There is a strong rationale for combining HER2-targeted therapies with cancer immunotherapy to increase efficacy in breast cancer, particularly in the early-stage setting, where the immune system has not been weakened by heavy pretreatment. ASTEFANIA aims to evaluate the efficacy of adjuvant atezolizumab in combination with ado-trastuzumab emtansine in patients with high-risk, HER2-positive early breast cancer and residual disease following HER2-based neoadjuvant therapy. Eligible patients will be randomized to receive ado-trastuzumab emtansine in combination with either atezolizumab or placebo for 14 cycles within 12 weeks of primary surgery. The primary outcome is invasive disease-free survival and secondary outcomes include additional efficacy end points, safety and pharmacokinetics. The study plans to enroll 1700 patients across 32 counties.

ASTEFANIA: adjuvant ado-trastuzumab emtansine and atezolizumab for high-risk, HER2-positive breast cancer / Hurvitz, S. A.; Bachelot, T.; Bianchini, G.; Harbeck, N.; Loi, S.; Park, Y. H.; Prat, A.; Gilham, L.; Boulet, T.; Monturus, N. G. E.; Lambertini, C.; Nyawira, B.; Knott, A.; Restuccia, E.; Schmid, P.. - In: FUTURE ONCOLOGY. - ISSN 1479-6694. - 18:32(2022), pp. 3563-3572. [10.2217/fon-2022-0485]

ASTEFANIA: adjuvant ado-trastuzumab emtansine and atezolizumab for high-risk, HER2-positive breast cancer

Bianchini G.;
2022-01-01

Abstract

There is a strong rationale for combining HER2-targeted therapies with cancer immunotherapy to increase efficacy in breast cancer, particularly in the early-stage setting, where the immune system has not been weakened by heavy pretreatment. ASTEFANIA aims to evaluate the efficacy of adjuvant atezolizumab in combination with ado-trastuzumab emtansine in patients with high-risk, HER2-positive early breast cancer and residual disease following HER2-based neoadjuvant therapy. Eligible patients will be randomized to receive ado-trastuzumab emtansine in combination with either atezolizumab or placebo for 14 cycles within 12 weeks of primary surgery. The primary outcome is invasive disease-free survival and secondary outcomes include additional efficacy end points, safety and pharmacokinetics. The study plans to enroll 1700 patients across 32 counties.
2022
Inglese
Newlands Press Ltd
18
32
3563
3572
10
Pubblicato
https://www.tandfonline.com/doi/full/10.2217/fon-2022-0485
Esperti anonimi
Internazionale
Goal 3: Good health and well-being
ado-trastuzumab emtansine
atezolizumab
cancer immunotherapy
early breast cancer
HER2
ASTEFANIA: adjuvant ado-trastuzumab emtansine and atezolizumab for high-risk, HER2-positive breast cancer / Hurvitz, S. A.; Bachelot, T.; Bianchini, G.; Harbeck, N.; Loi, S.; Park, Y. H.; Prat, A.; Gilham, L.; Boulet, T.; Monturus, N. G. E.; Lambertini, C.; Nyawira, B.; Knott, A.; Restuccia, E.; Schmid, P.. - In: FUTURE ONCOLOGY. - ISSN 1479-6694. - 18:32(2022), pp. 3563-3572. [10.2217/fon-2022-0485]
open
15
info:eu-repo/semantics/article
262
Hurvitz, S. A.; Bachelot, T.; Bianchini, G.; Harbeck, N.; Loi, S.; Park, Y. H.; Prat, A.; Gilham, L.; Boulet, T.; Monturus, N. G. E.; Lambertini, C.; ...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/161457
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