Claudin 18.2 targeting: overzicht van expressie, zolbetuximab en lopende pipeline-therapieën
Deze narratieve review belicht de expressie van Claudin 18.2 bij maag- en maag-darmovergangscarcinoom, met toenemende data voor pancreas- en ovariumcarcinoom. Na de FDA-goedkeuring van zolbetuximab in combinatie met chemotherapie op basis van de SPOTLIGHT- en GLOW-trials, worden diverse CLDN18.2-gerichte interventies zoals ADC's, CAR-T-cellen en bispecifieke antistoffen actief onderzocht.
Ondanks heterogeniteit en behandelingsgeïnduceerde expressieveranderingen, zijn de pipeline-therapieën over het algemeen goed verdraagbaar bij intensieve anti-emese. Voor optimale patiëntselectie en klinische toepassing zijn gestandaardiseerde biomarkerstrategieën en IHC-kwaliteitscontrole essentieel.
Abstract (original)
Claudin 18.2 (CLDN18.2) is exclusively expressed on gastric mucosal cell tight junctions with minimal expression in other healthy adult tissues. Prior studies assessed expression by immunohistochemistry, mainly membrane staining. The FDA CLDN18.2 threshold for zolbetuximab approval is ≥75% moderate to strong staining. Higher level expression has been seen in a number of cancers including (but not limited to) gastric, gastroesophageal junction (GEJ), pancreatic, and ovarian cancers. CLDN18.2 expression can change with treatment and can exhibit heterogeneity between tumor sites. Zolbetuximab is a recently FDA-approved anti-CLDN18.2 monoclonal antibody for first-line therapy of gastric/GEJ cancers in combination with chemotherapy based on the improvement in outcomes demonstrated in the biomarker selected populations of the SPOTLIGHT and GLOW trials. Given limited single-agent responses rates to zolbetuximab, a number of other CLDN18.2-directed therapies, including antibody-drug conjugates, CAR-T cells, and bispecific antibodies, are under exploration in clinical trials. Despite expression of CLDN18.2 on the gastric mucosa, these therapies have overall been tolerable in clinical trials, albeit with the use of aggressive anti-emetic regimens. Herein, we summarize CLDN18.2 expression in cancer along with clinical trials of zolbetuximab and other CLDN18.2-directed therapies. Given the variability in CLDN18.2 expression within and between tumor types, biomarker-driven approaches will be critical for patient selection in clinical trials and therapeutic approaches.
Dit artikel is een samenvatting van een publicatie in Clinical cancer research : an official journal of the American Association for Cancer Research. Voor het volledige artikel, alle details en referenties verwijzen wij u naar de oorspronkelijke bron.
Lees het volledige artikelDOI: 10.1158/1078-0432.CCR-26-0708