Evidence map›Paper›PMID 33802502›Full record

ArticleCancers2021

Use of Measurable Residual Disease to Evolve Transplant Policy in Acute Myeloid Leukemia: A 20-Year Monocentric Observation.

Francesco Buccisano, Raffaele Palmieri, Alfonso Piciocchi, Luca Maurillo, Maria Ilaria Del Principe, Giovangiacinto Paterno, Stefano Soddu, Raffaella Cerretti, Gottardo De Angelis, Benedetta Mariotti and 10 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

20 authors at 2 institutions in 1 country.

Francesco BuccisanoDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.ORCID 0000-0003-4320-9253
Raffaele PalmieriDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Alfonso PiciocchiCentro Dati Fondazione GIMEMA, 00100 Rome, Italy.
Luca MaurilloDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Maria Ilaria Del PrincipeDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Giovangiacinto PaternoDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Stefano SodduCentro Dati Fondazione GIMEMA, 00100 Rome, Italy.
Raffaella CerrettiDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Gottardo De AngelisDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Benedetta MariottiDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Maria Antonietta Irno ConsalvoDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Consuelo ContiDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Daniela FraboniDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Mariadomenica DivonaDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Tiziana OttoneDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Serena LavorgnaDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Paola PanettaDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Maria Teresa VosoDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
William ArceseDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.
Adriano VendittiDepartment of Biomedicine and Prevention, University Tor Vergata of Roma, 00133 Rome, Italy.ORCID 0000-0002-0245-0553
University of Rome Tor Vergata · ITFondazione Gimema Onlus · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Measurable residual disease (MRD) is increasingly employed as a biomarker of quality of complete remission (CR) in intensively treated acute myeloid leukemia (AML) patients. We evaluated if a MRD-driven transplant policy improved outcome as compared to a policy solely relying on a familiar donor availability. High-risk patients (adverse karyotype, FLT3-ITD) received allogeneic hematopoietic cell transplant (alloHCT) whereas for intermediate and low risk ones (CBF-AML and NPM1-mutated), alloHCT or autologous SCT was delivered depending on the post-consolidation measurable residual disease (MRD) status, as assessed by flow cytometry. For comparison, we analyzed a matched historical cohort of patients in whom alloHCT was delivered based on the sole availability of a matched sibling donor. Ten-years overall and disease-free survival were longer in the MRD-driven cohort as compared to the historical cohort (47.7% vs. 28.7%,

Indexed as

AMLbiomarkerscytogenetics and molecular markersMRDmultiparametric flow cytometry

Identifiers

PMID33802502
PMCPMC7959451
OpenAlexW3134236839

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.