Macroscopic and multiple metastases in sentinel lymph node biopsy are respectively associated with poor prognosis in early oral cancer

Background A multicenter, randomized controlled phase III trial was conducted on sentinel lymph node biopsy (SLNB) and elective neck dissection for T1 (depth of invasion ≥ 4 mm)–T2N0M0 oral cavity squamous cell carcinoma. This study identified factors associated with poor prognosis in patients who u...

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Veröffentlicht in:International journal of clinical oncology 2023-04, Vol.28 (4), p.512-520
Hauptverfasser: Kondo, Takahito, Tsukahara, Kiyoaki, Kawakita, Daisuke, Yoshimoto, Seiichi, Miura, Kouki, Sugasawa, Masashi, Chikamatsu, Kazuaki, Matsuzuka, Takashi, Oze, Isao, Kitamura, Morimasa, Murakami, Yoshiko, Otozai, Shinji, Shinozaki, Takeshi, Ohba, Shinichi, Araki, Koji, Mizumachi, Takatsugu, Sato, Dai, Wakisaka, Naohiro, Hirakawa, Hitoshi, Hasegawa, Yasuhisa
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container_issue 4
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container_title International journal of clinical oncology
container_volume 28
creator Kondo, Takahito
Tsukahara, Kiyoaki
Kawakita, Daisuke
Yoshimoto, Seiichi
Miura, Kouki
Sugasawa, Masashi
Chikamatsu, Kazuaki
Matsuzuka, Takashi
Oze, Isao
Kitamura, Morimasa
Murakami, Yoshiko
Otozai, Shinji
Shinozaki, Takeshi
Ohba, Shinichi
Araki, Koji
Mizumachi, Takatsugu
Sato, Dai
Wakisaka, Naohiro
Hirakawa, Hitoshi
Hasegawa, Yasuhisa
description Background A multicenter, randomized controlled phase III trial was conducted on sentinel lymph node biopsy (SLNB) and elective neck dissection for T1 (depth of invasion ≥ 4 mm)–T2N0M0 oral cavity squamous cell carcinoma. This study identified factors associated with poor prognosis in patients who underwent SLNB based on a subgroup analysis of this trial. Methods We analyzed 418 sentinel lymph nodes (SLNs) from 132 patients who underwent SLNB. The metastatic SLNs were classified into three categories based on size-isolated tumor cells: 
doi_str_mv 10.1007/s10147-023-02305-1
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This study identified factors associated with poor prognosis in patients who underwent SLNB based on a subgroup analysis of this trial. Methods We analyzed 418 sentinel lymph nodes (SLNs) from 132 patients who underwent SLNB. The metastatic SLNs were classified into three categories based on size-isolated tumor cells: &lt; 0.2 mm, micrometastasis: ≥ 0.2 mm and &lt; 2 mm, and macrometastasis: ≥ 2 mm. Three groups were formed based on the number of metastatic SLNs: no metastasis, 1 metastatic node, and ≥ 2 metastatic nodes. The size and number of metastatic SLNs on survival were evaluated using Cox proportional hazard models. Results Patients with macrometastasis and ≥ 2 metastatic SLNs had worse overall survival (OS) and disease-free survival (DFS) after adjustment for potential confounders (HR for OS: macrometastasis, 4.85; 95% CI 1.34–17.60; ≥ 2 metastatic SLN, 3.63; 95% CI 1.02–12.89; HR for DFS: macrometastasis, 2.94; 95% CI 1.16–7.44; ≥ 2 metastatic SLN, 2.97; 95% CI 1.18–7.51). Conclusions In patients who underwent SLNB, a poorer prognosis was associated with macrometastasis or having ≥ 2 metastatic SLNs.</description><identifier>ISSN: 1341-9625</identifier><identifier>EISSN: 1437-7772</identifier><identifier>DOI: 10.1007/s10147-023-02305-1</identifier><identifier>PMID: 36795281</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Biopsy ; Breast Neoplasms - pathology ; Cancer Research ; Cell size ; Disease-Free Survival ; Female ; Humans ; Lymph nodes ; Lymph Nodes - pathology ; Lymph Nodes - surgery ; Lymphatic Metastasis - pathology ; Lymphatic system ; Medical prognosis ; Medicine ; Medicine &amp; Public Health ; Metastases ; Metastasis ; Mouth Neoplasms - pathology ; Mouth Neoplasms - surgery ; Neck Dissection ; Oncology ; Oral cancer ; Oral carcinoma ; Oral cavity ; Original Article ; Prognosis ; Sentinel Lymph Node - pathology ; Sentinel Lymph Node - surgery ; Sentinel Lymph Node Biopsy ; Squamous cell carcinoma ; Surgical Oncology ; Tumor cells</subject><ispartof>International journal of clinical oncology, 2023-04, Vol.28 (4), p.512-520</ispartof><rights>The Author(s) under exclusive licence to Japan Society of Clinical Oncology 2023. 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This study identified factors associated with poor prognosis in patients who underwent SLNB based on a subgroup analysis of this trial. Methods We analyzed 418 sentinel lymph nodes (SLNs) from 132 patients who underwent SLNB. The metastatic SLNs were classified into three categories based on size-isolated tumor cells: &lt; 0.2 mm, micrometastasis: ≥ 0.2 mm and &lt; 2 mm, and macrometastasis: ≥ 2 mm. Three groups were formed based on the number of metastatic SLNs: no metastasis, 1 metastatic node, and ≥ 2 metastatic nodes. The size and number of metastatic SLNs on survival were evaluated using Cox proportional hazard models. Results Patients with macrometastasis and ≥ 2 metastatic SLNs had worse overall survival (OS) and disease-free survival (DFS) after adjustment for potential confounders (HR for OS: macrometastasis, 4.85; 95% CI 1.34–17.60; ≥ 2 metastatic SLN, 3.63; 95% CI 1.02–12.89; HR for DFS: macrometastasis, 2.94; 95% CI 1.16–7.44; ≥ 2 metastatic SLN, 2.97; 95% CI 1.18–7.51). Conclusions In patients who underwent SLNB, a poorer prognosis was associated with macrometastasis or having ≥ 2 metastatic SLNs.</description><subject>Biopsy</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer Research</subject><subject>Cell size</subject><subject>Disease-Free Survival</subject><subject>Female</subject><subject>Humans</subject><subject>Lymph nodes</subject><subject>Lymph Nodes - pathology</subject><subject>Lymph Nodes - surgery</subject><subject>Lymphatic Metastasis - pathology</subject><subject>Lymphatic system</subject><subject>Medical prognosis</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Mouth Neoplasms - pathology</subject><subject>Mouth Neoplasms - surgery</subject><subject>Neck Dissection</subject><subject>Oncology</subject><subject>Oral cancer</subject><subject>Oral carcinoma</subject><subject>Oral cavity</subject><subject>Original Article</subject><subject>Prognosis</subject><subject>Sentinel Lymph Node - pathology</subject><subject>Sentinel Lymph Node - surgery</subject><subject>Sentinel Lymph Node Biopsy</subject><subject>Squamous cell carcinoma</subject><subject>Surgical Oncology</subject><subject>Tumor cells</subject><issn>1341-9625</issn><issn>1437-7772</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kctu1TAQhi1ERS_wAiyQJTZsQseXxMkSVeUiFXVT1pZjT1pXjh3shOq8AM-NT08BiQWSLY_s7_89mp-Q1wzeMwB1XhgwqRrgYr-hbdgzcsKkUI1Sij-vtZCsGTreHpPTUu4BmOpa_oIci04NLe_ZCfn51dicik2Lt9RER-ctrH4JSGdcTakLC_WRFoyrjxho2M3LHY3JIR19WsqOmow0Y1nQrv4HhnpRSrLerOjog1_v6JJSpktOtzEV_-iGJlcuZROoNdFifkmOJhMKvno6z8i3j5c3F5-bq-tPXy4-XDVWSrE2xnFnW-NwYAijnRB7N3RmmoCjkGLsJIzQOcklH7kUnNc59CBa03cCcBDijLw7-NZ2vm9YVj37YjEEEzFtRVeBkiB7BhV9-w96n7Yca3ea9wNIEMCHSvEDtZ9iyTjpJfvZ5J1moPcp6UNKuiakH1PSrIrePFlv44zuj-R3LBUQB6DUp3iL-e_f_7H9BejTnz4</recordid><startdate>20230401</startdate><enddate>20230401</enddate><creator>Kondo, Takahito</creator><creator>Tsukahara, Kiyoaki</creator><creator>Kawakita, Daisuke</creator><creator>Yoshimoto, Seiichi</creator><creator>Miura, Kouki</creator><creator>Sugasawa, Masashi</creator><creator>Chikamatsu, Kazuaki</creator><creator>Matsuzuka, Takashi</creator><creator>Oze, Isao</creator><creator>Kitamura, Morimasa</creator><creator>Murakami, Yoshiko</creator><creator>Otozai, Shinji</creator><creator>Shinozaki, Takeshi</creator><creator>Ohba, Shinichi</creator><creator>Araki, Koji</creator><creator>Mizumachi, Takatsugu</creator><creator>Sato, Dai</creator><creator>Wakisaka, Naohiro</creator><creator>Hirakawa, Hitoshi</creator><creator>Hasegawa, Yasuhisa</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>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</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>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4198-9615</orcidid><orcidid>https://orcid.org/0000-0003-3794-2790</orcidid><orcidid>https://orcid.org/0000-0001-9323-3003</orcidid></search><sort><creationdate>20230401</creationdate><title>Macroscopic and multiple metastases in sentinel lymph node biopsy are respectively associated with poor prognosis in early oral cancer</title><author>Kondo, Takahito ; 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Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Mouth Neoplasms - pathology</topic><topic>Mouth Neoplasms - surgery</topic><topic>Neck Dissection</topic><topic>Oncology</topic><topic>Oral cancer</topic><topic>Oral carcinoma</topic><topic>Oral cavity</topic><topic>Original Article</topic><topic>Prognosis</topic><topic>Sentinel Lymph Node - pathology</topic><topic>Sentinel Lymph Node - surgery</topic><topic>Sentinel Lymph Node Biopsy</topic><topic>Squamous cell carcinoma</topic><topic>Surgical Oncology</topic><topic>Tumor cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kondo, Takahito</creatorcontrib><creatorcontrib>Tsukahara, Kiyoaki</creatorcontrib><creatorcontrib>Kawakita, Daisuke</creatorcontrib><creatorcontrib>Yoshimoto, Seiichi</creatorcontrib><creatorcontrib>Miura, Kouki</creatorcontrib><creatorcontrib>Sugasawa, Masashi</creatorcontrib><creatorcontrib>Chikamatsu, Kazuaki</creatorcontrib><creatorcontrib>Matsuzuka, Takashi</creatorcontrib><creatorcontrib>Oze, Isao</creatorcontrib><creatorcontrib>Kitamura, Morimasa</creatorcontrib><creatorcontrib>Murakami, Yoshiko</creatorcontrib><creatorcontrib>Otozai, Shinji</creatorcontrib><creatorcontrib>Shinozaki, Takeshi</creatorcontrib><creatorcontrib>Ohba, Shinichi</creatorcontrib><creatorcontrib>Araki, Koji</creatorcontrib><creatorcontrib>Mizumachi, Takatsugu</creatorcontrib><creatorcontrib>Sato, Dai</creatorcontrib><creatorcontrib>Wakisaka, Naohiro</creatorcontrib><creatorcontrib>Hirakawa, Hitoshi</creatorcontrib><creatorcontrib>Hasegawa, Yasuhisa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health &amp; 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This study identified factors associated with poor prognosis in patients who underwent SLNB based on a subgroup analysis of this trial. Methods We analyzed 418 sentinel lymph nodes (SLNs) from 132 patients who underwent SLNB. The metastatic SLNs were classified into three categories based on size-isolated tumor cells: &lt; 0.2 mm, micrometastasis: ≥ 0.2 mm and &lt; 2 mm, and macrometastasis: ≥ 2 mm. Three groups were formed based on the number of metastatic SLNs: no metastasis, 1 metastatic node, and ≥ 2 metastatic nodes. The size and number of metastatic SLNs on survival were evaluated using Cox proportional hazard models. Results Patients with macrometastasis and ≥ 2 metastatic SLNs had worse overall survival (OS) and disease-free survival (DFS) after adjustment for potential confounders (HR for OS: macrometastasis, 4.85; 95% CI 1.34–17.60; ≥ 2 metastatic SLN, 3.63; 95% CI 1.02–12.89; HR for DFS: macrometastasis, 2.94; 95% CI 1.16–7.44; ≥ 2 metastatic SLN, 2.97; 95% CI 1.18–7.51). Conclusions In patients who underwent SLNB, a poorer prognosis was associated with macrometastasis or having ≥ 2 metastatic SLNs.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>36795281</pmid><doi>10.1007/s10147-023-02305-1</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-4198-9615</orcidid><orcidid>https://orcid.org/0000-0003-3794-2790</orcidid><orcidid>https://orcid.org/0000-0001-9323-3003</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Biopsy
Breast Neoplasms - pathology
Cancer Research
Cell size
Disease-Free Survival
Female
Humans
Lymph nodes
Lymph Nodes - pathology
Lymph Nodes - surgery
Lymphatic Metastasis - pathology
Lymphatic system
Medical prognosis
Medicine
Medicine & Public Health
Metastases
Metastasis
Mouth Neoplasms - pathology
Mouth Neoplasms - surgery
Neck Dissection
Oncology
Oral cancer
Oral carcinoma
Oral cavity
Original Article
Prognosis
Sentinel Lymph Node - pathology
Sentinel Lymph Node - surgery
Sentinel Lymph Node Biopsy
Squamous cell carcinoma
Surgical Oncology
Tumor cells
title Macroscopic and multiple metastases in sentinel lymph node biopsy are respectively associated with poor prognosis in early oral cancer
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