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DRUG:

Kadcyla (ado-trastuzumab emtansine)

i
Other names: PRO132365, R3502, RG 3502, RG3502, T-DM1, trastuzumab-DM1, trastuzumab-MCC-DM1, trastuzumab-mertansine, Herceptin-DM1, RO5304020, PRO 132365, RO 5304020, PRO-132365, RO-5304020
Company:
AbbVie, Roche
Drug class:
Microtubule inhibitor, HER2-targeted antibody-drug conjugate
Related drugs:
6d
HER2 Therapies in Non-Small Cell Lung Cancer (NSCLC). (PubMed, Int J Mol Sci)
Concerning treatment, in advanced HER2-positive, Non-Squamous NSCLC tumors, the first-line treatment is Platinum-based + Pemetrexed chemotherapy, with or without immunotherapy, because no HER2-targeted antibody therapy has yet been approved for initial treatment. After progression, HER2-targeted antibody-drug conjugates like Trastuzumab-Deruxtecan and Ado Trastuzumab-Emtansine may offer patients clinical benefits. New HER2-selective tyrosine kinase inhibitors, such as zongertinib and sevabertinib, have shown promising results, including patients previously treated with antibody-drug conjugates (ADCs). Recent advances, including next-generation ADCs such as SHR-A1811 and A166, and bispecific antibodies, such as zenocutuzumab for NRG1 fusion-positive disease, which are also expanding treatment options. Overall, advances in diagnostics and new targeted therapies are changing how HER2-altered NSCLC is treated and are helping to make care more personalized.
Review • Journal • IO biomarker
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NRG1 (Neuregulin 1)
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HER-2 positive • HER-2 mutation • HER-2 expression • NRG1 fusion • HER-2 exon 20 mutation
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Kadcyla (ado-trastuzumab emtansine) • Enhertu (fam-trastuzumab deruxtecan-nxki) • pemetrexed • Bizengri (zenocutuzumab-zbco) • trastuzumab rezetecan (SHR-A1811) • Hernexeos (zongertinib) • Sertaly (trastuzumab botidotin) • Hyrnuo (sevabertinib)
6d
Prognostic Role of Inflammatory Indices and Real-World Outcomes in HER2-Positive Metastatic Breast Cancer Treated with Trastuzumab Emtansine. (PubMed, Diagnostics (Basel))
Treatment response was the main determinant of progression, while baseline inflammatory markers offered modest complementary prognostic value. These findings may aid patient selection for T-DM1, particularly in settings with limited access to trastuzumab deruxtecan.
Journal • Real-world evidence
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HER-2 (Human epidermal growth factor receptor 2)
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HER-2 positive
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Kadcyla (ado-trastuzumab emtansine) • Enhertu (fam-trastuzumab deruxtecan-nxki)
10d
Next-generation antibody-drug conjugates in drug-resistant solid tumors: promise, toxicity, and the emerging challenge of acquired resistance. (PubMed, Ann Med Surg (Lond))
Conventional chemotherapy and first-generation antibody-drug conjugates (ADCs), such as ado-trastuzumab emtansine (T-DM1), were limited by non-specific cytotoxicity, heterogeneous drug-antibody ratios, linker instability, and insufficient bystander killing, yielding modest efficacy in heavily pretreated populations...Clinically, trastuzumab deruxtecan demonstrated meaningful progression-free survival benefit in HER2-low metastatic breast cancer, while enfortumab vedotin reduced mortality risk in platinum- and immunotherapy-refractory urothelial carcinoma, establishing ADC efficacy across solid tumor histologies...Trastuzumab deruxtecan carries a 15.4% incidence of interstitial lung disease, including fatal events, and sacituzumab govitecan is associated with grade 3 or higher neutropenia in approximately 51% of patients. Furthermore, next-generation ADCs are not resistance-proof, with antigen downregulation, payload efflux, and impaired internalization emerging as clinically relevant escape mechanisms. Biomarker-driven patient selection, rigorous toxicity monitoring, and prospective trials addressing resistance will be essential to realizing the full and durable potential of this drug class.
Preclinical • Journal • IO biomarker
|
HER-2 (Human epidermal growth factor receptor 2)
|
Kadcyla (ado-trastuzumab emtansine) • Enhertu (fam-trastuzumab deruxtecan-nxki) • Trodelvy (sacituzumab govitecan-hziy) • Padcev (enfortumab vedotin-ejfv)
12d
Integrated metabolomics of tumor and plasma reveals local and systemic metabolic responses to T-DM1 therapy. (PubMed, J Chromatogr B Analyt Technol Biomed Life Sci)
These bidirectional changes indicate a metabolic coupling between tumor and circulation, driven by differential utilization and excretion processes during T-DM1 response. Collectively, our findings demonstrate that T-DM1 elicits coordinated local and systemic metabolic reprogramming, providing mechanistic insights into its antitumor activity and the metabolic coupling between tumor and circulation.
Journal • Metabolomic study
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HER-2 (Human epidermal growth factor receptor 2)
|
EGFR positive
|
Kadcyla (ado-trastuzumab emtansine)
14d
Loss of Flotillin-2 enhances trastuzumab emtansine internalization and cytotoxicity by relieving negative regulation of HER2 internalization in HER2-amplified cancers. (PubMed, bioRxiv)
Higher FLOT2 expression in nine HER2 amplified cell lines correlated with a higher T-DM1 IC50 in vitro , and breast cancer patients with high FLOT2 expression had worse survival when receiving either T-DXd (16.2 months (m) vs 18.3 m, p=0.04) or T-DM1 (38.0 m vs 41.3 m, p=0.1) in real-world Caris Life Sciences data. In conclusion, FLOT2 regulates the internalization and cytotoxicity of T-DM1 mediated by Cbl-dependent ubiquitination of HER2. Zoledronic acid disrupts the HER2/FLOT2 interaction, therefore increasing the internalization and cytotoxicity of T-DM1, providing proof of principle that a small molecule inhibitor of the HER2/FLOT2 interaction can enhance the activity of the HER2-targeting ADC.
Journal
|
EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2)
|
HER-2 amplification • HER-2 expression
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Kadcyla (ado-trastuzumab emtansine) • Enhertu (fam-trastuzumab deruxtecan-nxki) • zoledronic acid
14d
Safety of concurrent T-DM1 and radiation therapy in HER2-positive breast cancer with residual disease after neoadjuvant chemotherapy. (PubMed, Int J Radiat Biol)
Concurrent T-DM1 and RT was generally well tolerated. However, RP appeared more frequent in patients with pulmonary comorbidities and larger PTV, warranting careful selection and prospective validation.
Journal
|
HER-2 (Human epidermal growth factor receptor 2)
|
HER-2 positive
|
Kadcyla (ado-trastuzumab emtansine)
21d
New trial
|
HER-2 (Human epidermal growth factor receptor 2) • TACSTD2 (Tumor Associated Calcium Signal Transducer 2)
|
HER-2 positive • HER-2 expression
|
Kadcyla (ado-trastuzumab emtansine) • Enhertu (fam-trastuzumab deruxtecan-nxki)
24d
Breast cancer chemotherapy in transition: predictive markers, resistance mechanisms, and new treatment approaches. (PubMed, Front Oncol)
Recent therapeutic advances have focused on overcoming resistance through platinum agents, PARP inhibitors, immune checkpoint blockade, post-neoadjuvant escalation with capecitabine or trastuzumab emtansine, and emerging antibody-drug conjugates. This review summarizes the advancement of chemotherapy in breast cancer.
Review • Journal • BRCA Biomarker • PARP Biomarker
|
HER-2 (Human epidermal growth factor receptor 2) • BRCA1 (Breast cancer 1, early onset) • BRCA2 (Breast cancer 2, early onset) • HRD (Homologous Recombination Deficiency)
|
HER-2 positive • HR positive • HRD
|
Kadcyla (ado-trastuzumab emtansine) • capecitabine
24d
The prognostic value of peripheral blood inflammatory markers in patients with HER2-positive metastatic breast cancer treated with pyrotinib. (PubMed, Front Oncol)
Kaplan-Meier survival curve and Cox regression model was used to analyze the effect of different levels of NLR and LDH before T-DM1 treatment on the survival of patients. Elevated NLR and LDH were associated with poor PFS and OS. Future data are needed to validate and update our results.
Journal
|
HER-2 (Human epidermal growth factor receptor 2)
|
HER-2 positive
|
Kadcyla (ado-trastuzumab emtansine) • Irene (pyrotinib)
29d
New P1/2 trial
|
HER-2 (Human epidermal growth factor receptor 2)
|
HER-2 overexpression • HER-2 amplification
|
Herceptin (trastuzumab) • 5-fluorouracil • Kadcyla (ado-trastuzumab emtansine) • Enhertu (fam-trastuzumab deruxtecan-nxki) • capecitabine • oxaliplatin • Ziihera (zanidatamab-hrii) • Hernexeos (zongertinib)
1m
Cost-effectiveness analysis of the treatment pathway after trastuzumab treatment failure in patients with HER2-positive advanced breast cancer: a chinese health system perspective. (PubMed, BMC Health Serv Res)
In the context of the Chinese health system, none of the three alternative regimens-pyrotinib plus capecitabine, T-DM1, and T-DXd-demonstrated cost-effectiveness relative to lapatinib plus capecitabine at the current WTP threshold.
Journal • HEOR • Cost-effectiveness
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HER-2 (Human epidermal growth factor receptor 2)
|
HER-2 positive • EGFR positive
|
lapatinib • Kadcyla (ado-trastuzumab emtansine) • Enhertu (fam-trastuzumab deruxtecan-nxki) • capecitabine • Irene (pyrotinib)
1m
A Study of Trastuzumab Deruxtecan (T-DXd) Versus Trastuzumab Emtansine (T-DM1) in High-risk HER2-positive Participants With Residual Invasive Breast Cancer Following Neoadjuvant Therapy (DESTINY-Breast05) (clinicaltrials.gov)
P3, N=1635, Active, not recruiting, Daiichi Sankyo | Trial completion date: Dec 2030 --> Jun 2028 | Trial primary completion date: Dec 2025 --> Jul 2025
Trial completion date • Trial primary completion date
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HER-2 (Human epidermal growth factor receptor 2) • ER (Estrogen receptor) • PGR (Progesterone receptor)
|
HER-2 positive • HR positive • HER-2 expression • ER negative
|
Kadcyla (ado-trastuzumab emtansine) • Enhertu (fam-trastuzumab deruxtecan-nxki)