Evidence map›Paper›PMID 39500221›Full record

ReviewBreast (Edinburgh, Scotland)2024

Unveiling the future of breast cancer therapy: Cutting-edge antibody-drug conjugate strategies and clinical outcomes.

Lu Sun, Xiaomeng Jia, Kainan Wang, Man Li

Abstract readReview
In one paragraph

Review in Breast (Edinburgh, Scotland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  20. Escalation and optimisation of primary breast cancer treatment with antibody-drug conjugates.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Lu SunDepartment of Oncology, The Second Hospital of Dalian Medical University, Dalian, 116023, China. Electronic address: gddmusl@163.com.
Xiaomeng JiaDepartment of Oncology, The Second Hospital of Dalian Medical University, Dalian, 116023, China. Electronic address: jxm19970906@163.com.
Kainan WangDepartment of Oncology, The Second Hospital of Dalian Medical University, Dalian, 116023, China. Electronic address: kainan_wang@dmu.edu.cn.
Man LiDepartment of Oncology, The Second Hospital of Dalian Medical University, Dalian, 116023, China. Electronic address: man_li@dmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer has become the most prevalent malignant tumor worldwide and remains one of the leading causes of cancer-related mortality among women globally. The prognosis for patients with metastatic breast cancer remains poor, necessitating the exploration of novel therapeutic strategies to improve survival rates. In the era of precision medicine, antibody-drug conjugates (ADCs) have gained significant attention as a targeted therapeutic strategy in breast cancer treatment. ADCs, a relatively new treatment for breast cancer, deliver cytotoxic drugs (payloads), directly into the tumor space, turning chemotherapy into a targeted agent, which enables patients to experience significant improvements with manageable drug toxicity. For the treatment of breast cancer, there are three ADCs approved for breast cancer treatment: Trastuzumab emtansine (T-DM1), Trastuzumab Deruxtecan (T-Dxd) targeting HER-2, and Sacituzumab Govitecan (SG) targeting Trop-2. Recent clinical studies have demonstrated that the benefits of ADC therapies extend beyond HER2-positive breast cancer toinclude hormone receptor (HR)-positive breast cancer, triple-negative breast cancer (TNBC), and HER2-low expressing breast cancer. Notably, the DESTINY-Breast series of studies, particularly focusing on T-Dxd, encompass neoadjuvant, adjuvant, and multiple lines of therapy for advanced breast cancer. This marks the advent of a comprehensive ADC era in breast cancer treatment. This review summarizes the efficacy and adverse effects of ADC therapies that have completed or are currently undergoing phase I-III clinical trials. Additionally, it analyzes potential combination strategies to overcome ADC resistance, aiming to provide clinicians with a comprehensive clinical guide to the use of ADCs in breast cancer treatment.

Indexed as

Breast NeoplasmsImmunoconjugatesAdo-Trastuzumab EmtansineAntibodies, Monoclonal, HumanizedAntigens, NeoplasmAntineoplastic Agents, ImmunologicalCamptothecinCell Adhesion MoleculesErb-b2 Receptor Tyrosine KinasesFemaleHumansTrastuzumabTreatment OutcomeAdo-Trastuzumab EmtansineAntibodies, Monoclonal, HumanizedAntigens, NeoplasmAntineoplastic Agents, ImmunologicalCamptothecinCell Adhesion MoleculesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesImmunoconjugatessacituzumab govitecanTACSTD2 protein, humanTrastuzumabtrastuzumab deruxtecanAntibody-drug conjugateBreast cancerHER2HER2-LowHER2-Ultra-lowTargeted therapyTrop2

Identifiers

PMID39500221
PMCPMC11570738

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.