Datopotamab deruxtecan-dlnk

(Datroway®)

Datopotamab deruxtecan-dlnk

Drug updated on 1/31/2025

Dosage FormInjection (intravenous; 100 mg lyophilized powder in a single-dose vial)
Drug ClassTrop-2-directed antibodies and topoisomerase inhibitor conjugates
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • DATROWAY is indicated for the treatment of adult patients with unresectable or metastatic, hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative (IHC 0, IHC 1+ or IHC 2+/ISH-) breast cancer who have received prior endocrine-based therapy and chemotherapy for unresectable or metastatic disease

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Summary
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  • This summary is based on the review of one systematic review/meta-analysis. [1]
  • In HR+/HER2-low MBC, T-DXd and SG showed no significant difference in PFS or OS, though P-score analysis favored T-DXd for PFS (0.90 vs. 0.60) and OS (0.89 vs. 0.60); both significantly outperformed standard chemotherapy in PFS and OS (all p < 0.001), with Dato-DXd demonstrating the worst performance and T-DXd noted as the only ADC significantly outperforming chemotherapy in OS.
  • In TN/HER2-low MBC, T-DXd and SG showed no significant difference in PFS or OS, though P-score analysis favored SG for OS (0.80 vs. 0.69); both significantly outperformed standard chemotherapy in PFS and OS (all p < 0.001).
  • In HR+/HER2-low and TN/HER2-low MBC, SG showed higher rates of neutropenia, diarrhea, and alopecia.
  • T-DXd exhibited higher rates of thrombocytopenia, fatigue, and nausea, was associated with pneumonitis and cardiotoxicity, and had more toxicity-related discontinuations compared to SG.
  • In chemotherapy-pretreated patients, both ADCs improved PFS and OS with safety profiles consistent across these subgroups.

Product Monograph / Prescribing Information

Document TitleYearSource
Datroway (datopotamab deruxtecan-dlnk) Prescribing Information.2025Daiichi Sankyo, Inc., Basking Ridge, NJ 07920 AstraZeneca Pharmaceuticals LP, Wilmington, DE

Systematic Reviews / Meta-Analyses