chemotherapy as women with high-risk disease. Decisions to use adjuvant chemotherapy (AC) in these women should be mindful of this uncertainty, and the uncertainty regarding adverse events. Treatment of women with lower risk disease should be individualised to take into account individual factors.

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Conflict of interest statement

BWR has no known conflicts of interest. TL has no known conflicts of interest. PH has no known conflicts of interest. HK has no known conflicts of interest.

Figures

1
1
Study flow diagram of search results (up to August 2011).
2
2
Study flow diagram of the literature search results (24 March 2015).
3
3
'Risk of bias' summary: review authors' judgements about each 'Risk of bias' item for each included study.
4
4
Risk of death in the 10 years after surgery for women with early stage ovarian cancer treated with adjuvant chemotherapy: In the control group 33 women had died compared to 25 (20 to 31) out of 100 in the active treatment group.
5
5
Risk of cancer progression/recurrence in the 10 years after surgery for women with early stage ovarian cancer treated with adjuvant chemotherapy: in the control group 39 women had progressive disease compared to 28 (23 to 34) out of 100 in the active treatment group.
6
6
Risk of death in the 10 years after surgery for women with high risk early stage ovarian cancer treated with adjuvant chemotherapy: in the control group 44 people out of 100 died, compared to 32 (95% CI 23 to 43) out of 100 for the active treatment group.
7
7
Risk of cancer progression/recurrence in the 10 years after surgery for women with high risk early stage ovarian cancer treated with adjuvant chemotherapy: in the control group 50 women had progressive disease compared to 32 (23 to 45) out of 100 in the active treatment group.
1.1
1.1. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 1 Overall survival (5 yr).
1.2
1.2. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 2 Deaths total (5 yr).
1.3
1.3. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 3 Overall survival (10 yr).
1.4
1.4. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 4 Death total (10 yr).
1.5
1.5. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 5 Progression‐free survival (5 yr).
1.6
1.6. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 6 Progression total (5 yr).
1.7
1.7. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 7 Progression‐free survival (10 yr).
1.8
1.8. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 8 Progression total (10 yr).
1.9
1.9. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 9 Disease‐specific survival (5 yr).
1.10
1.10. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 10 Disease‐specific survival (10 yr).
1.11
1.11. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 11 Subgroup analysis by staging: 5‐yr OS.
1.12
1.12. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 12 Subgroup analysis by staging: 10 yr DSS.
1.13
1.13. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 13 Subgroup analysis by staging: death from ovarian cancer (10 years).
1.14
1.14. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 14 Subgroup analysis by staging: 5‐yr PFS.
1.15
1.15. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 15 Subgroup analysis by staging: 10‐yr PFS.
1.16
1.16. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 16 Subgroup analysis by staging: progression of ovarian cancer (10 years).
1.17
1.17. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 17 Subgroup analysis by risk: 10‐yr OS.
1.18
1.18. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 18 Subgroup analysis by risk: 10‐yr PFS.
1.19
1.19. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 19 Subgroup analysis by risk: progression at 10 yrs.
1.20
1.20. Analysis
Comparison 1 Adjuvant chemotherapy versus observation, Outcome 20 Subgroup analysis by risk: deaths by 10 yrs.

Update of

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Publication types