Braeden Freitas

ORCID: 0009-0005-2512-9112
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About
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Research Areas
  • Lung Cancer Research Studies
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Metastasis and carcinoma case studies
  • Lung Cancer Treatments and Mutations
  • Neuroendocrine Tumor Research Advances
  • Cancer therapeutics and mechanisms
  • Brain Metastases and Treatment
  • HER2/EGFR in Cancer Research
  • Cancer Treatment and Pharmacology

The University of Texas Southwestern Medical Center
2023-2024

Abstract Small cell lung cancer (SCLC) presents as a highly chemosensitive malignancy but acquires cross-resistance after relapse. This transformation is nearly inevitable in patients has been difficult to capture laboratory models. Here, we present preclinical system that recapitulates acquired cross-resistance, developed from 51 patient-derived xenograft (PDX) Each model was tested vivo against three clinical regimens: cisplatin plus etoposide, olaparib temozolomide, and topotecan. These...

10.1158/2159-8290.cd-23-0656 article EN cc-by-nc-nd Cancer Discovery 2024-02-21

ABSTRACT Small cell lung cancer (SCLC) presents as a highly chemosensitive malignancy but acquires cross-resistance after relapse. This transformation is nearly inevitable in patients has been difficult to capture laboratory models. Here we present pre-clinical system that recapitulates acquired SCLC, developed from 51 patient-derived xenografts (PDXs). Each model was tested for vivo sensitivity three clinical regimens: cisplatin plus etoposide, olaparib temozolomide, and topotecan. These...

10.1101/2023.06.23.546278 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2023-06-26

<div>Abstract<p>Small cell lung cancer (SCLC) presents as a highly chemosensitive malignancy but acquires cross-resistance after relapse. This transformation is nearly inevitable in patients has been difficult to capture laboratory models. Here, we present preclinical system that recapitulates acquired cross-resistance, developed from 51 patient-derived xenograft (PDX) Each model was tested <i>in vivo</i> against three clinical regimens: cisplatin plus etoposide,...

10.1158/2159-8290.c.7209241.v1 preprint EN 2024-05-01
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