DNA mismatch repair deficiency and outcomes of patients with locally advanced gastric cancer treated with preoperative docetaxel, oxaliplatin, and S-1 plus surgery and postoperative S-1 or surgery plus postoperative S-1: a sub-analysis of the phase 3 PRODIGY trial
Background The benefit of adjuvant chemotherapy for locally advanced gastric cancer (LAGC) patients with DNA mismatch repair (MMR) deficiency (D-MMR) is controversial due to concerns about its potential detrimental effect. The PRODIGY trial showed the survival benefit of adding preoperative docetaxe...
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Veröffentlicht in: | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2024, Vol.27 (1), p.110-117 |
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container_title | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association |
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creator | Hyung, Jaewon Cho, Hyungwoo Kim, Hyung-Don Park, Young Soo Moon, Meesun Ryu, Min-Hee Kang, Yoon-Koo |
description | Background
The benefit of adjuvant chemotherapy for locally advanced gastric cancer (LAGC) patients with DNA mismatch repair (MMR) deficiency (D-MMR) is controversial due to concerns about its potential detrimental effect. The PRODIGY trial showed the survival benefit of adding preoperative docetaxel, oxaliplatin, and S-1 (DOS) to surgery plus postoperative S-1 for LAGC patients. In this sub-analysis, we evaluated the benefit of preoperative DOS according to MMR status.
Methods
Among patients enrolled in the PRODIGY trial treated with either preoperative DOS followed by surgery and postoperative S-1 (CSC arm), or surgery and postoperative S-1 (SC arm) at Asan Medical Center (
n
= 249), those in the full analysis set with available tissue to assess MMR status were included in the present analysis.
Results
A total of 231 patients (CSC arm,
n
= 108; SC arm,
n
= 123) were included (median age, 58 years [range, 27–75]), and 21 patients (CSC arm,
n
= 8 [7.4%]; SC arm,
n
= 13 [10.6%]) had D-MMR tumors. Progression-free survival and overall survival tended to be superior in the CSC arm than in the SC arm among D-MMR patients (HR 0.48 [95% CI 0.09–2.50]; log-rank
P
= 0.37 and HR 0.55 [95% CI 0.11–2.86]; log-rank
P
= 0.46, respectively), as well as among proficient MMR (P-MMR) patients (HR 0.68 [95% CI 0.46–1.03]; log-rank
P
= 0.07 and HR 0.75 [95% CI 0.49–1.14]; log-rank
P
= 0.17, respectively).
Conclusion
Preoperative DOS followed by surgery and postoperative S-1 may be considered a treatment option for LAGC patients regardless of MMR status. |
doi_str_mv | 10.1007/s10120-023-01434-w |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2883581445</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2909154610</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-8f9dc9c0792508ec220f3030141c4d27a91ad64326620dfa0d8c69b28e6b88463</originalsourceid><addsrcrecordid>eNp9kk1v1DAQhgMCsaXwBzggS1w4NOCPxHG4VW0plSqK-DhwimbtSTeVNw620-3--3qTfkggcbI988w749GbZW8Y_cAorT4GRhmnOeUip6wQRb55mu2li8yFoOWz-zuv2SJ7GcIVpaysmXyRLUSlVC0k3XuyOP56SNZdWEPUK-JxgM4Tg22nO-z1lkBviBujdmsMxLVkgJgSMZBNF1fEOg3WJspcQ6_RkEsI0Xea6N3Tk-gRYgpP8ODRDeiTwDUS4zRGuEF7QNwN2G6wKd4fTP1-5IwMdgwkjP4S_TzE4EJ8LN8hzj8AE_0P8YlAIpY59GC3oZvmjyskwwoCEkG-fb84Pjv9nabswL7KnrdgA76-O_ezX59Pfh59yc8vTs-ODs9zLaoy5qqtja41rWpeUoWac9oKKtL-mS4Mr6BmYGQhuJScmhaoUVrWS65QLpUqpNjP3s-6g3d_RgyxSdvXaC306MbQcKVEqVhRlAl99xd65UafPpOomtasLCSjieIzpb0LwWPbDL5bg982jDY7nzSzT5rkk2bySbNJRW_vpMflGs1Dyb0xEiBmIKRUn5b82Ps_srcJiMvo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2909154610</pqid></control><display><type>article</type><title>DNA mismatch repair deficiency and outcomes of patients with locally advanced gastric cancer treated with preoperative docetaxel, oxaliplatin, and S-1 plus surgery and postoperative S-1 or surgery plus postoperative S-1: a sub-analysis of the phase 3 PRODIGY trial</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>SpringerLink Journals - AutoHoldings</source><creator>Hyung, Jaewon ; Cho, Hyungwoo ; Kim, Hyung-Don ; Park, Young Soo ; Moon, Meesun ; Ryu, Min-Hee ; Kang, Yoon-Koo</creator><creatorcontrib>Hyung, Jaewon ; Cho, Hyungwoo ; Kim, Hyung-Don ; Park, Young Soo ; Moon, Meesun ; Ryu, Min-Hee ; Kang, Yoon-Koo</creatorcontrib><description>Background
The benefit of adjuvant chemotherapy for locally advanced gastric cancer (LAGC) patients with DNA mismatch repair (MMR) deficiency (D-MMR) is controversial due to concerns about its potential detrimental effect. The PRODIGY trial showed the survival benefit of adding preoperative docetaxel, oxaliplatin, and S-1 (DOS) to surgery plus postoperative S-1 for LAGC patients. In this sub-analysis, we evaluated the benefit of preoperative DOS according to MMR status.
Methods
Among patients enrolled in the PRODIGY trial treated with either preoperative DOS followed by surgery and postoperative S-1 (CSC arm), or surgery and postoperative S-1 (SC arm) at Asan Medical Center (
n
= 249), those in the full analysis set with available tissue to assess MMR status were included in the present analysis.
Results
A total of 231 patients (CSC arm,
n
= 108; SC arm,
n
= 123) were included (median age, 58 years [range, 27–75]), and 21 patients (CSC arm,
n
= 8 [7.4%]; SC arm,
n
= 13 [10.6%]) had D-MMR tumors. Progression-free survival and overall survival tended to be superior in the CSC arm than in the SC arm among D-MMR patients (HR 0.48 [95% CI 0.09–2.50]; log-rank
P
= 0.37 and HR 0.55 [95% CI 0.11–2.86]; log-rank
P
= 0.46, respectively), as well as among proficient MMR (P-MMR) patients (HR 0.68 [95% CI 0.46–1.03]; log-rank
P
= 0.07 and HR 0.75 [95% CI 0.49–1.14]; log-rank
P
= 0.17, respectively).
Conclusion
Preoperative DOS followed by surgery and postoperative S-1 may be considered a treatment option for LAGC patients regardless of MMR status.</description><identifier>ISSN: 1436-3291</identifier><identifier>EISSN: 1436-3305</identifier><identifier>DOI: 10.1007/s10120-023-01434-w</identifier><identifier>PMID: 37889360</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Abdominal Surgery ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Cancer Research ; Chemotherapy ; Chemotherapy, Adjuvant ; DNA - therapeutic use ; DNA Mismatch Repair ; DNA repair ; Docetaxel ; Drug therapy ; Fluorouracil ; Gastric cancer ; Gastroenterology ; Humans ; Medicine ; Medicine & Public Health ; Middle Aged ; Mismatch repair ; Oncology ; Original Article ; Oxaliplatin ; Patients ; Postoperative period ; Prodigies ; Stomach Neoplasms - drug therapy ; Stomach Neoplasms - genetics ; Stomach Neoplasms - surgery ; Surgery ; Surgical Oncology ; Surgical techniques ; Survival ; Yeast</subject><ispartof>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2024, Vol.27 (1), p.110-117</ispartof><rights>The Author(s) under exclusive licence to The International Gastric Cancer Association and The Japanese Gastric Cancer Association 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s) under exclusive licence to The International Gastric Cancer Association and The Japanese Gastric Cancer Association.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-8f9dc9c0792508ec220f3030141c4d27a91ad64326620dfa0d8c69b28e6b88463</citedby><cites>FETCH-LOGICAL-c375t-8f9dc9c0792508ec220f3030141c4d27a91ad64326620dfa0d8c69b28e6b88463</cites><orcidid>0000-0003-0783-6583</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10120-023-01434-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10120-023-01434-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37889360$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hyung, Jaewon</creatorcontrib><creatorcontrib>Cho, Hyungwoo</creatorcontrib><creatorcontrib>Kim, Hyung-Don</creatorcontrib><creatorcontrib>Park, Young Soo</creatorcontrib><creatorcontrib>Moon, Meesun</creatorcontrib><creatorcontrib>Ryu, Min-Hee</creatorcontrib><creatorcontrib>Kang, Yoon-Koo</creatorcontrib><title>DNA mismatch repair deficiency and outcomes of patients with locally advanced gastric cancer treated with preoperative docetaxel, oxaliplatin, and S-1 plus surgery and postoperative S-1 or surgery plus postoperative S-1: a sub-analysis of the phase 3 PRODIGY trial</title><title>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</title><addtitle>Gastric Cancer</addtitle><addtitle>Gastric Cancer</addtitle><description>Background
The benefit of adjuvant chemotherapy for locally advanced gastric cancer (LAGC) patients with DNA mismatch repair (MMR) deficiency (D-MMR) is controversial due to concerns about its potential detrimental effect. The PRODIGY trial showed the survival benefit of adding preoperative docetaxel, oxaliplatin, and S-1 (DOS) to surgery plus postoperative S-1 for LAGC patients. In this sub-analysis, we evaluated the benefit of preoperative DOS according to MMR status.
Methods
Among patients enrolled in the PRODIGY trial treated with either preoperative DOS followed by surgery and postoperative S-1 (CSC arm), or surgery and postoperative S-1 (SC arm) at Asan Medical Center (
n
= 249), those in the full analysis set with available tissue to assess MMR status were included in the present analysis.
Results
A total of 231 patients (CSC arm,
n
= 108; SC arm,
n
= 123) were included (median age, 58 years [range, 27–75]), and 21 patients (CSC arm,
n
= 8 [7.4%]; SC arm,
n
= 13 [10.6%]) had D-MMR tumors. Progression-free survival and overall survival tended to be superior in the CSC arm than in the SC arm among D-MMR patients (HR 0.48 [95% CI 0.09–2.50]; log-rank
P
= 0.37 and HR 0.55 [95% CI 0.11–2.86]; log-rank
P
= 0.46, respectively), as well as among proficient MMR (P-MMR) patients (HR 0.68 [95% CI 0.46–1.03]; log-rank
P
= 0.07 and HR 0.75 [95% CI 0.49–1.14]; log-rank
P
= 0.17, respectively).
Conclusion
Preoperative DOS followed by surgery and postoperative S-1 may be considered a treatment option for LAGC patients regardless of MMR status.</description><subject>Abdominal Surgery</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Cancer Research</subject><subject>Chemotherapy</subject><subject>Chemotherapy, Adjuvant</subject><subject>DNA - therapeutic use</subject><subject>DNA Mismatch Repair</subject><subject>DNA repair</subject><subject>Docetaxel</subject><subject>Drug therapy</subject><subject>Fluorouracil</subject><subject>Gastric cancer</subject><subject>Gastroenterology</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Mismatch repair</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Oxaliplatin</subject><subject>Patients</subject><subject>Postoperative period</subject><subject>Prodigies</subject><subject>Stomach Neoplasms - drug therapy</subject><subject>Stomach Neoplasms - genetics</subject><subject>Stomach Neoplasms - surgery</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Surgical techniques</subject><subject>Survival</subject><subject>Yeast</subject><issn>1436-3291</issn><issn>1436-3305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kk1v1DAQhgMCsaXwBzggS1w4NOCPxHG4VW0plSqK-DhwimbtSTeVNw620-3--3qTfkggcbI988w749GbZW8Y_cAorT4GRhmnOeUip6wQRb55mu2li8yFoOWz-zuv2SJ7GcIVpaysmXyRLUSlVC0k3XuyOP56SNZdWEPUK-JxgM4Tg22nO-z1lkBviBujdmsMxLVkgJgSMZBNF1fEOg3WJspcQ6_RkEsI0Xea6N3Tk-gRYgpP8ODRDeiTwDUS4zRGuEF7QNwN2G6wKd4fTP1-5IwMdgwkjP4S_TzE4EJ8LN8hzj8AE_0P8YlAIpY59GC3oZvmjyskwwoCEkG-fb84Pjv9nabswL7KnrdgA76-O_ezX59Pfh59yc8vTs-ODs9zLaoy5qqtja41rWpeUoWac9oKKtL-mS4Mr6BmYGQhuJScmhaoUVrWS65QLpUqpNjP3s-6g3d_RgyxSdvXaC306MbQcKVEqVhRlAl99xd65UafPpOomtasLCSjieIzpb0LwWPbDL5bg982jDY7nzSzT5rkk2bySbNJRW_vpMflGs1Dyb0xEiBmIKRUn5b82Ps_srcJiMvo</recordid><startdate>2024</startdate><enddate>2024</enddate><creator>Hyung, Jaewon</creator><creator>Cho, Hyungwoo</creator><creator>Kim, Hyung-Don</creator><creator>Park, Young Soo</creator><creator>Moon, Meesun</creator><creator>Ryu, Min-Hee</creator><creator>Kang, Yoon-Koo</creator><general>Springer Nature Singapore</general><general>Springer Nature B.V</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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0783-6583</orcidid></search><sort><creationdate>2024</creationdate><title>DNA mismatch repair deficiency and outcomes of patients with locally advanced gastric cancer treated with preoperative docetaxel, oxaliplatin, and S-1 plus surgery and postoperative S-1 or surgery plus postoperative S-1: a sub-analysis of the phase 3 PRODIGY trial</title><author>Hyung, Jaewon ; Cho, Hyungwoo ; Kim, Hyung-Don ; Park, Young Soo ; Moon, Meesun ; Ryu, Min-Hee ; Kang, Yoon-Koo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-8f9dc9c0792508ec220f3030141c4d27a91ad64326620dfa0d8c69b28e6b88463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Abdominal Surgery</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Cancer Research</topic><topic>Chemotherapy</topic><topic>Chemotherapy, Adjuvant</topic><topic>DNA - therapeutic use</topic><topic>DNA Mismatch Repair</topic><topic>DNA repair</topic><topic>Docetaxel</topic><topic>Drug therapy</topic><topic>Fluorouracil</topic><topic>Gastric cancer</topic><topic>Gastroenterology</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Mismatch repair</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Oxaliplatin</topic><topic>Patients</topic><topic>Postoperative period</topic><topic>Prodigies</topic><topic>Stomach Neoplasms - drug therapy</topic><topic>Stomach Neoplasms - genetics</topic><topic>Stomach Neoplasms - surgery</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Surgical techniques</topic><topic>Survival</topic><topic>Yeast</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hyung, Jaewon</creatorcontrib><creatorcontrib>Cho, Hyungwoo</creatorcontrib><creatorcontrib>Kim, Hyung-Don</creatorcontrib><creatorcontrib>Park, Young Soo</creatorcontrib><creatorcontrib>Moon, Meesun</creatorcontrib><creatorcontrib>Ryu, Min-Hee</creatorcontrib><creatorcontrib>Kang, Yoon-Koo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hyung, Jaewon</au><au>Cho, Hyungwoo</au><au>Kim, Hyung-Don</au><au>Park, Young Soo</au><au>Moon, Meesun</au><au>Ryu, Min-Hee</au><au>Kang, Yoon-Koo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>DNA mismatch repair deficiency and outcomes of patients with locally advanced gastric cancer treated with preoperative docetaxel, oxaliplatin, and S-1 plus surgery and postoperative S-1 or surgery plus postoperative S-1: a sub-analysis of the phase 3 PRODIGY trial</atitle><jtitle>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</jtitle><stitle>Gastric Cancer</stitle><addtitle>Gastric Cancer</addtitle><date>2024</date><risdate>2024</risdate><volume>27</volume><issue>1</issue><spage>110</spage><epage>117</epage><pages>110-117</pages><issn>1436-3291</issn><eissn>1436-3305</eissn><abstract>Background
The benefit of adjuvant chemotherapy for locally advanced gastric cancer (LAGC) patients with DNA mismatch repair (MMR) deficiency (D-MMR) is controversial due to concerns about its potential detrimental effect. The PRODIGY trial showed the survival benefit of adding preoperative docetaxel, oxaliplatin, and S-1 (DOS) to surgery plus postoperative S-1 for LAGC patients. In this sub-analysis, we evaluated the benefit of preoperative DOS according to MMR status.
Methods
Among patients enrolled in the PRODIGY trial treated with either preoperative DOS followed by surgery and postoperative S-1 (CSC arm), or surgery and postoperative S-1 (SC arm) at Asan Medical Center (
n
= 249), those in the full analysis set with available tissue to assess MMR status were included in the present analysis.
Results
A total of 231 patients (CSC arm,
n
= 108; SC arm,
n
= 123) were included (median age, 58 years [range, 27–75]), and 21 patients (CSC arm,
n
= 8 [7.4%]; SC arm,
n
= 13 [10.6%]) had D-MMR tumors. Progression-free survival and overall survival tended to be superior in the CSC arm than in the SC arm among D-MMR patients (HR 0.48 [95% CI 0.09–2.50]; log-rank
P
= 0.37 and HR 0.55 [95% CI 0.11–2.86]; log-rank
P
= 0.46, respectively), as well as among proficient MMR (P-MMR) patients (HR 0.68 [95% CI 0.46–1.03]; log-rank
P
= 0.07 and HR 0.75 [95% CI 0.49–1.14]; log-rank
P
= 0.17, respectively).
Conclusion
Preoperative DOS followed by surgery and postoperative S-1 may be considered a treatment option for LAGC patients regardless of MMR status.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>37889360</pmid><doi>10.1007/s10120-023-01434-w</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0783-6583</orcidid></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; SpringerLink Journals - AutoHoldings |
subjects | Abdominal Surgery Antineoplastic Combined Chemotherapy Protocols - therapeutic use Cancer Research Chemotherapy Chemotherapy, Adjuvant DNA - therapeutic use DNA Mismatch Repair DNA repair Docetaxel Drug therapy Fluorouracil Gastric cancer Gastroenterology Humans Medicine Medicine & Public Health Middle Aged Mismatch repair Oncology Original Article Oxaliplatin Patients Postoperative period Prodigies Stomach Neoplasms - drug therapy Stomach Neoplasms - genetics Stomach Neoplasms - surgery Surgery Surgical Oncology Surgical techniques Survival Yeast |
title | DNA mismatch repair deficiency and outcomes of patients with locally advanced gastric cancer treated with preoperative docetaxel, oxaliplatin, and S-1 plus surgery and postoperative S-1 or surgery plus postoperative S-1: a sub-analysis of the phase 3 PRODIGY trial |
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