Evidence map›Paper›PMID 27133819›Full record

Trial reportLeukemia2016

PML-RARα kinetics and impact of FLT3-ITD mutations in newly diagnosed acute promyelocytic leukaemia treated with ATRA and ATO or ATRA and chemotherapy.

L Cicconi, M Divona, C Ciardi, T Ottone, A Ferrantini, S Lavorgna, V Alfonso, F Paoloni, A Piciocchi, G Avvisati and 14 more

Open access · greenAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Leukemia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 82 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Atypical singleBlood neoplasia · 2026
    Article
  5. Discrepancies in the Detection ofDiseases (Basel, Switzerland) · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Critical transition and reversion of tumorigenesis.Experimental & molecular medicine · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Significance of Dysplastic Neutrophils with Multiple Auer Rods in Post-therapy Acute Promyelocytic Leukemia.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

24 authors at 12 institutions in 1 country.

L CicconiDipartimento di Biomedicina e Prevenzione, Università degli studi Tor Vergata, Roma, Italy.
M DivonaLaboratorio di Oncoematologia, Policlinico Tor Vergata, Roma, Italy.
C CiardiDipartimento di Biomedicina e Prevenzione, Università degli studi Tor Vergata, Roma, Italy.
T OttoneDipartimento di Biomedicina e Prevenzione, Università degli studi Tor Vergata, Roma, Italy.
A FerrantiniDipartimento di Biomedicina e Prevenzione, Università degli studi Tor Vergata, Roma, Italy.
S LavorgnaDipartimento di Biomedicina e Prevenzione, Università degli studi Tor Vergata, Roma, Italy.
V AlfonsoDipartimento di Biomedicina e Prevenzione, Università degli studi Tor Vergata, Roma, Italy.
F PaoloniGruppo Italiano Malattie EMatologiche dell'Adulto (GIMEMA) Data Center, Rome, Italy.
A PiciocchiGruppo Italiano Malattie EMatologiche dell'Adulto (GIMEMA) Data Center, Rome, Italy.
G AvvisatiDipartimento di Ematologia, Università Campus Biomedico, Rome, Italy.
F FerraraDipartimento di Ematologia e Trapianto di Cellule Staminali, Ospedale Cardarelli, Napoli, Italy.
E Di BonaDipartimento di Terapie cellulari ed Ematologia, Unità Operativa di Ematologia, Vicenza, Italy.
F AlbanoDipartimento di Ematologia, Università di Bari, Bari, Italy.
M BrecciaDipartimento di Biotecnologie Cellulari ed Ematologia, Università La Sapienza, Roma, Italy.
E CerquiDipartimento di Ematologia, Spedali Civili, Brescia, Italy.
M SborgiaDipartimento di Ematologia, Ospedale Civile, Pescara, Italy.
M G KroppAzienda Ospedaliera Pugliese Ciaccio, Catanzaro, Italy.
A SantoroDivisione di Ematologia e Unità di Trapianti di Midollo Osseo, Ospedale Riuniti Villa Sofia-Cervello, Palermo, Italy.
A LevisDipartimento di Oncoematologia, Sopedale SS Antonio e Biagio, Alessandria, Italy.
S SicaUniversità Cattolica Sacro Cuore, Roma.
S AmadoriDipartimento di Biomedicina e Prevenzione, Università degli studi Tor Vergata, Roma, Italy.
M T VosoDipartimento di Biomedicina e Prevenzione, Università degli studi Tor Vergata, Roma, Italy.
F MandelliGruppo Italiano Malattie EMatologiche dell'Adulto (GIMEMA) Data Center, Rome, Italy.
F Lo-CocoDipartimento di Biomedicina e Prevenzione, Università degli studi Tor Vergata, Roma, Italy.
University of Rome Tor Vergata · ITFondazione Gimema Onlus · ITAzienda Ospedaliera Pugliese Ciaccio · ITAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITFondazione Santa Lucia · ITOspedale Antonio Cardarelli · ITOspedale Vincenzo Cervello · ITPoliclinico Tor Vergata · ITSapienza University of Rome · ITUniversità Campus Bio-Medico · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Bari Aldo Moro · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The APL0406 study showed that arsenic trioxide (ATO) and all-trans retinoic acid (ATRA) are not inferior to standard ATRA and chemotherapy (CHT) in newly diagnosed, low-intermediaterisk acute promyelocytic leukaemia (APL). We analysed the kinetics of promyelocytic leukaemia-retinoic acid receptor-α (PML-RARα) transcripts by real-time quantitative PCR (RQ-PCR) in bone marrow samples from 184 patients and assessed the prognostic impact of fms-related tyrosine kinase 3-internal tandem duplication (FLT3-ITD) in 159 patients enrolled in this trial in Italy. After induction therapy, the reduction of PML-RARα transcripts was significantly greater in patients receiving ATRA-CHT as compared with those treated with ATRA-ATO (3.4 vs 2.9 logs; P=0.0182). Conversely, at the end of consolidation, a greater log reduction of PML-RARα transcripts was detected in the ATRA-ATO as compared with the ATRA-CHT group (6.3 vs 5.3 logs; P=0.0024). FLT3-ITD mutations had no significant impact on either event-free survival (EFS) or cumulative incidence of relapse in patients receiving ATRA-ATO, whereas a trend for inferior EFS was observed in FLT3-ITD-positive patients receiving ATRA-CHT. Our study shows at the molecular level that ATRA-ATO exerts at least equal and probably superior antileukaemic efficacy compared with ATRA-CHT in low-intermediaterisk APL. The data also suggest that ATRA-ATO may abrogate the negative prognostic impact of FLT3-ITD.

Indexed as

AdolescentAdultAgedArsenicalsArsenic TrioxideDisease-Free SurvivalFemalefms-Like Tyrosine Kinase 3HumansInduction ChemotherapyItalyKineticsLeukemia, Promyelocytic, AcuteMaleMiddle AgedMutationArsenicalsArsenic Trioxidefms-Like Tyrosine Kinase 3Oncogene Proteins, FusionOxidespromyelocytic leukemia-retinoic acid receptor alpha fusion oncoproteinTretinoin

Identifiers

PMID27133819
OpenAlexW2344085448

What OpenQuestion holds

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Registered trials

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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.