학술논문

Treatments and outcomes in high‐risk gestational trophoblastic neoplasia: A systematic review and meta‐analysis.
Document Type
Article
Source
BJOG: An International Journal of Obstetrics & Gynaecology. Apr2023, Vol. 130 Issue 5, p443-453. 11p.
Subject
*MOLAR pregnancy
*GESTATIONAL trophoblastic disease
*THERAPEUTICS
Language
ISSN
1470-0328
Abstract
Background: High‐risk gestational trophoblastic neoplasia (GTN) is rare and treated with diverse approaches. Limited published institutional data has yet to be systematically reviewed. Objectives: To compile global high‐risk GTN (prognostic score ≥7) cohorts to summarise treatments and outcomes by disease characteristics and primary chemotherapy. Search Strategy: MEDLINE, Embase, Scopus, ClinicalTrials.gov and Cochrane were searched through March 2021. Selection Criteria: Full‐text manuscripts reporting mortality among ≥10 high‐risk GTN patients. Data Collection and Analysis: Binomial proportions were summed, and random‐effects meta‐analyses performed. Main Results: From 1137 records, we included 35 studies, representing 20 countries. Among 2276 unique high‐risk GTN patients, 99.7% received chemotherapy, 35.8% surgery and 4.9% radiation. Mortality was 10.9% (243/2236; meta‐analysis: 10%, 95% confidence interval [CI] 7–12%) and likelihood of complete response to primary chemotherapy was 79.7% (1506/1890; meta‐analysis: 78%, 95% CI: 74–83%). Across 24 reporting studies, modern preferred chemotherapy (EMA/CO or EMA/EP) was associated with lower mortality (overall: 8.8 versus 9.5%; comparative meta‐analysis: 8.1 versus 12.4%, OR 0.42, 95% CI: 0.20–0.90%, 14 studies) and higher likelihood of complete response (overall: 76.6 versus 72.8%; comparative meta‐analysis: 75.9 versus 60.7%, OR 2.98, 95% CI: 1.06–8.35%, 14 studies), though studies focused on non‐preferred regimens reported comparable outcomes. Mortality was increased for ultra‐high‐risk disease (30 versus 7.5% high‐risk; meta‐analysis OR 7.44, 95% CI: 4.29–12.9%) and disease following term delivery (20.8 versus 7.3% following molar pregnancy; meta‐analysis OR 2.64, 95% CI: 1.10–6.31%). Relapse rate estimates ranged from 3 to 6%. Conclusions: High‐risk GTN is responsive to several chemotherapy regimens, with EMA/CO or EMA/EP associated with improved outcomes. Mortality is increased in patients with ultra‐high‐risk, relapsed and post‐term pregnancy disease. Linked article: This article is commented on by Lawrence Impey, pp. 494 in this issue. To view this mini commentary visit https://doi.org/10.1111/1471‐0528.17383 [ABSTRACT FROM AUTHOR]