Antitumor activity and safety of trastuzumab deruxtecan in patients with HER2-low-expressing advanced breast cancer: Results from a phase Ib study Journal Article


Authors: Modi, S.; Park, H.; Murthy, R. K.; Iwata, H.; Tamura, K.; Tsurutani, J.; Moreno-Aspitia, A.; Doi, T.; Sagara, Y.; Redfern, C.; Krop, I. E.; Lee, C.; Fujisaki, Y.; Sugihara, M.; Zhang, L.; Shahidi, J.; Takahashi, S.
Article Title: Antitumor activity and safety of trastuzumab deruxtecan in patients with HER2-low-expressing advanced breast cancer: Results from a phase Ib study
Abstract: PURPOSETrastuzumab deruxtecan (T-DXd, formerly DS-8201a) is a novel human epidermal growth factor receptor 2 (HER2)-targeted antibody drug conjugate (ADC) with a topoisomerase I inhibitor payload. A dose escalation and expansion phase I study evaluated the safety and activity of T-DXd in patients with advanced HER2-expressing/mutated solid tumors. Here, results for T-DXd at the recommended doses for expansion (RDE) in patients with HER2-low (immunohistochemistry [IHC] 1+ or IHC 2+/in situ hybridization-) breast cancer (ClinicalTrials.gov identifier: NCT02564900) are reported.PATIENTS AND METHODSEligible patients had advanced/metastatic HER2-low-expressing breast cancer refractory to standard therapies. The RDE of 5.4 or 6.4 mg/kg T-DXd were administered intravenously once every 3 weeks until withdrawal of consent, unacceptable toxicity, or progressive disease. Antitumor activity and safety were assessed.RESULTSBetween August 2016 and August 2018, 54 patients were enrolled and received >= 1 dose of T-DXd at the RDE. Patients were extensively pretreated (median, 7.5 prior therapies). The confirmed objective response rate by independent central review was 20/54 (37.0%; 95% CI, 24.3% to 51.3%) with median duration of response of 10.4 months (95% CI, 8.8 month to not evaluable). Most patients (53/54; 98.1%) experienced >= 1 treatment-emergent adverse event (TEAE; grade >= 3; 34/54; 63.0%). Common (>= 5%) grade >= 3 TEAEs included decreases in neutrophil, platelet, and WBC counts; anemia; hypokalemia; AST increase; decreased appetite; and diarrhea. Three patients treated at 6.4 mg/kg suffered fatal events associated with T-DXd-induced interstitial lung disease (ILD)/pneumonitis as determined by an independent adjudication committee.CONCLUSIONThe novel HER2-targeted ADC, T-DXd, demonstrated promising preliminary antitumor activity in patients with HER2-low breast cancer. Most toxicities were GI or hematologic in nature. ILD is an important identified risk and should be monitored closely and proactively managed.
Keywords: experience; anthracycline; in-situ; her2; hybridization; efficacy; cohort; therapies; interstitial lung-disease; antibody-drug conjugate; ds-8201a
Journal Title: Journal of Clinical Oncology
Volume: 38
Issue: 17
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2020-06-10
Start Page: 1887
End Page: 1896
Language: English
ACCESSION: WOS:000540597700003
DOI: 10.1200/jco.19.02318
PROVIDER: wos
PMCID: PMC7280051
PUBMED: 32058843
Notes: Article -- Source: Wos
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  1. Shanu Modi
    265 Modi