Evidence map›Paper›PMID 26648836›Full record

ArticleMolecular syndromology2015

Cytogenetic and Molecular Findings in Children with Acute Lymphoblastic Leukemia: Experience of a Single Institution in Argentina.

Mariela C Coccé, Cristina N Alonso, Jorge G Rossi, Andrea R Bernasconi, Maria A Rampazzi, Maria S Felice, Patricia L Rubio, Silvia Eandi Eberle, Adriana Medina, Marta S Gallego

Open access · bronzeAbstract read
In one paragraph

Article in Molecular syndromology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. NovelExperimental hematology & oncology · 2019
    Article
  6. Susceptibility to thiopurine toxicity byColombia medica (Cali, Colombia)
    Observational
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

10 authors at 2 institutions in 2 countries.

Mariela C CoccéCytogenetics Laboratory, Genetics Department, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Cristina N AlonsoDepartment of Hematology and Oncology, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Jorge G RossiDepartment of Immunology and Rheumatology, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Andrea R BernasconiDepartment of Immunology and Rheumatology, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Maria A RampazziCytogenetics Laboratory, Genetics Department, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Maria S FeliceDepartment of Hematology and Oncology, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Patricia L RubioDepartment of Hematology and Oncology, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Silvia Eandi EberleDepartment of Hematology and Oncology, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Adriana MedinaDepartment of Hematology and Oncology, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Marta S GallegoCytogenetics Laboratory, Genetics Department, Hospital de Pediatría 'Prof Dr. Juan P. Garrahan', Buenos Aires, Argentina.
Palmetto Hematology Oncology · USGarrahan Hospital · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of the current study was to evaluate the cytogenetic findings in 1,057 children with acute lymphoblastic leukemia (ALL) referred to the cytogenetics laboratory at the Hospital de Pediatría Dr. Juan P. Garrahan, between 1991 and 2014. Chromosomal abnormalities were evaluated by G-banding and FISH. Since December 2002, RT-PCR determinations were systematically carried out for BCR-ABL1, KMT2A-AFF1, ETV6-RUNX1, and TCF3-PBX1 rearrangements in children, adding KMT2A-MLLT3 and KMT2A-MLLT1 in infants. The percentage of abnormalities detected by cytogenetics was 70.1%. Four novel abnormalities, t(2;8)(p11.2;p22), inv(4)(p16q25), t(1;7)(q25;q32), and t(5;6)(q21;q21), were found in this cohort. We compared cytogenetic and RT-PCR results for BCR-ABL1, KMT2A-AFF1 and TCF3-PBX1 rearrangements in 497 children evaluated by both methods. The results were highly concordant (p < 0.7), and interestingly, FISH was relevant to confirm G-banding findings that were discordant with RT-PCR studies. This study showed the importance of performing G-banding, FISH and RT-PCR simultaneously to improve the detection of chromosomal abnormalities considering their important value in the diagnosis and prognosis of childhood ALL patients. Finally, to the best of our knowledge, this is the first series of cytogenetic findings in children with ALL reported in Argentina.

Indexed as

Childhood acute lymphoblastic leukemiaChromosomal abnormalitiesFISHRT-PCR

Identifiers

PMID26648836
PMCPMC4662297
OpenAlexW2259739371

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.