<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Overman MJ</submitter><funding>American Cancer Society</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>139-144</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5834085</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Hypermethylation of promoter CpG islands [CpG island methylator phenotype (CIMP)] represents a unique pathway for the development of colorectal cancer (CRC), characterized by lack of chromosomal instability and a low rate of adenomatous polyposis coli (APC) mutations, which have both been correlated with taxane resistance. Similarly, small bowel adenocarcinoma (SBA), a rare tumor, also has a low rate of APC mutations. This phase II study evaluated taxane sensitivity in SBA and CIMP-high CRC.&lt;h4>Patients and methods&lt;/h4>The primary objective was Response Evaluation Criteria in Solid Tumors version 1.1 response rate. Eligibility included Eastern Cooperative Oncology Group performance status 0/1, refractory disease, and SBA or CIMP-high metastatic CRC. Nab-paclitaxel was in</pubmed_abstract><journal>Annals of oncology : official journal of the European Society for Medical Oncology</journal><pubmed_title>Phase II study of nab-paclitaxel in refractory small bowel adenocarcinoma and CpG island methylator phenotype (CIMP)-high colorectal cancer.</pubmed_title><pmcid>PMC5834085</pmcid><funding_grant_id>P30 CA016672</funding_grant_id><funding_grant_id>127343-RSG-15-068-01-TBG</funding_grant_id><pubmed_authors>Adam L</pubmed_authors><pubmed_authors>Kopetz S</pubmed_authors><pubmed_authors>Azad N</pubmed_authors><pubmed_authors>Vilar E</pubmed_authors><pubmed_authors>Overman MJ</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Wolff R</pubmed_authors><pubmed_authors>Pisanic TR</pubmed_authors><pubmed_authors>Fogelman D</pubmed_authors><pubmed_authors>Dasari A</pubmed_authors><pubmed_authors>Raghav K</pubmed_authors><pubmed_authors>Morris J</pubmed_authors><pubmed_authors>Shroff R</pubmed_authors><pubmed_authors>Karunasena E</pubmed_authors><pubmed_authors>Kee B</pubmed_authors><pubmed_authors>Eng C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phase II study of nab-paclitaxel in refractory small bowel adenocarcinoma and CpG island methylator phenotype (CIMP)-high colorectal cancer.</name><description>&lt;h4>Background&lt;/h4>Hypermethylation of promoter CpG islands [CpG island methylator phenotype (CIMP)] represents a unique pathway for the development of colorectal cancer (CRC), characterized by lack of chromosomal instability and a low rate of adenomatous polyposis coli (APC) mutations, which have both been correlated with taxane resistance. Similarly, small bowel adenocarcinoma (SBA), a rare tumor, also has a low rate of APC mutations. This phase II study evaluated taxane sensitivity in SBA and CIMP-high CRC.&lt;h4>Patients and methods&lt;/h4>The primary objective was Response Evaluation Criteria in Solid Tumors version 1.1 response rate. Eligibility included Eastern Cooperative Oncology Group performance status 0/1, refractory disease, and SBA or CIMP-high metastatic CRC. Nab-paclitaxel was in</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jan</publication><modification>2025-04-19T15:17:39.04Z</modification><creation>2019-03-26T22:26:58Z</creation></dates><accession>S-EPMC5834085</accession><cross_references><pubmed>29069279</pubmed><doi>10.1093/annonc/mdx688</doi></cross_references></HashMap>