Orthotopic xenografts models in relapse/refractory lymphomas: a preclinical model for therapeutic, mechanistic and functional studies

Introduction: Novel targeted therapies have improved the treatment of relapse/refractory lymphomas, although overcoming therapy resistance is still a main clinical challenge and an overriding priority for patients and treating physicians. Patient-derived orthotopic xenografts (PDOXs), in which a human tumor biopsy is implanted in an immunodeficient mice in the same organ as the tumor is grown in the patient, are the most advanced in vivotumor preclinical models, as they reproduce better patient tumor behavior and therapeutic responses. Aim: To generate and characterize PDOXs for refractory and relapsed lymphomas from different histologies and to derive cell lines from these PDOX in order to obtain advanced preclinical models to examine the mechanisms involved in drug resistance through therapeutic, mechanistic and functional studies. Material and Methods: Systematic and prospective study in which a fragment of the patients' biopsy has been used to generate PDOXs. Fresh tumor biopsies were grafted in spleen and/or mesenteric lymph nodes or in extranodal sites (according to the location where the tumor grow in the patient), in 1–3 (depending on tissue availability) NOD/LtSz-scid/IL-2Rγchainnull (NSG) mice. Once the tumor grows, the animal was sacrificed and the tumor was re-implanted (2–3 fragments) in the same location in additional animals to expand it for histological, IHQ and molecular characterizations and posterior therapeutic studies. Genetic match between the PDOX and the paired patient tumor from which they derived was assessed using 6 microsatellites by PCR followed by capillary electrophoresis with fluorescence detection. Fusions, point mutations, and expression levels in 125 genes linked to lymphomas were simultaneously detected using Archer® FusionPlex® Lymphoma Kit. Results: We have generated 15 patient derived xenografts (PDX) based in orthotopic implantation from aggressive B and T cell lymphomas, including resistant DLBCLs, adult Burkitt's lymphoma, Hodgkin lymphoma, marginal zone lymphomas and aggressive anaplastic and angioimmunoblastic T-cell lymphomas, among other histologies (Table). All of them mimic the histology of the tumor there were derived and showed genetic match with their respective patient tumor. From 10 of these orthotopic PDX, we have derived cell lines to have paired in vitro and in vivo models. These models are now molecularly characterized using a targeted next generation sequencing assay. In vivo massive pharmacologic screening in this models are ongoing. Keywords: Patient-Derived Xenograft (PDX) Models, Tumor Biology and Heterogeneity No conflicts of interests pertinent to the abstract.