Scott Barker

ORCID: 0000-0001-9372-6932
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Lung Cancer Treatments and Mutations
  • Lung Cancer Research Studies
  • Colorectal Cancer Treatments and Studies
  • Lung Cancer Diagnosis and Treatment
  • Cancer Genomics and Diagnostics
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Neuroblastoma Research and Treatments
  • CAR-T cell therapy research
  • Platelet Disorders and Treatments
  • PI3K/AKT/mTOR signaling in cancer
  • Glutathione Transferases and Polymorphisms
  • Cancer, Hypoxia, and Metabolism
  • Lymphoma Diagnosis and Treatment
  • Adrenal and Paraganglionic Tumors
  • Glioma Diagnosis and Treatment
  • Advanced Breast Cancer Therapies
  • Health Systems, Economic Evaluations, Quality of Life
  • Brain Metastases and Treatment
  • Blood disorders and treatments
  • Peptidase Inhibition and Analysis
  • Gastric Cancer Management and Outcomes
  • Renal cell carcinoma treatment
  • Sarcoma Diagnosis and Treatment
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Chronic Myeloid Leukemia Treatments

Eli Lilly (United States)
2013-2025

Loxo Oncology at Lilly (United States)
2023

Selpercatinib is a highly selective and potent CNS-active RET kinase inhibitor approved for the treatment of fusion-positive NSCLC based on results phase I/II trial LIBRETTO-001 (NCT03157128). The final data reported. Patients with advanced, (identified by NGS, PCR or FISH) who were naïve had previously received platinum-based chemotherapy enrolled at selpercatinib dose 160 mg BID. primary end point was objective response rate (ORR) RECIST 1.1 assessed an independent review committee....

10.1016/j.esmoop.2024.102614 article EN cc-by-nc-nd ESMO Open 2024-03-01

LIBRETTO-001 (ClinicalTrials.gov identifier: NCT03157128 ) is a registrational phase I/II, single-arm, open-label trial of selpercatinib in RET-dependent cancers. With 19 months additional follow-up, we report the final efficacy and safety results patients with RET fusion–positive non–small cell lung cancer (NSCLC) who had previously received platinum-based chemotherapy (N = 247) or were treatment-naïve 69). The objective response rate (ORR) was 62% for pretreated 83% patients. Duration...

10.1200/jco-24-02076 article EN Journal of Clinical Oncology 2025-02-21

746 Background: Selpercatinib, a first-in-class highly selective and potent RET kinase inhibitor with CNS activity, is approved in multiple countries for the treatment of RET-activated cancers. This update includes more patients (pts, n=52) 16 months (mo) longer follow-up (data cut-off: 13Jan2023) fusion+ solid tumors other than lung/thyroid focus on GI histologies. Methods: The phase 1/2 LIBRETTO-001 trial (NCT03157128) enrolled pts locally advanced/metastatic tumors. 51/52 received...

10.1200/jco.2024.42.3_suppl.746 article EN Journal of Clinical Oncology 2024-01-20

"HSR24-128: Real-World Treatment Patterns and Effectiveness of Selpercatinib in Patients With Locally Advanced/Metastatic Non–Small Cell Lung Cancer the US" published on 05 Apr 2024 by National Comprehensive Network.

10.6004/jnccn.2023.7200 article EN Journal of the National Comprehensive Cancer Network 2024-04-05

10009 Background: Activating RET alterations are oncogenic drivers of select pediatric and adult cancers. Selpercatinib is a first-in-class, highly selective potent, CNS active kinase inhibitor. The manageable toxicity profile durable anti-tumor activity in RET-altered cancers demonstrated the LIBRETTO-001 phase 1/2 trial led to global approvals selpercatinib adults adolescents with thyroid cancer NSCLC. Methods: LIBRETTO-121 (JZJJ) multicenter pts 0.5-21 years (yrs) age advanced, solid or...

10.1200/jco.2021.39.15_suppl.10009 article EN Journal of Clinical Oncology 2021-05-20

Selpercatinib is indicated for locally advanced/metastatic RET-activated solid tumors after progression or following prior systemic therapies. Until the recently published data from LIBRETTO-431 and LIBRETTO-531, there were limited effectiveness comparing selpercatinib with other first-line treatments in non-small cell lung cancer (NSCLC), medullary thyroid (MTC), (TC). This study analyzed patient LIBRETTO-001 compared outcomes (time to treatment discontinuation {TTD}, time next death...

10.3390/cancers16010140 article EN Cancers 2023-12-27

Olaratumab is a human monoclonal immunoglobulin G1 antibody against platelet-derived growth factor receptor-α. We report the nature and frequency of infusion-related reactions (IRRs) with olaratumab in clinical trials postmarketing reports.Data from patients exposed to across nine were reviewed for IRRs. Blood samples also analyzed pre-existing E anti-galactose-α-1,3-galactose (anti-α-Gal) antibodies.In trials, IRRs identified 70 485 (14.4%). The most frequent symptoms included flushing,...

10.1200/jop.18.00761 article EN cc-by-nc-nd Journal of Oncology Practice 2019-07-03

•Long-term patient-reported outcomes (PROs) in patients with RET-driven cancers from the LIBRETTO-001 trial were reported.•Most had improved or stable quality of life during long-term treatment selpercatinib.•Physical function and symptoms such as dyspnea, appetite loss, insomnia, fatigue, pain also remained stable.•These findings further support selpercatinib standard care for advanced cancers. BackgroundThis post-hoc retrospective study describes REarranged Transfection (RET)-altered...

10.1016/j.esmoop.2024.103444 article EN cc-by-nc-nd ESMO Open 2024-05-01

3150 Background: Selpercatinib, a first-in-class highly selective and potent RET kinase inhibitor with CNS activity, is approved in multiple countries for the treatment of RET-activated cancers. Current indications mutant disease are limited to MTC. This analysis examined if selpercatinib was effective non-MTC, mutation positive tumors whether certain mutations demonstrated better activity (n=23; data cut-off: 13Jan2023). Methods: The phase 1/2 LIBRETTO-001 trial (NCT03157128) enrolled pts...

10.1200/jco.2024.42.16_suppl.3150 article EN Journal of Clinical Oncology 2024-06-01

Selpercatinib is a selective RET inhibitor approved for treatment of RET-activated cancers. Adverse events (AEs) are manageable with dose modifications. This post hoc analysis characterized selpercatinib's clinical safety profile after long-term follow-up in the population LIBRETTO-001.

10.1093/oncolo/oyae282 article EN cc-by-nc The Oncologist 2024-10-29

This study described real-world patient characteristics and outcomes among selpercatinib-treated patients in the United States, using Flatiron Health electronic health record-derived deidentified database (FHD) for advanced/metastatic non-small cell lung cancer (a/mNSCLC) Optum's de-identified Clinformatics

10.3390/cancers16223835 article EN Cancers 2024-11-15

This study was designed to describe demographic and clinical characteristics of patients diagnosed with advanced or metastatic soft tissue sarcoma (STS) examine treatment healthcare resource utilization patterns this patient population in a United States (US) community-based oncology practice setting over time.

10.1155/2020/1765319 article EN cc-by Sarcoma 2020-03-01

"HSR22-130: A Retrospective Cohort Study of Selpercatinib-Treated Patients With Advanced/Metastatic Non-Small Cell Lung Cancer: Preliminary Findings From a Real-World Database in the United States" published on 31 Mar 2022 by National Comprehensive Cancer Network.

10.6004/jnccn.2021.7179 article EN Journal of the National Comprehensive Cancer Network 2022-03-31
Coming Soon ...