Tumor Treating Fields Combine with Temozolomide for Newly Diagnosed Glioblastoma: A Retrospective Analysis of Chinese Patients in a Single Center
Introduction: TTFields plus Temozolomide (TTFields/TMZ) extended survival versus TMZ alone in newly diagnosed glioblastoma (GBM) patients in the EF-14 trial. We have reported a retrospective analysis of newly diagnosed Chinese GBM patients who received TTFields/TMZ treatment and TMZ treatment from A...
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Veröffentlicht in: | Journal of clinical medicine 2022-10, Vol.11 (19), p.5855 |
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description | Introduction: TTFields plus Temozolomide (TTFields/TMZ) extended survival versus TMZ alone in newly diagnosed glioblastoma (GBM) patients in the EF-14 trial. We have reported a retrospective analysis of newly diagnosed Chinese GBM patients who received TTFields/TMZ treatment and TMZ treatment from August 2018 to May 2021 in Huashan hospital in Shanghai. Methods: Overall survival (OS) and progression-free survival (PFS) curves were constructed using the Kaplan−Meier method. A Cox proportional hazards regression model, propensity score matched data, and inverse probability of treatment weighting (IPTW) based on propensity score were used to assess the effect of TTFields and account for confounding factors. Results: In the preliminary analysis, the median PFS in TTFields/TMZ group was 16 months (95% CI, 9.6−24.6) versus 11 months (95% CI, 9−12) in TMZ group (p < 0.05). Median overall survival was 21.8 months (95% CI, 17.4-NA) with TTFields/TMZ versus 15 months (HR = 0.43; 95% CI, 13−18) with TMZ alone. The multivariate analysis identified surgery type, STUPP scheme, IDH status, and TTFields use as favorable prognostic factors. After PSM adjustment, the variate among the groups was similar, except that the methylation rate of MGMT promoter remained high in the TMZ group (12 v 32 months; p = 0.011). Upon IPTW Survival analysis, TTFields was associated with a significantly lower risk of death (HR = 0.19 in OS; 95% CI, 0.09−0.41) and progression (HR = 0.35; 95% CI 0.14−0.9) compared with TMZ group. Conclusion: In the final analysis of our single-center Chinese patients with glioblastoma, adding TTFields to temozolomide chemotherapy resulted in statistically significant improvement in PFS and OS. |
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We have reported a retrospective analysis of newly diagnosed Chinese GBM patients who received TTFields/TMZ treatment and TMZ treatment from August 2018 to May 2021 in Huashan hospital in Shanghai. Methods: Overall survival (OS) and progression-free survival (PFS) curves were constructed using the Kaplan−Meier method. A Cox proportional hazards regression model, propensity score matched data, and inverse probability of treatment weighting (IPTW) based on propensity score were used to assess the effect of TTFields and account for confounding factors. Results: In the preliminary analysis, the median PFS in TTFields/TMZ group was 16 months (95% CI, 9.6−24.6) versus 11 months (95% CI, 9−12) in TMZ group (p < 0.05). Median overall survival was 21.8 months (95% CI, 17.4-NA) with TTFields/TMZ versus 15 months (HR = 0.43; 95% CI, 13−18) with TMZ alone. The multivariate analysis identified surgery type, STUPP scheme, IDH status, and TTFields use as favorable prognostic factors. After PSM adjustment, the variate among the groups was similar, except that the methylation rate of MGMT promoter remained high in the TMZ group (12 v 32 months; p = 0.011). Upon IPTW Survival analysis, TTFields was associated with a significantly lower risk of death (HR = 0.19 in OS; 95% CI, 0.09−0.41) and progression (HR = 0.35; 95% CI 0.14−0.9) compared with TMZ group. Conclusion: In the final analysis of our single-center Chinese patients with glioblastoma, adding TTFields to temozolomide chemotherapy resulted in statistically significant improvement in PFS and OS.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm11195855</identifier><identifier>PMID: 36233722</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Brain cancer ; Chemotherapy ; Clinical medicine ; Datasets ; Hospitals ; Medical prognosis ; Multivariate analysis ; Mutation ; Patients ; Statistical analysis ; Surgery</subject><ispartof>Journal of clinical medicine, 2022-10, Vol.11 (19), p.5855</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-e7eff8ff1d439f7518105fec51d8e10e59afb339056b1b09bca7614f310b820c3</citedby><cites>FETCH-LOGICAL-c409t-e7eff8ff1d439f7518105fec51d8e10e59afb339056b1b09bca7614f310b820c3</cites><orcidid>0000-0002-7890-3707 ; 0000-0003-4205-8852</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570572/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570572/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,27926,27927,53793,53795</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36233722$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Chunjui</creatorcontrib><creatorcontrib>Xu, Hao</creatorcontrib><creatorcontrib>Song, Kun</creatorcontrib><creatorcontrib>Zhang, Yi</creatorcontrib><creatorcontrib>Zhang, Junyan</creatorcontrib><creatorcontrib>Wang, Yang</creatorcontrib><creatorcontrib>Sheng, Xiaofang</creatorcontrib><creatorcontrib>Chen, Lingchao</creatorcontrib><creatorcontrib>Qin, Zhiyong</creatorcontrib><title>Tumor Treating Fields Combine with Temozolomide for Newly Diagnosed Glioblastoma: A Retrospective Analysis of Chinese Patients in a Single Center</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>Introduction: TTFields plus Temozolomide (TTFields/TMZ) extended survival versus TMZ alone in newly diagnosed glioblastoma (GBM) patients in the EF-14 trial. We have reported a retrospective analysis of newly diagnosed Chinese GBM patients who received TTFields/TMZ treatment and TMZ treatment from August 2018 to May 2021 in Huashan hospital in Shanghai. Methods: Overall survival (OS) and progression-free survival (PFS) curves were constructed using the Kaplan−Meier method. A Cox proportional hazards regression model, propensity score matched data, and inverse probability of treatment weighting (IPTW) based on propensity score were used to assess the effect of TTFields and account for confounding factors. Results: In the preliminary analysis, the median PFS in TTFields/TMZ group was 16 months (95% CI, 9.6−24.6) versus 11 months (95% CI, 9−12) in TMZ group (p < 0.05). Median overall survival was 21.8 months (95% CI, 17.4-NA) with TTFields/TMZ versus 15 months (HR = 0.43; 95% CI, 13−18) with TMZ alone. The multivariate analysis identified surgery type, STUPP scheme, IDH status, and TTFields use as favorable prognostic factors. After PSM adjustment, the variate among the groups was similar, except that the methylation rate of MGMT promoter remained high in the TMZ group (12 v 32 months; p = 0.011). Upon IPTW Survival analysis, TTFields was associated with a significantly lower risk of death (HR = 0.19 in OS; 95% CI, 0.09−0.41) and progression (HR = 0.35; 95% CI 0.14−0.9) compared with TMZ group. Conclusion: In the final analysis of our single-center Chinese patients with glioblastoma, adding TTFields to temozolomide chemotherapy resulted in statistically significant improvement in PFS and OS.</description><subject>Brain cancer</subject><subject>Chemotherapy</subject><subject>Clinical medicine</subject><subject>Datasets</subject><subject>Hospitals</subject><subject>Medical prognosis</subject><subject>Multivariate analysis</subject><subject>Mutation</subject><subject>Patients</subject><subject>Statistical analysis</subject><subject>Surgery</subject><issn>2077-0383</issn><issn>2077-0383</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkV9rFDEUxQdRbGn75LsEfBFk2_yZbBIfhGW0VSgquj6HTOZmN0tmsiYzLdtv0W_c1Naympcbcn-cc3NuVb0i-JQxhc82tieEKC45f1YdUizEDDPJnu_dD6qTnDe4HClrSsTL6oDNKWOC0sPqdjn1MaFlAjP6YYXOPYQuoyb2rR8AXftxjZbQx5sYYu87QK7QX-E67NBHb1ZDzNChi-BjG0weY2_eowX6AWOKeQt29FeAFoMJu-wzig4166KaAX0vbjCMGfkBGfSzOAdATXmBdFy9cCZkOHmsR9Wv80_L5vPs8tvFl2ZxObM1VuMMBDgnnSNdzZQTnEiCuQPLSSeBYODKuPY-Ij5vSYtVa42Yk9oxgltJsWVH1YcH3e3U9tDZYp5M0Nvke5N2Ohqv_-0Mfq1X8UorLjAXtAi8fRRI8fcEedS9zxZCMAPEKWsqKCdKKiwL-uY_dBOnVHL5Q9V0zlhNCvXugbIlvZzAPQ1DsL7_it7bdqFf78__xP7dLbsD60aneg</recordid><startdate>20221003</startdate><enddate>20221003</enddate><creator>Chen, Chunjui</creator><creator>Xu, Hao</creator><creator>Song, Kun</creator><creator>Zhang, Yi</creator><creator>Zhang, Junyan</creator><creator>Wang, Yang</creator><creator>Sheng, Xiaofang</creator><creator>Chen, Lingchao</creator><creator>Qin, Zhiyong</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</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>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7890-3707</orcidid><orcidid>https://orcid.org/0000-0003-4205-8852</orcidid></search><sort><creationdate>20221003</creationdate><title>Tumor Treating Fields Combine with Temozolomide for Newly Diagnosed Glioblastoma: A Retrospective Analysis of Chinese Patients in a Single Center</title><author>Chen, Chunjui ; Xu, Hao ; Song, Kun ; Zhang, Yi ; Zhang, Junyan ; Wang, Yang ; Sheng, Xiaofang ; Chen, Lingchao ; Qin, Zhiyong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-e7eff8ff1d439f7518105fec51d8e10e59afb339056b1b09bca7614f310b820c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Brain cancer</topic><topic>Chemotherapy</topic><topic>Clinical medicine</topic><topic>Datasets</topic><topic>Hospitals</topic><topic>Medical prognosis</topic><topic>Multivariate analysis</topic><topic>Mutation</topic><topic>Patients</topic><topic>Statistical analysis</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Chunjui</creatorcontrib><creatorcontrib>Xu, Hao</creatorcontrib><creatorcontrib>Song, Kun</creatorcontrib><creatorcontrib>Zhang, Yi</creatorcontrib><creatorcontrib>Zhang, Junyan</creatorcontrib><creatorcontrib>Wang, Yang</creatorcontrib><creatorcontrib>Sheng, Xiaofang</creatorcontrib><creatorcontrib>Chen, Lingchao</creatorcontrib><creatorcontrib>Qin, Zhiyong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Access via ProQuest (Open Access)</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><jtitle>Journal of clinical medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Chunjui</au><au>Xu, Hao</au><au>Song, Kun</au><au>Zhang, Yi</au><au>Zhang, Junyan</au><au>Wang, Yang</au><au>Sheng, Xiaofang</au><au>Chen, Lingchao</au><au>Qin, Zhiyong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor Treating Fields Combine with Temozolomide for Newly Diagnosed Glioblastoma: A Retrospective Analysis of Chinese Patients in a Single Center</atitle><jtitle>Journal of clinical medicine</jtitle><addtitle>J Clin Med</addtitle><date>2022-10-03</date><risdate>2022</risdate><volume>11</volume><issue>19</issue><spage>5855</spage><pages>5855-</pages><issn>2077-0383</issn><eissn>2077-0383</eissn><abstract>Introduction: TTFields plus Temozolomide (TTFields/TMZ) extended survival versus TMZ alone in newly diagnosed glioblastoma (GBM) patients in the EF-14 trial. We have reported a retrospective analysis of newly diagnosed Chinese GBM patients who received TTFields/TMZ treatment and TMZ treatment from August 2018 to May 2021 in Huashan hospital in Shanghai. Methods: Overall survival (OS) and progression-free survival (PFS) curves were constructed using the Kaplan−Meier method. A Cox proportional hazards regression model, propensity score matched data, and inverse probability of treatment weighting (IPTW) based on propensity score were used to assess the effect of TTFields and account for confounding factors. Results: In the preliminary analysis, the median PFS in TTFields/TMZ group was 16 months (95% CI, 9.6−24.6) versus 11 months (95% CI, 9−12) in TMZ group (p < 0.05). Median overall survival was 21.8 months (95% CI, 17.4-NA) with TTFields/TMZ versus 15 months (HR = 0.43; 95% CI, 13−18) with TMZ alone. The multivariate analysis identified surgery type, STUPP scheme, IDH status, and TTFields use as favorable prognostic factors. After PSM adjustment, the variate among the groups was similar, except that the methylation rate of MGMT promoter remained high in the TMZ group (12 v 32 months; p = 0.011). Upon IPTW Survival analysis, TTFields was associated with a significantly lower risk of death (HR = 0.19 in OS; 95% CI, 0.09−0.41) and progression (HR = 0.35; 95% CI 0.14−0.9) compared with TMZ group. Conclusion: In the final analysis of our single-center Chinese patients with glioblastoma, adding TTFields to temozolomide chemotherapy resulted in statistically significant improvement in PFS and OS.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36233722</pmid><doi>10.3390/jcm11195855</doi><orcidid>https://orcid.org/0000-0002-7890-3707</orcidid><orcidid>https://orcid.org/0000-0003-4205-8852</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Brain cancer Chemotherapy Clinical medicine Datasets Hospitals Medical prognosis Multivariate analysis Mutation Patients Statistical analysis Surgery |
title | Tumor Treating Fields Combine with Temozolomide for Newly Diagnosed Glioblastoma: A Retrospective Analysis of Chinese Patients in a Single Center |
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