Randomized study of Lapatinib alone or in combination with trastuzumab in women with ErbB2-positive, trastuzumab-refractory metastatic breast cancer.
By K. Blackwell, H. Burstein, A. Storniolo, H. Rugo, G. Sledge, M. Koehler, C. Ellis, M. Casey, S. Vukelja, J. Bischoff and 2 more. Journal of Clinical Oncology, 2010
977 citations recorded by the source corpus.
Subfields: Cancer Research, Oncology
View Paper: https://www.semanticscholar.org/paper/d2e57b189b240c45008a591b127cfa06b81dac5f
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Citations in the corpus
- A standardised, generic, validated approach to stratify the magnitude of clinical benefit that can be anticipated from anti-cancer therapies: the European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS). (2015, neutral): “97) 4 [95, 96]”
- Molecular biology in breast cancer: intrinsic subtypes and signaling pathways. (2012, background): “This set researchers to investigate the possibilities of dual targeting of the HER-2 receptor.(60) The Neo-ALTTO trial(32) proved that a dual inhibition achieves a greater rate of pCR.”
- Antibodies and cancer therapy: versatile platforms for cancer immunotherapy (2010, background): “A recent Phase III clinical trial showed that trastuzumab and lapatinib combination therapy improved progression-free survival compared with lapatinib monotherapy in patients with HER2-positive, trastuzumab-refractory metastatic breast cance”
- ERBB receptors: From oncogene discovery to basic science to mechanism-based cancer therapeutics (2014, background): “For example, the combination of trastuzumab and lapatinib is superior to each agent alone in both the metastatic (Blackwell et al., 2010) and neoadjuvant (Baselga et al.”
- Treatment of HER2-positive breast cancer: current status and future perspectives (2012, background): “A subsequent randomized trial also showed that the combination of lapatinib and trastuzumab had better efficacy than lapatinib alone in patients whose disease had progressed on trastuzumab”