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pmid: 35665782
pmc: PMC10561652
Among breast cancers without human epidermal growth factor receptor 2 (HER2) amplification, overexpression, or both, a large proportion express low levels of HER2 that may be targetable. Currently available HER2-directed therapies have been ineffective in patients with these "HER2-low" cancers.We conducted a phase 3 trial involving patients with HER2-low metastatic breast cancer who had received one or two previous lines of chemotherapy. (Low expression of HER2 was defined as a score of 1+ on immunohistochemical [IHC] analysis or as an IHC score of 2+ and negative results on in situ hybridization.) Patients were randomly assigned in a 2:1 ratio to receive trastuzumab deruxtecan or the physician's choice of chemotherapy. The primary end point was progression-free survival in the hormone receptor-positive cohort. The key secondary end points were progression-free survival among all patients and overall survival in the hormone receptor-positive cohort and among all patients.Of 557 patients who underwent randomization, 494 (88.7%) had hormone receptor-positive disease and 63 (11.3%) had hormone receptor-negative disease. In the hormone receptor-positive cohort, the median progression-free survival was 10.1 months in the trastuzumab deruxtecan group and 5.4 months in the physician's choice group (hazard ratio for disease progression or death, 0.51; P<0.001), and overall survival was 23.9 months and 17.5 months, respectively (hazard ratio for death, 0.64; P = 0.003). Among all patients, the median progression-free survival was 9.9 months in the trastuzumab deruxtecan group and 5.1 months in the physician's choice group (hazard ratio for disease progression or death, 0.50; P<0.001), and overall survival was 23.4 months and 16.8 months, respectively (hazard ratio for death, 0.64; P = 0.001). Adverse events of grade 3 or higher occurred in 52.6% of the patients who received trastuzumab deruxtecan and 67.4% of those who received the physician's choice of chemotherapy. Adjudicated, drug-related interstitial lung disease or pneumonitis occurred in 12.1% of the patients who received trastuzumab deruxtecan; 0.8% had grade 5 events.In this trial involving patients with HER2-low metastatic breast cancer, trastuzumab deruxtecan resulted in significantly longer progression-free and overall survival than the physician's choice of chemotherapy. (Funded by Daiichi Sankyo and AstraZeneca; DESTINY-Breast04 ClinicalTrials.gov number, NCT03734029.).
Immunoconjugates, Breast Neoplasms* / secondary, Receptor, ErbB-2, Humanized / adverse effects, ErbB-2* / genetics, 610, Antineoplastic Agents, Breast Neoplasms, Antibodies, Monoclonal, Humanized, Antibodies, Càncer de mama, Immunological* / therapeutic use, Breast cancer, Antineoplastic Agents, Immunological, Immunological* / adverse effects, Monoclonal, Humanized / therapeutic use, Antineoplastic Combined Chemotherapy Protocols / adverse effects, Antineoplastic Combined Chemotherapy Protocols / therapeutic use, Antineoplastic Combined Chemotherapy Protocols, Breast Neoplasms* / genetics, Camptothecin / analogs & derivatives, Humans, ErbB-2* / analysis, Breast Neoplasms* / metabolism, Trastuzumab* / adverse effects, Trastuzumab* / therapeutic use, Immunoconjugates / adverse effects, Sciences bio-médicales et agricoles, Trastuzumab, Immunohistochemistry, Immunoconjugates / therapeutic use, ErbB-2* / biosynthesis, Disease Progression, Monoclonal antibodies, Camptothecin, Female, Anticossos monoclonals, Breast Neoplasms* / drug therapy, Receptor
Immunoconjugates, Breast Neoplasms* / secondary, Receptor, ErbB-2, Humanized / adverse effects, ErbB-2* / genetics, 610, Antineoplastic Agents, Breast Neoplasms, Antibodies, Monoclonal, Humanized, Antibodies, Càncer de mama, Immunological* / therapeutic use, Breast cancer, Antineoplastic Agents, Immunological, Immunological* / adverse effects, Monoclonal, Humanized / therapeutic use, Antineoplastic Combined Chemotherapy Protocols / adverse effects, Antineoplastic Combined Chemotherapy Protocols / therapeutic use, Antineoplastic Combined Chemotherapy Protocols, Breast Neoplasms* / genetics, Camptothecin / analogs & derivatives, Humans, ErbB-2* / analysis, Breast Neoplasms* / metabolism, Trastuzumab* / adverse effects, Trastuzumab* / therapeutic use, Immunoconjugates / adverse effects, Sciences bio-médicales et agricoles, Trastuzumab, Immunohistochemistry, Immunoconjugates / therapeutic use, ErbB-2* / biosynthesis, Disease Progression, Monoclonal antibodies, Camptothecin, Female, Anticossos monoclonals, Breast Neoplasms* / drug therapy, Receptor
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popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 0.01% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 0.1% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 0.01% |
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