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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.
Afiliação
  • Lang JE; University of Southern California, Los Angeles, USA. LANGJ2@ccf.org.
  • Forero-Torres A; University of Alabama at Birmingham, Birmingham, USA.
  • Yee D; University of Minnesota, Minneapolis, USA.
  • Yau C; University of California San Francisco, San Francisco, USA.
  • Wolf D; University of California San Francisco, San Francisco, USA.
  • Park J; University of California San Francisco, San Francisco, USA.
  • Parker BA; University of California San Diego, San Diego, USA.
  • Chien AJ; University of California San Francisco, San Francisco, USA.
  • Wallace AM; University of California San Francisco, San Francisco, USA.
  • Murthy R; University of Texas MD Anderson Cancer Center, Houston, USA.
  • Albain KS; Loyola University Chicago Stritch School of Medicine, Maywood, USA.
  • Ellis ED; Swedish Cancer Institute, Seattle, USA.
  • Beckwith H; University of Minnesota, Minneapolis, USA.
  • Haley BB; University of Texas Southwestern, Dallas, USA.
  • Elias AD; University of Colorado, Boulder, USA.
  • Boughey JC; Mayo Clinic Rochester, Rochester, USA.
  • Yung RL; University of Washington, Seattle, USA.
  • Isaacs C; University of Georgetown, Washington, DC, USA.
  • Clark AS; University of Pennsylvania, Philadelphia, USA.
  • Han HS; Moffitt Cancer Center, Tampa, USA.
  • Nanda R; University of Chicago, Chicago, USA.
  • Khan QJ; University of Kansas, Lawrence, USA.
  • Edmiston KK; Inova Health System, Virginia, USA.
  • Stringer-Reasor E; University of Alabama at Birmingham, Birmingham, USA.
  • Price E; University of California San Francisco, San Francisco, USA.
  • Joe B; University of California San Francisco, San Francisco, USA.
  • Liu MC; Mayo Clinic Rochester, Rochester, USA.
  • Brown-Swigart L; University of California San Francisco, San Francisco, USA.
  • Petricoin EF; George Mason University, Fairfax, USA.
  • Wulfkuhle JD; George Mason University, Fairfax, USA.
  • Buxton M; University of California San Francisco, San Francisco, USA.
  • Clennell JL; University of California San Francisco, San Francisco, USA.
  • Sanil A; Berry Consultants, LLC, Austin, USA.
  • Berry S; Berry Consultants, LLC, Austin, USA.
  • Asare SM; Quantum Leap Healthcare Collaborative, San Francisco, USA.
  • Wilson A; Quantum Leap Healthcare Collaborative, San Francisco, USA.
  • Hirst GL; University of California San Francisco, San Francisco, USA.
  • Singhrao R; University of California San Francisco, San Francisco, USA.
  • Asare AL; Quantum Leap Healthcare Collaborative, San Francisco, USA.
  • Matthews JB; University of California San Francisco, San Francisco, USA.
  • Melisko M; University of California San Francisco, San Francisco, USA.
  • Perlmutter J; Gemini Group, Michigan, USA.
  • Rugo HS; University of California San Francisco, San Francisco, USA.
  • Symmans WF; University of Texas MD Anderson Cancer Center, Houston, USA.
  • van 't Veer LJ; University of California San Francisco, San Francisco, USA.
  • Hylton NM; University of California San Francisco, San Francisco, USA.
  • DeMichele AM; University of Pennsylvania, Philadelphia, USA.
  • Berry DA; Berry Consultants, LLC, Austin, USA.
  • Esserman LJ; University of California San Francisco, San Francisco, USA.
NPJ Breast Cancer ; 8(1): 128, 2022 Dec 01.
Article em En | MEDLINE | ID: mdl-36456573
ABSTRACT
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/m2 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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: NPJ Breast Cancer Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: NPJ Breast Cancer Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos