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Walter M. Stadler

Researcher at University of Chicago

Publications -  513
Citations -  37554

Walter M. Stadler is an academic researcher from University of Chicago. The author has contributed to research in topics: Cancer & Prostate cancer. The author has an hindex of 88, co-authored 494 publications receiving 34323 citations. Previous affiliations of Walter M. Stadler include Cleveland Clinic & Northwestern University.

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Journal Article

Increased p16 Levels Correlate with pRb Alterations in Human Urothelial Cells

TL;DR: The hypothesis that p16 mediated cell cycle inhibition, as well as p16 regulation, occurs via pRb dependent pathway(s) is supported.

Vorinostat in Advanced Prostate Cancer Patients Progressing on Prior Chemotherapy (National Cancer

TL;DR: In this article, a phase 2 trial was designed to evaluate the efficacy of vorinostat in chemotherapy-pretreated patients with metastatic castration-resistant prostate cancer.
Journal Article

Transcriptional Profiles in Peripheral Blood Mononuclear Cells Prognostic of Clinical Outcomes in Patients with Advanced Renal Cell Carcinoma

TL;DR: In this paper, the authors evaluated the association of expression profiles in peripheral blood mononuclear cells (PBMCs) with clinical outcomes in patients with advanced renal cell cancer and found that the expression levels of many PBMC transcripts were predictors for the patient outcomes of time to progression and overall survival (time to death).
Journal ArticleDOI

Afatinib Activity in Platinum-Refractory Metastatic Urothelial Carcinoma in Patients With ERBB Alterations

TL;DR: Afatinib demonstrated significant activity in patients with platinum-refractory UC with HER2 or ERBB3 alterations and deserves further investigation in molecularly selected UC.
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Cabozantinib in advanced non-clear-cell renal cell carcinoma: a multicentre, retrospective, cohort study.

TL;DR: This real-world study provides evidence supporting the antitumour activity and safety of cabozantinib across non-clear-cell renal cell carcinoma subtypes and specific molecular alterations.