Amide proton transfer imaging in differentiation of type II and type I endometrial carcinoma: a pilot study

Purpose This study aimed at evaluating the efficacy of amide proton transfer (APT) imaging in differentiation of type II and type I uterine endometrial carcinoma. Materials and methods Thirty-three patients diagnosed with uterine endometrial carcinoma, including 24 with type I and 9 with type II car...

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Veröffentlicht in:Japanese journal of radiology 2022-02, Vol.40 (2), p.184-191
Hauptverfasser: Ochiai, Ryoya, Mukuda, Naoko, Yunaga, Hiroto, Kitao, Shinichiro, Okuda, Kyohei, Sato, Shinya, Oishi, Tetsuro, Miyoshi, Mitsuharu, Nozaki, Atsushi, Fujii, Shinya
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Sprache:eng
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Zusammenfassung:Purpose This study aimed at evaluating the efficacy of amide proton transfer (APT) imaging in differentiation of type II and type I uterine endometrial carcinoma. Materials and methods Thirty-three patients diagnosed with uterine endometrial carcinoma, including 24 with type I and 9 with type II carcinomas, underwent APT imaging. Two readers evaluated the magnetization transfer ratio at 3.5 ppm [MTR asym (3.5 ppm)] in each type of carcinoma. The average MTR asym (APT mean ) and the maximum MTR asym (APT max ) were analyzed. The receiver operating characteristic (ROC) curve analysis was performed. Results The APT max was significantly higher in type II carcinomas than in type I carcinomas (reader1, p  = 0.004; reader 2, p  = 0.014; respectively). However, APT mean showed no significant difference between type I and II carcinomas. Based on the results reported by reader 1, the area under the curve (AUC) pertaining to the APT max for distinguishing type I from type II carcinomas was 0.826, with a cut-off, sensitivity, and specificity of 9.90%, 66.7%, and 91.3%, respectively. Moreover, based on the results reported by reader 2, the AUC was 0.750, with a cut-off, sensitivity, and specificity of 9.80%, 62.5%, and 87.5%, respectively. Conclusion APT imaging has the potential to determine the type of endometrial cancer.
ISSN:1867-1071
1867-108X
DOI:10.1007/s11604-021-01197-3