The gray area of RQ-PCR-based measurable residual disease: subdividing the “positive, below quantitative range” category
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Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41375-024-02265-z.pdf
Reference10 articles.
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2. Fronkova E, Muzikova K, Mejstrikova E, Kovac M, Formankova R, Sedlacek P, et al. B-cell reconstitution after allogeneic SCT impairs minimal residual disease monitoring in children with ALL. Bone Marrow Transpl. 2008;42:187–96.
3. Kotrova M, van der Velden VHJ, van Dongen JJM, Formankova R, Sedlacek P, Brüggemann M, et al. Next-generation sequencing indicates false-positive MRD results and better predicts prognosis after SCT in patients with childhood ALL. Bone Marrow Transpl. 2017;52:962–8.
4. van der Velden VHJ, Wijkhuijs JM, van Dongen JJM. Non-specific amplification of patient-specific Ig/TCR gene rearrangements depends on the time point during therapy: implications for minimal residual disease monitoring. Leukemia. 2008;22:641–4.
5. Schwinghammer C, Koopmann J, Chitadze G, Karawajew L, Brüggemann M, Eckert C. A new view on minimal residual disease quantification in acute lymphoblastic leukemia using droplet digital PCR. J Mol Diagn. 2022;24:856–66.
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