Prospective experimental treatment of colorectal cancer patients based on organoid drug responses
Organoid technology has recently emerged as a powerful tool to assess drug sensitivity of individual patient tumors in vitro. Organoids may therefore represent a new avenue for precision medicine, as this circumvents many of the complexities associated with DNA- or transcriptional-profiling. The SEN...
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creator | Ooft, S.N. Weeber, F. Schipper, L. Dijkstra, K.K. McLean, C.M. Kaing, S. van de Haar, J. Prevoo, W. van Werkhoven, E. Snaebjornsson, P. Hoes, L.R. Chalabi, M. van der Velden, D. van Leerdam, M. Boot, H. Grootscholten, C. Huitema, A.D.R. Bloemendal, H.J. Cuppen, E. Voest, E.E. |
description | Organoid technology has recently emerged as a powerful tool to assess drug sensitivity of individual patient tumors in vitro. Organoids may therefore represent a new avenue for precision medicine, as this circumvents many of the complexities associated with DNA- or transcriptional-profiling.
The SENSOR trial was a single-arm, single-center, prospective intervention trial to evaluate the feasibility of patient-derived organoids to allocate patients for treatment with off-label or investigational agents. The primary endpoint was an objective response rate of ≥20%. Patients underwent a biopsy for culture before commencing their last round standard of care. Organoids were exposed to a panel of eight drugs and patients were treated after progression on standard-of-care treatment and when a clear signal of antitumor activity was identified in vitro.
Sixty-one patients were included and we generated 31 organoids of 54 eligible patients. Twenty-five cultures were subjected to drug screening and 19 organoids exhibited substantial responses to one or more drugs. Three patients underwent treatment with vistusertib and three with capivasertib. Despite drug sensitivity of organoids, patients did not demonstrate objective clinical responses to the recommended treatment.
Organoid technology had limited value as a tool for precision medicine in this patient population because a large fraction of patients could not undergo treatment or because the recommended treatment did not elicit an objective response. We identified several essential parameters, such as the culture success rate, clinical deterioration of patients during standard of care, and rational design of drug panels that need to be accounted for in organoid-guided clinical studies.
•The first prospective clinical trial that leverages tumor organoids to guide experimental treatment decisions.•Clinical implementation of tumor-organoid-guided treatment is challenging.•Patients that received organoid-informed treatment did not experience clinical benefit.•Organoid drug screening can distinguish differential drug responses in identical genetic genotypes. |
doi_str_mv | 10.1016/j.esmoop.2021.100103 |
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The SENSOR trial was a single-arm, single-center, prospective intervention trial to evaluate the feasibility of patient-derived organoids to allocate patients for treatment with off-label or investigational agents. The primary endpoint was an objective response rate of ≥20%. Patients underwent a biopsy for culture before commencing their last round standard of care. Organoids were exposed to a panel of eight drugs and patients were treated after progression on standard-of-care treatment and when a clear signal of antitumor activity was identified in vitro.
Sixty-one patients were included and we generated 31 organoids of 54 eligible patients. Twenty-five cultures were subjected to drug screening and 19 organoids exhibited substantial responses to one or more drugs. Three patients underwent treatment with vistusertib and three with capivasertib. Despite drug sensitivity of organoids, patients did not demonstrate objective clinical responses to the recommended treatment.
Organoid technology had limited value as a tool for precision medicine in this patient population because a large fraction of patients could not undergo treatment or because the recommended treatment did not elicit an objective response. We identified several essential parameters, such as the culture success rate, clinical deterioration of patients during standard of care, and rational design of drug panels that need to be accounted for in organoid-guided clinical studies.
•The first prospective clinical trial that leverages tumor organoids to guide experimental treatment decisions.•Clinical implementation of tumor-organoid-guided treatment is challenging.•Patients that received organoid-informed treatment did not experience clinical benefit.•Organoid drug screening can distinguish differential drug responses in identical genetic genotypes.</description><identifier>ISSN: 2059-7029</identifier><identifier>EISSN: 2059-7029</identifier><identifier>DOI: 10.1016/j.esmoop.2021.100103</identifier><identifier>PMID: 33887686</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>clinical trial ; colorectal cancer ; drug screening ; experimental treatment ; Original Research ; precision medicine ; tumor organoids</subject><ispartof>ESMO open, 2021-06, Vol.6 (3), p.100103, Article 100103</ispartof><rights>2021 The Author(s)</rights><rights>Copyright © 2021 The Author(s). Published by Elsevier Ltd.. All rights reserved.</rights><rights>2021 The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-d394fcc283259879ba6fc66adc81eff157eef42d219ea858240417910da19d693</citedby><cites>FETCH-LOGICAL-c463t-d394fcc283259879ba6fc66adc81eff157eef42d219ea858240417910da19d693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8086019/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8086019/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33887686$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ooft, S.N.</creatorcontrib><creatorcontrib>Weeber, F.</creatorcontrib><creatorcontrib>Schipper, L.</creatorcontrib><creatorcontrib>Dijkstra, K.K.</creatorcontrib><creatorcontrib>McLean, C.M.</creatorcontrib><creatorcontrib>Kaing, S.</creatorcontrib><creatorcontrib>van de Haar, J.</creatorcontrib><creatorcontrib>Prevoo, W.</creatorcontrib><creatorcontrib>van Werkhoven, E.</creatorcontrib><creatorcontrib>Snaebjornsson, P.</creatorcontrib><creatorcontrib>Hoes, L.R.</creatorcontrib><creatorcontrib>Chalabi, M.</creatorcontrib><creatorcontrib>van der Velden, D.</creatorcontrib><creatorcontrib>van Leerdam, M.</creatorcontrib><creatorcontrib>Boot, H.</creatorcontrib><creatorcontrib>Grootscholten, C.</creatorcontrib><creatorcontrib>Huitema, A.D.R.</creatorcontrib><creatorcontrib>Bloemendal, H.J.</creatorcontrib><creatorcontrib>Cuppen, E.</creatorcontrib><creatorcontrib>Voest, E.E.</creatorcontrib><title>Prospective experimental treatment of colorectal cancer patients based on organoid drug responses</title><title>ESMO open</title><addtitle>ESMO Open</addtitle><description>Organoid technology has recently emerged as a powerful tool to assess drug sensitivity of individual patient tumors in vitro. Organoids may therefore represent a new avenue for precision medicine, as this circumvents many of the complexities associated with DNA- or transcriptional-profiling.
The SENSOR trial was a single-arm, single-center, prospective intervention trial to evaluate the feasibility of patient-derived organoids to allocate patients for treatment with off-label or investigational agents. The primary endpoint was an objective response rate of ≥20%. Patients underwent a biopsy for culture before commencing their last round standard of care. Organoids were exposed to a panel of eight drugs and patients were treated after progression on standard-of-care treatment and when a clear signal of antitumor activity was identified in vitro.
Sixty-one patients were included and we generated 31 organoids of 54 eligible patients. Twenty-five cultures were subjected to drug screening and 19 organoids exhibited substantial responses to one or more drugs. Three patients underwent treatment with vistusertib and three with capivasertib. Despite drug sensitivity of organoids, patients did not demonstrate objective clinical responses to the recommended treatment.
Organoid technology had limited value as a tool for precision medicine in this patient population because a large fraction of patients could not undergo treatment or because the recommended treatment did not elicit an objective response. We identified several essential parameters, such as the culture success rate, clinical deterioration of patients during standard of care, and rational design of drug panels that need to be accounted for in organoid-guided clinical studies.
•The first prospective clinical trial that leverages tumor organoids to guide experimental treatment decisions.•Clinical implementation of tumor-organoid-guided treatment is challenging.•Patients that received organoid-informed treatment did not experience clinical benefit.•Organoid drug screening can distinguish differential drug responses in identical genetic genotypes.</description><subject>clinical trial</subject><subject>colorectal cancer</subject><subject>drug screening</subject><subject>experimental treatment</subject><subject>Original Research</subject><subject>precision medicine</subject><subject>tumor organoids</subject><issn>2059-7029</issn><issn>2059-7029</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kM9OwzAMxiMEYtPYGyCUF9hI0jZNLkho4p80CQ5wjrLEHZm6pkq6Cd6eVIUxLpxs2f4-2z-ELimZU0L59WYOcet9O2eE0VQilGQnaMxIIWclYfL0KB-haYwbkmbKPBX5ORplmRAlF3yM9EvwsQXTuT1g-GghuC00na5xF0B3fY59hY2vfUhTqW50YyDgVncuNSNe6QgW-wb7sNaNdxbbsFvjALH1TYR4gc4qXUeYfscJeru_e108zpbPD0-L2-XM5DzrZjaTeWUMExkrpCjlSvPKcK6tERSqihYlQJUzy6gELQrBcpLTUlJiNZWWy2yCbgbfdrfagjXpuKBr1aaHdPhUXjv1t9O4d7X2eyWI4IT2BvlgYBKSGKA6aClRPXW1UQN11VNXA_UkuzreexD9MP49DNL3ewdBRZPQGbCuR6qsd_9v-AJcRJi1</recordid><startdate>20210601</startdate><enddate>20210601</enddate><creator>Ooft, S.N.</creator><creator>Weeber, F.</creator><creator>Schipper, L.</creator><creator>Dijkstra, K.K.</creator><creator>McLean, C.M.</creator><creator>Kaing, S.</creator><creator>van de Haar, J.</creator><creator>Prevoo, W.</creator><creator>van Werkhoven, E.</creator><creator>Snaebjornsson, P.</creator><creator>Hoes, L.R.</creator><creator>Chalabi, M.</creator><creator>van der Velden, D.</creator><creator>van Leerdam, M.</creator><creator>Boot, H.</creator><creator>Grootscholten, C.</creator><creator>Huitema, A.D.R.</creator><creator>Bloemendal, H.J.</creator><creator>Cuppen, E.</creator><creator>Voest, E.E.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20210601</creationdate><title>Prospective experimental treatment of colorectal cancer patients based on organoid drug responses</title><author>Ooft, S.N. ; Weeber, F. ; Schipper, L. ; Dijkstra, K.K. ; McLean, C.M. ; Kaing, S. ; van de Haar, J. ; Prevoo, W. ; van Werkhoven, E. ; Snaebjornsson, P. ; Hoes, L.R. ; Chalabi, M. ; van der Velden, D. ; van Leerdam, M. ; Boot, H. ; Grootscholten, C. ; Huitema, A.D.R. ; Bloemendal, H.J. ; Cuppen, E. ; Voest, E.E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-d394fcc283259879ba6fc66adc81eff157eef42d219ea858240417910da19d693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>clinical trial</topic><topic>colorectal cancer</topic><topic>drug screening</topic><topic>experimental treatment</topic><topic>Original Research</topic><topic>precision medicine</topic><topic>tumor organoids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ooft, S.N.</creatorcontrib><creatorcontrib>Weeber, F.</creatorcontrib><creatorcontrib>Schipper, L.</creatorcontrib><creatorcontrib>Dijkstra, K.K.</creatorcontrib><creatorcontrib>McLean, C.M.</creatorcontrib><creatorcontrib>Kaing, S.</creatorcontrib><creatorcontrib>van de Haar, J.</creatorcontrib><creatorcontrib>Prevoo, W.</creatorcontrib><creatorcontrib>van Werkhoven, E.</creatorcontrib><creatorcontrib>Snaebjornsson, P.</creatorcontrib><creatorcontrib>Hoes, L.R.</creatorcontrib><creatorcontrib>Chalabi, M.</creatorcontrib><creatorcontrib>van der Velden, D.</creatorcontrib><creatorcontrib>van Leerdam, M.</creatorcontrib><creatorcontrib>Boot, H.</creatorcontrib><creatorcontrib>Grootscholten, C.</creatorcontrib><creatorcontrib>Huitema, A.D.R.</creatorcontrib><creatorcontrib>Bloemendal, H.J.</creatorcontrib><creatorcontrib>Cuppen, E.</creatorcontrib><creatorcontrib>Voest, E.E.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>ESMO open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ooft, S.N.</au><au>Weeber, F.</au><au>Schipper, L.</au><au>Dijkstra, K.K.</au><au>McLean, C.M.</au><au>Kaing, S.</au><au>van de Haar, J.</au><au>Prevoo, W.</au><au>van Werkhoven, E.</au><au>Snaebjornsson, P.</au><au>Hoes, L.R.</au><au>Chalabi, M.</au><au>van der Velden, D.</au><au>van Leerdam, M.</au><au>Boot, H.</au><au>Grootscholten, C.</au><au>Huitema, A.D.R.</au><au>Bloemendal, H.J.</au><au>Cuppen, E.</au><au>Voest, E.E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prospective experimental treatment of colorectal cancer patients based on organoid drug responses</atitle><jtitle>ESMO open</jtitle><addtitle>ESMO Open</addtitle><date>2021-06-01</date><risdate>2021</risdate><volume>6</volume><issue>3</issue><spage>100103</spage><pages>100103-</pages><artnum>100103</artnum><issn>2059-7029</issn><eissn>2059-7029</eissn><abstract>Organoid technology has recently emerged as a powerful tool to assess drug sensitivity of individual patient tumors in vitro. Organoids may therefore represent a new avenue for precision medicine, as this circumvents many of the complexities associated with DNA- or transcriptional-profiling.
The SENSOR trial was a single-arm, single-center, prospective intervention trial to evaluate the feasibility of patient-derived organoids to allocate patients for treatment with off-label or investigational agents. The primary endpoint was an objective response rate of ≥20%. Patients underwent a biopsy for culture before commencing their last round standard of care. Organoids were exposed to a panel of eight drugs and patients were treated after progression on standard-of-care treatment and when a clear signal of antitumor activity was identified in vitro.
Sixty-one patients were included and we generated 31 organoids of 54 eligible patients. Twenty-five cultures were subjected to drug screening and 19 organoids exhibited substantial responses to one or more drugs. Three patients underwent treatment with vistusertib and three with capivasertib. Despite drug sensitivity of organoids, patients did not demonstrate objective clinical responses to the recommended treatment.
Organoid technology had limited value as a tool for precision medicine in this patient population because a large fraction of patients could not undergo treatment or because the recommended treatment did not elicit an objective response. We identified several essential parameters, such as the culture success rate, clinical deterioration of patients during standard of care, and rational design of drug panels that need to be accounted for in organoid-guided clinical studies.
•The first prospective clinical trial that leverages tumor organoids to guide experimental treatment decisions.•Clinical implementation of tumor-organoid-guided treatment is challenging.•Patients that received organoid-informed treatment did not experience clinical benefit.•Organoid drug screening can distinguish differential drug responses in identical genetic genotypes.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>33887686</pmid><doi>10.1016/j.esmoop.2021.100103</doi><oa>free_for_read</oa></addata></record> |
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subjects | clinical trial colorectal cancer drug screening experimental treatment Original Research precision medicine tumor organoids |
title | Prospective experimental treatment of colorectal cancer patients based on organoid drug responses |
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