Loading…

Proof of Principle of Combining Fluorescence-Guided Surgery with Photoimmunotherapy to Improve the Outcome of Pancreatic Cancer Therapy in an Orthotopic Mouse Model

Background Pancreatic cancer is a recalcitrant disease in which R0 resection is often not achieved owing to difficulty in visualization of the tumor margins and proximity of adjacent vessels. To improve outcomes, we have developed fluorescence-guided surgery (FGS) and photoimmunotherapy (PIT) using...

Full description

Saved in:
Bibliographic Details
Published in:Annals of surgical oncology 2023-01, Vol.30 (1), p.618-625
Main Authors: Nishino, Hiroto, Turner, Michael A., Amirfakhri, Siamak, Lwin, Thinzar M., Hosseini, Mojgan, Singer, Bernhard B., Hoffman, Robert M., Bouvet, Michael
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c404t-f8598bc2572fd704fbfeb79a95c708a3e7df60b5d4f500050b684bef708be013
cites cdi_FETCH-LOGICAL-c404t-f8598bc2572fd704fbfeb79a95c708a3e7df60b5d4f500050b684bef708be013
container_end_page 625
container_issue 1
container_start_page 618
container_title Annals of surgical oncology
container_volume 30
creator Nishino, Hiroto
Turner, Michael A.
Amirfakhri, Siamak
Lwin, Thinzar M.
Hosseini, Mojgan
Singer, Bernhard B.
Hoffman, Robert M.
Bouvet, Michael
description Background Pancreatic cancer is a recalcitrant disease in which R0 resection is often not achieved owing to difficulty in visualization of the tumor margins and proximity of adjacent vessels. To improve outcomes, we have developed fluorescence-guided surgery (FGS) and photoimmunotherapy (PIT) using a fluorescent tumor-specific antibody. Methods Nude mice received surgical orthotopic implantation (SOI) of the human pancreatic cancer cell line BxPC-3 expressing green fluorescent protein. An anti-carcinoembryonic antigen-related cell adhesion molecule (CEACAM) monoclonal antibody (6G5j) was conjugated to the 700-nm fluorescent dye IR700DyeDX (6G5j-IR700DX). Three weeks after SOI, 16 mice received 50 μg 6G5j-IR700DX via the tail vein 24 h before surgery and were randomized to two groups: FGS-only ( n = 8) and FGS + PIT ( n = 8). All tumors were imaged with the Pearl Trilogy imaging system and resected under the guidance of the FLARE imaging system. The FGS + PIT group received PIT of the post-surgical bed at an intensity of 150 mW/cm 2 for 30 min. Mice were sacrificed 4 weeks after initial surgery, and tumors were imaged with a Dino-Lite digital microscope, excised, and weighed. Results The 6G5j-IR700DX dye illuminated the orthotopic pancreatic tumors for FGS and PIT. The metastatic recurrence rate was 100.0% for FGS-only and 25.0% for FGS + PIT ( p = 0.007). The average total recurrent tumor weight was 2370.3 ± 1907.8 mg for FGS-only and 705.5 ± 1200.0 mg for FGS + PIT ( p = 0.039). Conclusions FGS and adjuvant PIT can be combined by using a single antibody–fluorophore conjugate to significantly reduce the frequency of pancreatic cancer recurrence.
doi_str_mv 10.1245/s10434-022-12466-4
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9726788</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2747121318</sourcerecordid><originalsourceid>FETCH-LOGICAL-c404t-f8598bc2572fd704fbfeb79a95c708a3e7df60b5d4f500050b684bef708be013</originalsourceid><addsrcrecordid>eNp9Uk1v1DAQjRCIlsIf4IAsceESsB07Ti5IaEVLpaJdqXu3HGey6yqxg5202v_DD2W2u7SUQyXLno83zx7Py7L3jH5mXMgviVFRiJxynqNflrl4kZ0yiSFRVuwl2rSs8pqX8iR7k9INpUwVVL7OToqSSlXV9Wn2exVD6AiuVXTeurGHvbMIQ-O88xty3s8hQrLgLeQXs2uhJddz3EDckTs3bclqG6bghmH2YdpCNOOOTIFcDmMMt0AwRJbzZMNwz7sy3kYwk7NkgSZEsj7WOE-MJ8s47elGzP8McwLcW-jfZq860yd4dzzPsvX59_XiR361vLhcfLvKraBiyrtK1lVjuVS8axUVXdNBo2pTS6toZQpQbVfSRraik5RSSZuyEg10mGyAsuIs-3qgHedmgBZbnqLp9RjdYOJOB-P004x3W70Jt7pWvFRVhQSfjgQx_JohTXpw-HN9bzxgN5orWitRKE4R-vE_6E2Yo8fuECUU46xge0J-QNkYUorQPTyGUb3XgD5oQKMG9L0GtMCiD_-28VDyd-gIKA6AhCmPk3y8-xnaP17gwMs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2747121318</pqid></control><display><type>article</type><title>Proof of Principle of Combining Fluorescence-Guided Surgery with Photoimmunotherapy to Improve the Outcome of Pancreatic Cancer Therapy in an Orthotopic Mouse Model</title><source>Springer Nature</source><creator>Nishino, Hiroto ; Turner, Michael A. ; Amirfakhri, Siamak ; Lwin, Thinzar M. ; Hosseini, Mojgan ; Singer, Bernhard B. ; Hoffman, Robert M. ; Bouvet, Michael</creator><creatorcontrib>Nishino, Hiroto ; Turner, Michael A. ; Amirfakhri, Siamak ; Lwin, Thinzar M. ; Hosseini, Mojgan ; Singer, Bernhard B. ; Hoffman, Robert M. ; Bouvet, Michael</creatorcontrib><description>Background Pancreatic cancer is a recalcitrant disease in which R0 resection is often not achieved owing to difficulty in visualization of the tumor margins and proximity of adjacent vessels. To improve outcomes, we have developed fluorescence-guided surgery (FGS) and photoimmunotherapy (PIT) using a fluorescent tumor-specific antibody. Methods Nude mice received surgical orthotopic implantation (SOI) of the human pancreatic cancer cell line BxPC-3 expressing green fluorescent protein. An anti-carcinoembryonic antigen-related cell adhesion molecule (CEACAM) monoclonal antibody (6G5j) was conjugated to the 700-nm fluorescent dye IR700DyeDX (6G5j-IR700DX). Three weeks after SOI, 16 mice received 50 μg 6G5j-IR700DX via the tail vein 24 h before surgery and were randomized to two groups: FGS-only ( n = 8) and FGS + PIT ( n = 8). All tumors were imaged with the Pearl Trilogy imaging system and resected under the guidance of the FLARE imaging system. The FGS + PIT group received PIT of the post-surgical bed at an intensity of 150 mW/cm 2 for 30 min. Mice were sacrificed 4 weeks after initial surgery, and tumors were imaged with a Dino-Lite digital microscope, excised, and weighed. Results The 6G5j-IR700DX dye illuminated the orthotopic pancreatic tumors for FGS and PIT. The metastatic recurrence rate was 100.0% for FGS-only and 25.0% for FGS + PIT ( p = 0.007). The average total recurrent tumor weight was 2370.3 ± 1907.8 mg for FGS-only and 705.5 ± 1200.0 mg for FGS + PIT ( p = 0.039). Conclusions FGS and adjuvant PIT can be combined by using a single antibody–fluorophore conjugate to significantly reduce the frequency of pancreatic cancer recurrence.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1245/s10434-022-12466-4</identifier><identifier>PMID: 36057899</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Animals ; Antibodies ; Cancer therapies ; Carcinoembryonic antigen ; Cell adhesion molecules ; Dyes ; Fluorescent indicators ; Green fluorescent protein ; Humans ; Medicine ; Medicine &amp; Public Health ; Metastases ; Mice ; Mice, Nude ; Monoclonal antibodies ; Oncology ; Pancreatic cancer ; Pancreatic Neoplasms - surgery ; Surgery ; Surgical Oncology ; Translational Research ; Tumors</subject><ispartof>Annals of surgical oncology, 2023-01, Vol.30 (1), p.618-625</ispartof><rights>The Author(s) 2022</rights><rights>2022. The Author(s).</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-f8598bc2572fd704fbfeb79a95c708a3e7df60b5d4f500050b684bef708be013</citedby><cites>FETCH-LOGICAL-c404t-f8598bc2572fd704fbfeb79a95c708a3e7df60b5d4f500050b684bef708be013</cites><orcidid>0000-0002-0086-2159</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36057899$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nishino, Hiroto</creatorcontrib><creatorcontrib>Turner, Michael A.</creatorcontrib><creatorcontrib>Amirfakhri, Siamak</creatorcontrib><creatorcontrib>Lwin, Thinzar M.</creatorcontrib><creatorcontrib>Hosseini, Mojgan</creatorcontrib><creatorcontrib>Singer, Bernhard B.</creatorcontrib><creatorcontrib>Hoffman, Robert M.</creatorcontrib><creatorcontrib>Bouvet, Michael</creatorcontrib><title>Proof of Principle of Combining Fluorescence-Guided Surgery with Photoimmunotherapy to Improve the Outcome of Pancreatic Cancer Therapy in an Orthotopic Mouse Model</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><addtitle>Ann Surg Oncol</addtitle><description>Background Pancreatic cancer is a recalcitrant disease in which R0 resection is often not achieved owing to difficulty in visualization of the tumor margins and proximity of adjacent vessels. To improve outcomes, we have developed fluorescence-guided surgery (FGS) and photoimmunotherapy (PIT) using a fluorescent tumor-specific antibody. Methods Nude mice received surgical orthotopic implantation (SOI) of the human pancreatic cancer cell line BxPC-3 expressing green fluorescent protein. An anti-carcinoembryonic antigen-related cell adhesion molecule (CEACAM) monoclonal antibody (6G5j) was conjugated to the 700-nm fluorescent dye IR700DyeDX (6G5j-IR700DX). Three weeks after SOI, 16 mice received 50 μg 6G5j-IR700DX via the tail vein 24 h before surgery and were randomized to two groups: FGS-only ( n = 8) and FGS + PIT ( n = 8). All tumors were imaged with the Pearl Trilogy imaging system and resected under the guidance of the FLARE imaging system. The FGS + PIT group received PIT of the post-surgical bed at an intensity of 150 mW/cm 2 for 30 min. Mice were sacrificed 4 weeks after initial surgery, and tumors were imaged with a Dino-Lite digital microscope, excised, and weighed. Results The 6G5j-IR700DX dye illuminated the orthotopic pancreatic tumors for FGS and PIT. The metastatic recurrence rate was 100.0% for FGS-only and 25.0% for FGS + PIT ( p = 0.007). The average total recurrent tumor weight was 2370.3 ± 1907.8 mg for FGS-only and 705.5 ± 1200.0 mg for FGS + PIT ( p = 0.039). Conclusions FGS and adjuvant PIT can be combined by using a single antibody–fluorophore conjugate to significantly reduce the frequency of pancreatic cancer recurrence.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Cancer therapies</subject><subject>Carcinoembryonic antigen</subject><subject>Cell adhesion molecules</subject><subject>Dyes</subject><subject>Fluorescent indicators</subject><subject>Green fluorescent protein</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Metastases</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Monoclonal antibodies</subject><subject>Oncology</subject><subject>Pancreatic cancer</subject><subject>Pancreatic Neoplasms - surgery</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Translational Research</subject><subject>Tumors</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9Uk1v1DAQjRCIlsIf4IAsceESsB07Ti5IaEVLpaJdqXu3HGey6yqxg5202v_DD2W2u7SUQyXLno83zx7Py7L3jH5mXMgviVFRiJxynqNflrl4kZ0yiSFRVuwl2rSs8pqX8iR7k9INpUwVVL7OToqSSlXV9Wn2exVD6AiuVXTeurGHvbMIQ-O88xty3s8hQrLgLeQXs2uhJddz3EDckTs3bclqG6bghmH2YdpCNOOOTIFcDmMMt0AwRJbzZMNwz7sy3kYwk7NkgSZEsj7WOE-MJ8s47elGzP8McwLcW-jfZq860yd4dzzPsvX59_XiR361vLhcfLvKraBiyrtK1lVjuVS8axUVXdNBo2pTS6toZQpQbVfSRraik5RSSZuyEg10mGyAsuIs-3qgHedmgBZbnqLp9RjdYOJOB-P004x3W70Jt7pWvFRVhQSfjgQx_JohTXpw-HN9bzxgN5orWitRKE4R-vE_6E2Yo8fuECUU46xge0J-QNkYUorQPTyGUb3XgD5oQKMG9L0GtMCiD_-28VDyd-gIKA6AhCmPk3y8-xnaP17gwMs</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Nishino, Hiroto</creator><creator>Turner, Michael A.</creator><creator>Amirfakhri, Siamak</creator><creator>Lwin, Thinzar M.</creator><creator>Hosseini, Mojgan</creator><creator>Singer, Bernhard B.</creator><creator>Hoffman, Robert M.</creator><creator>Bouvet, Michael</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>C6C</scope><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>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-0086-2159</orcidid></search><sort><creationdate>20230101</creationdate><title>Proof of Principle of Combining Fluorescence-Guided Surgery with Photoimmunotherapy to Improve the Outcome of Pancreatic Cancer Therapy in an Orthotopic Mouse Model</title><author>Nishino, Hiroto ; Turner, Michael A. ; Amirfakhri, Siamak ; Lwin, Thinzar M. ; Hosseini, Mojgan ; Singer, Bernhard B. ; Hoffman, Robert M. ; Bouvet, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-f8598bc2572fd704fbfeb79a95c708a3e7df60b5d4f500050b684bef708be013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Cancer therapies</topic><topic>Carcinoembryonic antigen</topic><topic>Cell adhesion molecules</topic><topic>Dyes</topic><topic>Fluorescent indicators</topic><topic>Green fluorescent protein</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Metastases</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Monoclonal antibodies</topic><topic>Oncology</topic><topic>Pancreatic cancer</topic><topic>Pancreatic Neoplasms - surgery</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Translational Research</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nishino, Hiroto</creatorcontrib><creatorcontrib>Turner, Michael A.</creatorcontrib><creatorcontrib>Amirfakhri, Siamak</creatorcontrib><creatorcontrib>Lwin, Thinzar M.</creatorcontrib><creatorcontrib>Hosseini, Mojgan</creatorcontrib><creatorcontrib>Singer, Bernhard B.</creatorcontrib><creatorcontrib>Hoffman, Robert M.</creatorcontrib><creatorcontrib>Bouvet, Michael</creatorcontrib><collection>SpringerOpen</collection><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>ProQuest Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of surgical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nishino, Hiroto</au><au>Turner, Michael A.</au><au>Amirfakhri, Siamak</au><au>Lwin, Thinzar M.</au><au>Hosseini, Mojgan</au><au>Singer, Bernhard B.</au><au>Hoffman, Robert M.</au><au>Bouvet, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proof of Principle of Combining Fluorescence-Guided Surgery with Photoimmunotherapy to Improve the Outcome of Pancreatic Cancer Therapy in an Orthotopic Mouse Model</atitle><jtitle>Annals of surgical oncology</jtitle><stitle>Ann Surg Oncol</stitle><addtitle>Ann Surg Oncol</addtitle><date>2023-01-01</date><risdate>2023</risdate><volume>30</volume><issue>1</issue><spage>618</spage><epage>625</epage><pages>618-625</pages><issn>1068-9265</issn><eissn>1534-4681</eissn><abstract>Background Pancreatic cancer is a recalcitrant disease in which R0 resection is often not achieved owing to difficulty in visualization of the tumor margins and proximity of adjacent vessels. To improve outcomes, we have developed fluorescence-guided surgery (FGS) and photoimmunotherapy (PIT) using a fluorescent tumor-specific antibody. Methods Nude mice received surgical orthotopic implantation (SOI) of the human pancreatic cancer cell line BxPC-3 expressing green fluorescent protein. An anti-carcinoembryonic antigen-related cell adhesion molecule (CEACAM) monoclonal antibody (6G5j) was conjugated to the 700-nm fluorescent dye IR700DyeDX (6G5j-IR700DX). Three weeks after SOI, 16 mice received 50 μg 6G5j-IR700DX via the tail vein 24 h before surgery and were randomized to two groups: FGS-only ( n = 8) and FGS + PIT ( n = 8). All tumors were imaged with the Pearl Trilogy imaging system and resected under the guidance of the FLARE imaging system. The FGS + PIT group received PIT of the post-surgical bed at an intensity of 150 mW/cm 2 for 30 min. Mice were sacrificed 4 weeks after initial surgery, and tumors were imaged with a Dino-Lite digital microscope, excised, and weighed. Results The 6G5j-IR700DX dye illuminated the orthotopic pancreatic tumors for FGS and PIT. The metastatic recurrence rate was 100.0% for FGS-only and 25.0% for FGS + PIT ( p = 0.007). The average total recurrent tumor weight was 2370.3 ± 1907.8 mg for FGS-only and 705.5 ± 1200.0 mg for FGS + PIT ( p = 0.039). Conclusions FGS and adjuvant PIT can be combined by using a single antibody–fluorophore conjugate to significantly reduce the frequency of pancreatic cancer recurrence.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>36057899</pmid><doi>10.1245/s10434-022-12466-4</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-0086-2159</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1068-9265
ispartof Annals of surgical oncology, 2023-01, Vol.30 (1), p.618-625
issn 1068-9265
1534-4681
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9726788
source Springer Nature
subjects Animals
Antibodies
Cancer therapies
Carcinoembryonic antigen
Cell adhesion molecules
Dyes
Fluorescent indicators
Green fluorescent protein
Humans
Medicine
Medicine & Public Health
Metastases
Mice
Mice, Nude
Monoclonal antibodies
Oncology
Pancreatic cancer
Pancreatic Neoplasms - surgery
Surgery
Surgical Oncology
Translational Research
Tumors
title Proof of Principle of Combining Fluorescence-Guided Surgery with Photoimmunotherapy to Improve the Outcome of Pancreatic Cancer Therapy in an Orthotopic Mouse Model
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T00%3A02%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Proof%20of%20Principle%20of%20Combining%20Fluorescence-Guided%20Surgery%20with%20Photoimmunotherapy%20to%20Improve%20the%20Outcome%20of%20Pancreatic%20Cancer%20Therapy%20in%20an%20Orthotopic%20Mouse%20Model&rft.jtitle=Annals%20of%20surgical%20oncology&rft.au=Nishino,%20Hiroto&rft.date=2023-01-01&rft.volume=30&rft.issue=1&rft.spage=618&rft.epage=625&rft.pages=618-625&rft.issn=1068-9265&rft.eissn=1534-4681&rft_id=info:doi/10.1245/s10434-022-12466-4&rft_dat=%3Cproquest_pubme%3E2747121318%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c404t-f8598bc2572fd704fbfeb79a95c708a3e7df60b5d4f500050b684bef708be013%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2747121318&rft_id=info:pmid/36057899&rfr_iscdi=true