'Targeting' Improved Outcomes with Antibody-Drug Conjugates in Non-Small Cell Lung Cancer-An Updated Review
Saurav Verma1,2, Daniel Breadner1,2, Jacques Raphael1,2
1Division of Medical Oncology, Department of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada.
Abstract:
Antibody-Drug conjugates (ADCs) are a relatively new class of drugs with a promise to improve the outcomes in specific cancers. By delivering the cytotoxic agent to tumor cells expressing specific antigens, ADCs achieve a better therapeutic index and more potency. ADCs have been approved for several hematological and solid malignancies, including breast, urothelial and gastric carcinoma. Recently, trastuzumab deruxtecan (TDXd) was the first ADC approved for previously treated metastatic HER2-mutant non-small cell lung cancer (NSCLC). Many promising ADCs are in the pipeline for clinical development in non-small cell lung cancer, including sacituzumab govitecan, patritumab deruxtecan, datopotamab deruxtecan and tusamitamab ravtansine. There is a hope that these drugs would cater to the unmet need of specific patient populations, including patients with currently untargetable mutations. We hope these drugs, e.g., TROP2 targeted ADCs, will also give more options for therapy in NSCLC to improve outcomes for patients. In this comprehensive review, we will be discussing the recent evidence including targets, efficacy and the safety of newer ADC candidates in NSCLC. We will also briefly discuss the specific toxicities, novel biomarkers, overcoming resistance mechanisms, challenges and the way forward, as these new ADCs and combinations find a way into the clinical practice.
Insights
Antibody-drug conjugates (ADCs) offer new hope for non-small cell lung cancer (NSCLC) treatment. This review covers emerging ADCs targeting specific mutations and antigens to improve patient outcomes.
Area of Science:
- Oncology
- Pharmacology
- Biotechnology
Background:
- Antibody-drug conjugates (ADCs) represent a novel therapeutic class for cancer treatment.
- ADCs enhance drug potency and therapeutic index by targeting tumor-specific antigens.
- Approved ADCs have shown efficacy in various hematological and solid tumors.
Purpose of the Study:
- To review recent advancements in ADCs for non-small cell lung cancer (NSCLC).
- To discuss emerging ADC candidates, their targets, efficacy, and safety profiles in NSCLC.
- To explore challenges, biomarkers, and future directions for ADCs in NSCLC treatment.
Main Methods:
- Comprehensive literature review of recent clinical evidence on ADCs in NSCLC.
- Analysis of data on ADC targets, efficacy, and safety.
- Discussion of specific toxicities, resistance mechanisms, and biomarkers.
Main Results:
- Trastuzumab deruxtecan (TDXd) is the first ADC approved for HER2-mutant NSCLC.
- Several promising ADCs (e.g., sacituzumab govitecan, TROP2-targeted agents) are in clinical development for NSCLC.
- These agents aim to address unmet needs in patient populations with currently untargetable mutations.
Conclusions:
- Emerging ADCs hold significant promise for improving outcomes in NSCLC.
- Further research into targets, biomarkers, and resistance mechanisms is crucial for optimizing ADC therapy.
- ADCs are expected to expand therapeutic options and improve patient care in NSCLC.
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