<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14</volume><submitter>Benner B</submitter><pubmed_abstract>Tenosynovial giant cell tumor (TGCT) is a rare benign tumor that involves the synovium, bursa, and tendon sheath, resulting in reduced mobility of the affected joint or limb. The current standard of care for TGCT is surgical resection. However, some patients have tumor recurrence, present with unresectable tumors, or have tumors that are in locations where resection could result in amputations or significant debility. Therefore, the development of systemic agents with activity against TGCT to expand treatment options is a highly unmet medical need. Pathologically, TGCT is characterized by the overexpression of colony﻿-stimulating factor 1 (CSF-1), which leads to the recruitment of colony﻿-stimulating factor-1 receptor (CSF-1R) expressing macrophages that make up the primary cell type withi</pubmed_abstract><journal>Drug design, development and therapy</journal><pagination>1693-1704</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7210448</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pexidartinib, a Novel Small Molecule CSF-1R Inhibitor in Use for Tenosynovial Giant Cell Tumor: A Systematic Review of Pre-Clinical and Clinical Development.</pubmed_title><pmcid>PMC7210448</pmcid><pubmed_authors>Good L</pubmed_authors><pubmed_authors>Quiroga D</pubmed_authors><pubmed_authors>Schultz TE</pubmed_authors><pubmed_authors>Wesolowski R</pubmed_authors><pubmed_authors>Benner B</pubmed_authors><pubmed_authors>Sardesai S</pubmed_authors><pubmed_authors>Cherian MA</pubmed_authors><pubmed_authors>Carson WE</pubmed_authors><pubmed_authors>Kassem M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pexidartinib, a Novel Small Molecule CSF-1R Inhibitor in Use for Tenosynovial Giant Cell Tumor: A Systematic Review of Pre-Clinical and Clinical Development.</name><description>Tenosynovial giant cell tumor (TGCT) is a rare benign tumor that involves the synovium, bursa, and tendon sheath, resulting in reduced mobility of the affected joint or limb. The current standard of care for TGCT is surgical resection. However, some patients have tumor recurrence, present with unresectable tumors, or have tumors that are in locations where resection could result in amputations or significant debility. Therefore, the development of systemic agents with activity against TGCT to expand treatment options is a highly unmet medical need. Pathologically, TGCT is characterized by the overexpression of colony﻿-stimulating factor 1 (CSF-1), which leads to the recruitment of colony﻿-stimulating factor-1 receptor (CSF-1R) expressing macrophages that make up the primary cell type withi</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2025-04-26T00:25:23.912Z</modification><creation>2020-05-25T07:07:10Z</creation></dates><accession>S-EPMC7210448</accession><cross_references><pubmed>32440095</pubmed><doi>10.2147/DDDT.S253232</doi></cross_references></HashMap>