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Inhibition of WEE1 Is Effective in TP53- and RAS-Mutant Metastatic Colorectal Cancer: A Randomized Trial (FOCUS4-C) Comparing Adavosertib (AZD1775) With Active Monitoring

Outcomes in RAS-mutant metastatic colorectal cancer (mCRC) remain poor and patients have limited therapeutic options. Adavosertib is the first small-molecule inhibitor of WEE1 kinase. We hypothesized that aberrations in DNA replication seen in mCRC with both RAS and TP53 mutations would sensitize tu...

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Autores principales: Seligmann, Jenny F., Fisher, David J., Brown, Louise C., Adams, Richard A., Graham, Janet, Quirke, Philip, Richman, Susan D., Butler, Rachel, Domingo, Enric, Blake, Andrew, Yates, Emma, Braun, Michael, Collinson, Fiona, Jones, Rob, Brown, Ewan, de Winton, Emma, Humphrey, Timothy C., Parmar, Mahesh, Kaplan, Richard, Wilson, Richard H., Seymour, Matthew, Maughan, Timothy S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601321/
https://www.ncbi.nlm.nih.gov/pubmed/34538072
http://dx.doi.org/10.1200/JCO.21.01435
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author Seligmann, Jenny F.
Fisher, David J.
Brown, Louise C.
Adams, Richard A.
Graham, Janet
Quirke, Philip
Richman, Susan D.
Butler, Rachel
Domingo, Enric
Blake, Andrew
Yates, Emma
Braun, Michael
Collinson, Fiona
Jones, Rob
Brown, Ewan
de Winton, Emma
Humphrey, Timothy C.
Parmar, Mahesh
Kaplan, Richard
Wilson, Richard H.
Seymour, Matthew
Maughan, Timothy S.
author_facet Seligmann, Jenny F.
Fisher, David J.
Brown, Louise C.
Adams, Richard A.
Graham, Janet
Quirke, Philip
Richman, Susan D.
Butler, Rachel
Domingo, Enric
Blake, Andrew
Yates, Emma
Braun, Michael
Collinson, Fiona
Jones, Rob
Brown, Ewan
de Winton, Emma
Humphrey, Timothy C.
Parmar, Mahesh
Kaplan, Richard
Wilson, Richard H.
Seymour, Matthew
Maughan, Timothy S.
author_sort Seligmann, Jenny F.
collection PubMed
description Outcomes in RAS-mutant metastatic colorectal cancer (mCRC) remain poor and patients have limited therapeutic options. Adavosertib is the first small-molecule inhibitor of WEE1 kinase. We hypothesized that aberrations in DNA replication seen in mCRC with both RAS and TP53 mutations would sensitize tumors to WEE1 inhibition. METHODS: Patients with newly diagnosed mCRC were registered into FOCUS4 and tested for TP53 and RAS mutations. Those with both mutations who were stable or responding after 16 weeks of chemotherapy were randomly assigned 2:1 between adavosertib and active monitoring (AM). Adavosertib (250 mg or 300 mg) was taken orally once on days 1-5 and days 8-12 of a 3-week cycle. The primary outcome was progression-free survival (PFS), with a target hazard ratio (HR) of 0.5 and 80% power with a one-sided 0.025 significance level. RESULTS: FOCUS4-C was conducted between April 2017 and Mar 2020 during which time 718 patients were registered; 247 (34%) were RAS/TP53-mutant. Sixty-nine patients were randomly assigned from 25 UK hospitals (adavosertib = 44; AM = 25). Adavosertib was associated with a PFS improvement over AM (median 3.61 v 1.87 months; HR = 0.35; 95% CI, 0.18 to 0.68; P = .0022). Overall survival (OS) was not improved with adavosertib versus AM (median 14.0 v 12.8 months; HR = 0.92; 95% CI, 0.44 to 1.94; P = .93). In prespecified subgroup analysis, adavosertib activity was greater in left-sided tumors (HR = 0.24; 95% CI, 0.11 to 0.51), versus right-sided (HR = 1.02; 95% CI, 0.41 to 2.56; interaction P = .043). Adavosertib was well-tolerated; grade 3 toxicities were diarrhea (9%), nausea (5%), and neutropenia (7%). CONCLUSION: In this phase II randomized trial, adavosertib improved PFS compared with AM and demonstrates potential as a well-tolerated therapy for RAS/TP53-mutant mCRC. Further testing is required in this sizable population of unmet need.
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spelling pubmed-86013212022-07-01 Inhibition of WEE1 Is Effective in TP53- and RAS-Mutant Metastatic Colorectal Cancer: A Randomized Trial (FOCUS4-C) Comparing Adavosertib (AZD1775) With Active Monitoring Seligmann, Jenny F. Fisher, David J. Brown, Louise C. Adams, Richard A. Graham, Janet Quirke, Philip Richman, Susan D. Butler, Rachel Domingo, Enric Blake, Andrew Yates, Emma Braun, Michael Collinson, Fiona Jones, Rob Brown, Ewan de Winton, Emma Humphrey, Timothy C. Parmar, Mahesh Kaplan, Richard Wilson, Richard H. Seymour, Matthew Maughan, Timothy S. J Clin Oncol ORIGINAL REPORTS Outcomes in RAS-mutant metastatic colorectal cancer (mCRC) remain poor and patients have limited therapeutic options. Adavosertib is the first small-molecule inhibitor of WEE1 kinase. We hypothesized that aberrations in DNA replication seen in mCRC with both RAS and TP53 mutations would sensitize tumors to WEE1 inhibition. METHODS: Patients with newly diagnosed mCRC were registered into FOCUS4 and tested for TP53 and RAS mutations. Those with both mutations who were stable or responding after 16 weeks of chemotherapy were randomly assigned 2:1 between adavosertib and active monitoring (AM). Adavosertib (250 mg or 300 mg) was taken orally once on days 1-5 and days 8-12 of a 3-week cycle. The primary outcome was progression-free survival (PFS), with a target hazard ratio (HR) of 0.5 and 80% power with a one-sided 0.025 significance level. RESULTS: FOCUS4-C was conducted between April 2017 and Mar 2020 during which time 718 patients were registered; 247 (34%) were RAS/TP53-mutant. Sixty-nine patients were randomly assigned from 25 UK hospitals (adavosertib = 44; AM = 25). Adavosertib was associated with a PFS improvement over AM (median 3.61 v 1.87 months; HR = 0.35; 95% CI, 0.18 to 0.68; P = .0022). Overall survival (OS) was not improved with adavosertib versus AM (median 14.0 v 12.8 months; HR = 0.92; 95% CI, 0.44 to 1.94; P = .93). In prespecified subgroup analysis, adavosertib activity was greater in left-sided tumors (HR = 0.24; 95% CI, 0.11 to 0.51), versus right-sided (HR = 1.02; 95% CI, 0.41 to 2.56; interaction P = .043). Adavosertib was well-tolerated; grade 3 toxicities were diarrhea (9%), nausea (5%), and neutropenia (7%). CONCLUSION: In this phase II randomized trial, adavosertib improved PFS compared with AM and demonstrates potential as a well-tolerated therapy for RAS/TP53-mutant mCRC. Further testing is required in this sizable population of unmet need. Wolters Kluwer Health 2021-11-20 2021-09-18 /pmc/articles/PMC8601321/ /pubmed/34538072 http://dx.doi.org/10.1200/JCO.21.01435 Text en © 2021 by American Society of Clinical Oncology https://creativecommons.org/licenses/by/4.0/Licensed under the Creative Commons Attribution 4.0 License: https://creativecommons.org/licenses/by/4.0/
spellingShingle ORIGINAL REPORTS
Seligmann, Jenny F.
Fisher, David J.
Brown, Louise C.
Adams, Richard A.
Graham, Janet
Quirke, Philip
Richman, Susan D.
Butler, Rachel
Domingo, Enric
Blake, Andrew
Yates, Emma
Braun, Michael
Collinson, Fiona
Jones, Rob
Brown, Ewan
de Winton, Emma
Humphrey, Timothy C.
Parmar, Mahesh
Kaplan, Richard
Wilson, Richard H.
Seymour, Matthew
Maughan, Timothy S.
Inhibition of WEE1 Is Effective in TP53- and RAS-Mutant Metastatic Colorectal Cancer: A Randomized Trial (FOCUS4-C) Comparing Adavosertib (AZD1775) With Active Monitoring
title Inhibition of WEE1 Is Effective in TP53- and RAS-Mutant Metastatic Colorectal Cancer: A Randomized Trial (FOCUS4-C) Comparing Adavosertib (AZD1775) With Active Monitoring
title_full Inhibition of WEE1 Is Effective in TP53- and RAS-Mutant Metastatic Colorectal Cancer: A Randomized Trial (FOCUS4-C) Comparing Adavosertib (AZD1775) With Active Monitoring
title_fullStr Inhibition of WEE1 Is Effective in TP53- and RAS-Mutant Metastatic Colorectal Cancer: A Randomized Trial (FOCUS4-C) Comparing Adavosertib (AZD1775) With Active Monitoring
title_full_unstemmed Inhibition of WEE1 Is Effective in TP53- and RAS-Mutant Metastatic Colorectal Cancer: A Randomized Trial (FOCUS4-C) Comparing Adavosertib (AZD1775) With Active Monitoring
title_short Inhibition of WEE1 Is Effective in TP53- and RAS-Mutant Metastatic Colorectal Cancer: A Randomized Trial (FOCUS4-C) Comparing Adavosertib (AZD1775) With Active Monitoring
title_sort inhibition of wee1 is effective in tp53- and ras-mutant metastatic colorectal cancer: a randomized trial (focus4-c) comparing adavosertib (azd1775) with active monitoring
topic ORIGINAL REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601321/
https://www.ncbi.nlm.nih.gov/pubmed/34538072
http://dx.doi.org/10.1200/JCO.21.01435
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