Meihui Jessica Shi

ORCID: 0009-0008-2985-4858
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About
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Research Areas
  • Glioma Diagnosis and Treatment
  • Cancer, Hypoxia, and Metabolism
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Adrenal and Paraganglionic Tumors
  • Microtubule and mitosis dynamics
  • Radiomics and Machine Learning in Medical Imaging
  • Neurofibromatosis and Schwannoma Cases
  • Lung Cancer Diagnosis and Treatment
  • Gastric Cancer Management and Outcomes
  • Endometrial and Cervical Cancer Treatments
  • Breast Cancer Treatment Studies
  • Breast Implant and Reconstruction
  • Sarcoma Diagnosis and Treatment

Xijing Hospital
2023

Sidney Kimmel Comprehensive Cancer Center
2023

Johns Hopkins University
2023

Air Force Medical University
2023

Abstract Purpose: Isocitrate dehydrogenase (IDH)-mutant gliomas are usually treated with radiotherapy and chemotherapy, which increases the risk for neurocognitive sequelae during patients’ most productive years. We report our experience using off-label first-in-class mutant IDH1 inhibitor ivosidenib its impact on tumor volume in IDH-mutant gliomas. Experimental Design: retrospectively analyzed patients ages ≥18 years radiation/chemotherapy-naïve, IDH1, nonenhancing, radiographically active,...

10.1158/1078-0432.ccr-23-0585 article EN Clinical Cancer Research 2023-06-29

<div>Abstract<p>Purpose: Isocitrate dehydrogenase (IDH) mutant gliomas are usually treated with radiotherapy and chemotherapy, which increases the risk for neurocognitive sequelae during patients’ most productive years. We report our experience using off-label first-inclass IDH1mut-inhibitor ivosidenib its impact on tumor volume in IDHmut gliomas. Experimental Design: retrospectively analyzed patients aged ≥18 years radiation/chemotherapy-naïve, IDH1mut, non-enhancing,...

10.1158/1078-0432.c.6749981.v3 preprint EN 2024-09-16

<div>Abstract<p>Purpose: Isocitrate dehydrogenase (IDH) mutant gliomas are usually treated with radiotherapy and chemotherapy, which increases the risk for neurocognitive sequelae during patients’ most productive years. We report our experience using off-label first-inclass IDH1mut-inhibitor ivosidenib its impact on tumor volume in IDHmut gliomas. Experimental Design: retrospectively analyzed patients aged ≥18 years radiation/chemotherapy-naïve, IDH1mut, non-enhancing,...

10.1158/1078-0432.c.6749981 preprint EN 2023-07-19

<div>AbstractPurpose:<p>Isocitrate dehydrogenase (IDH)-mutant gliomas are usually treated with radiotherapy and chemotherapy, which increases the risk for neurocognitive sequelae during patients’ most productive years. We report our experience using off-label first-in-class mutant IDH1 inhibitor ivosidenib its impact on tumor volume in IDH-mutant gliomas.</p>Experimental Design:<p>We retrospectively analyzed patients ages ≥18 years radiation/chemotherapy-naïve, IDH1,...

10.1158/1078-0432.c.6749981.v1 preprint EN 2023-07-19

<div>AbstractPurpose:<p>Isocitrate dehydrogenase (IDH)-mutant gliomas are usually treated with radiotherapy and chemotherapy, which increases the risk for neurocognitive sequelae during patients’ most productive years. We report our experience using off-label first-in-class mutant IDH1 inhibitor ivosidenib its impact on tumor volume in IDH-mutant gliomas.</p>Experimental Design:<p>We retrospectively analyzed patients ages ≥18 years radiation/chemotherapy-naïve, IDH1,...

10.1158/1078-0432.c.6749981.v2 preprint EN 2023-12-01
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