Neoadjuvant docetaxel, oxaliplatin and S‑1 (DOS) combination chemotherapy for patients with resectable adenocarcinoma of esophagogastric junction
Backgrounds Since the prognosis of patients with adenocarcinoma of the esophagogastric junction (AEG) remains poor, more intensive treatments, including neoadjuvant chemotherapy (NAC), should be developed. We retrospectively examined whether neoadjuvant docetaxel, oxaliplatin, and S‑1 (DOS) combinat...
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Veröffentlicht in: | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2022-09, Vol.25 (5), p.966-972 |
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creator | Saito, Takuro Kurokawa, Yukinori Takahashi, Tsuyoshi Yamamoto, Kazuyoshi Yamashita, Kotaro Tanaka, Koji Makino, Tomoki Nakajima, Kiyokazu Eguchi, Hidetoshi Doki, Yuichiro |
description | Backgrounds
Since the prognosis of patients with adenocarcinoma of the esophagogastric junction (AEG) remains poor, more intensive treatments, including neoadjuvant chemotherapy (NAC), should be developed. We retrospectively examined whether neoadjuvant docetaxel, oxaliplatin, and S‑1 (DOS) combination chemotherapy resulted in a favorable clinical response and acceptable toxicity in patients with AEG.
Methods
This retrospective cohort study included 36 consecutive patients with cStage IIB–IV AEG (Siewert types I–III). Regarding stage IV disease, patients with resectable distant lymph node metastasis (M1-LYM) were eligible. Patients underwent three 3-week cycles of docetaxel (40 mg/m
2
) and oxaliplatin (100 mg/m
2
) on day 1 plus oral S-1 (80–120 mg according to body surface area) from day 1 to 14. Surgical resection was performed within 2–4 weeks after completion of NAC.
Results
Three cycles of neoadjuvant DOS were completed in 28 (78%) patients. Grade 3–4 neutropenia, anorexia, and diarrhea were observed in 26 (72%), 7 (19%), and 4 (11%) patients, respectively. Febrile neutropenia occurred in six (17%) patients. There were no treatment-related deaths. R0 resection was achieved in 35 (97%) patients, and postoperative morbidities of Clavien–Dindo grade III or higher were observed in 6 (17%) patients. Pathological complete response was observed in 11 (31%) of 36 patients. Pathological response rates of grade ≥ 2 and grade ≥ 1b were 47 and 72%, respectively. Two-year progression-free and overall survival rates were 60.1 and 81.2%, respectively.
Conclusions
Neoadjuvant DOS therapy for AEG produced high pathological response rates with an acceptable safety profile, and may be a promising treatment strategy. |
doi_str_mv | 10.1007/s10120-022-01300-1 |
format | Article |
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Since the prognosis of patients with adenocarcinoma of the esophagogastric junction (AEG) remains poor, more intensive treatments, including neoadjuvant chemotherapy (NAC), should be developed. We retrospectively examined whether neoadjuvant docetaxel, oxaliplatin, and S‑1 (DOS) combination chemotherapy resulted in a favorable clinical response and acceptable toxicity in patients with AEG.
Methods
This retrospective cohort study included 36 consecutive patients with cStage IIB–IV AEG (Siewert types I–III). Regarding stage IV disease, patients with resectable distant lymph node metastasis (M1-LYM) were eligible. Patients underwent three 3-week cycles of docetaxel (40 mg/m
2
) and oxaliplatin (100 mg/m
2
) on day 1 plus oral S-1 (80–120 mg according to body surface area) from day 1 to 14. Surgical resection was performed within 2–4 weeks after completion of NAC.
Results
Three cycles of neoadjuvant DOS were completed in 28 (78%) patients. Grade 3–4 neutropenia, anorexia, and diarrhea were observed in 26 (72%), 7 (19%), and 4 (11%) patients, respectively. Febrile neutropenia occurred in six (17%) patients. There were no treatment-related deaths. R0 resection was achieved in 35 (97%) patients, and postoperative morbidities of Clavien–Dindo grade III or higher were observed in 6 (17%) patients. Pathological complete response was observed in 11 (31%) of 36 patients. Pathological response rates of grade ≥ 2 and grade ≥ 1b were 47 and 72%, respectively. Two-year progression-free and overall survival rates were 60.1 and 81.2%, respectively.
Conclusions
Neoadjuvant DOS therapy for AEG produced high pathological response rates with an acceptable safety profile, and may be a promising treatment strategy.</description><identifier>ISSN: 1436-3291</identifier><identifier>EISSN: 1436-3305</identifier><identifier>DOI: 10.1007/s10120-022-01300-1</identifier><identifier>PMID: 35488968</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Abdominal Surgery ; Adenocarcinoma ; Anorexia ; Cancer ; Cancer Research ; Chemotherapy ; Diarrhea ; Gastric cancer ; Gastroenterology ; Lymph nodes ; Medical prognosis ; Medicine ; Medicine & Public Health ; Metastases ; Neutropenia ; Oncology ; Original Article ; Oxaliplatin ; Patients ; Response rates ; Surgical Oncology ; Toxicity</subject><ispartof>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2022-09, Vol.25 (5), p.966-972</ispartof><rights>The Author(s) under exclusive licence to The International Gastric Cancer Association and The Japanese Gastric Cancer Association 2022</rights><rights>2022. The Author(s) under exclusive licence to The International Gastric Cancer Association and The Japanese Gastric Cancer Association.</rights><rights>The Author(s) under exclusive licence to The International Gastric Cancer Association and The Japanese Gastric Cancer Association 2022.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-d81e3b0f5a98743be35f6ffec34d1b56598575396bfa009f233f3d9ebfb082e03</citedby><cites>FETCH-LOGICAL-c443t-d81e3b0f5a98743be35f6ffec34d1b56598575396bfa009f233f3d9ebfb082e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10120-022-01300-1$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10120-022-01300-1$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27906,27907,41470,42539,51301</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35488968$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saito, Takuro</creatorcontrib><creatorcontrib>Kurokawa, Yukinori</creatorcontrib><creatorcontrib>Takahashi, Tsuyoshi</creatorcontrib><creatorcontrib>Yamamoto, Kazuyoshi</creatorcontrib><creatorcontrib>Yamashita, Kotaro</creatorcontrib><creatorcontrib>Tanaka, Koji</creatorcontrib><creatorcontrib>Makino, Tomoki</creatorcontrib><creatorcontrib>Nakajima, Kiyokazu</creatorcontrib><creatorcontrib>Eguchi, Hidetoshi</creatorcontrib><creatorcontrib>Doki, Yuichiro</creatorcontrib><title>Neoadjuvant docetaxel, oxaliplatin and S‑1 (DOS) combination chemotherapy for patients with resectable adenocarcinoma of esophagogastric junction</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>Backgrounds
Since the prognosis of patients with adenocarcinoma of the esophagogastric junction (AEG) remains poor, more intensive treatments, including neoadjuvant chemotherapy (NAC), should be developed. We retrospectively examined whether neoadjuvant docetaxel, oxaliplatin, and S‑1 (DOS) combination chemotherapy resulted in a favorable clinical response and acceptable toxicity in patients with AEG.
Methods
This retrospective cohort study included 36 consecutive patients with cStage IIB–IV AEG (Siewert types I–III). Regarding stage IV disease, patients with resectable distant lymph node metastasis (M1-LYM) were eligible. Patients underwent three 3-week cycles of docetaxel (40 mg/m
2
) and oxaliplatin (100 mg/m
2
) on day 1 plus oral S-1 (80–120 mg according to body surface area) from day 1 to 14. Surgical resection was performed within 2–4 weeks after completion of NAC.
Results
Three cycles of neoadjuvant DOS were completed in 28 (78%) patients. Grade 3–4 neutropenia, anorexia, and diarrhea were observed in 26 (72%), 7 (19%), and 4 (11%) patients, respectively. Febrile neutropenia occurred in six (17%) patients. There were no treatment-related deaths. R0 resection was achieved in 35 (97%) patients, and postoperative morbidities of Clavien–Dindo grade III or higher were observed in 6 (17%) patients. Pathological complete response was observed in 11 (31%) of 36 patients. Pathological response rates of grade ≥ 2 and grade ≥ 1b were 47 and 72%, respectively. Two-year progression-free and overall survival rates were 60.1 and 81.2%, respectively.
Conclusions
Neoadjuvant DOS therapy for AEG produced high pathological response rates with an acceptable safety profile, and may be a promising treatment strategy.</description><subject>Abdominal Surgery</subject><subject>Adenocarcinoma</subject><subject>Anorexia</subject><subject>Cancer</subject><subject>Cancer Research</subject><subject>Chemotherapy</subject><subject>Diarrhea</subject><subject>Gastric cancer</subject><subject>Gastroenterology</subject><subject>Lymph nodes</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Neutropenia</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Oxaliplatin</subject><subject>Patients</subject><subject>Response rates</subject><subject>Surgical Oncology</subject><subject>Toxicity</subject><issn>1436-3291</issn><issn>1436-3305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kctu1TAQhi0EoqXwAiyQJTatRMCXOJdl1QsgVXRRWFsTZ3xOjhI72A60u74C6hvyJPhwWpBYsPLI881vaz5CXnL2ljNWv4ucccEKJkTBuGSs4I_IPi9lVUjJ1OOHWrR8jzyLccMYVy2vnpI9qcqmaatmn9x9Qg_9ZvkGLtHeG0xwjeMb6q9hHOYR0uAouJ5e_bz9wenh6eXVETV-6gaXW95Rs8bJpzUGmG-o9YHO-R5divT7kNY0YESToBuRQo_OGwhmcH4C6i3F6Oc1rPwKYgqDoZvFmW3oc_LEwhjxxf15QL6cn30--VBcXL7_eHJ8UZiylKnoG46yY1ZB29Sl7FAqW1mLRpY971Sl2kbVSrZVZ4Gx1goprexb7GzHGoFMHpDDXe4c_NcFY9LTEA2OIzj0S9SiUo3I26vrjL7-B934Jbj8Oy3q7ELxSvJMiR1lgo8xoNVzGCYIN5ozvVWmd8p0VqZ_K9PboVf30Us3Yf9n5MFRBuQOiLnlVhj-vv2f2F-15qSN</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Saito, Takuro</creator><creator>Kurokawa, Yukinori</creator><creator>Takahashi, Tsuyoshi</creator><creator>Yamamoto, Kazuyoshi</creator><creator>Yamashita, Kotaro</creator><creator>Tanaka, Koji</creator><creator>Makino, Tomoki</creator><creator>Nakajima, Kiyokazu</creator><creator>Eguchi, Hidetoshi</creator><creator>Doki, Yuichiro</creator><general>Springer Nature Singapore</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20220901</creationdate><title>Neoadjuvant docetaxel, oxaliplatin and S‑1 (DOS) combination chemotherapy for patients with resectable adenocarcinoma of esophagogastric junction</title><author>Saito, Takuro ; Kurokawa, Yukinori ; Takahashi, Tsuyoshi ; Yamamoto, Kazuyoshi ; Yamashita, Kotaro ; Tanaka, Koji ; Makino, Tomoki ; Nakajima, Kiyokazu ; Eguchi, Hidetoshi ; Doki, Yuichiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-d81e3b0f5a98743be35f6ffec34d1b56598575396bfa009f233f3d9ebfb082e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Abdominal Surgery</topic><topic>Adenocarcinoma</topic><topic>Anorexia</topic><topic>Cancer</topic><topic>Cancer Research</topic><topic>Chemotherapy</topic><topic>Diarrhea</topic><topic>Gastric cancer</topic><topic>Gastroenterology</topic><topic>Lymph nodes</topic><topic>Medical prognosis</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Neutropenia</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Oxaliplatin</topic><topic>Patients</topic><topic>Response rates</topic><topic>Surgical Oncology</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saito, Takuro</creatorcontrib><creatorcontrib>Kurokawa, Yukinori</creatorcontrib><creatorcontrib>Takahashi, Tsuyoshi</creatorcontrib><creatorcontrib>Yamamoto, Kazuyoshi</creatorcontrib><creatorcontrib>Yamashita, Kotaro</creatorcontrib><creatorcontrib>Tanaka, Koji</creatorcontrib><creatorcontrib>Makino, Tomoki</creatorcontrib><creatorcontrib>Nakajima, Kiyokazu</creatorcontrib><creatorcontrib>Eguchi, Hidetoshi</creatorcontrib><creatorcontrib>Doki, Yuichiro</creatorcontrib><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>Saito, Takuro</au><au>Kurokawa, Yukinori</au><au>Takahashi, Tsuyoshi</au><au>Yamamoto, Kazuyoshi</au><au>Yamashita, Kotaro</au><au>Tanaka, Koji</au><au>Makino, Tomoki</au><au>Nakajima, Kiyokazu</au><au>Eguchi, Hidetoshi</au><au>Doki, Yuichiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neoadjuvant docetaxel, oxaliplatin and S‑1 (DOS) combination chemotherapy for patients with resectable adenocarcinoma of esophagogastric junction</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>2022-09-01</date><risdate>2022</risdate><volume>25</volume><issue>5</issue><spage>966</spage><epage>972</epage><pages>966-972</pages><issn>1436-3291</issn><eissn>1436-3305</eissn><abstract>Backgrounds
Since the prognosis of patients with adenocarcinoma of the esophagogastric junction (AEG) remains poor, more intensive treatments, including neoadjuvant chemotherapy (NAC), should be developed. We retrospectively examined whether neoadjuvant docetaxel, oxaliplatin, and S‑1 (DOS) combination chemotherapy resulted in a favorable clinical response and acceptable toxicity in patients with AEG.
Methods
This retrospective cohort study included 36 consecutive patients with cStage IIB–IV AEG (Siewert types I–III). Regarding stage IV disease, patients with resectable distant lymph node metastasis (M1-LYM) were eligible. Patients underwent three 3-week cycles of docetaxel (40 mg/m
2
) and oxaliplatin (100 mg/m
2
) on day 1 plus oral S-1 (80–120 mg according to body surface area) from day 1 to 14. Surgical resection was performed within 2–4 weeks after completion of NAC.
Results
Three cycles of neoadjuvant DOS were completed in 28 (78%) patients. Grade 3–4 neutropenia, anorexia, and diarrhea were observed in 26 (72%), 7 (19%), and 4 (11%) patients, respectively. Febrile neutropenia occurred in six (17%) patients. There were no treatment-related deaths. R0 resection was achieved in 35 (97%) patients, and postoperative morbidities of Clavien–Dindo grade III or higher were observed in 6 (17%) patients. Pathological complete response was observed in 11 (31%) of 36 patients. Pathological response rates of grade ≥ 2 and grade ≥ 1b were 47 and 72%, respectively. Two-year progression-free and overall survival rates were 60.1 and 81.2%, respectively.
Conclusions
Neoadjuvant DOS therapy for AEG produced high pathological response rates with an acceptable safety profile, and may be a promising treatment strategy.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>35488968</pmid><doi>10.1007/s10120-022-01300-1</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | SpringerLink Journals; EZB-FREE-00999 freely available EZB journals |
subjects | Abdominal Surgery Adenocarcinoma Anorexia Cancer Cancer Research Chemotherapy Diarrhea Gastric cancer Gastroenterology Lymph nodes Medical prognosis Medicine Medicine & Public Health Metastases Neutropenia Oncology Original Article Oxaliplatin Patients Response rates Surgical Oncology Toxicity |
title | Neoadjuvant docetaxel, oxaliplatin and S‑1 (DOS) combination chemotherapy for patients with resectable adenocarcinoma of esophagogastric junction |
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