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Meta-Analysis
. 2016 Jan 9;2016(1):CD006014.
doi: 10.1002/14651858.CD006014.pub7.

Interval debulking surgery for advanced epithelial ovarian cancer

Affiliations
Meta-Analysis

Interval debulking surgery for advanced epithelial ovarian cancer

Siriwan Tangjitgamol et al. Cochrane Database Syst Rev. .

Abstract

Background: Interval debulking surgery (IDS), following induction or neoadjuvant chemotherapy, may have a role in treating advanced epithelial ovarian cancer (stage III to IV) where primary debulking surgery is not an option.

Objectives: To assess the effectiveness and complications of IDS for women with advanced stage epithelial ovarian cancer.

Search methods: We searched the Cochrane Gynaecological Cancer Group's Specialised Register, the Cochrane Central Register of Controlled Trials (CENTRAL) 2012, Issue 6, MEDLINE and EMBASE for the original review in to June 2012. We updated the searches in June 2009, 2012 and 2015 for the review updates.

Selection criteria: Randomised controlled trials (RCTs) comparing survival of women with advanced epithelial ovarian cancer, who had IDS performed between cycles of chemotherapy after primary surgery with survival of women who had conventional treatment (primary debulking surgery and adjuvant chemotherapy).

Data collection and analysis: Two review authors independently assessed trial quality and extracted data. Searches for additional information from study authors were attempted. We performed meta-analysis of overall and progression-free survival (PFS), using random-effects models.

Main results: Three RCTs randomising 853 women, of whom 781 were evaluated, met the inclusion criteria. Meta-analysis of three trials for overall survival (OS) found no statistically significant difference between IDS and chemotherapy alone (hazard ratio (HR) = 0.80, 95% confidence interval (CI) 0.61 to 1.06, I² = 58%). Subgroup analysis for OS in two trials, where the primary surgery was not performed by gynaecologic oncologists or was less extensive, showed a benefit of IDS (HR = 0.68, 95% CI 0.53 to 0.87, I² = 0%). Meta-analysis of two trials for PFS found no statistically significant difference between IDS and chemotherapy alone (HR = 0.88, 95% CI 0.57 to 1.33, I² = 83%). Rates of toxic reactions to chemotherapy were similar in both arms (risk ratio = 1.19, 95% CI 0.53 to 2.66, I² = 0%), but little information was available for other adverse events or quality or life (QoL).

Authors' conclusions: We found no conclusive evidence to determine whether IDS between cycles of chemotherapy would improve or decrease the survival rates of women with advanced ovarian cancer, compared with conventional treatment of primary surgery followed by adjuvant chemotherapy. IDS appeared to yield benefit only in women whose primary surgery was not performed by gynaecologic oncologists or was less extensive. Data on QoL and adverse events were inconclusive.

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Conflict of interest statement

There is no known conflict of interest among the authors of this review.

Figures

1
1
Methodological quality graph: review authors' judgements about each methodological quality item presented as percentages across all included studies.
2
2
Methodological quality summary: review authors' judgements about each methodological quality item for each included study.
3
3
Study flow diagram.
1.1
1.1. Analysis
Comparison 1 IDS vs chemotherapy only, Outcome 1 Overall survival.
1.2
1.2. Analysis
Comparison 1 IDS vs chemotherapy only, Outcome 2 Progression‐free survival.
1.3
1.3. Analysis
Comparison 1 IDS vs chemotherapy only, Outcome 3 Toxic reactions to chemotherapy.
1.4
1.4. Analysis
Comparison 1 IDS vs chemotherapy only, Outcome 4 Peripheral neuropathy of grade 2 or higher.
1.5
1.5. Analysis
Comparison 1 IDS vs chemotherapy only, Outcome 5 Grade 3 or 4 gastrointestinal adverse events.
1.6
1.6. Analysis
Comparison 1 IDS vs chemotherapy only, Outcome 6 Grade 4 pulmonary adverse events.
1.7
1.7. Analysis
Comparison 1 IDS vs chemotherapy only, Outcome 7 Grade 4 cardiovascular adverse events.

Update of

References

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