TY - CHAP
T1 - Droplet digital PCR for minimal residual disease detection in mature lymphoproliferative disorders
AU - Drandi, Daniela
AU - Ferrero, Simone
AU - Ladetto, Marco
N1 - Publisher Copyright:
© Springer Science+Business Media, LLC, part of Springer Nature 2018.
PY - 2018
Y1 - 2018
N2 - Minimal residual disease (MRD) detection has a powerful prognostic relevance for response evaluation and prediction of relapse in hematological malignancies. Real-time quantitative PCR (qPCR) has become the settled and standardized method for MRD assessment in lymphoid disorders. However, qPCR is a relative quantification approach, since it requires a reference standard curve. Droplet digital™ PCR (ddPCR™) allows a reliable absolute tumor burden quantification withdrawing the need for preparing, for each experiment, a tumor-specific standard curve. We have recently shown that ddPCR has a good concordance with qPCR and could be a feasible and reliable tool for MRD monitoring in mature lymphoproliferative disorders. In this chapter we describe the experimental workflow, from the detection of the clonal molecular marker to the MRD monitoring by ddPCR, in patients affected by multiple myeloma, mantle cell lymphoma and follicular lymphoma. However, standardization programs among different laboratories are needed in order to ensure the reliability and reproducibility of ddPCR-based MRD results.
AB - Minimal residual disease (MRD) detection has a powerful prognostic relevance for response evaluation and prediction of relapse in hematological malignancies. Real-time quantitative PCR (qPCR) has become the settled and standardized method for MRD assessment in lymphoid disorders. However, qPCR is a relative quantification approach, since it requires a reference standard curve. Droplet digital™ PCR (ddPCR™) allows a reliable absolute tumor burden quantification withdrawing the need for preparing, for each experiment, a tumor-specific standard curve. We have recently shown that ddPCR has a good concordance with qPCR and could be a feasible and reliable tool for MRD monitoring in mature lymphoproliferative disorders. In this chapter we describe the experimental workflow, from the detection of the clonal molecular marker to the MRD monitoring by ddPCR, in patients affected by multiple myeloma, mantle cell lymphoma and follicular lymphoma. However, standardization programs among different laboratories are needed in order to ensure the reliability and reproducibility of ddPCR-based MRD results.
KW - BCL1/IGH
KW - BCL2/IGH
KW - Droplet digital PCR
KW - Follicular lymphoma (FL)
KW - Immunoglobulin heavy-chain gene (IGH)
KW - Mantle cell lymphoma (MCL)
KW - Minimal residual disease (MRD)
KW - Multiple myeloma (MM)
KW - T(11;14) translocation
KW - T(14;18) translocation
UR - http://www.scopus.com/inward/record.url?scp=85046334645&partnerID=8YFLogxK
U2 - 10.1007/978-1-4939-7778-9_14
DO - 10.1007/978-1-4939-7778-9_14
M3 - Chapter
T3 - Methods in Molecular Biology
SP - 229
EP - 256
BT - Methods in Molecular Biology
PB - Humana Press Inc.
ER -