The DOI matches its Crossref record; 102 of the 102 references it cites were found in a registry or an index.
Antibody–Drug Conjugates (ADCs) for Personalized Treatment of Solid Tumors: A Review
Open accessAbstract
Attaching a cytotoxic "payload" to an antibody to form an antibody-drug conjugate (ADC) provides a mechanism for selective delivery of the cytotoxic agent to cancer cells via the specific binding of the antibody to cancer-selective cell surface molecules. The first ADC to receive marketing authorization was gemtuzumab ozogamicin, which comprises an anti-CD33 antibody conjugated to a highly potent DNA-targeting antibiotic, calicheamicin, approved in 2000 for treating acute myeloid leukemia. It was withdrawn from the US market in 2010 following an unsuccessful confirmatory trial. The development of two classes of highly potent microtubule-disrupting agents, maytansinoids and auristatins, as payloads for ADCs resulted in approval of brentuximab vedotin in 2011 for treating Hodgkin lymphoma and anaplastic large cell lymphoma, and approval of ado-trastuzumab emtansine in 2013 for treating HER2-positive breast cancer. Their success stimulated much research into the ADC approach, with >60 ADCs currently in clinical evaluation, mostly targeting solid tumors. Five ADCs have advanced into pivotal clinical trials for treating various solid tumors-platinum-resistant ovarian cancer, mesothelioma, triple-negative breast cancer, glioblastoma, and small cell lung cancer. The level of target expression is a key parameter in predicting the likelihood of patient benefit for all these ADCs, as well as for the approved compound, ado-trastuzumab emtansine. The development of a patient selection strategy linked to target expression on the tumor is thus critically important for identifying the population appropriate for receiving treatment.
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“They bind to cell surface receptors that are upregulated by mutant RAS and exhibit potent antitumor activity, demonstrating their efficacy in targeting undruggable proteins outside the cell.645–649”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [646]
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“They bind to cell surface receptors that are upregulated by mutant RAS and exhibit potent antitumor activity, demonstrating their efficacy in targeting undruggable proteins outside the cell.645–649”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [646]
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“They bind to cell surface receptors that are upregulated by mutant RAS and exhibit potent antitumor activity, demonstrating their efficacy in targeting undruggable proteins outside the cell.645–649”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [646]
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Vandraas, K. F., Naume, B., Sætersdal, A. B., & Blix, E. S. (2026) · Tidsskrift for Den norske legeforening · doi:10.4045/tidsskr.26.0199
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Metadata
- Authors
- Lambert, J. M., & Morris, C. Q.
- Affiliations
- ImmunoGen (United States) (US)
- Corresponding author
- Lambert, John M.
- Venue
- Advances in Therapy
- Published
- 2017-03-30
- Volume
- 34
- Issue
- 5
- Pages
- 1015-1035
- ISSN
- 0741-238X (ISSN-L)
- 1865-8652
- PMC
- PMC5427099
- OpenAlex
- W2603088210
- Cited by
- 304
- References
- 102
- Citations by year
- 2026: 30 · 2025: 21 · 2024: 18 · 2023: 24 · 2022: 16 · 2021: 49 · 2020: 48 · 2019: 45 · 2018: 45 · 2017: 7
- FWCI
- 5.99
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Advances in Therapy (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Monoclonal and Polyclonal Antibodies Research
- Life Sciences › Immunology and Microbiology › Immunology › Toxin Mechanisms and Immunotoxins
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Keywords
- antibody-drug conjugates, solid tumors, precision oncology, targeted drug delivery, maytansinoids, auristatin, calicheamicin, gemtuzumab ozogamicin, brentuximab vedotin, trastuzumab emtansine, target expression, patient selection, platinum-resistant ovarian cancer, mesothelioma, triple-negative breast cancer, glioblastoma, small cell lung cancer, cytotoxic payloads
- MeSH terms
- Trastuzumab, Gemtuzumab, Ado-Trastuzumab Emtansine, Aminoglycosides, Antineoplastic Agents, Humans, Maytansine, Neoplasms, Oligopeptides, Immunoconjugates, Antibodies, Monoclonal, Humanized, Aminobenzoates, Sialic Acid Binding Ig-like Lectin 3
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