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Safety and efficacy of HSP90 inhibitor ganetespib for neoadjuvant treatment of stage II/III breast cancer

HSP90 inhibitors destabilize oncoproteins associated with cell cycle, angiogenesis, RAS-MAPK activity, histone modification, kinases and growth factors. We evaluated the HSP90-inhibitor ganetespib in combination with standard chemotherapy in patients with high-risk early-stage breast cancer. I-SPY2...

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Autores principales: Lang, Julie E., Forero-Torres, Andres, Yee, Douglas, Yau, Christina, Wolf, Denise, Park, John, Parker, Barbara A., Chien, A. Jo, Wallace, Anne M., Murthy, Rashmi, Albain, Kathy S., Ellis, Erin D., Beckwith, Heather, Haley, Barbara B., Elias, Anthony D., Boughey, Judy C., Yung, Rachel L., Isaacs, Claudine, Clark, Amy S., Han, Hyo S., Nanda, Rita, Khan, Qamar J., Edmiston, Kristen K., Stringer-Reasor, Erica, Price, Elissa, Joe, Bonnie, Liu, Minetta C., Brown-Swigart, Lamorna, Petricoin, Emanuel F., Wulfkuhle, Julia D., Buxton, Meredith, Clennell, Julia L., Sanil, Ashish, Berry, Scott, Asare, Smita M., Wilson, Amy, Hirst, Gillian L., Singhrao, Ruby, Asare, Adam L., Matthews, Jeffrey B., Melisko, Michelle, Perlmutter, Jane, Rugo, Hope S., Symmans, W. Fraser, van ‘t Veer, Laura J., Hylton, Nola M., DeMichele, Angela M., Berry, Donald A., Esserman, Laura J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715670/
https://www.ncbi.nlm.nih.gov/pubmed/36456573
http://dx.doi.org/10.1038/s41523-022-00493-z
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author Lang, Julie E.
Forero-Torres, Andres
Yee, Douglas
Yau, Christina
Wolf, Denise
Park, John
Parker, Barbara A.
Chien, A. Jo
Wallace, Anne M.
Murthy, Rashmi
Albain, Kathy S.
Ellis, Erin D.
Beckwith, Heather
Haley, Barbara B.
Elias, Anthony D.
Boughey, Judy C.
Yung, Rachel L.
Isaacs, Claudine
Clark, Amy S.
Han, Hyo S.
Nanda, Rita
Khan, Qamar J.
Edmiston, Kristen K.
Stringer-Reasor, Erica
Price, Elissa
Joe, Bonnie
Liu, Minetta C.
Brown-Swigart, Lamorna
Petricoin, Emanuel F.
Wulfkuhle, Julia D.
Buxton, Meredith
Clennell, Julia L.
Sanil, Ashish
Berry, Scott
Asare, Smita M.
Wilson, Amy
Hirst, Gillian L.
Singhrao, Ruby
Asare, Adam L.
Matthews, Jeffrey B.
Melisko, Michelle
Perlmutter, Jane
Rugo, Hope S.
Symmans, W. Fraser
van ‘t Veer, Laura J.
Hylton, Nola M.
DeMichele, Angela M.
Berry, Donald A.
Esserman, Laura J.
author_facet Lang, Julie E.
Forero-Torres, Andres
Yee, Douglas
Yau, Christina
Wolf, Denise
Park, John
Parker, Barbara A.
Chien, A. Jo
Wallace, Anne M.
Murthy, Rashmi
Albain, Kathy S.
Ellis, Erin D.
Beckwith, Heather
Haley, Barbara B.
Elias, Anthony D.
Boughey, Judy C.
Yung, Rachel L.
Isaacs, Claudine
Clark, Amy S.
Han, Hyo S.
Nanda, Rita
Khan, Qamar J.
Edmiston, Kristen K.
Stringer-Reasor, Erica
Price, Elissa
Joe, Bonnie
Liu, Minetta C.
Brown-Swigart, Lamorna
Petricoin, Emanuel F.
Wulfkuhle, Julia D.
Buxton, Meredith
Clennell, Julia L.
Sanil, Ashish
Berry, Scott
Asare, Smita M.
Wilson, Amy
Hirst, Gillian L.
Singhrao, Ruby
Asare, Adam L.
Matthews, Jeffrey B.
Melisko, Michelle
Perlmutter, Jane
Rugo, Hope S.
Symmans, W. Fraser
van ‘t Veer, Laura J.
Hylton, Nola M.
DeMichele, Angela M.
Berry, Donald A.
Esserman, Laura J.
author_sort Lang, Julie E.
collection PubMed
description HSP90 inhibitors destabilize oncoproteins associated with cell cycle, angiogenesis, RAS-MAPK activity, histone modification, kinases and growth factors. We evaluated the HSP90-inhibitor ganetespib in combination with standard chemotherapy in patients with high-risk early-stage breast cancer. I-SPY2 is a multicenter, phase II adaptively randomized neoadjuvant (NAC) clinical trial enrolling patients with stage II-III breast cancer with tumors 2.5 cm or larger on the basis of hormone receptors (HR), HER2 and Mammaprint status. Multiple novel investigational agents plus standard chemotherapy are evaluated in parallel for the primary endpoint of pathologic complete response (pCR). Patients with HER2-negative breast cancer were eligible for randomization to ganetespib from October 2014 to October 2015. Of 233 women included in the final analysis, 140 were randomized to the standard NAC control; 93 were randomized to receive 150 mg/m(2) ganetespib every 3 weeks with weekly paclitaxel over 12 weeks, followed by AC. Arms were balanced for hormone receptor status (51–52% HR-positive). Ganetespib did not graduate in any of the biomarker signatures studied before reaching maximum enrollment. Final estimated pCR rates were 26% vs. 18% HER2-negative, 38% vs. 22% HR-negative/HER2-negative, and 15% vs. 14% HR-positive/HER2-negative for ganetespib vs control, respectively. The predicted probability of success in phase 3 testing was 47% HER2-negative, 72% HR-negative/HER2-negative, and 19% HR-positive/HER2-negative. Ganetespib added to standard therapy is unlikely to yield substantially higher pCR rates in HER2-negative breast cancer compared to standard NAC, and neither HSP90 pathway nor replicative stress expression markers predicted response. HSP90 inhibitors remain of limited clinical interest in breast cancer, potentially in other clinical settings such as HER2-positive disease or in combination with anti-PD1 neoadjuvant chemotherapy in triple negative breast cancer. Trial registration: www.clinicaltrials.gov/ct2/show/NCT01042379
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spelling pubmed-97156702022-12-03 Safety and efficacy of HSP90 inhibitor ganetespib for neoadjuvant treatment of stage II/III breast cancer Lang, Julie E. Forero-Torres, Andres Yee, Douglas Yau, Christina Wolf, Denise Park, John Parker, Barbara A. Chien, A. Jo Wallace, Anne M. Murthy, Rashmi Albain, Kathy S. Ellis, Erin D. Beckwith, Heather Haley, Barbara B. Elias, Anthony D. Boughey, Judy C. Yung, Rachel L. Isaacs, Claudine Clark, Amy S. Han, Hyo S. Nanda, Rita Khan, Qamar J. Edmiston, Kristen K. Stringer-Reasor, Erica Price, Elissa Joe, Bonnie Liu, Minetta C. Brown-Swigart, Lamorna Petricoin, Emanuel F. Wulfkuhle, Julia D. Buxton, Meredith Clennell, Julia L. Sanil, Ashish Berry, Scott Asare, Smita M. Wilson, Amy Hirst, Gillian L. Singhrao, Ruby Asare, Adam L. Matthews, Jeffrey B. Melisko, Michelle Perlmutter, Jane Rugo, Hope S. Symmans, W. Fraser van ‘t Veer, Laura J. Hylton, Nola M. DeMichele, Angela M. Berry, Donald A. Esserman, Laura J. NPJ Breast Cancer Article HSP90 inhibitors destabilize oncoproteins associated with cell cycle, angiogenesis, RAS-MAPK activity, histone modification, kinases and growth factors. We evaluated the HSP90-inhibitor ganetespib in combination with standard chemotherapy in patients with high-risk early-stage breast cancer. I-SPY2 is a multicenter, phase II adaptively randomized neoadjuvant (NAC) clinical trial enrolling patients with stage II-III breast cancer with tumors 2.5 cm or larger on the basis of hormone receptors (HR), HER2 and Mammaprint status. Multiple novel investigational agents plus standard chemotherapy are evaluated in parallel for the primary endpoint of pathologic complete response (pCR). Patients with HER2-negative breast cancer were eligible for randomization to ganetespib from October 2014 to October 2015. Of 233 women included in the final analysis, 140 were randomized to the standard NAC control; 93 were randomized to receive 150 mg/m(2) ganetespib every 3 weeks with weekly paclitaxel over 12 weeks, followed by AC. Arms were balanced for hormone receptor status (51–52% HR-positive). Ganetespib did not graduate in any of the biomarker signatures studied before reaching maximum enrollment. Final estimated pCR rates were 26% vs. 18% HER2-negative, 38% vs. 22% HR-negative/HER2-negative, and 15% vs. 14% HR-positive/HER2-negative for ganetespib vs control, respectively. The predicted probability of success in phase 3 testing was 47% HER2-negative, 72% HR-negative/HER2-negative, and 19% HR-positive/HER2-negative. Ganetespib added to standard therapy is unlikely to yield substantially higher pCR rates in HER2-negative breast cancer compared to standard NAC, and neither HSP90 pathway nor replicative stress expression markers predicted response. HSP90 inhibitors remain of limited clinical interest in breast cancer, potentially in other clinical settings such as HER2-positive disease or in combination with anti-PD1 neoadjuvant chemotherapy in triple negative breast cancer. Trial registration: www.clinicaltrials.gov/ct2/show/NCT01042379 Nature Publishing Group UK 2022-12-01 /pmc/articles/PMC9715670/ /pubmed/36456573 http://dx.doi.org/10.1038/s41523-022-00493-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lang, Julie E.
Forero-Torres, Andres
Yee, Douglas
Yau, Christina
Wolf, Denise
Park, John
Parker, Barbara A.
Chien, A. Jo
Wallace, Anne M.
Murthy, Rashmi
Albain, Kathy S.
Ellis, Erin D.
Beckwith, Heather
Haley, Barbara B.
Elias, Anthony D.
Boughey, Judy C.
Yung, Rachel L.
Isaacs, Claudine
Clark, Amy S.
Han, Hyo S.
Nanda, Rita
Khan, Qamar J.
Edmiston, Kristen K.
Stringer-Reasor, Erica
Price, Elissa
Joe, Bonnie
Liu, Minetta C.
Brown-Swigart, Lamorna
Petricoin, Emanuel F.
Wulfkuhle, Julia D.
Buxton, Meredith
Clennell, Julia L.
Sanil, Ashish
Berry, Scott
Asare, Smita M.
Wilson, Amy
Hirst, Gillian L.
Singhrao, Ruby
Asare, Adam L.
Matthews, Jeffrey B.
Melisko, Michelle
Perlmutter, Jane
Rugo, Hope S.
Symmans, W. Fraser
van ‘t Veer, Laura J.
Hylton, Nola M.
DeMichele, Angela M.
Berry, Donald A.
Esserman, Laura J.
Safety and efficacy of HSP90 inhibitor ganetespib for neoadjuvant treatment of stage II/III breast cancer
title Safety and efficacy of HSP90 inhibitor ganetespib for neoadjuvant treatment of stage II/III breast cancer
title_full Safety and efficacy of HSP90 inhibitor ganetespib for neoadjuvant treatment of stage II/III breast cancer
title_fullStr Safety and efficacy of HSP90 inhibitor ganetespib for neoadjuvant treatment of stage II/III breast cancer
title_full_unstemmed Safety and efficacy of HSP90 inhibitor ganetespib for neoadjuvant treatment of stage II/III breast cancer
title_short Safety and efficacy of HSP90 inhibitor ganetespib for neoadjuvant treatment of stage II/III breast cancer
title_sort safety and efficacy of hsp90 inhibitor ganetespib for neoadjuvant treatment of stage ii/iii breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715670/
https://www.ncbi.nlm.nih.gov/pubmed/36456573
http://dx.doi.org/10.1038/s41523-022-00493-z
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