Datopotamab deruxtecan: a new era in targeted therapy for metastatic breast cancer

Datopotamab deruxtecan (Datroway) is approved by the FDA to treat hormone receptor-positive, human epidermal growth factor receptor 2-negative breast cancer that is metastatic or incurable. This antibody-drug combination consists of a linker, the cytotoxic compound DXd, and a monoclonal antibody (mAb) that targets TROP2. Following internalization facilitated by the mAb's binding to TROP2 on cancer cells, DXd is released, causing cell death. Dato-DXd outperformed traditional chemotherapy in the TROPION-Breast01 study. With better efficacy than conventional treatments, it offers a possible alternative for individuals who have not responded to previous endocrine or chemotherapy therapies. This manuscript reviews the mechanisms of action, clinical efficacy, safety profiles, and trials of Dato-DXd and T-DXd, highlighting their transformative potential and positioning in current breast cancer treatment algorithms.

Authors

Institutions

Publication Details

Journal
Annals of Medicine and Surgery
Published
2025-09-12
DOI
https://doi.org/10.1097/ms9.0000000000003857
Primary Topic
Cancer Treatment and Pharmacology
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Datopotamab deruxtecan: a new era in targeted therapy for metastatic breast cancer

Iqbal Habib, Ihsan Qamar, Waseem Sajjad, Shakeel Ahmad et al.
Annals of Medicine and Surgery
Cancer Treatment and Pharmacology
article

Datopotamab deruxtecan: a new era in targeted therapy for metastatic breast cancer

Iqbal Habib, Ihsan Qamar, Waseem Sajjad, Shakeel Ahmad, Areeba Inam, Huda Tarique, Maryam Mobashir
article en

Abstract

Datopotamab deruxtecan (Datroway) is approved by the FDA to treat hormone receptor-positive, human epidermal growth factor receptor 2-negative breast cancer that is metastatic or incurable. This antibody-drug combination consists of a linker, the cytotoxic compound DXd, and a monoclonal antibody (mAb) that targets TROP2. Following internalization facilitated by the mAb's binding to TROP2 on cancer cells, DXd is released, causing cell death. Dato-DXd outperformed traditional chemotherapy in the TROPION-Breast01 study. With better efficacy than conventional treatments, it offers a possible alternative for individuals who have not responded to previous endocrine or chemotherapy therapies. This manuscript reviews the mechanisms of action, clinical efficacy, safety profiles, and trials of Dato-DXd and T-DXd, highlighting their transformative potential and positioning in current breast cancer treatment algorithms.

Annals of Medicine and SurgeryVol. 87(11)
Ayub Medical College (PK), King Edward Medical University (PK), Kabul University (AF), Saidu Teaching Hospital (PK), Jinnah Sindh Medical University (PK), Dow University of Health Sciences (PK), Mayo Hospital (PK)
Openalex Percentile: Top 66%
Cancer Treatment and Pharmacology
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Datopotamab deruxtecan: a new era in targeted therapy for metastatic breast cancer — Iqbal Habib, Ihsan Qamar, et al. · Annals of Medicine and Surgery (2025) | TGRS Research Map | TGRS