. The most used techniques to evaluate MRD are multiparametric flow cytometry (MFC), quantitative reverse transcription polymerase chain reaction (RT-qPCR), and high-throughput next-generation sequencing (NGS). Each method varies in terms of advantages, disadvantages, and MRD sensitivity. MRD negativity after induction treatment and after allogeneic hematopoietic cell transplantation (HCT) is an important prognostic marker that has consistently been shown to be associated with improved outcomes. Blinatumomab, a new targeted therapy for Ph + ALL, demonstrates high efficacy in eradicating MRD and improving patient outcomes. In the relapsed/refractory setting, the use of inotuzumab ozogamicin and tisagenlecleucel has shown promise in eradicating MRD. The presence of MRD has become an important predictive measure in Ph + ALL. Current studies evaluate the use of MRD in treatment decisions, especially in expanding therapeutic options for Ph + ALL, including tyrosine kinase inhibitors, targeted antibody therapies, chimeric antigen receptor cell therapy, and HCT.
Keyphrases
- acute lymphoblastic leukemia
- cell therapy
- flow cytometry
- stem cells
- bone marrow
- stem cell transplantation
- mesenchymal stem cells
- cancer therapy
- low dose
- diffuse large b cell lymphoma
- type diabetes
- dna methylation
- skeletal muscle
- big data
- mass spectrometry
- drug delivery
- machine learning
- signaling pathway
- cell death
- high dose
- replacement therapy
- hodgkin lymphoma
- circulating tumor cells