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Updated: Jul 10, 2026

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
New developments in multitargeted therapy for patients with solid tumours
C Le Tourneau1, S Faivre, E Raymond
1Service Inter-Hospitalier de Cancérologie Beaujon-Bichat, Hôpital Beaujon, 100, Boulevard du Général Leclerc, Clichy, France. christophe.le-tourneau@bjn.aphp.fr
Abstract:
Molecularly targeted anticancer therapies are now available that have been rationally designed to interact with specific proteins associated with tumour development or progression. The main purpose of this article is to review the rationale and phase II/III clinical data for approved and emerging multitargeted agents used in the treatment of solid tumours. Imatinib, sunitinib, sorafenib, and dasatinib have all produced advances in the treatment of the indications for which they are licensed and show promising activity in other tumour types. Newer multitargeted agents in development appear, from preliminary phase I and II data, to be active in a broad range of tumour types, although the clinical relevance of this activity is as yet unproven. The challenge for the future is to ensure that the potential of multitargeted agents is maximised by selecting the patient populations most likely to derive clinical benefit, by optimising the dose schedules used, and by investigating multitargeted therapies combined with other agents of the same type or with conventional chemotherapy and/or other treatment modalities.
Insights
Molecularly targeted therapies offer new ways to treat solid tumors by targeting specific proteins. Future research should focus on patient selection and combination therapies to maximize benefits.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Molecularly targeted anticancer therapies are rationally designed to interact with specific proteins involved in tumor development and progression.
- These targeted agents represent a significant advancement over traditional chemotherapy.
Purpose of the Study:
- To review the rationale and clinical data (Phase II/III) for approved and emerging multitargeted agents in solid tumor treatment.
- To discuss future challenges and strategies for optimizing the use of these agents.
Main Methods:
- Review of published Phase I, II, and III clinical trial data for approved and investigational multitargeted agents.
- Analysis of drug mechanisms of action and clinical efficacy in various solid tumor types.
Main Results:
- Approved agents like imatinib, sunitinib, sorafenib, and dasatinib have shown efficacy in licensed indications and promise in other tumor types.
- Emerging multitargeted agents demonstrate broad-spectrum activity in early-phase trials, though clinical relevance requires further validation.
Conclusions:
- Multitargeted agents have advanced cancer treatment, with approved drugs showing significant clinical benefits.
- Future efforts should focus on personalized medicine approaches, including patient selection, optimized dosing, and combination strategies to enhance therapeutic outcomes.
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