A Comprehensive ddPCR Strategy for Sensitive and Reliable Monitoring of CAR-T Cell Kinetics in Clinical Applications

Author:

Wiedemann Gertrud12ORCID,Bacher Ulrike1ORCID,Joncourt Raphael1,Solly Françoise3,Widmer Corinne C.456,Zeerleder Sacha2,Novak Urban78,Pabst Thomas78ORCID,Porret Naomi A.12ORCID

Affiliation:

1. Department of Hematology and Central Hematological Laboratory, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland

2. Department for BioMedical Research, University of Bern, 3008 Bern, Switzerland

3. Service and Central Laboratory of Hematology, Lausanne University Hospital (CHUV), 1011 Lausanne, Switzerland

4. Department of Medical Oncology and Hematology, University Hospital Zurich, 8091 Zurich, Switzerland

5. Department of Hematology, University Hospital of Basel, 4031 Basel, Switzerland

6. Laboratory Medicine, Diagnostic Hematology, 4031 Basel, Switzerland

7. Department of Medical Oncology, Inselspital, University Hospital of Bern, 3010 Bern, Switzerland

8. Center for Hemato-Oncology, University Cancer Center, 3010 Bern, Switzerland

Abstract

In this study, we present the design, implementation, and successful use of digital droplet PCR (ddPCR) for the monitoring of chimeric antigen receptor T-cell (CAR-T) expansion in patients with B-cell malignancies treated with different CAR-T products at our clinical center. Initially, we designed a specific and highly sensitive ddPCR assay targeting the junction between the 4-1BB and CD3ζ domains of tisa-cel, normalized with RPP30, and validated it using blood samples from the first tisa-cel-treated patient in Switzerland. We further compared this assay with a published qPCR (quantitative real-time PCR) design. Both assays showed reliable quantification of CAR-T copies down to 20 copies/µg DNA. The reproducibility and precision were confirmed through extensive testing and inter-laboratory comparisons. With the introduction of other CAR-T products, we also developed a corresponding ddPCR assay targeting axi-cel and brexu-cel, demonstrating high specificity and sensitivity with a limit of detection of 20 copies/µg DNA. These assays are suitable for CAR-T copy number quantification across multiple sample types, including peripheral blood, bone marrow, and lymph node biopsy material, showing robust performance and indicating the presence of CAR-T cells not only in the blood but also in target tissues. Longitudinal monitoring of CAR-T cell kinetics in 141 patients treated with tisa-cel, axi-cel, or brexu-cel revealed significant expansion and long-term persistence. Peak expansion correlated with clinical outcomes and adverse effects, as is now well known. Additionally, we quantified the CAR-T mRNA expression, showing a high correlation with DNA copy numbers and confirming active transgene expression. Our results highlight the quality of ddPCR for CAR-T monitoring, providing a sensitive, precise, and reproducible method suitable for clinical applications. This approach can be adapted for future CAR-T products and will support the monitoring and the management of CAR-T cell therapies.

Publisher

MDPI AG

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