Loading…

Distinctive grade based on Ki67 index and immune microenvironment of metastatic pancreatic neuroendocrine tumors responding to capecitabine plus temozolomide

Ki67 index changes during the treatment of metastatic pancreatic neuroendocrine tumor (PanNET) treatment. The study aimed to detect alterations of grade based on Ki67 index and immune microenvironment in PanNET responding to capecitabine/temozolomide (CapTem). Retrospective data of patients with Pan...

Full description

Saved in:
Bibliographic Details
Published in:BMC cancer 2024-11, Vol.24 (1), p.1362-10, Article 1362
Main Authors: Gao, Heli, Zhang, Wuhu, Li, Zheng, Liu, Wensheng, Liu, Mengqi, Zhuo, Qifeng, Shi, Yihua, Xu, Wenyan, Zhou, Chenjie, Qin, Yi, Xu, Jin, Chen, Jie, Yu, Xianjun, Xu, Xiaowu, Ji, Shunrong
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c510t-86f77a5d7af7954a221ec37221f858f95e0eab9a2285e7fdf40994665289bfeb3
container_end_page 10
container_issue 1
container_start_page 1362
container_title BMC cancer
container_volume 24
creator Gao, Heli
Zhang, Wuhu
Li, Zheng
Liu, Wensheng
Liu, Mengqi
Zhuo, Qifeng
Shi, Yihua
Xu, Wenyan
Zhou, Chenjie
Qin, Yi
Xu, Jin
Chen, Jie
Yu, Xianjun
Xu, Xiaowu
Ji, Shunrong
description Ki67 index changes during the treatment of metastatic pancreatic neuroendocrine tumor (PanNET) treatment. The study aimed to detect alterations of grade based on Ki67 index and immune microenvironment in PanNET responding to capecitabine/temozolomide (CapTem). Retrospective data of patients with PanNET were collected. In control group, 35 patients underwent surgery immediately after biopsy. In CapTem group, 38 patients received CapTem after biopsy and responded well to treatment (defined as either stable disease or partial response), and subsequently underwent surgery. All patients have pathological Ki67 index at biopsy and after surgery. CD163 + CD68 + CD206 + M2 macrophages, CD68 + CD86 + CD80 + M1 macrophages, CD11b + CD33 + myeloid-derived suppressor cells, and CD4 + CD25 + regulatory T cells were stained using multiplex immunofluorescence. In control group, the paired grade based on Ki67 index directly after surgery showed no upgrade or downgrade compared to biopsy. In patients who responded well to CapTem, the grade based on Ki67 index before and after CapTem was altered. Thirteen patients had upgraded Ki67 index and 11 patients had downgraded. The proportion of stable disease was higher in the upgraded group compared to downgraded group (p = 0.0155). And upgraded group had a significantly shorter mPFS than patients in the downgrade group (8.5 months vs. 20 months, HR 4.834, 95% CI 1.414 to 16.53, p = 0.012). M1 macrophages was significantly lower in the downgraded group than in the Ki67 upgraded group (p 
doi_str_mv 10.1186/s12885-024-13117-5
format article
fullrecord <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_07be9ba86f7a4a8dbe7f208d56ee4cc4</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A815234573</galeid><doaj_id>oai_doaj_org_article_07be9ba86f7a4a8dbe7f208d56ee4cc4</doaj_id><sourcerecordid>A815234573</sourcerecordid><originalsourceid>FETCH-LOGICAL-c510t-86f77a5d7af7954a221ec37221f858f95e0eab9a2285e7fdf40994665289bfeb3</originalsourceid><addsrcrecordid>eNptkl2L1DAUhoso7rr6B7yQgCB60bVpmya9kmX9GlwQ_LgOp8npTIY2mU3SYfW_-F9NZ9Z1RiQXCSfPeUPe82bZU1qcUyqa14GWQrC8KOucVpTynN3LTmnNaV7WBb9_cD7JHoWwLgrKRSEeZidVyyhljJ1mv96aEI1V0WyRLD1oJB0E1MRZ8sk0nBir8YaA1cSM42SRjEZ5h3ZrvLMj2khcT0aMECJEo8gGrPK4O1qcZlI75U1qjNPofCAew8ZZbeySREcUbFCZCN1MbIYpkIij--kGNxqNj7MHPQwBn9zuZ9n39---XX7Mrz5_WFxeXOWK0SLmouk5B6Y59LxlNZQlRVXxtPWCib5lWCB0baoLhrzXfV20bd00rBRt12NXnWWLva52sJYbb0bwP6QDI3cF55cSfPrSgLLgHbYdzE9CDUJ3SbAshGYNYq1UnbTe7LU2UzeiVskiD8OR6PGNNSu5dFuZJlKXlWiTwstbBe-uJwxRjiYoHAaw6KYgqzT3qmRlyxL6_B907SZvk1cz1dQpAaz9Sy0h_cDY3qWH1SwqLwRlZVUzXiXq_D9UWhrTzJ3F3qT6UcOro4bERLyJS5hCkIuvX47ZFwfsCmGIq-CGKRpnwzFY7sGUshA89nfO0ULOsZf72MsUe7mLvZxteHbo-V3Ln5xXvwHT-v9L</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3126414759</pqid></control><display><type>article</type><title>Distinctive grade based on Ki67 index and immune microenvironment of metastatic pancreatic neuroendocrine tumors responding to capecitabine plus temozolomide</title><source>Open Access: PubMed Central</source><source>Publicly Available Content (ProQuest)</source><creator>Gao, Heli ; Zhang, Wuhu ; Li, Zheng ; Liu, Wensheng ; Liu, Mengqi ; Zhuo, Qifeng ; Shi, Yihua ; Xu, Wenyan ; Zhou, Chenjie ; Qin, Yi ; Xu, Jin ; Chen, Jie ; Yu, Xianjun ; Xu, Xiaowu ; Ji, Shunrong</creator><creatorcontrib>Gao, Heli ; Zhang, Wuhu ; Li, Zheng ; Liu, Wensheng ; Liu, Mengqi ; Zhuo, Qifeng ; Shi, Yihua ; Xu, Wenyan ; Zhou, Chenjie ; Qin, Yi ; Xu, Jin ; Chen, Jie ; Yu, Xianjun ; Xu, Xiaowu ; Ji, Shunrong</creatorcontrib><description>Ki67 index changes during the treatment of metastatic pancreatic neuroendocrine tumor (PanNET) treatment. The study aimed to detect alterations of grade based on Ki67 index and immune microenvironment in PanNET responding to capecitabine/temozolomide (CapTem). Retrospective data of patients with PanNET were collected. In control group, 35 patients underwent surgery immediately after biopsy. In CapTem group, 38 patients received CapTem after biopsy and responded well to treatment (defined as either stable disease or partial response), and subsequently underwent surgery. All patients have pathological Ki67 index at biopsy and after surgery. CD163 + CD68 + CD206 + M2 macrophages, CD68 + CD86 + CD80 + M1 macrophages, CD11b + CD33 + myeloid-derived suppressor cells, and CD4 + CD25 + regulatory T cells were stained using multiplex immunofluorescence. In control group, the paired grade based on Ki67 index directly after surgery showed no upgrade or downgrade compared to biopsy. In patients who responded well to CapTem, the grade based on Ki67 index before and after CapTem was altered. Thirteen patients had upgraded Ki67 index and 11 patients had downgraded. The proportion of stable disease was higher in the upgraded group compared to downgraded group (p = 0.0155). And upgraded group had a significantly shorter mPFS than patients in the downgrade group (8.5 months vs. 20 months, HR 4.834, 95% CI 1.414 to 16.53, p = 0.012). M1 macrophages was significantly lower in the downgraded group than in the Ki67 upgraded group (p &lt; 0.001). Grade based on Ki67 index and immune environment change in PanNET patients responding well to CapTem. Patients with downgraded had longer mPFS compared to those with upgraded. It is necessary to reassess the Ki67 index after CapTem treatment, even in patients responding well to CapTem.</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-024-13117-5</identifier><identifier>PMID: 39511555</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adult ; Aged ; Antimitotic agents ; Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biopsy ; Capecitabine - administration &amp; dosage ; Capecitabine - therapeutic use ; Capecitabine/temozolomide ; Care and treatment ; CD11b antigen ; CD163 antigen ; CD25 antigen ; CD4 antigen ; CD80 antigen ; CD86 antigen ; Chemotherapy ; Development and progression ; Diagnosis ; Dosage and administration ; Female ; Humans ; Immunofluorescence ; Immunoregulation ; Ki-67 Antigen - metabolism ; Ki67 index ; Liver ; Lymphocytes T ; Macrophages ; Male ; Medical prognosis ; Metastases ; Metastasis ; Microenvironments ; Middle Aged ; Neoplasm Grading ; Neuroendocrine tumors ; Neuroendocrine Tumors - drug therapy ; Neuroendocrine Tumors - immunology ; Neuroendocrine Tumors - pathology ; Pancreas ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - immunology ; Pancreatic Neoplasms - pathology ; Pancreatic neuroendocrine tumor ; Pancreatic tumors ; Patients ; Retrospective Studies ; Suppressor cells ; Surgery ; Temozolomide ; Temozolomide - administration &amp; dosage ; Temozolomide - pharmacology ; Temozolomide - therapeutic use ; Testing ; Treatment Outcome ; Tumor antigens ; Tumor microenvironment ; Tumor Microenvironment - drug effects ; Tumor Microenvironment - immunology ; Upgrading ; Variance analysis</subject><ispartof>BMC cancer, 2024-11, Vol.24 (1), p.1362-10, Article 1362</ispartof><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2024 BioMed Central Ltd.</rights><rights>2024. This work is licensed under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2024 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c510t-86f77a5d7af7954a221ec37221f858f95e0eab9a2285e7fdf40994665289bfeb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11542389/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3126414759?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39511555$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gao, Heli</creatorcontrib><creatorcontrib>Zhang, Wuhu</creatorcontrib><creatorcontrib>Li, Zheng</creatorcontrib><creatorcontrib>Liu, Wensheng</creatorcontrib><creatorcontrib>Liu, Mengqi</creatorcontrib><creatorcontrib>Zhuo, Qifeng</creatorcontrib><creatorcontrib>Shi, Yihua</creatorcontrib><creatorcontrib>Xu, Wenyan</creatorcontrib><creatorcontrib>Zhou, Chenjie</creatorcontrib><creatorcontrib>Qin, Yi</creatorcontrib><creatorcontrib>Xu, Jin</creatorcontrib><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Yu, Xianjun</creatorcontrib><creatorcontrib>Xu, Xiaowu</creatorcontrib><creatorcontrib>Ji, Shunrong</creatorcontrib><title>Distinctive grade based on Ki67 index and immune microenvironment of metastatic pancreatic neuroendocrine tumors responding to capecitabine plus temozolomide</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>Ki67 index changes during the treatment of metastatic pancreatic neuroendocrine tumor (PanNET) treatment. The study aimed to detect alterations of grade based on Ki67 index and immune microenvironment in PanNET responding to capecitabine/temozolomide (CapTem). Retrospective data of patients with PanNET were collected. In control group, 35 patients underwent surgery immediately after biopsy. In CapTem group, 38 patients received CapTem after biopsy and responded well to treatment (defined as either stable disease or partial response), and subsequently underwent surgery. All patients have pathological Ki67 index at biopsy and after surgery. CD163 + CD68 + CD206 + M2 macrophages, CD68 + CD86 + CD80 + M1 macrophages, CD11b + CD33 + myeloid-derived suppressor cells, and CD4 + CD25 + regulatory T cells were stained using multiplex immunofluorescence. In control group, the paired grade based on Ki67 index directly after surgery showed no upgrade or downgrade compared to biopsy. In patients who responded well to CapTem, the grade based on Ki67 index before and after CapTem was altered. Thirteen patients had upgraded Ki67 index and 11 patients had downgraded. The proportion of stable disease was higher in the upgraded group compared to downgraded group (p = 0.0155). And upgraded group had a significantly shorter mPFS than patients in the downgrade group (8.5 months vs. 20 months, HR 4.834, 95% CI 1.414 to 16.53, p = 0.012). M1 macrophages was significantly lower in the downgraded group than in the Ki67 upgraded group (p &lt; 0.001). Grade based on Ki67 index and immune environment change in PanNET patients responding well to CapTem. Patients with downgraded had longer mPFS compared to those with upgraded. It is necessary to reassess the Ki67 index after CapTem treatment, even in patients responding well to CapTem.</description><subject>Adult</subject><subject>Aged</subject><subject>Antimitotic agents</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biopsy</subject><subject>Capecitabine - administration &amp; dosage</subject><subject>Capecitabine - therapeutic use</subject><subject>Capecitabine/temozolomide</subject><subject>Care and treatment</subject><subject>CD11b antigen</subject><subject>CD163 antigen</subject><subject>CD25 antigen</subject><subject>CD4 antigen</subject><subject>CD80 antigen</subject><subject>CD86 antigen</subject><subject>Chemotherapy</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Dosage and administration</subject><subject>Female</subject><subject>Humans</subject><subject>Immunofluorescence</subject><subject>Immunoregulation</subject><subject>Ki-67 Antigen - metabolism</subject><subject>Ki67 index</subject><subject>Liver</subject><subject>Lymphocytes T</subject><subject>Macrophages</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Microenvironments</subject><subject>Middle Aged</subject><subject>Neoplasm Grading</subject><subject>Neuroendocrine tumors</subject><subject>Neuroendocrine Tumors - drug therapy</subject><subject>Neuroendocrine Tumors - immunology</subject><subject>Neuroendocrine Tumors - pathology</subject><subject>Pancreas</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - immunology</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Pancreatic neuroendocrine tumor</subject><subject>Pancreatic tumors</subject><subject>Patients</subject><subject>Retrospective Studies</subject><subject>Suppressor cells</subject><subject>Surgery</subject><subject>Temozolomide</subject><subject>Temozolomide - administration &amp; dosage</subject><subject>Temozolomide - pharmacology</subject><subject>Temozolomide - therapeutic use</subject><subject>Testing</subject><subject>Treatment Outcome</subject><subject>Tumor antigens</subject><subject>Tumor microenvironment</subject><subject>Tumor Microenvironment - drug effects</subject><subject>Tumor Microenvironment - immunology</subject><subject>Upgrading</subject><subject>Variance analysis</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl2L1DAUhoso7rr6B7yQgCB60bVpmya9kmX9GlwQ_LgOp8npTIY2mU3SYfW_-F9NZ9Z1RiQXCSfPeUPe82bZU1qcUyqa14GWQrC8KOucVpTynN3LTmnNaV7WBb9_cD7JHoWwLgrKRSEeZidVyyhljJ1mv96aEI1V0WyRLD1oJB0E1MRZ8sk0nBir8YaA1cSM42SRjEZ5h3ZrvLMj2khcT0aMECJEo8gGrPK4O1qcZlI75U1qjNPofCAew8ZZbeySREcUbFCZCN1MbIYpkIij--kGNxqNj7MHPQwBn9zuZ9n39---XX7Mrz5_WFxeXOWK0SLmouk5B6Y59LxlNZQlRVXxtPWCib5lWCB0baoLhrzXfV20bd00rBRt12NXnWWLva52sJYbb0bwP6QDI3cF55cSfPrSgLLgHbYdzE9CDUJ3SbAshGYNYq1UnbTe7LU2UzeiVskiD8OR6PGNNSu5dFuZJlKXlWiTwstbBe-uJwxRjiYoHAaw6KYgqzT3qmRlyxL6_B907SZvk1cz1dQpAaz9Sy0h_cDY3qWH1SwqLwRlZVUzXiXq_D9UWhrTzJ3F3qT6UcOro4bERLyJS5hCkIuvX47ZFwfsCmGIq-CGKRpnwzFY7sGUshA89nfO0ULOsZf72MsUe7mLvZxteHbo-V3Ln5xXvwHT-v9L</recordid><startdate>20241107</startdate><enddate>20241107</enddate><creator>Gao, Heli</creator><creator>Zhang, Wuhu</creator><creator>Li, Zheng</creator><creator>Liu, Wensheng</creator><creator>Liu, Mengqi</creator><creator>Zhuo, Qifeng</creator><creator>Shi, Yihua</creator><creator>Xu, Wenyan</creator><creator>Zhou, Chenjie</creator><creator>Qin, Yi</creator><creator>Xu, Jin</creator><creator>Chen, Jie</creator><creator>Yu, Xianjun</creator><creator>Xu, Xiaowu</creator><creator>Ji, Shunrong</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20241107</creationdate><title>Distinctive grade based on Ki67 index and immune microenvironment of metastatic pancreatic neuroendocrine tumors responding to capecitabine plus temozolomide</title><author>Gao, Heli ; Zhang, Wuhu ; Li, Zheng ; Liu, Wensheng ; Liu, Mengqi ; Zhuo, Qifeng ; Shi, Yihua ; Xu, Wenyan ; Zhou, Chenjie ; Qin, Yi ; Xu, Jin ; Chen, Jie ; Yu, Xianjun ; Xu, Xiaowu ; Ji, Shunrong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-86f77a5d7af7954a221ec37221f858f95e0eab9a2285e7fdf40994665289bfeb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antimitotic agents</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biopsy</topic><topic>Capecitabine - administration &amp; dosage</topic><topic>Capecitabine - therapeutic use</topic><topic>Capecitabine/temozolomide</topic><topic>Care and treatment</topic><topic>CD11b antigen</topic><topic>CD163 antigen</topic><topic>CD25 antigen</topic><topic>CD4 antigen</topic><topic>CD80 antigen</topic><topic>CD86 antigen</topic><topic>Chemotherapy</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Dosage and administration</topic><topic>Female</topic><topic>Humans</topic><topic>Immunofluorescence</topic><topic>Immunoregulation</topic><topic>Ki-67 Antigen - metabolism</topic><topic>Ki67 index</topic><topic>Liver</topic><topic>Lymphocytes T</topic><topic>Macrophages</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Microenvironments</topic><topic>Middle Aged</topic><topic>Neoplasm Grading</topic><topic>Neuroendocrine tumors</topic><topic>Neuroendocrine Tumors - drug therapy</topic><topic>Neuroendocrine Tumors - immunology</topic><topic>Neuroendocrine Tumors - pathology</topic><topic>Pancreas</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Pancreatic Neoplasms - immunology</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Pancreatic neuroendocrine tumor</topic><topic>Pancreatic tumors</topic><topic>Patients</topic><topic>Retrospective Studies</topic><topic>Suppressor cells</topic><topic>Surgery</topic><topic>Temozolomide</topic><topic>Temozolomide - administration &amp; dosage</topic><topic>Temozolomide - pharmacology</topic><topic>Temozolomide - therapeutic use</topic><topic>Testing</topic><topic>Treatment Outcome</topic><topic>Tumor antigens</topic><topic>Tumor microenvironment</topic><topic>Tumor Microenvironment - drug effects</topic><topic>Tumor Microenvironment - immunology</topic><topic>Upgrading</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gao, Heli</creatorcontrib><creatorcontrib>Zhang, Wuhu</creatorcontrib><creatorcontrib>Li, Zheng</creatorcontrib><creatorcontrib>Liu, Wensheng</creatorcontrib><creatorcontrib>Liu, Mengqi</creatorcontrib><creatorcontrib>Zhuo, Qifeng</creatorcontrib><creatorcontrib>Shi, Yihua</creatorcontrib><creatorcontrib>Xu, Wenyan</creatorcontrib><creatorcontrib>Zhou, Chenjie</creatorcontrib><creatorcontrib>Qin, Yi</creatorcontrib><creatorcontrib>Xu, Jin</creatorcontrib><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Yu, Xianjun</creatorcontrib><creatorcontrib>Xu, Xiaowu</creatorcontrib><creatorcontrib>Ji, Shunrong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health &amp; Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gao, Heli</au><au>Zhang, Wuhu</au><au>Li, Zheng</au><au>Liu, Wensheng</au><au>Liu, Mengqi</au><au>Zhuo, Qifeng</au><au>Shi, Yihua</au><au>Xu, Wenyan</au><au>Zhou, Chenjie</au><au>Qin, Yi</au><au>Xu, Jin</au><au>Chen, Jie</au><au>Yu, Xianjun</au><au>Xu, Xiaowu</au><au>Ji, Shunrong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinctive grade based on Ki67 index and immune microenvironment of metastatic pancreatic neuroendocrine tumors responding to capecitabine plus temozolomide</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2024-11-07</date><risdate>2024</risdate><volume>24</volume><issue>1</issue><spage>1362</spage><epage>10</epage><pages>1362-10</pages><artnum>1362</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>Ki67 index changes during the treatment of metastatic pancreatic neuroendocrine tumor (PanNET) treatment. The study aimed to detect alterations of grade based on Ki67 index and immune microenvironment in PanNET responding to capecitabine/temozolomide (CapTem). Retrospective data of patients with PanNET were collected. In control group, 35 patients underwent surgery immediately after biopsy. In CapTem group, 38 patients received CapTem after biopsy and responded well to treatment (defined as either stable disease or partial response), and subsequently underwent surgery. All patients have pathological Ki67 index at biopsy and after surgery. CD163 + CD68 + CD206 + M2 macrophages, CD68 + CD86 + CD80 + M1 macrophages, CD11b + CD33 + myeloid-derived suppressor cells, and CD4 + CD25 + regulatory T cells were stained using multiplex immunofluorescence. In control group, the paired grade based on Ki67 index directly after surgery showed no upgrade or downgrade compared to biopsy. In patients who responded well to CapTem, the grade based on Ki67 index before and after CapTem was altered. Thirteen patients had upgraded Ki67 index and 11 patients had downgraded. The proportion of stable disease was higher in the upgraded group compared to downgraded group (p = 0.0155). And upgraded group had a significantly shorter mPFS than patients in the downgrade group (8.5 months vs. 20 months, HR 4.834, 95% CI 1.414 to 16.53, p = 0.012). M1 macrophages was significantly lower in the downgraded group than in the Ki67 upgraded group (p &lt; 0.001). Grade based on Ki67 index and immune environment change in PanNET patients responding well to CapTem. Patients with downgraded had longer mPFS compared to those with upgraded. It is necessary to reassess the Ki67 index after CapTem treatment, even in patients responding well to CapTem.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>39511555</pmid><doi>10.1186/s12885-024-13117-5</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1471-2407
ispartof BMC cancer, 2024-11, Vol.24 (1), p.1362-10, Article 1362
issn 1471-2407
1471-2407
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_07be9ba86f7a4a8dbe7f208d56ee4cc4
source Open Access: PubMed Central; Publicly Available Content (ProQuest)
subjects Adult
Aged
Antimitotic agents
Antineoplastic agents
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biopsy
Capecitabine - administration & dosage
Capecitabine - therapeutic use
Capecitabine/temozolomide
Care and treatment
CD11b antigen
CD163 antigen
CD25 antigen
CD4 antigen
CD80 antigen
CD86 antigen
Chemotherapy
Development and progression
Diagnosis
Dosage and administration
Female
Humans
Immunofluorescence
Immunoregulation
Ki-67 Antigen - metabolism
Ki67 index
Liver
Lymphocytes T
Macrophages
Male
Medical prognosis
Metastases
Metastasis
Microenvironments
Middle Aged
Neoplasm Grading
Neuroendocrine tumors
Neuroendocrine Tumors - drug therapy
Neuroendocrine Tumors - immunology
Neuroendocrine Tumors - pathology
Pancreas
Pancreatic Neoplasms - drug therapy
Pancreatic Neoplasms - immunology
Pancreatic Neoplasms - pathology
Pancreatic neuroendocrine tumor
Pancreatic tumors
Patients
Retrospective Studies
Suppressor cells
Surgery
Temozolomide
Temozolomide - administration & dosage
Temozolomide - pharmacology
Temozolomide - therapeutic use
Testing
Treatment Outcome
Tumor antigens
Tumor microenvironment
Tumor Microenvironment - drug effects
Tumor Microenvironment - immunology
Upgrading
Variance analysis
title Distinctive grade based on Ki67 index and immune microenvironment of metastatic pancreatic neuroendocrine tumors responding to capecitabine plus temozolomide
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T17%3A03%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Distinctive%20grade%20based%20on%20Ki67%20index%20and%20immune%20microenvironment%20of%20metastatic%20pancreatic%20neuroendocrine%20tumors%20responding%20to%20capecitabine%20plus%20temozolomide&rft.jtitle=BMC%20cancer&rft.au=Gao,%20Heli&rft.date=2024-11-07&rft.volume=24&rft.issue=1&rft.spage=1362&rft.epage=10&rft.pages=1362-10&rft.artnum=1362&rft.issn=1471-2407&rft.eissn=1471-2407&rft_id=info:doi/10.1186/s12885-024-13117-5&rft_dat=%3Cgale_doaj_%3EA815234573%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c510t-86f77a5d7af7954a221ec37221f858f95e0eab9a2285e7fdf40994665289bfeb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3126414759&rft_id=info:pmid/39511555&rft_galeid=A815234573&rfr_iscdi=true