Evidence map›Paper›PMID 26565002›Full record

ArticleHaematologica2016

Clinical significance of bax/bcl-2 ratio in chronic lymphocytic leukemia.

Maria Ilaria Del Principe, Michele Dal Bo, Tamara Bittolo, Francesco Buccisano, Francesca Maria Rossi, Antonella Zucchetto, Davide Rossi, Riccardo Bomben, Luca Maurillo, Mariagiovanna Cefalo and 7 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 61 citations in OpenAlex.

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  18. Formaldehyde exposure and leukemia risk: a comprehensive review and network-based toxicogenomic approach.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2021
    Review
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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 at 3 institutions in 1 country.

Maria Ilaria Del PrincipeEmatologia, Dipartimento di Biomedicina e Prevenzione, S. Eugenio Hospital and Università Tor Vergata, Roma, Italy.
Michele Dal BoUnità Clinica e Sperimentale Onco-Ematologica, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Italy.
Tamara BittoloUnità Clinica e Sperimentale Onco-Ematologica, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Italy.
Francesco BuccisanoEmatologia, Dipartimento di Biomedicina e Prevenzione, S. Eugenio Hospital and Università Tor Vergata, Roma, Italy.
Francesca Maria RossiUnità Clinica e Sperimentale Onco-Ematologica, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Italy.
Antonella ZucchettoUnità Clinica e Sperimentale Onco-Ematologica, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Italy.
Davide RossiEmatologia, Università del Piemonte Orientale, Novara, Italy.
Riccardo BombenUnità Clinica e Sperimentale Onco-Ematologica, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Italy.
Luca MaurilloEmatologia, Dipartimento di Biomedicina e Prevenzione, S. Eugenio Hospital and Università Tor Vergata, Roma, Italy.
Mariagiovanna CefaloEmatologia, Dipartimento di Biomedicina e Prevenzione, S. Eugenio Hospital and Università Tor Vergata, Roma, Italy.
Giovanna De SantisEmatologia, Dipartimento di Biomedicina e Prevenzione, S. Eugenio Hospital and Università Tor Vergata, Roma, Italy.
Adriano VendittiEmatologia, Dipartimento di Biomedicina e Prevenzione, S. Eugenio Hospital and Università Tor Vergata, Roma, Italy.
Gianluca GaidanoEmatologia, Università del Piemonte Orientale, Novara, Italy.
Sergio AmadoriEmatologia, Dipartimento di Biomedicina e Prevenzione, S. Eugenio Hospital and Università Tor Vergata, Roma, Italy.
Paolo de FabritiisEmatologia, Dipartimento di Biomedicina e Prevenzione, S. Eugenio Hospital and Università Tor Vergata, Roma, Italy.
Valter GatteiUnità Clinica e Sperimentale Onco-Ematologica, Centro di Riferimento Oncologico, I.R.C.C.S., Aviano, Italy.
Giovanni Del PoetaEmatologia, Dipartimento di Biomedicina e Prevenzione, S. Eugenio Hospital and Università Tor Vergata, Roma, Italy g.delpoeta@tin.it del.principe@med.uniroma2.it.
St. Eugenio Hospital · ITCentro di Riferimento Oncologico · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In chronic lymphocytic leukemia the balance between the pro-apoptotic and anti-apoptotic members of the bcl-2 family is involved in the pathogenesis, chemorefractoriness and clinical outcome. Moreover, the recently proposed anti-bcl-2 molecules, such as ABT-199, have emphasized the potential role of of bcl-2 family proteins in the context of target therapies. We investigated bax/bcl-2 ratio by flow cytometry in 502 patients and identified a cut off of 1.50 to correlate bax/bcl-2 ratio with well-established clinical and biological prognosticators. Bax/bcl-2 was 1.50 or over in 263 patients (52%) with chronic lymphocytic leukemia. Higher bax/bcl-2 was associated with low Rai stage, lymphocyte doubling time over 12 months, beta-2 microglobulin less than 2.2 mg/dL, soluble CD23 less than 70 U/mL and a low risk cytogenetic profile (P<0.0001). On the other hand, lower bax/bcl-2 was correlated with unmutated IGHV (P<0.0001), mutated NOTCH1 (P<0.0001) and mutated TP53 (P=0.00007). Significant shorter progression-free survival and overall survival were observed in patients with lower bax/bcl-2 (P<0.0001). Moreover, within IGHV unmutated (168 patients) and TP53 mutated (37 patients) subgroups, higher bax/bcl-2 identified cases with significant longer PFS (P=0.00002 and P=0.039). In multivariate analysis of progression-free survival and overall survival, bax/bcl-2 was an independent prognostic factor (P=0.0002 and P=0.002). In conclusion, we defined the prognostic power of bax/bcl-2 ratio, as determined by a flow cytometric approach, and highlighted a correlation with chemoresistance and outcome in chronic lymphocytic leukemia. Finally, the recently proposed new therapies employing bcl-2 inhibitors prompted the potential use of bax/bcl-2 ratio to identify patients putatively resistant to these molecules.

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy Protocolsbcl-2-Associated X ProteinChlorambucilDisease-Free SurvivalFemaleHumansMaleMiddle AgedPredictive Value of TestsPrednisoloneProto-Oncogene Proteins c-bcl-2Retrospective StudiesBAX protein, humanbcl-2-Associated X ProteinBCL2 protein, humanChlorambucilfludarabinePrednisoloneProto-Oncogene Proteins c-bcl-2RituximabVidarabine

Identifiers

PMID26565002
PMCPMC4697894
OpenAlexW2258708832

What OpenQuestion holds

Textmetadata
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.