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Cisplatin-docetaxel induction chemotherapy for patients with nasopharyngeal carcinoma in a non-endemic cohort
This is the report on our clinic's 15 years of experience (2004-2018) on nasopharyngeal carcinoma (NPC), treated with induction chemotherapy (IC) and subsequent concomitant chemoradiotherapy (CCRT), comprising population characteristics and treatment outcomes of 203 patients with non-metastatic...
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Published in: | Journal of chemotherapy (Florence) 2024-04, Vol.ahead-of-print (ahead-of-print), p.1-10 |
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container_title | Journal of chemotherapy (Florence) |
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creator | Özkaya Toraman, Kübra Meral, Rasim Karadeniz, Ahmet Nafiz Kaval, Gizem Başaran, Mert Ekenel, Meltem Altun, Musa |
description | This is the report on our clinic's 15 years of experience (2004-2018) on nasopharyngeal carcinoma (NPC), treated with induction chemotherapy (IC) and subsequent concomitant chemoradiotherapy (CCRT), comprising population characteristics and treatment outcomes of 203 patients with non-metastatic NPC. IC comprised docetaxel (75 mg/m
2
) and cisplatin (75 mg/m
2
) combination (TP). Concurrent cisplatin (P) was applied either weekly (40 mg/m
2
, 32 cases) or every-3-week (100 mg/m
2
, 171 cases). The median follow-up duration was 85 months (range, 5-204 months). Overall and distant failure rates were observed in 27.1% (n = 55) and 13.8% (n = 28) patients, respectively. The 5-year locoregional recurrence-free survival (LRRFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), and overall survival (OS) rates were 84.1%, 86.4%, 75%, and 78.7% respectively. The overall stage was an independent prognostic factor for the LRRFS, DMFS, DFS, and OS. The WHO histological type was a prognostic factor for the LRRFS, DFS, and OS. Age was a prognostic factor for the DMFS, DFS, and OS. Concurrent P schedule was independent prognostic only the LRRFS. |
doi_str_mv | 10.1080/1120009X.2023.2215090 |
format | article |
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2
) and cisplatin (75 mg/m
2
) combination (TP). Concurrent cisplatin (P) was applied either weekly (40 mg/m
2
, 32 cases) or every-3-week (100 mg/m
2
, 171 cases). The median follow-up duration was 85 months (range, 5-204 months). Overall and distant failure rates were observed in 27.1% (n = 55) and 13.8% (n = 28) patients, respectively. The 5-year locoregional recurrence-free survival (LRRFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), and overall survival (OS) rates were 84.1%, 86.4%, 75%, and 78.7% respectively. The overall stage was an independent prognostic factor for the LRRFS, DMFS, DFS, and OS. The WHO histological type was a prognostic factor for the LRRFS, DFS, and OS. Age was a prognostic factor for the DMFS, DFS, and OS. Concurrent P schedule was independent prognostic only the LRRFS.</description><identifier>ISSN: 1120-009X</identifier><identifier>EISSN: 1973-9478</identifier><identifier>DOI: 10.1080/1120009X.2023.2215090</identifier><identifier>PMID: 37211862</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Chemoradiotherapy ; Cisplatin ; concomitant chemoradiotherapy ; docetaxel ; Docetaxel - therapeutic use ; Humans ; Induction Chemotherapy ; Kaplan-Meier Estimate ; Nasopharyngeal carcinoma ; Nasopharyngeal Carcinoma - drug therapy ; Nasopharyngeal Carcinoma - etiology ; Nasopharyngeal Neoplasms - drug therapy ; Nasopharyngeal Neoplasms - pathology ; Retrospective Studies</subject><ispartof>Journal of chemotherapy (Florence), 2024-04, Vol.ahead-of-print (ahead-of-print), p.1-10</ispartof><rights>2023 Edizioni Scientifiche per l'Informazione su Farmaci e Terapia (Italian Society of Chemotherapy) 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c314t-64d9ec86c957ca866d16622f3a094bd799296ebece4c340d9d51b2faa818c7403</cites><orcidid>0000-0003-0943-7287 ; 0000-0003-1887-5561 ; 0000-0003-2518-5980 ; 0000-0002-6585-4598 ; 0000-0003-1006-1942 ; 0000-0001-5437-134X ; 0000-0002-4921-6975</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37211862$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Özkaya Toraman, Kübra</creatorcontrib><creatorcontrib>Meral, Rasim</creatorcontrib><creatorcontrib>Karadeniz, Ahmet Nafiz</creatorcontrib><creatorcontrib>Kaval, Gizem</creatorcontrib><creatorcontrib>Başaran, Mert</creatorcontrib><creatorcontrib>Ekenel, Meltem</creatorcontrib><creatorcontrib>Altun, Musa</creatorcontrib><title>Cisplatin-docetaxel induction chemotherapy for patients with nasopharyngeal carcinoma in a non-endemic cohort</title><title>Journal of chemotherapy (Florence)</title><addtitle>J Chemother</addtitle><description>This is the report on our clinic's 15 years of experience (2004-2018) on nasopharyngeal carcinoma (NPC), treated with induction chemotherapy (IC) and subsequent concomitant chemoradiotherapy (CCRT), comprising population characteristics and treatment outcomes of 203 patients with non-metastatic NPC. IC comprised docetaxel (75 mg/m
2
) and cisplatin (75 mg/m
2
) combination (TP). Concurrent cisplatin (P) was applied either weekly (40 mg/m
2
, 32 cases) or every-3-week (100 mg/m
2
, 171 cases). The median follow-up duration was 85 months (range, 5-204 months). Overall and distant failure rates were observed in 27.1% (n = 55) and 13.8% (n = 28) patients, respectively. The 5-year locoregional recurrence-free survival (LRRFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), and overall survival (OS) rates were 84.1%, 86.4%, 75%, and 78.7% respectively. The overall stage was an independent prognostic factor for the LRRFS, DMFS, DFS, and OS. The WHO histological type was a prognostic factor for the LRRFS, DFS, and OS. Age was a prognostic factor for the DMFS, DFS, and OS. Concurrent P schedule was independent prognostic only the LRRFS.</description><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Chemoradiotherapy</subject><subject>Cisplatin</subject><subject>concomitant chemoradiotherapy</subject><subject>docetaxel</subject><subject>Docetaxel - therapeutic use</subject><subject>Humans</subject><subject>Induction Chemotherapy</subject><subject>Kaplan-Meier Estimate</subject><subject>Nasopharyngeal carcinoma</subject><subject>Nasopharyngeal Carcinoma - drug therapy</subject><subject>Nasopharyngeal Carcinoma - etiology</subject><subject>Nasopharyngeal Neoplasms - drug therapy</subject><subject>Nasopharyngeal Neoplasms - pathology</subject><subject>Retrospective Studies</subject><issn>1120-009X</issn><issn>1973-9478</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kMtuFDEQRS1ERKKQTwjykk1P_Oj2YwcaEUCKxAak7CyPXU0bdduN7VGYv49HM2GZVdXi3Fuqg9AtJRtKFLmjlBFC9OOGEcY3jNGBaPIGXVEtead7qd62vTHdEbpEN6X8aTwRTHIt3qFLLhmlSrArtGxDWWdbQ-x8clDtP5hxiH7vakgRuwmWVCfIdj3gMWW8NhRiLfgp1AlHW9I62XyIv8HO2NnsQkyLbQ3Y4phiB9HDEhx2aUq5vkcXo50L3JznNfp1_-Xn9lv38OPr9-3nh85x2tdO9F6DU8LpQTqrhPBUCMZGbonud15qzbSAHTjoHe-J136gOzZaq6hysif8Gn089a45_d1DqWYJxcE82whpXwxTVEqpCBsaOpxQl1MpGUaz5rC0lwwl5ijbvMg2R9nmLLvlPpxP7HcL-P-pF7UN-HQCQmziFvuU8uxNtYc55THb6EIx_PUbz4HokDg</recordid><startdate>202404</startdate><enddate>202404</enddate><creator>Özkaya Toraman, Kübra</creator><creator>Meral, Rasim</creator><creator>Karadeniz, Ahmet Nafiz</creator><creator>Kaval, Gizem</creator><creator>Başaran, Mert</creator><creator>Ekenel, Meltem</creator><creator>Altun, Musa</creator><general>Taylor & Francis</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>7X8</scope><orcidid>https://orcid.org/0000-0003-0943-7287</orcidid><orcidid>https://orcid.org/0000-0003-1887-5561</orcidid><orcidid>https://orcid.org/0000-0003-2518-5980</orcidid><orcidid>https://orcid.org/0000-0002-6585-4598</orcidid><orcidid>https://orcid.org/0000-0003-1006-1942</orcidid><orcidid>https://orcid.org/0000-0001-5437-134X</orcidid><orcidid>https://orcid.org/0000-0002-4921-6975</orcidid></search><sort><creationdate>202404</creationdate><title>Cisplatin-docetaxel induction chemotherapy for patients with nasopharyngeal carcinoma in a non-endemic cohort</title><author>Özkaya Toraman, Kübra ; Meral, Rasim ; Karadeniz, Ahmet Nafiz ; Kaval, Gizem ; Başaran, Mert ; Ekenel, Meltem ; Altun, Musa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-64d9ec86c957ca866d16622f3a094bd799296ebece4c340d9d51b2faa818c7403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Chemoradiotherapy</topic><topic>Cisplatin</topic><topic>concomitant chemoradiotherapy</topic><topic>docetaxel</topic><topic>Docetaxel - therapeutic use</topic><topic>Humans</topic><topic>Induction Chemotherapy</topic><topic>Kaplan-Meier Estimate</topic><topic>Nasopharyngeal carcinoma</topic><topic>Nasopharyngeal Carcinoma - drug therapy</topic><topic>Nasopharyngeal Carcinoma - etiology</topic><topic>Nasopharyngeal Neoplasms - drug therapy</topic><topic>Nasopharyngeal Neoplasms - pathology</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Özkaya Toraman, Kübra</creatorcontrib><creatorcontrib>Meral, Rasim</creatorcontrib><creatorcontrib>Karadeniz, Ahmet Nafiz</creatorcontrib><creatorcontrib>Kaval, Gizem</creatorcontrib><creatorcontrib>Başaran, Mert</creatorcontrib><creatorcontrib>Ekenel, Meltem</creatorcontrib><creatorcontrib>Altun, Musa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of chemotherapy (Florence)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Özkaya Toraman, Kübra</au><au>Meral, Rasim</au><au>Karadeniz, Ahmet Nafiz</au><au>Kaval, Gizem</au><au>Başaran, Mert</au><au>Ekenel, Meltem</au><au>Altun, Musa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cisplatin-docetaxel induction chemotherapy for patients with nasopharyngeal carcinoma in a non-endemic cohort</atitle><jtitle>Journal of chemotherapy (Florence)</jtitle><addtitle>J Chemother</addtitle><date>2024-04</date><risdate>2024</risdate><volume>ahead-of-print</volume><issue>ahead-of-print</issue><spage>1</spage><epage>10</epage><pages>1-10</pages><issn>1120-009X</issn><eissn>1973-9478</eissn><abstract>This is the report on our clinic's 15 years of experience (2004-2018) on nasopharyngeal carcinoma (NPC), treated with induction chemotherapy (IC) and subsequent concomitant chemoradiotherapy (CCRT), comprising population characteristics and treatment outcomes of 203 patients with non-metastatic NPC. IC comprised docetaxel (75 mg/m
2
) and cisplatin (75 mg/m
2
) combination (TP). Concurrent cisplatin (P) was applied either weekly (40 mg/m
2
, 32 cases) or every-3-week (100 mg/m
2
, 171 cases). The median follow-up duration was 85 months (range, 5-204 months). Overall and distant failure rates were observed in 27.1% (n = 55) and 13.8% (n = 28) patients, respectively. The 5-year locoregional recurrence-free survival (LRRFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), and overall survival (OS) rates were 84.1%, 86.4%, 75%, and 78.7% respectively. The overall stage was an independent prognostic factor for the LRRFS, DMFS, DFS, and OS. The WHO histological type was a prognostic factor for the LRRFS, DFS, and OS. Age was a prognostic factor for the DMFS, DFS, and OS. Concurrent P schedule was independent prognostic only the LRRFS.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>37211862</pmid><doi>10.1080/1120009X.2023.2215090</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-0943-7287</orcidid><orcidid>https://orcid.org/0000-0003-1887-5561</orcidid><orcidid>https://orcid.org/0000-0003-2518-5980</orcidid><orcidid>https://orcid.org/0000-0002-6585-4598</orcidid><orcidid>https://orcid.org/0000-0003-1006-1942</orcidid><orcidid>https://orcid.org/0000-0001-5437-134X</orcidid><orcidid>https://orcid.org/0000-0002-4921-6975</orcidid></addata></record> |
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subjects | Antineoplastic Combined Chemotherapy Protocols - adverse effects Chemoradiotherapy Cisplatin concomitant chemoradiotherapy docetaxel Docetaxel - therapeutic use Humans Induction Chemotherapy Kaplan-Meier Estimate Nasopharyngeal carcinoma Nasopharyngeal Carcinoma - drug therapy Nasopharyngeal Carcinoma - etiology Nasopharyngeal Neoplasms - drug therapy Nasopharyngeal Neoplasms - pathology Retrospective Studies |
title | Cisplatin-docetaxel induction chemotherapy for patients with nasopharyngeal carcinoma in a non-endemic cohort |
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