The paradox-breaking panRAF plus SRC family kinase inhibitor, CCT3833, is effective in mutant KRAS-driven cancers
KRAS is mutated in ∼90% of pancreatic ductal adenocarcinomas, ∼35% of colorectal cancers and ∼20% of non-small-cell lung cancers. There has been recent progress in targeting G12CKRAS specifically, but therapeutic options for other mutant forms of KRAS are limited, largely because the complexity of d...
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Veröffentlicht in: | Annals of oncology 2021-02, Vol.32 (2), p.269-278 |
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creator | Saturno, G. Lopes, F. Niculescu-Duvaz, I. Niculescu-Duvaz, D. Zambon, A. Davies, L. Johnson, L. Preece, N. Lee, R. Viros, A. Holovanchuk, D. Pedersen, M. McLeary, R. Lorigan, P. Dhomen, N. Fisher, C. Banerji, U. Dean, E. Krebs, M.G. Gore, M. Larkin, J. Marais, R. Springer, C. |
description | KRAS is mutated in ∼90% of pancreatic ductal adenocarcinomas, ∼35% of colorectal cancers and ∼20% of non-small-cell lung cancers. There has been recent progress in targeting G12CKRAS specifically, but therapeutic options for other mutant forms of KRAS are limited, largely because the complexity of downstream signaling and feedback mechanisms mean that targeting individual pathway components is ineffective.
The protein kinases RAF and SRC are validated therapeutic targets in KRAS-mutant pancreatic ductal adenocarcinomas, colorectal cancers and non-small-cell lung cancers and we show that both must be inhibited to block growth of these cancers. We describe CCT3833, a new drug that inhibits both RAF and SRC, which may be effective in KRAS-mutant cancers.
We show that CCT3833 inhibits RAF and SRC in KRAS-mutant tumors in vitro and in vivo, and that it inhibits tumor growth at well-tolerated doses in mice. CCT3833 has been evaluated in a phase I clinical trial (NCT02437227) and we report here that it significantly prolongs progression-free survival of a patient with a G12VKRAS spindle cell sarcoma who did not respond to a multikinase inhibitor and therefore had limited treatment options.
New drug CCT3833 elicits significant preclinical therapeutic efficacy in KRAS-mutant colorectal, lung and pancreatic tumor xenografts, demonstrating a treatment option for several areas of unmet clinical need. Based on these preclinical data and the phase I clinical unconfirmed response in a patient with KRAS-mutant spindle cell sarcoma, CCT3833 requires further evaluation in patients with other KRAS-mutant cancers.
•We synthesized new drug, CCT3833, that inhibits both RAF and SRC, and so may be effective in KRAS-mutant cancers.•CCT3833 inhibits both signaling pathways in vitro and in vivo, inhibits tumor growth and leads to regressions in mice.•CCT3833 significantly prolonged progression-free survival of a patient with a G12VKRAS spindle cell sarcoma.•CCT3833 is a potential treatment option for several areas of unmet clinical need. |
doi_str_mv | 10.1016/j.annonc.2020.10.483 |
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The protein kinases RAF and SRC are validated therapeutic targets in KRAS-mutant pancreatic ductal adenocarcinomas, colorectal cancers and non-small-cell lung cancers and we show that both must be inhibited to block growth of these cancers. We describe CCT3833, a new drug that inhibits both RAF and SRC, which may be effective in KRAS-mutant cancers.
We show that CCT3833 inhibits RAF and SRC in KRAS-mutant tumors in vitro and in vivo, and that it inhibits tumor growth at well-tolerated doses in mice. CCT3833 has been evaluated in a phase I clinical trial (NCT02437227) and we report here that it significantly prolongs progression-free survival of a patient with a G12VKRAS spindle cell sarcoma who did not respond to a multikinase inhibitor and therefore had limited treatment options.
New drug CCT3833 elicits significant preclinical therapeutic efficacy in KRAS-mutant colorectal, lung and pancreatic tumor xenografts, demonstrating a treatment option for several areas of unmet clinical need. Based on these preclinical data and the phase I clinical unconfirmed response in a patient with KRAS-mutant spindle cell sarcoma, CCT3833 requires further evaluation in patients with other KRAS-mutant cancers.
•We synthesized new drug, CCT3833, that inhibits both RAF and SRC, and so may be effective in KRAS-mutant cancers.•CCT3833 inhibits both signaling pathways in vitro and in vivo, inhibits tumor growth and leads to regressions in mice.•CCT3833 significantly prolonged progression-free survival of a patient with a G12VKRAS spindle cell sarcoma.•CCT3833 is a potential treatment option for several areas of unmet clinical need.</description><identifier>ISSN: 0923-7534</identifier><identifier>EISSN: 1569-8041</identifier><identifier>DOI: 10.1016/j.annonc.2020.10.483</identifier><identifier>PMID: 33130216</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - genetics ; Cell Line, Tumor ; Cell Proliferation ; CRC ; Humans ; KRAS ; Lung Neoplasms - drug therapy ; Lung Neoplasms - genetics ; Mice ; Mutation ; NSCLC ; Original ; panRAF/SRC inhibitor ; PDAC ; Protein Kinase Inhibitors - pharmacology ; Protein Kinase Inhibitors - therapeutic use ; Proto-Oncogene Proteins p21(ras) - genetics ; src-Family Kinases - genetics</subject><ispartof>Annals of oncology, 2021-02, Vol.32 (2), p.269-278</ispartof><rights>2020 The Authors</rights><rights>Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><rights>2020 The Authors 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-c4df1989ebe65c1c6918ecd9812c7b9cc4369aa35320ebb91e4809c477608263</citedby><cites>FETCH-LOGICAL-c463t-c4df1989ebe65c1c6918ecd9812c7b9cc4369aa35320ebb91e4809c477608263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33130216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saturno, G.</creatorcontrib><creatorcontrib>Lopes, F.</creatorcontrib><creatorcontrib>Niculescu-Duvaz, I.</creatorcontrib><creatorcontrib>Niculescu-Duvaz, D.</creatorcontrib><creatorcontrib>Zambon, A.</creatorcontrib><creatorcontrib>Davies, L.</creatorcontrib><creatorcontrib>Johnson, L.</creatorcontrib><creatorcontrib>Preece, N.</creatorcontrib><creatorcontrib>Lee, R.</creatorcontrib><creatorcontrib>Viros, A.</creatorcontrib><creatorcontrib>Holovanchuk, D.</creatorcontrib><creatorcontrib>Pedersen, M.</creatorcontrib><creatorcontrib>McLeary, R.</creatorcontrib><creatorcontrib>Lorigan, P.</creatorcontrib><creatorcontrib>Dhomen, N.</creatorcontrib><creatorcontrib>Fisher, C.</creatorcontrib><creatorcontrib>Banerji, U.</creatorcontrib><creatorcontrib>Dean, E.</creatorcontrib><creatorcontrib>Krebs, M.G.</creatorcontrib><creatorcontrib>Gore, M.</creatorcontrib><creatorcontrib>Larkin, J.</creatorcontrib><creatorcontrib>Marais, R.</creatorcontrib><creatorcontrib>Springer, C.</creatorcontrib><title>The paradox-breaking panRAF plus SRC family kinase inhibitor, CCT3833, is effective in mutant KRAS-driven cancers</title><title>Annals of oncology</title><addtitle>Ann Oncol</addtitle><description>KRAS is mutated in ∼90% of pancreatic ductal adenocarcinomas, ∼35% of colorectal cancers and ∼20% of non-small-cell lung cancers. There has been recent progress in targeting G12CKRAS specifically, but therapeutic options for other mutant forms of KRAS are limited, largely because the complexity of downstream signaling and feedback mechanisms mean that targeting individual pathway components is ineffective.
The protein kinases RAF and SRC are validated therapeutic targets in KRAS-mutant pancreatic ductal adenocarcinomas, colorectal cancers and non-small-cell lung cancers and we show that both must be inhibited to block growth of these cancers. We describe CCT3833, a new drug that inhibits both RAF and SRC, which may be effective in KRAS-mutant cancers.
We show that CCT3833 inhibits RAF and SRC in KRAS-mutant tumors in vitro and in vivo, and that it inhibits tumor growth at well-tolerated doses in mice. CCT3833 has been evaluated in a phase I clinical trial (NCT02437227) and we report here that it significantly prolongs progression-free survival of a patient with a G12VKRAS spindle cell sarcoma who did not respond to a multikinase inhibitor and therefore had limited treatment options.
New drug CCT3833 elicits significant preclinical therapeutic efficacy in KRAS-mutant colorectal, lung and pancreatic tumor xenografts, demonstrating a treatment option for several areas of unmet clinical need. Based on these preclinical data and the phase I clinical unconfirmed response in a patient with KRAS-mutant spindle cell sarcoma, CCT3833 requires further evaluation in patients with other KRAS-mutant cancers.
•We synthesized new drug, CCT3833, that inhibits both RAF and SRC, and so may be effective in KRAS-mutant cancers.•CCT3833 inhibits both signaling pathways in vitro and in vivo, inhibits tumor growth and leads to regressions in mice.•CCT3833 significantly prolonged progression-free survival of a patient with a G12VKRAS spindle cell sarcoma.•CCT3833 is a potential treatment option for several areas of unmet clinical need.</description><subject>Animals</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>CRC</subject><subject>Humans</subject><subject>KRAS</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - genetics</subject><subject>Mice</subject><subject>Mutation</subject><subject>NSCLC</subject><subject>Original</subject><subject>panRAF/SRC inhibitor</subject><subject>PDAC</subject><subject>Protein Kinase Inhibitors - pharmacology</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Proto-Oncogene Proteins p21(ras) - genetics</subject><subject>src-Family Kinases - genetics</subject><issn>0923-7534</issn><issn>1569-8041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UV2L1DAUDaK44-o_EMmjD9sxX02TF2EorooLwuy8hzS93cnYprNJO7j_3pRZV30RQgLnnnvuzTkIvaVkTQmVHw5rG8IY3JoRtkBrofgztKKl1IUigj5HK6IZL6qSiwv0KqUDIURqpl-iC84pJ4zKFbrf7QEfbbTt-LNoItgfPtxlIGw31_jYzwnfbmvc2cH3DzjXbALsw943fhrjFa7rHVecX2GfMHQduMmfFgIe5smGCX_bbm6LNmYwYGeDg5heoxed7RO8eXwv0e76067-Utx8__y13twUTkg-5bvtqFYaGpClo05qqsC1WlHmqkY7J7jU1vKSMwJNoykIRbQTVSWJYpJfoo9n2ePcDNA6CFO0vTlGP9j4YEbrzb-V4PfmbjyZSnGdTxZ4_ygQx_sZ0mQGnxz0vQ0wzskwUUolK85Epooz1cUxpQjd0xhKzBKWOZhzWGYJa0FzWLnt3d8rPjX9TufPHyD7dPIQTXIesoutj9lq047-_xN-AefDp7o</recordid><startdate>202102</startdate><enddate>202102</enddate><creator>Saturno, G.</creator><creator>Lopes, F.</creator><creator>Niculescu-Duvaz, I.</creator><creator>Niculescu-Duvaz, D.</creator><creator>Zambon, A.</creator><creator>Davies, L.</creator><creator>Johnson, L.</creator><creator>Preece, N.</creator><creator>Lee, R.</creator><creator>Viros, A.</creator><creator>Holovanchuk, D.</creator><creator>Pedersen, M.</creator><creator>McLeary, R.</creator><creator>Lorigan, P.</creator><creator>Dhomen, N.</creator><creator>Fisher, C.</creator><creator>Banerji, U.</creator><creator>Dean, E.</creator><creator>Krebs, M.G.</creator><creator>Gore, M.</creator><creator>Larkin, J.</creator><creator>Marais, R.</creator><creator>Springer, C.</creator><general>Elsevier Ltd</general><general>Oxford University Press</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>5PM</scope></search><sort><creationdate>202102</creationdate><title>The paradox-breaking panRAF plus SRC family kinase inhibitor, CCT3833, is effective in mutant KRAS-driven cancers</title><author>Saturno, G. ; Lopes, F. ; Niculescu-Duvaz, I. ; Niculescu-Duvaz, D. ; Zambon, A. ; Davies, L. ; Johnson, L. ; Preece, N. ; Lee, R. ; Viros, A. ; Holovanchuk, D. ; Pedersen, M. ; McLeary, R. ; Lorigan, P. ; Dhomen, N. ; Fisher, C. ; Banerji, U. ; Dean, E. ; Krebs, M.G. ; Gore, M. ; Larkin, J. ; Marais, R. ; Springer, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-c4df1989ebe65c1c6918ecd9812c7b9cc4369aa35320ebb91e4809c477608263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>CRC</topic><topic>Humans</topic><topic>KRAS</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - genetics</topic><topic>Mice</topic><topic>Mutation</topic><topic>NSCLC</topic><topic>Original</topic><topic>panRAF/SRC inhibitor</topic><topic>PDAC</topic><topic>Protein Kinase Inhibitors - pharmacology</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Proto-Oncogene Proteins p21(ras) - genetics</topic><topic>src-Family Kinases - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saturno, G.</creatorcontrib><creatorcontrib>Lopes, F.</creatorcontrib><creatorcontrib>Niculescu-Duvaz, I.</creatorcontrib><creatorcontrib>Niculescu-Duvaz, D.</creatorcontrib><creatorcontrib>Zambon, A.</creatorcontrib><creatorcontrib>Davies, L.</creatorcontrib><creatorcontrib>Johnson, L.</creatorcontrib><creatorcontrib>Preece, N.</creatorcontrib><creatorcontrib>Lee, R.</creatorcontrib><creatorcontrib>Viros, A.</creatorcontrib><creatorcontrib>Holovanchuk, D.</creatorcontrib><creatorcontrib>Pedersen, M.</creatorcontrib><creatorcontrib>McLeary, R.</creatorcontrib><creatorcontrib>Lorigan, P.</creatorcontrib><creatorcontrib>Dhomen, N.</creatorcontrib><creatorcontrib>Fisher, C.</creatorcontrib><creatorcontrib>Banerji, U.</creatorcontrib><creatorcontrib>Dean, E.</creatorcontrib><creatorcontrib>Krebs, M.G.</creatorcontrib><creatorcontrib>Gore, M.</creatorcontrib><creatorcontrib>Larkin, J.</creatorcontrib><creatorcontrib>Marais, R.</creatorcontrib><creatorcontrib>Springer, C.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saturno, G.</au><au>Lopes, F.</au><au>Niculescu-Duvaz, I.</au><au>Niculescu-Duvaz, D.</au><au>Zambon, A.</au><au>Davies, L.</au><au>Johnson, L.</au><au>Preece, N.</au><au>Lee, R.</au><au>Viros, A.</au><au>Holovanchuk, D.</au><au>Pedersen, M.</au><au>McLeary, R.</au><au>Lorigan, P.</au><au>Dhomen, N.</au><au>Fisher, C.</au><au>Banerji, U.</au><au>Dean, E.</au><au>Krebs, M.G.</au><au>Gore, M.</au><au>Larkin, J.</au><au>Marais, R.</au><au>Springer, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The paradox-breaking panRAF plus SRC family kinase inhibitor, CCT3833, is effective in mutant KRAS-driven cancers</atitle><jtitle>Annals of oncology</jtitle><addtitle>Ann Oncol</addtitle><date>2021-02</date><risdate>2021</risdate><volume>32</volume><issue>2</issue><spage>269</spage><epage>278</epage><pages>269-278</pages><issn>0923-7534</issn><eissn>1569-8041</eissn><abstract>KRAS is mutated in ∼90% of pancreatic ductal adenocarcinomas, ∼35% of colorectal cancers and ∼20% of non-small-cell lung cancers. There has been recent progress in targeting G12CKRAS specifically, but therapeutic options for other mutant forms of KRAS are limited, largely because the complexity of downstream signaling and feedback mechanisms mean that targeting individual pathway components is ineffective.
The protein kinases RAF and SRC are validated therapeutic targets in KRAS-mutant pancreatic ductal adenocarcinomas, colorectal cancers and non-small-cell lung cancers and we show that both must be inhibited to block growth of these cancers. We describe CCT3833, a new drug that inhibits both RAF and SRC, which may be effective in KRAS-mutant cancers.
We show that CCT3833 inhibits RAF and SRC in KRAS-mutant tumors in vitro and in vivo, and that it inhibits tumor growth at well-tolerated doses in mice. CCT3833 has been evaluated in a phase I clinical trial (NCT02437227) and we report here that it significantly prolongs progression-free survival of a patient with a G12VKRAS spindle cell sarcoma who did not respond to a multikinase inhibitor and therefore had limited treatment options.
New drug CCT3833 elicits significant preclinical therapeutic efficacy in KRAS-mutant colorectal, lung and pancreatic tumor xenografts, demonstrating a treatment option for several areas of unmet clinical need. Based on these preclinical data and the phase I clinical unconfirmed response in a patient with KRAS-mutant spindle cell sarcoma, CCT3833 requires further evaluation in patients with other KRAS-mutant cancers.
•We synthesized new drug, CCT3833, that inhibits both RAF and SRC, and so may be effective in KRAS-mutant cancers.•CCT3833 inhibits both signaling pathways in vitro and in vivo, inhibits tumor growth and leads to regressions in mice.•CCT3833 significantly prolonged progression-free survival of a patient with a G12VKRAS spindle cell sarcoma.•CCT3833 is a potential treatment option for several areas of unmet clinical need.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>33130216</pmid><doi>10.1016/j.annonc.2020.10.483</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - genetics Cell Line, Tumor Cell Proliferation CRC Humans KRAS Lung Neoplasms - drug therapy Lung Neoplasms - genetics Mice Mutation NSCLC Original panRAF/SRC inhibitor PDAC Protein Kinase Inhibitors - pharmacology Protein Kinase Inhibitors - therapeutic use Proto-Oncogene Proteins p21(ras) - genetics src-Family Kinases - genetics |
title | The paradox-breaking panRAF plus SRC family kinase inhibitor, CCT3833, is effective in mutant KRAS-driven cancers |
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