
Mark Alan Rosen
University of Pennsylvania · Rehabilitation Medicine
Active 1973–2024
Research topics
- Internal medicine
- Medicine
- Biochemistry
- Materials science
- Chemistry
- Oncology
- Pathology
Selected publications
ACS Nano · 2020 · 173 citations
- Medicine
- Materials science
- Pathology
CT imaging was done with both healthy mice and a dextran sodium sulfate induced colitis mouse model. Dex-CeNP's CT contrast generation and accumulation in inflammation sites were compared with iopamidol, an FDA approved CT contrast agent. Dex-CeNP was found to be protective against oxidative damage. Dex-CeNP produced strong CT contrast and accumulated in the colitis area of large intestines. In addition, >97% of oral doses were cleared from the body within 24 h. Therefore, Dex-CeNP can be used as a potential CT contrast agent for imaging GIT with IBD while protecting against oxidative damage.
npj Breast Cancer · 2020 · 81 citations
- Medicine
- Oncology
- Internal medicine
Dynamic contrast-enhanced (DCE) MRI provides both morphological and functional information regarding breast tumor response to neoadjuvant chemotherapy (NAC). The purpose of this retrospective study is to test if prediction models combining multiple MRI features outperform models with single features. Four features were quantitatively calculated in each MRI exam: functional tumor volume, longest diameter, sphericity, and contralateral background parenchymal enhancement. Logistic regression analysis was used to study the relationship between MRI variables and pathologic complete response (pCR). Predictive performance was estimated using the area under the receiver operating characteristic curve (AUC). The full cohort was stratified by hormone receptor (HR) and human epidermal growth factor receptor 2 (HER2) status (positive or negative). A total of 384 patients (median age: 49 y/o) were included. Results showed analysis with combined features achieved higher AUCs than analysis with any feature alone. AUCs estimated for the combined versus highest AUCs among single features were 0.81 (95% confidence interval [CI]: 0.76, 0.86) versus 0.79 (95% CI: 0.73, 0.85) in the full cohort, 0.83 (95% CI: 0.77, 0.92) versus 0.73 (95% CI: 0.61, 0.84) in HR-positive/HER2-negative, 0.88 (95% CI: 0.79, 0.97) versus 0.78 (95% CI: 0.63, 0.89) in HR-positive/HER2-positive, 0.83 (95% CI not available) versus 0.75 (95% CI: 0.46, 0.81) in HR-negative/HER2-positive, and 0.82 (95% CI: 0.74, 0.91) versus 0.75 (95% CI: 0.64, 0.83) in triple negatives. Multi-feature MRI analysis improved pCR prediction over analysis of any individual feature that we examined. Additionally, the improvements in prediction were more notable when analysis was conducted according to cancer subtype.
Recent grants
NIH · $652k · 2013
Imaging and Radiation Oncology Core (IROC) Group
NIH · $107.5M · 2014–2026
Penn Quantitative MRI Resource for Pancreatic Cancer
NIH · $573k · 2018–2023
NIH · $8.8M · 2015
Penn Quantitative MRI Resource for Pancreatic Cancer
NIH · $2.4M · 2018–2024
Frequent coauthors
- 78 shared
Mitchell D. Schnall
University of Pennsylvania
- 75 shared
Peter J. O’Dwyer
University of Pennsylvania
- 67 shared
Angela DeMichele
University of Pennsylvania
- 61 shared
M. Giulia Cicchetti
University of Massachusetts Chan Medical School
- 61 shared
Janaki Moni
University of Massachusetts Chan Medical School
- 61 shared
Thomas J. FitzGerald
University of Massachusetts Chan Medical School
- 61 shared
Jeff M. Michalski
Washington University in St. Louis
- 59 shared
Fran Laurie
University of Massachusetts Chan Medical School
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