In this conference update video, Profs. Michael Gnant and Giuseppe Curigliano provide key insights from the highly anticipated 19th St. Gallen Breast Cancer Conference (SGBCC) Satellite Symposium, sponsored by Menarini Stemline. 

In this conference update video, Profs. Michael Gnant and Giuseppe Curigliano provide key insights from the highly anticipated 19th St. Gallen Breast Cancer Conference (SGBCC) Satellite Symposium, sponsored by Menarini Stemline. 

Key topics included: 

  • Defining recurrence risk in high- vs low-risk groups 
  • Review of current treatment guidelines 
  • Ongoing clinical trials evaluating oral SERDs in the adjuvant early breast cancer setting 

 

Clinical takeaways

  • Risk assessment enables personalized treatment approaches, optimizing therapeutic outcomes  
  • High-risk patients exhibit significantly lower invasive disease-free survival than intermediate/low-risk groups, underscoring the need for enhanced treatment strategies 
  • Adjuvant ET intensification with CDK4/6 inhibitors has shown clinical benefit; however, emerging resistance remains a challenge, contributing to disease recurrence  
  • Oral SERDs have shown evidence of superior efficacy over SOC in metastatic settings, particularly in the presence of ESR1-mut and are now being explored in early-stage disease as either an upfront or switch treatment strategy  
  • Elacestrant is the only oral SERD with agonistic properties being investigated as a switch strategy in a “pure high-risk population” following demonstration of CCCA rate reduction, substantial Ki-67 suppression, and activity in ESR1 wild-type breast cancer  

Full Professor of Surgery at the Medical University of Vienna, Austria, where he also serves as President of the Austrian Breast and Colorectal Cancer Study Group. He has been co-chairing and hosting St. Gallen International Consensus Panel for Early Breast Cancer since 2015 and is involved in many scientific societies including ASCO, AACR, ACS, BIG, EORTC, ESSO, EUSOMA, and UICC.​

Prof. Michael Gnant has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies:

Amgen, AstraZeneca, Bayer, Daiichi Sankyo, Eli Lilly, EPG Health (IQVIA), Menarini Stemline, MSD, Novartis, Pierre Fabre, and Veracyte​

Director of the Early Drug Development Division and Co-Chair for the Experimental Therapeutics Program at the European Institute of Oncology, a comprehensive cancer center in Milan, Italy. He is a steering committee member of the Department of Oncology and Hemato-Oncology at the University of Milan. Moreover, he is a member of the Italian National Health Council, serving as an adviser to the Ministry of Health for cancer policy issues.

Prof. Giuseppe Curigliano has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies:

AstraZeneca, BMS, Celcuity, Daiichi Sankyo, Exact Sciences, Menarini, Merck, Novartis, Pfizer, Roche, Ellipsis, Astellas, Blueprint Medicines, BMS, Kymab, Philogen, Relay Therapeutics and Sanofi​

Key topics included: 

  • Defining recurrence risk in high- vs low-risk groups 
  • Review of current treatment guidelines 
  • Ongoing clinical trials evaluating oral SERDs in the adjuvant early breast cancer setting 

 

Clinical takeaways

  • Risk assessment enables personalized treatment approaches, optimizing therapeutic outcomes  
  • High-risk patients exhibit significantly lower invasive disease-free survival than intermediate/low-risk groups, underscoring the need for enhanced treatment strategies 
  • Adjuvant ET intensification with CDK4/6 inhibitors has shown clinical benefit; however, emerging resistance remains a challenge, contributing to disease recurrence  
  • Oral SERDs have shown evidence of superior efficacy over SOC in metastatic settings, particularly in the presence of ESR1-mut and are now being explored in early-stage disease as either an upfront or switch treatment strategy  
  • Elacestrant is the only oral SERD with agonistic properties being investigated as a switch strategy in a “pure high-risk population” following demonstration of CCCA rate reduction, substantial Ki-67 suppression, and activity in ESR1 wild-type breast cancer  

Full Professor of Surgery at the Medical University of Vienna, Austria, where he also serves as President of the Austrian Breast and Colorectal Cancer Study Group. He has been co-chairing and hosting St. Gallen International Consensus Panel for Early Breast Cancer since 2015 and is involved in many scientific societies including ASCO, AACR, ACS, BIG, EORTC, ESSO, EUSOMA, and UICC.​

Prof. Michael Gnant has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies:

Amgen, AstraZeneca, Bayer, Daiichi Sankyo, Eli Lilly, EPG Health (IQVIA), Menarini Stemline, MSD, Novartis, Pierre Fabre, and Veracyte​

Director of the Early Drug Development Division and Co-Chair for the Experimental Therapeutics Program at the European Institute of Oncology, a comprehensive cancer center in Milan, Italy. He is a steering committee member of the Department of Oncology and Hemato-Oncology at the University of Milan. Moreover, he is a member of the Italian National Health Council, serving as an adviser to the Ministry of Health for cancer policy issues.

Prof. Giuseppe Curigliano has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies:

AstraZeneca, BMS, Celcuity, Daiichi Sankyo, Exact Sciences, Menarini, Merck, Novartis, Pfizer, Roche, Ellipsis, Astellas, Blueprint Medicines, BMS, Kymab, Philogen, Relay Therapeutics and Sanofi​

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