Application of accelerated quantitative magnetic resonance imaging in predicting drug resistance in pituitary prolactinomas
Motivation: Predicting and managing dopamine agonists (DA) resistance of prolactinomas remain a challenge. There is no reliable quantitative imaging marker. Goal(s): The goal is to use accelerated quantitative T2 mapping(GRAPPATNI) for early diagnosis of drug resistance in pituitary prolactinomas to guide treatment. Approach: This is a cross-sectional study. It will analyze the differences in T2 values between drug-resistant and sensitive groups and explore their diagnostic value in predicting drug sensitivity. Results: Quantitative T2 values have better sensitivity than T2 signal intensity (SI) in predicting drug resistance in pituitary prolactinoma. Impact: This is the first study to apply GRAPPATINI in prolactinoma. We found that T2 values of tumors were lower in drug-resistant prolactinoma than sensitive patients. T2 values might be a promising predictive imaging tool.
Authors
- Thomas J. Hwang (ORCID: https://orcid.org/0000-0003-0717-1497)
- Lijin Ji (ORCID: https://orcid.org/0000-0002-0243-6399)
- Zheyuan Wu (ORCID: https://orcid.org/0000-0002-8381-5605)
- Rong Lü (ORCID: https://orcid.org/0000-0001-8768-9303)
- Ying‐Hua Chu (ORCID: https://orcid.org/0000-0002-5574-4053)
- Tobias Kober (ORCID: https://orcid.org/0000-0001-7598-9456)
- Qing Li (ORCID: https://orcid.org/0000-0002-2338-150X)
- Shuzhen Shi (ORCID: https://orcid.org/0000-0002-0841-4270)
- Weijun Tang (ORCID: https://orcid.org/0000-0002-3726-5243)
- Caixia Fu (ORCID: https://orcid.org/0000-0002-5595-6347)
- Tom Hibert
Publication Details
- Journal
- Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
- Published
- 2024-11-26
- DOI
- https://doi.org/10.58530/2024/0405
- Primary Topic
- Pituitary Gland Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00