Details

Autor(en) / Beteiligte

• Decary, Stéphanie
• Berne, Pierre-François
• Nicolazzi, Céline
• Lefebvre, Anne-Marie
• Dabdoubi, Tarik
• Cameron, Béatrice
• Rival, Pierrick
• Devaud, Catherine
• Prades, Catherine
• Bouchard, Hervé
• Cassé, Alhassan
• Henry, Christophe
• Amara, Céline
• Brillac, Claire
• Ferrari, Paul
• Maçon, Laetitia
• Lacoste, Eric
• Combeau, Cecile
• Beys, Eric
• Naimi, Souad
• García-Echeverría, Carlos
• Mayaux, Jean-François
• Blanc, Véronique

Titel

Preclinical Activity of SAR408701: A Novel Anti-CEACAM5-maytansinoid Antibody-drug Conjugate for the Treatment of CEACAM5-positive Epithelial Tumors

Ist Teil von

• Clinical cancer research, 2020-12, Vol.26 (24), p.6589-6599

Ort / Verlag

United States

Erscheinungsjahr

2020

Link zum Volltext

Quelle

MEDLINE

Beschreibungen/Notizen

• Carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5) is a glycoprotein that has limited expression in normal adult tissues, but is overexpressed in carcinomas of the gastrointestinal tract, the genitourinary and respiratory systems, and breast cancer. As such, CEACAM5 is an attractive target for antibody-based therapies designed to selectively deliver cytotoxic drugs to certain epithelial tumors. Here, we describe preclinical data for a novel antibody-drug conjugate (ADC), SAR408701, which consists of an anti-CEACAM5 antibody (SAR408377) coupled to a maytansinoid agent DM4 via a cleavable linker. The specificity and binding affinity of SAR408701 to human and cynomolgus monkey CEACAM5 were tested . The cytotoxic activity of SAR408701 was assessed in CEACAM5-expressing tumor cell lines and using patient-derived xenograft mouse models of CEACAM5-positive tumors. Pharmacokinetic-pharmacodynamic and pharmacokinetic-efficacy relationships were established. SAR408701 toxicity was evaluated in cynomolgus monkey. SAR408701 bound selectively to human and cynomolgus monkey CEACAM5 with similar apparent Kd values (0.017 nmol/L and 0.024 nmol/L, respectively). Both and evaluations showed that SAR408701 has cytotoxic activity, leading to efficacy in single and repeated dosing. Single doses of SAR408701 induced significant increases in the tumor expression of phosphorylated histone H3, confirming the tubulin-targeting mechanism of action. The overall toxicity profile of SAR408701 in cynomolgus monkey was similar to that observed after intravenous administration of DM4 alone. On the basis of these preclinical data, the ADC SAR408701 is a promising candidate for development as a potential treatment for patients with CEACAM5-positive tumors.