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Updated: Jun 10, 2026

Initial Evaluation of Antibody-conjugates Modified with Viral-derived Peptides for Increasing Cellular Accumulation and Improving Tumor Targeting
Published on: March 8, 2018
Antibody-drug conjugates: targeted drug delivery for cancer
Stephen C Alley1, Nicole M Okeley, Peter D Senter
1Seattle Genetics, Inc., 21823 30th Drive SE, Bothell, WA 98021, United States. SAlley@seagen.com
Abstract:
The antibody-drug conjugate field has made significant progress recently owing to careful optimization of several parameters, including mAb specificity, drug potency, linker technology, and the stoichiometry and placement of conjugated drugs. The underlying reason for this has been obtained in pre-clinical biodistribution and pharmacokinetics studies showing that targeted delivery leads to high intratumoral free drug concentrations, while non-target tissues are largely spared from chemotherapeutic exposure. Recent developments in the field have led to an increase in the number of ADCs being tested clinically, with 3 in late stage clinical trials: brentuximab vedotin (also referred to as SGN-35) for Hodgkin lymphoma; Trastuzumab-DM1 for breast cancer; and Inotuzumab ozogamicin for non-Hodgkin lymphoma. This review highlights the recent pre-clinical and clinical advances that have been made.
Insights
Antibody-drug conjugates (ADCs) show promise in cancer therapy due to targeted drug delivery. Recent advances in ADCs have led to increased clinical trials for various lymphomas and breast cancer.
Area of Science:
- Oncology
- Pharmacology
- Biotechnology
Background:
- The field of antibody-drug conjugates (ADCs) has advanced significantly.
- Progress is attributed to optimizing mAb specificity, drug potency, linker technology, and drug conjugation.
- Pre-clinical studies demonstrate targeted delivery of high intratumoral drug concentrations with minimal exposure to non-target tissues.
Purpose of the Study:
- To review recent pre-clinical and clinical advances in the antibody-drug conjugate field.
- To highlight key developments driving the increased clinical testing of ADCs.
Main Methods:
- Review of pre-clinical biodistribution and pharmacokinetic studies.
- Analysis of recent clinical trial data for antibody-drug conjugates.
Main Results:
- Optimized ADC parameters lead to effective targeted drug delivery.
- High intratumoral drug concentrations achieved with reduced systemic toxicity.
- Three ADCs (brentuximab vedotin, Trastuzumab-DM1, Inotuzumab ozogamicin) are in late-stage clinical trials for Hodgkin lymphoma, breast cancer, and non-Hodgkin lymphoma, respectively.
Conclusions:
- Antibody-drug conjugate technology is rapidly advancing.
- Targeted delivery strategies are improving therapeutic efficacy and safety profiles.
- Increased clinical development signifies the growing potential of ADCs in cancer treatment.
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