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Feasibility and therapeutic potential of [177Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma
Introduction The unique expression pattern of fibroblast activation protein (FAP) in stromal and tumor cells, particularly in sarcomas, and its absence in normal tissues, have positioned it as a promising theragnostic approach for the detection and treatment of various cancer types. The objective of...
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Published in: | European journal of nuclear medicine and molecular imaging 2024-12, Vol.52 (1), p.237-246 |
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creator | Banihashemian, Seyedeh Somayyeh Akbari, Mohammad Esmaeil Pirayesh, Elahe Divband, Ghasemali Abolhosseini Shahrnoy, Abdolghafar Nami, Reza Mazidi, Seyed Mohammad Nasiri, Meysam |
description | Introduction
The unique expression pattern of fibroblast activation protein (FAP) in stromal and tumor cells, particularly in sarcomas, and its absence in normal tissues, have positioned it as a promising theragnostic approach for the detection and treatment of various cancer types. The objective of this prospective study is to assess the feasibility, safety, biodistribution, and therapeutic efficacy of [
177
Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma.
Patients and Methods
Eight patients with advanced metastatic sarcoma, who were unresectable or had experienced disease recurrence following conventional treatments, underwent PTRT (peptide-targeted radionuclide therapy) using [
177
Lu]Lu-FAPI-2286. Prior to the treatment, confirmation of tumor uptake was obtained through [
68
Ga]Ga-FAPI-2286 PET/CT.
Results
After four cycles of PTRT with [
177
Lu]Lu-FAPI-2286 (6660–7400 MBq), with a 6-8-week interval between each cycle, no grade 3 or 4 side effects were observed in the patients, and the treatment was well tolerated by all participants. The results demonstrated a 52.37% reduction in the average volume of the primary tumor, accompanied by a significant decrease in SUV
max
and TBR of the metastatic lesions (29.67% and 43.66% respectively), especially in cases of lung metastasis. Furthermore, besides the improvement in physical capacity, there was a noticeable reduction in pain, an increase in overall survival, and enhanced satisfaction with the treatment reported by the patients.
Conclusion
[
177
Lu]Lu-FAPI-2286 PTRT, utilized for diverse cancer types, exhibited favorable tolerability in sarcoma patients, with minimal side effects, long-lasting retention of the radiopeptide within the tumor, and promising therapeutic effects. Preliminary findings of this prospective study need to be confirmed through further clinical trials. |
doi_str_mv | 10.1007/s00259-024-06795-7 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_3133051417</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3133051417</sourcerecordid><originalsourceid>FETCH-LOGICAL-c223t-2a3e1c9aaba178c20feb9984990a6e803f2c8eeb0d9fc2659e985e4833e0b8733</originalsourceid><addsrcrecordid>eNp9kE1P3DAQhq2qqHy0f6AHZKln07G9ie0jQl1AWqkc4ISQNXEmxWg3CbYD4t-TZSm99TQjzfO-Iz2MfZdwIgHMzwygKidALQTUxlXCfGIHspZOGLDu88duYJ8d5vwAIK2y7gvb1w5q0MYcsLgkzLGJ61heOPYtL_eUcKSpxMDHoVBfIq750PFbacxqultNYnl6dSmUsjWPPR-xxBnK_DmWe47tE_aBWr6hgrngtiVjCsMGv7K9DteZvr3PI3az_HV9diFWv88vz05XIiili1CoSQaH2KA0NijoqHHOLpwDrMmC7lSwRA20rguqrhw5W9HCak3QWKP1Efux6x3T8DhRLv5hmFI_v_Raag2VXEgzU2pHhTTknKjzY4obTC9egt_a9Tu7frbr3-z6bej4vXpqNtR-RP7qnAG9A_J86v9Q-vf7P7WvwZaEqw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3133051417</pqid></control><display><type>article</type><title>Feasibility and therapeutic potential of [177Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma</title><source>Springer Nature</source><creator>Banihashemian, Seyedeh Somayyeh ; Akbari, Mohammad Esmaeil ; Pirayesh, Elahe ; Divband, Ghasemali ; Abolhosseini Shahrnoy, Abdolghafar ; Nami, Reza ; Mazidi, Seyed Mohammad ; Nasiri, Meysam</creator><creatorcontrib>Banihashemian, Seyedeh Somayyeh ; Akbari, Mohammad Esmaeil ; Pirayesh, Elahe ; Divband, Ghasemali ; Abolhosseini Shahrnoy, Abdolghafar ; Nami, Reza ; Mazidi, Seyed Mohammad ; Nasiri, Meysam</creatorcontrib><description>Introduction
The unique expression pattern of fibroblast activation protein (FAP) in stromal and tumor cells, particularly in sarcomas, and its absence in normal tissues, have positioned it as a promising theragnostic approach for the detection and treatment of various cancer types. The objective of this prospective study is to assess the feasibility, safety, biodistribution, and therapeutic efficacy of [
177
Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma.
Patients and Methods
Eight patients with advanced metastatic sarcoma, who were unresectable or had experienced disease recurrence following conventional treatments, underwent PTRT (peptide-targeted radionuclide therapy) using [
177
Lu]Lu-FAPI-2286. Prior to the treatment, confirmation of tumor uptake was obtained through [
68
Ga]Ga-FAPI-2286 PET/CT.
Results
After four cycles of PTRT with [
177
Lu]Lu-FAPI-2286 (6660–7400 MBq), with a 6-8-week interval between each cycle, no grade 3 or 4 side effects were observed in the patients, and the treatment was well tolerated by all participants. The results demonstrated a 52.37% reduction in the average volume of the primary tumor, accompanied by a significant decrease in SUV
max
and TBR of the metastatic lesions (29.67% and 43.66% respectively), especially in cases of lung metastasis. Furthermore, besides the improvement in physical capacity, there was a noticeable reduction in pain, an increase in overall survival, and enhanced satisfaction with the treatment reported by the patients.
Conclusion
[
177
Lu]Lu-FAPI-2286 PTRT, utilized for diverse cancer types, exhibited favorable tolerability in sarcoma patients, with minimal side effects, long-lasting retention of the radiopeptide within the tumor, and promising therapeutic effects. Preliminary findings of this prospective study need to be confirmed through further clinical trials.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-024-06795-7</identifier><identifier>PMID: 39060377</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adult ; Aged ; Cancer ; Cardiology ; Cell activation ; Clinical trials ; Feasibility Studies ; Female ; Fibroblast activation protein ; Health services ; Humans ; Imaging ; Lutetium - therapeutic use ; Lutetium isotopes ; Male ; Medicine ; Medicine & Public Health ; Metastases ; Metastasis ; Middle Aged ; Neoplasm Metastasis ; Nuclear Medicine ; Oncology ; Original Article ; Orthopedics ; Patients ; Positron Emission Tomography Computed Tomography ; Radiation therapy ; Radioisotopes ; Radioisotopes - adverse effects ; Radioisotopes - therapeutic use ; Radiology ; Radiopharmaceuticals - therapeutic use ; Sarcoma ; Sarcoma - diagnostic imaging ; Sarcoma - radiotherapy ; Side effects ; Tissue Distribution ; Treatment Outcome ; Tumor cells ; Tumors</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2024-12, Vol.52 (1), p.237-246</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024. 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>2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c223t-2a3e1c9aaba178c20feb9984990a6e803f2c8eeb0d9fc2659e985e4833e0b8733</cites><orcidid>0000-0002-9938-3587</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27913,27914</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39060377$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Banihashemian, Seyedeh Somayyeh</creatorcontrib><creatorcontrib>Akbari, Mohammad Esmaeil</creatorcontrib><creatorcontrib>Pirayesh, Elahe</creatorcontrib><creatorcontrib>Divband, Ghasemali</creatorcontrib><creatorcontrib>Abolhosseini Shahrnoy, Abdolghafar</creatorcontrib><creatorcontrib>Nami, Reza</creatorcontrib><creatorcontrib>Mazidi, Seyed Mohammad</creatorcontrib><creatorcontrib>Nasiri, Meysam</creatorcontrib><title>Feasibility and therapeutic potential of [177Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma</title><title>European journal of nuclear medicine and molecular imaging</title><addtitle>Eur J Nucl Med Mol Imaging</addtitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><description>Introduction
The unique expression pattern of fibroblast activation protein (FAP) in stromal and tumor cells, particularly in sarcomas, and its absence in normal tissues, have positioned it as a promising theragnostic approach for the detection and treatment of various cancer types. The objective of this prospective study is to assess the feasibility, safety, biodistribution, and therapeutic efficacy of [
177
Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma.
Patients and Methods
Eight patients with advanced metastatic sarcoma, who were unresectable or had experienced disease recurrence following conventional treatments, underwent PTRT (peptide-targeted radionuclide therapy) using [
177
Lu]Lu-FAPI-2286. Prior to the treatment, confirmation of tumor uptake was obtained through [
68
Ga]Ga-FAPI-2286 PET/CT.
Results
After four cycles of PTRT with [
177
Lu]Lu-FAPI-2286 (6660–7400 MBq), with a 6-8-week interval between each cycle, no grade 3 or 4 side effects were observed in the patients, and the treatment was well tolerated by all participants. The results demonstrated a 52.37% reduction in the average volume of the primary tumor, accompanied by a significant decrease in SUV
max
and TBR of the metastatic lesions (29.67% and 43.66% respectively), especially in cases of lung metastasis. Furthermore, besides the improvement in physical capacity, there was a noticeable reduction in pain, an increase in overall survival, and enhanced satisfaction with the treatment reported by the patients.
Conclusion
[
177
Lu]Lu-FAPI-2286 PTRT, utilized for diverse cancer types, exhibited favorable tolerability in sarcoma patients, with minimal side effects, long-lasting retention of the radiopeptide within the tumor, and promising therapeutic effects. Preliminary findings of this prospective study need to be confirmed through further clinical trials.</description><subject>Adult</subject><subject>Aged</subject><subject>Cancer</subject><subject>Cardiology</subject><subject>Cell activation</subject><subject>Clinical trials</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>Fibroblast activation protein</subject><subject>Health services</subject><subject>Humans</subject><subject>Imaging</subject><subject>Lutetium - therapeutic use</subject><subject>Lutetium isotopes</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Neoplasm Metastasis</subject><subject>Nuclear Medicine</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Patients</subject><subject>Positron Emission Tomography Computed Tomography</subject><subject>Radiation therapy</subject><subject>Radioisotopes</subject><subject>Radioisotopes - adverse effects</subject><subject>Radioisotopes - therapeutic use</subject><subject>Radiology</subject><subject>Radiopharmaceuticals - therapeutic use</subject><subject>Sarcoma</subject><subject>Sarcoma - diagnostic imaging</subject><subject>Sarcoma - radiotherapy</subject><subject>Side effects</subject><subject>Tissue Distribution</subject><subject>Treatment Outcome</subject><subject>Tumor cells</subject><subject>Tumors</subject><issn>1619-7070</issn><issn>1619-7089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1P3DAQhq2qqHy0f6AHZKln07G9ie0jQl1AWqkc4ISQNXEmxWg3CbYD4t-TZSm99TQjzfO-Iz2MfZdwIgHMzwygKidALQTUxlXCfGIHspZOGLDu88duYJ8d5vwAIK2y7gvb1w5q0MYcsLgkzLGJ61heOPYtL_eUcKSpxMDHoVBfIq750PFbacxqultNYnl6dSmUsjWPPR-xxBnK_DmWe47tE_aBWr6hgrngtiVjCsMGv7K9DteZvr3PI3az_HV9diFWv88vz05XIiili1CoSQaH2KA0NijoqHHOLpwDrMmC7lSwRA20rguqrhw5W9HCak3QWKP1Efux6x3T8DhRLv5hmFI_v_Raag2VXEgzU2pHhTTknKjzY4obTC9egt_a9Tu7frbr3-z6bej4vXpqNtR-RP7qnAG9A_J86v9Q-vf7P7WvwZaEqw</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Banihashemian, Seyedeh Somayyeh</creator><creator>Akbari, Mohammad Esmaeil</creator><creator>Pirayesh, Elahe</creator><creator>Divband, Ghasemali</creator><creator>Abolhosseini Shahrnoy, Abdolghafar</creator><creator>Nami, Reza</creator><creator>Mazidi, Seyed Mohammad</creator><creator>Nasiri, Meysam</creator><general>Springer Berlin Heidelberg</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>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope><orcidid>https://orcid.org/0000-0002-9938-3587</orcidid></search><sort><creationdate>20241201</creationdate><title>Feasibility and therapeutic potential of [177Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma</title><author>Banihashemian, Seyedeh Somayyeh ; Akbari, Mohammad Esmaeil ; Pirayesh, Elahe ; Divband, Ghasemali ; Abolhosseini Shahrnoy, Abdolghafar ; Nami, Reza ; Mazidi, Seyed Mohammad ; Nasiri, Meysam</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c223t-2a3e1c9aaba178c20feb9984990a6e803f2c8eeb0d9fc2659e985e4833e0b8733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Cancer</topic><topic>Cardiology</topic><topic>Cell activation</topic><topic>Clinical trials</topic><topic>Feasibility Studies</topic><topic>Female</topic><topic>Fibroblast activation protein</topic><topic>Health services</topic><topic>Humans</topic><topic>Imaging</topic><topic>Lutetium - therapeutic use</topic><topic>Lutetium isotopes</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Neoplasm Metastasis</topic><topic>Nuclear Medicine</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Patients</topic><topic>Positron Emission Tomography Computed Tomography</topic><topic>Radiation therapy</topic><topic>Radioisotopes</topic><topic>Radioisotopes - adverse effects</topic><topic>Radioisotopes - therapeutic use</topic><topic>Radiology</topic><topic>Radiopharmaceuticals - therapeutic use</topic><topic>Sarcoma</topic><topic>Sarcoma - diagnostic imaging</topic><topic>Sarcoma - radiotherapy</topic><topic>Side effects</topic><topic>Tissue Distribution</topic><topic>Treatment Outcome</topic><topic>Tumor cells</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Banihashemian, Seyedeh Somayyeh</creatorcontrib><creatorcontrib>Akbari, Mohammad Esmaeil</creatorcontrib><creatorcontrib>Pirayesh, Elahe</creatorcontrib><creatorcontrib>Divband, Ghasemali</creatorcontrib><creatorcontrib>Abolhosseini Shahrnoy, Abdolghafar</creatorcontrib><creatorcontrib>Nami, Reza</creatorcontrib><creatorcontrib>Mazidi, Seyed Mohammad</creatorcontrib><creatorcontrib>Nasiri, Meysam</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>European journal of nuclear medicine and molecular imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Banihashemian, Seyedeh Somayyeh</au><au>Akbari, Mohammad Esmaeil</au><au>Pirayesh, Elahe</au><au>Divband, Ghasemali</au><au>Abolhosseini Shahrnoy, Abdolghafar</au><au>Nami, Reza</au><au>Mazidi, Seyed Mohammad</au><au>Nasiri, Meysam</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Feasibility and therapeutic potential of [177Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma</atitle><jtitle>European journal of nuclear medicine and molecular imaging</jtitle><stitle>Eur J Nucl Med Mol Imaging</stitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>52</volume><issue>1</issue><spage>237</spage><epage>246</epage><pages>237-246</pages><issn>1619-7070</issn><eissn>1619-7089</eissn><abstract>Introduction
The unique expression pattern of fibroblast activation protein (FAP) in stromal and tumor cells, particularly in sarcomas, and its absence in normal tissues, have positioned it as a promising theragnostic approach for the detection and treatment of various cancer types. The objective of this prospective study is to assess the feasibility, safety, biodistribution, and therapeutic efficacy of [
177
Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma.
Patients and Methods
Eight patients with advanced metastatic sarcoma, who were unresectable or had experienced disease recurrence following conventional treatments, underwent PTRT (peptide-targeted radionuclide therapy) using [
177
Lu]Lu-FAPI-2286. Prior to the treatment, confirmation of tumor uptake was obtained through [
68
Ga]Ga-FAPI-2286 PET/CT.
Results
After four cycles of PTRT with [
177
Lu]Lu-FAPI-2286 (6660–7400 MBq), with a 6-8-week interval between each cycle, no grade 3 or 4 side effects were observed in the patients, and the treatment was well tolerated by all participants. The results demonstrated a 52.37% reduction in the average volume of the primary tumor, accompanied by a significant decrease in SUV
max
and TBR of the metastatic lesions (29.67% and 43.66% respectively), especially in cases of lung metastasis. Furthermore, besides the improvement in physical capacity, there was a noticeable reduction in pain, an increase in overall survival, and enhanced satisfaction with the treatment reported by the patients.
Conclusion
[
177
Lu]Lu-FAPI-2286 PTRT, utilized for diverse cancer types, exhibited favorable tolerability in sarcoma patients, with minimal side effects, long-lasting retention of the radiopeptide within the tumor, and promising therapeutic effects. Preliminary findings of this prospective study need to be confirmed through further clinical trials.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>39060377</pmid><doi>10.1007/s00259-024-06795-7</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9938-3587</orcidid></addata></record> |
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subjects | Adult Aged Cancer Cardiology Cell activation Clinical trials Feasibility Studies Female Fibroblast activation protein Health services Humans Imaging Lutetium - therapeutic use Lutetium isotopes Male Medicine Medicine & Public Health Metastases Metastasis Middle Aged Neoplasm Metastasis Nuclear Medicine Oncology Original Article Orthopedics Patients Positron Emission Tomography Computed Tomography Radiation therapy Radioisotopes Radioisotopes - adverse effects Radioisotopes - therapeutic use Radiology Radiopharmaceuticals - therapeutic use Sarcoma Sarcoma - diagnostic imaging Sarcoma - radiotherapy Side effects Tissue Distribution Treatment Outcome Tumor cells Tumors |
title | Feasibility and therapeutic potential of [177Lu]Lu-FAPI-2286 in patients with advanced metastatic sarcoma |
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