Evaluation of serum mid-infrared spectroscopy as new prognostic marker for first-line bevacizumab-based chemotherapy in metastatic colorectal cancer
Bevacizumab-based chemotherapy is a recommended first-line treatment for metastatic colorectal cancer (mCRC). Robust biomarkers with clinical practice applicability have not been identified for patients with this treatment. We aimed to evaluate the prognostic yield of serum mid-infrared spectroscopy...
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creator | Chautard, Romain Caulet, Morgane Bouché, Olivier Borg, Christophe Manfredi, Sylvain Capitain, Olivier Spano, Jean-Philippe Raoul, William Guéguinou, Maxime Herault, Olivier Ferru, Aurélie Pobel, Cédric Sire, Olivier Lecomte, Thierry |
description | Bevacizumab-based chemotherapy is a recommended first-line treatment for metastatic colorectal cancer (mCRC). Robust biomarkers with clinical practice applicability have not been identified for patients with this treatment. We aimed to evaluate the prognostic yield of serum mid-infrared spectroscopy (MIRS) on patients receiving first-line bevacizumab-based chemotherapy for mCRC.
We conducted an ancillary analysis from a multicentre prospective study (NCT00489697). All baseline serums were screened by attenuated total reflection method. Principal component analysis and unsupervised k-mean partitioning methods were performed blinded to all patients’ data. Endpoints were progression-free survival (PFS) and overall survival (OS).
From the 108 included patients, MIRS discriminated two prognostic groups. First group patients had significantly lower body mass index (p = 0.026) and albumin levels (p < 0.001), and higher levels of angiogenic markers, lactate dehydrogenase and carcinoembryonic antigen (p < 0.001). In univariate analysis, their OS and PFS were shorter with respective medians: 17.6 vs 27.9 months (p = 0.02) and 8.7 vs 11.3 months (p = 0.03). In multivariate analysis, PFS was significantly shorter (HR = 1.74, p = 0.025) with a similar trend for OS (HR = 1.69, p = 0.061).
By metabolomic fingerprinting, MIRS proves to be a promising prognostic tool for patients receiving first-line bevacizumab-based chemotherapy for mCRC. |
doi_str_mv | 10.1016/j.dld.2024.07.022 |
format | Article |
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We conducted an ancillary analysis from a multicentre prospective study (NCT00489697). All baseline serums were screened by attenuated total reflection method. Principal component analysis and unsupervised k-mean partitioning methods were performed blinded to all patients’ data. Endpoints were progression-free survival (PFS) and overall survival (OS).
From the 108 included patients, MIRS discriminated two prognostic groups. First group patients had significantly lower body mass index (p = 0.026) and albumin levels (p < 0.001), and higher levels of angiogenic markers, lactate dehydrogenase and carcinoembryonic antigen (p < 0.001). In univariate analysis, their OS and PFS were shorter with respective medians: 17.6 vs 27.9 months (p = 0.02) and 8.7 vs 11.3 months (p = 0.03). In multivariate analysis, PFS was significantly shorter (HR = 1.74, p = 0.025) with a similar trend for OS (HR = 1.69, p = 0.061).
By metabolomic fingerprinting, MIRS proves to be a promising prognostic tool for patients receiving first-line bevacizumab-based chemotherapy for mCRC.</description><identifier>ISSN: 1590-8658</identifier><identifier>ISSN: 1878-3562</identifier><identifier>EISSN: 1878-3562</identifier><identifier>DOI: 10.1016/j.dld.2024.07.022</identifier><identifier>PMID: 39164167</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Bevacizumab ; Bevacizumab - administration & dosage ; Bevacizumab - therapeutic use ; Biomarker ; Biomarkers, Tumor - blood ; Cancer ; Colorectal Neoplasms - blood ; Colorectal Neoplasms - drug therapy ; Colorectal Neoplasms - pathology ; Engineering Sciences ; Female ; Humans ; Life Sciences ; Male ; Metastatic colorectal cancer ; Mid-infrared spectroscopy ; Middle Aged ; Optics ; Photonic ; Prognosis ; Progression-Free Survival ; Prospective Studies</subject><ispartof>Digestive and liver disease, 2025-01, Vol.57 (1), p.141-148</ispartof><rights>2024</rights><rights>Copyright © 2024. Published by Elsevier Ltd.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2272-8aaa112d2838c40be5fba852be47ba9882a6708f0876b2b83b3035ea8419d1e13</cites><orcidid>0000-0001-5093-0212 ; 0000-0001-6030-5621 ; 0000-0001-6251-622X ; 0000-0002-5040-3372 ; 0000-0001-5439-7179 ; 0000-0002-3921-2479 ; 0000-0002-7419-1124</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1590865824008867$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39164167$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-tours.hal.science/hal-04888278$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Chautard, Romain</creatorcontrib><creatorcontrib>Caulet, Morgane</creatorcontrib><creatorcontrib>Bouché, Olivier</creatorcontrib><creatorcontrib>Borg, Christophe</creatorcontrib><creatorcontrib>Manfredi, Sylvain</creatorcontrib><creatorcontrib>Capitain, Olivier</creatorcontrib><creatorcontrib>Spano, Jean-Philippe</creatorcontrib><creatorcontrib>Raoul, William</creatorcontrib><creatorcontrib>Guéguinou, Maxime</creatorcontrib><creatorcontrib>Herault, Olivier</creatorcontrib><creatorcontrib>Ferru, Aurélie</creatorcontrib><creatorcontrib>Pobel, Cédric</creatorcontrib><creatorcontrib>Sire, Olivier</creatorcontrib><creatorcontrib>Lecomte, Thierry</creatorcontrib><title>Evaluation of serum mid-infrared spectroscopy as new prognostic marker for first-line bevacizumab-based chemotherapy in metastatic colorectal cancer</title><title>Digestive and liver disease</title><addtitle>Dig Liver Dis</addtitle><description>Bevacizumab-based chemotherapy is a recommended first-line treatment for metastatic colorectal cancer (mCRC). Robust biomarkers with clinical practice applicability have not been identified for patients with this treatment. We aimed to evaluate the prognostic yield of serum mid-infrared spectroscopy (MIRS) on patients receiving first-line bevacizumab-based chemotherapy for mCRC.
We conducted an ancillary analysis from a multicentre prospective study (NCT00489697). All baseline serums were screened by attenuated total reflection method. Principal component analysis and unsupervised k-mean partitioning methods were performed blinded to all patients’ data. Endpoints were progression-free survival (PFS) and overall survival (OS).
From the 108 included patients, MIRS discriminated two prognostic groups. First group patients had significantly lower body mass index (p = 0.026) and albumin levels (p < 0.001), and higher levels of angiogenic markers, lactate dehydrogenase and carcinoembryonic antigen (p < 0.001). In univariate analysis, their OS and PFS were shorter with respective medians: 17.6 vs 27.9 months (p = 0.02) and 8.7 vs 11.3 months (p = 0.03). In multivariate analysis, PFS was significantly shorter (HR = 1.74, p = 0.025) with a similar trend for OS (HR = 1.69, p = 0.061).
By metabolomic fingerprinting, MIRS proves to be a promising prognostic tool for patients receiving first-line bevacizumab-based chemotherapy for mCRC.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Bevacizumab</subject><subject>Bevacizumab - administration & dosage</subject><subject>Bevacizumab - therapeutic use</subject><subject>Biomarker</subject><subject>Biomarkers, Tumor - blood</subject><subject>Cancer</subject><subject>Colorectal Neoplasms - blood</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Engineering Sciences</subject><subject>Female</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Metastatic colorectal cancer</subject><subject>Mid-infrared spectroscopy</subject><subject>Middle Aged</subject><subject>Optics</subject><subject>Photonic</subject><subject>Prognosis</subject><subject>Progression-Free Survival</subject><subject>Prospective Studies</subject><issn>1590-8658</issn><issn>1878-3562</issn><issn>1878-3562</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc2OFCEURonROOPoA7gxLHVRJVA_UHE1mYyOSSdudE0ucMumpYoWqtqMz-EDS6XHWbogEHI45H4fIa85qznj_ftD7YKrBRNtzWTNhHhCLrmSqmq6Xjwt525gleo7dUFe5HxgTPC-Y8_JRTPwvuW9vCR_bk8QVlh8nGkcaca0TnTyrvLzmCCho_mIdkkx23i8p5DpjL_oMcXvc8yLt3SC9AMTHWNZPuWlCn5GavAE1v9eJzCVgVw0do9TXPaYoGj8TCdcIC-wKWwMMZVPIFALs8X0kjwbIWR89bBfkW8fb7_e3FW7L58-31zvKiuEFJUCAM6FE6pRtmUGu9GA6oTBVhoYlBLQS6ZGpmRvhFGNaVjTIaiWD44jb67Iu7N3D0Efky-z3OsIXt9d7_R2x1pVLFKdNvbtmS2z_1wxL3ry2WIIMGNcs27Y0HHZDrItKD-jtsSWE46Pbs70Vpw-6FKc3orTTOpSXHnz5kG_mgnd44t_TRXgwxnAEsjJY9LZeixpOb9lp130_9H_Becpq1M</recordid><startdate>202501</startdate><enddate>202501</enddate><creator>Chautard, Romain</creator><creator>Caulet, Morgane</creator><creator>Bouché, Olivier</creator><creator>Borg, Christophe</creator><creator>Manfredi, Sylvain</creator><creator>Capitain, Olivier</creator><creator>Spano, Jean-Philippe</creator><creator>Raoul, William</creator><creator>Guéguinou, Maxime</creator><creator>Herault, Olivier</creator><creator>Ferru, Aurélie</creator><creator>Pobel, Cédric</creator><creator>Sire, Olivier</creator><creator>Lecomte, Thierry</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-5093-0212</orcidid><orcidid>https://orcid.org/0000-0001-6030-5621</orcidid><orcidid>https://orcid.org/0000-0001-6251-622X</orcidid><orcidid>https://orcid.org/0000-0002-5040-3372</orcidid><orcidid>https://orcid.org/0000-0001-5439-7179</orcidid><orcidid>https://orcid.org/0000-0002-3921-2479</orcidid><orcidid>https://orcid.org/0000-0002-7419-1124</orcidid></search><sort><creationdate>202501</creationdate><title>Evaluation of serum mid-infrared spectroscopy as new prognostic marker for first-line bevacizumab-based chemotherapy in metastatic colorectal cancer</title><author>Chautard, Romain ; 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Robust biomarkers with clinical practice applicability have not been identified for patients with this treatment. We aimed to evaluate the prognostic yield of serum mid-infrared spectroscopy (MIRS) on patients receiving first-line bevacizumab-based chemotherapy for mCRC.
We conducted an ancillary analysis from a multicentre prospective study (NCT00489697). All baseline serums were screened by attenuated total reflection method. Principal component analysis and unsupervised k-mean partitioning methods were performed blinded to all patients’ data. Endpoints were progression-free survival (PFS) and overall survival (OS).
From the 108 included patients, MIRS discriminated two prognostic groups. First group patients had significantly lower body mass index (p = 0.026) and albumin levels (p < 0.001), and higher levels of angiogenic markers, lactate dehydrogenase and carcinoembryonic antigen (p < 0.001). In univariate analysis, their OS and PFS were shorter with respective medians: 17.6 vs 27.9 months (p = 0.02) and 8.7 vs 11.3 months (p = 0.03). In multivariate analysis, PFS was significantly shorter (HR = 1.74, p = 0.025) with a similar trend for OS (HR = 1.69, p = 0.061).
By metabolomic fingerprinting, MIRS proves to be a promising prognostic tool for patients receiving first-line bevacizumab-based chemotherapy for mCRC.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>39164167</pmid><doi>10.1016/j.dld.2024.07.022</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5093-0212</orcidid><orcidid>https://orcid.org/0000-0001-6030-5621</orcidid><orcidid>https://orcid.org/0000-0001-6251-622X</orcidid><orcidid>https://orcid.org/0000-0002-5040-3372</orcidid><orcidid>https://orcid.org/0000-0001-5439-7179</orcidid><orcidid>https://orcid.org/0000-0002-3921-2479</orcidid><orcidid>https://orcid.org/0000-0002-7419-1124</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Antineoplastic Combined Chemotherapy Protocols - therapeutic use Bevacizumab Bevacizumab - administration & dosage Bevacizumab - therapeutic use Biomarker Biomarkers, Tumor - blood Cancer Colorectal Neoplasms - blood Colorectal Neoplasms - drug therapy Colorectal Neoplasms - pathology Engineering Sciences Female Humans Life Sciences Male Metastatic colorectal cancer Mid-infrared spectroscopy Middle Aged Optics Photonic Prognosis Progression-Free Survival Prospective Studies |
title | Evaluation of serum mid-infrared spectroscopy as new prognostic marker for first-line bevacizumab-based chemotherapy in metastatic colorectal cancer |
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