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The objective is to test the role of baseline endogenous testosterone (ET) in discriminating adverse tumor grades and predicting disease progression in prostate cancer (PCa) patients, who harbored organ-confined disease at radical prostatectomy (RP). Between November 2014 and December 2019, data on PCa patients treated with robot-assisted RP at a single tertiary referral center were retrospectively analyzed. Baseline ET levels were coded as abnormal (≤ 350 ng/dL) vs. normal (> 350 ng/dL) according to a standard consensus. In the surgical specimen, the International Society of Urological Pathology (ISUP) grade groups 3 and 4/5 were classified as unfavorable tumor grades. Disease progression was defined as biochemical recurrence/persistence and/or local recurrence and/or distant metastases. Multivariable logistic and Cox regression models were used. Overall, 460 patients were included. In the surgical specimen, adverse tumor grades were detected in 198 (43.0%) patients of whom 60 (13.0%) harbored ISUP grade group 4/5. Disease progression occurred in 62 (13.5%) patients. In multivariable regression models that adjusted for other available clinical and pathological factors, patients with abnormal baseline ET levels were less likely to associate with unfavorable tumor grades, as well as to experience PCa progression (hazard ratio: 0.49; 95% CI: 0.26-0.92; = 0.026). In pathological organ-confined PCa, baseline ET levels predicted disease progression after discriminating unfavorable tumor grades. Accordingly, baseline ET is a risk factor that might further stratify patients diagnosed with PCa.
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http://dx.doi.org/10.1007/s13193-024-02109-3 | DOI Listing |
Pathol Res Pract
September 2025
Department of Pathology, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China. Electronic address:
Our research aims to ascertain the value of precursor and outgrowth lepidic in aiding the confirmation of multiple lung adenocarcinomas as separate primary lung cancers (SPLC). A total of 151 patients with metachronous multiple invasive adenocarcinomas were included in this study. Driver mutation tests(at least five genes: EGFR, ALK, KRAS, BRAF, and ROS1) were conducted on 302 tumors collected from 151 patients.
View Article and Find Full Text PDFJCO Clin Cancer Inform
September 2025
USC Institute of Urology and Catherine and Joseph Aresty Department of Urology, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Purpose: To evaluate a generative artificial intelligence (GAI) framework for creating readable lay abstracts and summaries (LASs) of urologic oncology research, while maintaining accuracy, completeness, and clarity, for the purpose of assessing their comprehension and perception among patients and caregivers.
Methods: Forty original abstracts (OAs) on prostate, bladder, kidney, and testis cancers from leading journals were selected. LASs were generated using a free GAI tool, with three versions per abstract for consistency.
J Bras Pneumol
September 2025
. Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brasil.
Clin Cancer Res
September 2025
Amgen (United States), Thousand Oaks, CA, United States.
Purpose: Tarlatamab is a first-in-class, half-life extended bispecific T-cell engager (BiTE®) immunotherapy targeting delta-like ligand 3 (DLL3) currently approved for the treatment of adult patients with small cell lung cancer (SCLC) with disease progression on or after platinum-based chemotherapy. Here we report tarlatamab exposure-response relationships to inform dose selection in patients with SCLC.
Experimental Design: Pharmacokinetic data were correlated with therapeutic effect [exposure-response (ER) analyses] for efficacy and safety measures using pooled data from DeLLphi-300 and DeLLphi-301 studies.
Ann Acad Med Singap
August 2025
Division of Medical Oncology, National Cancer Centre Singapore, Singapore.
Introduction: Trastuzumab deruxtecan (T-DXd) has revolutionised treatment for metastatic breast cancer (MBC). While effective, its high cost and toxicities, such as fatigue and nausea, pose challenges.
Method: Medical records from the Joint Breast Cancer Registry in Singapore were used to study MBC patients treated with T-DXd (February 2021-June 2024).