scispace - formally typeset
A

Alexander F. Lovejoy

Researcher at Stanford University

Publications -  20
Citations -  3245

Alexander F. Lovejoy is an academic researcher from Stanford University. The author has contributed to research in topics: Lung cancer & RNA. The author has an hindex of 10, co-authored 17 publications receiving 2436 citations.

Papers
More filters
Journal ArticleDOI

Dynamic Noninvasive Genomic Monitoring for Outcome Prediction in Diffuse Large B-Cell Lymphoma

TL;DR: Given its high specificity and large dynamic range, ctDNA provides an opportunity to monitor the dynamics of therapeutic response in patients with DLBCL, and a multi-compartmental ordinary-differential equation model of tumor dynamics capturing tumor volume, cTDNA, and the effect of chemotherapy is developed.
Journal ArticleDOI

Risk profiling of patients with relapsed/refractory diffuse large B-cell lymphoma by measuring circulating tumor DNA

TL;DR: The level of baseline ct DNA correlated with PFS and OS in patients with R/R DLBCL receiving pola plus BR or BR alone and patients with a CR had a significantly greater median decrease in ctDNA levels at end of treatment than patients without a CR.
Journal ArticleDOI

Analysis of circulating tumor DNA in localized lung cancer for detection of molecular residual disease and personalization of adjuvant strategies.

TL;DR: This clinical trial aimed at identifying patients with residual disease following curative intent therapy with localized non-small cell lung cancer (NSCLC) and aims to provide real-time information on the progression-free survival and quality of life of these patients.
Proceedings ArticleDOI

Abstract 1034: Role of KEAP1/NRF2 and TP53 mutations in lung squamous cell carcinoma development and radiation resistance

TL;DR: Novel, clinically relevant murine LSCC models driven by inactivation of Trp53 with or without Keap1 are described and KEAP1/NRF2 mutations are identified as predictive biomarkers that could be used for personalization of therapeutic strategies for NSCLCs, and likely other cancers in which they are recurrently mutated.