Evidence map›Paper›PMID 33255857›Full record

ArticleJournal of clinical medicine2020

Assessment of Minimal Residual Disease by Next Generation Sequencing in Peripheral Blood as a Complementary Tool for Personalized Transplant Monitoring in Myeloid Neoplasms.

Paula Aguirre-Ruiz, Beñat Ariceta, María Cruz Viguria, María Teresa Zudaire, Zuriñe Blasco-Iturri, Patricia Arnedo, Almudena Aguilera-Diaz, Axier Jauregui, Amagoia Mañú, Felipe Prosper and 7 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Paula Aguirre-RuizHematological Diseases Laboratory, CIMA LAB Diagnostics, University of Navarra, 31008 Pamplona, Navarra, Spain.
Beñat AricetaHematological Diseases Laboratory, CIMA LAB Diagnostics, University of Navarra, 31008 Pamplona, Navarra, Spain.
María Cruz ViguriaNavarra Institute for Health Research (IdiSNA), 31008 Pamplona, Navarra, Spain.ORCID 0000-0002-6092-5393
María Teresa ZudaireNavarra Institute for Health Research (IdiSNA), 31008 Pamplona, Navarra, Spain.
Zuriñe Blasco-IturriHematological Diseases Laboratory, CIMA LAB Diagnostics, University of Navarra, 31008 Pamplona, Navarra, Spain.
Patricia ArnedoHematology Department, Complejo Hospitalario de Navarra, 31008 Pamplona, Navarra, Spain.
Almudena Aguilera-DiazNavarra Institute for Health Research (IdiSNA), 31008 Pamplona, Navarra, Spain.ORCID 0000-0002-1897-3914
Axier JaureguiHematology Department, Complejo Hospitalario de Navarra, 31008 Pamplona, Navarra, Spain.
Amagoia MañúHematological Diseases Laboratory, CIMA LAB Diagnostics, University of Navarra, 31008 Pamplona, Navarra, Spain.
Felipe ProsperNavarra Institute for Health Research (IdiSNA), 31008 Pamplona, Navarra, Spain.ORCID 0000-0001-6115-8790
María Carmen MateosNavarra Institute for Health Research (IdiSNA), 31008 Pamplona, Navarra, Spain.
Marta Fernández-MercadoHematological Diseases Laboratory, CIMA LAB Diagnostics, University of Navarra, 31008 Pamplona, Navarra, Spain.ORCID 0000-0003-3458-9231
María José LarráyozHematological Diseases Laboratory, CIMA LAB Diagnostics, University of Navarra, 31008 Pamplona, Navarra, Spain.
Margarita RedondoNavarra Institute for Health Research (IdiSNA), 31008 Pamplona, Navarra, Spain.
María José CalasanzHematological Diseases Laboratory, CIMA LAB Diagnostics, University of Navarra, 31008 Pamplona, Navarra, Spain.ORCID 0000-0002-0374-3008
Iria VázquezHematological Diseases Laboratory, CIMA LAB Diagnostics, University of Navarra, 31008 Pamplona, Navarra, Spain.ORCID 0000-0003-0027-6384
Eva BandrésNavarra Institute for Health Research (IdiSNA), 31008 Pamplona, Navarra, Spain.ORCID 0000-0002-9497-5356

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with myeloid neoplasms who relapsed after allogenic hematopoietic stem cell transplant (HSCT) have poor prognosis. Monitoring of chimerism and specific molecular markers as a surrogate measure of relapse is not always helpful; therefore, improved systems to detect early relapse are needed. We hypothesized that the use of next generation sequencing (NGS) could be a suitable approach for personalized follow-up post-HSCT. To validate our hypothesis, we analyzed by NGS, a retrospective set of peripheral blood (PB) DNA samples previously evaluated by high-sensitive quantitative PCR analysis using insertion/deletion polymorphisms (indel-qPCR) chimerism engraftment. Post-HCST allelic burdens assessed by NGS and chimerism status showed a similar time-course pattern. At time of clinical relapse in 8/12 patients, we detected positive NGS-based minimal residual disease (NGS-MRD). Importantly, in 6/8 patients, we were able to detect NGS-MRD at time points collected prior to clinical relapse. We also confirmed the disappearance of post-HCST allelic burden in non-relapsed patients, indicating true clinical specificity. This study highlights the clinical utility of NGS-based post-HCST monitoring in myeloid neoplasia as a complementary specific analysis to high-sensitive engraftment testing. Overall, NGS-MRD testing in PB is widely applicable for the evaluation of patients following HSCT and highly valuable to personalized early treatment intervention when mixed chimerism is detected.

Indexed as

chimerismhematopoietic stem cell transplant (HSCT)minimal residual disease (MRD)myeloid leukemianext generation sequencing (NGS)

Identifiers

PMID33255857
PMCPMC7760908

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.