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Magnetic resonance imaging-radiomics in endometrial cancer: a systematic review and meta-analysis

期刊

INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER
卷 33, 期 7, 页码 1070-1076

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/ijgc-2023-004313

关键词

Endometrial Neoplasms; Lymph Nodes; Sentinel Lymph Node; Uterine Cancer; Uterine Neoplasms

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This study aimed to assess the role of radiomics analysis in pre-operatively predicting molecular or clinicopathological prognostic factors in patients with endometrial carcinoma. The results showed that MRI has high sensitivity and specificity in predicting high-grade endometrial carcinoma, deep myometrial invasion, lymphovascular space invasion, and nodal metastasis.
ObjectiveEndometrial carcinoma is the most common gynecological tumor in developed countries. Clinicopathological factors and molecular subtypes are used to stratify the risk of recurrence and to tailor adjuvant treatment. The present study aimed to assess the role of radiomics analysis in pre-operatively predicting molecular or clinicopathological prognostic factors in patients with endometrial carcinoma. MethodsLiterature was searched for publications reporting radiomics analysis in assessing diagnostic performance of MRI for different outcomes. Diagnostic accuracy performance of risk prediction models was pooled using the metandi command in Stata. ResultsA search of MEDLINE (PubMed) resulted in 153 relevant articles. Fifteen articles met the inclusion criteria, for a total of 3608 patients. MRI showed pooled sensitivity and specificity 0.785 and 0.814, respectively, in predicting high-grade endometrial carcinoma, deep myometrial invasion (pooled sensitivity and specificity 0.743 and 0.816, respectively), lymphovascular space invasion (pooled sensitivity and specificity 0.656 and 0.753, respectively), and nodal metastasis (pooled sensitivity and specificity 0.831 and 0.736, respectively). ConclusionsPre-operative MRI-radiomics analyses in patients with endometrial carcinoma is a good predictor of tumor grading, deep myometrial invasion, lymphovascular space invasion, and nodal metastasis.

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