Evidence map›Paper›PMID 33542480›Full record

Observational studyLeukemia2021

Lymphocyte doubling time in chronic lymphocytic leukemia modern era: a real-life study in 848 unselected patients.

Tycho Baumann, Riccardo Moia, Gianluca Gaidano, Julio Delgado, Adalgisa Condoluci, Neus Villamor, Anil Babu Payedimarri, Dolors Costa, Andrea Patriarca, Carlos Jiménez-Vicente and 2 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Leukemia, 2021. 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
2.0field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 20 citations in OpenAlex.

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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

12 authors at 5 institutions in 3 countries.

Tycho Baumann *Department of Hematology, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Riccardo Moia *Division of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.
Gianluca GaidanoDivision of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.ORCID http://orcid.org/0000-0002-4681-0151
Julio DelgadoDepartment of Hematology, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Adalgisa CondoluciDivision of Hematology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Neus VillamorDepartment of Pathology, Hospital Clinic, University of Barcelona, Barcelona, Spain.ORCID http://orcid.org/0000-0001-6538-4111
Anil Babu PayedimarriDivision of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.ORCID http://orcid.org/0000-0003-4298-1305
Dolors CostaCancer Cytogenetics, Department of Pathology, Hospital Clinic, Barcelona, Spain.
Andrea PatriarcaDivision of Hematology, Department of Translational Medicine, University of Eastern Piedmont, Novara, Italy.
Carlos Jiménez-VicenteDepartment of Hematology, Hospital Clinic, University of Barcelona, Barcelona, Spain.
Davide RossiDivision of Hematology, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Emili MontserratDepartment of Hematology, Hospital Clinic, University of Barcelona, Barcelona, Spain. emontse@clinic.cat.
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversitat de Barcelona · ESHospital Clínic de Barcelona · ESInstitute of Oncology Research · CHHospital Universitario 12 De Octubre · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prognostic significance of lymphocyte doubling time (LDT) in chronic lymphocytic leukemia (CLL) was identified when the biology of the disease was poorly understood and therapy was not effective. We assessed the clinical and biological significance of LDT in 848 CLL patients in a real-life setting and the context of new biomarkers and effective therapy. A short LDT (≤12 months) was enriched for adverse biomarkers. Patients with a rapid LDT did need therapy shortly after diagnosis (median 23 months vs. not reached; p < 0.001) and had a poorer overall survival (median 95 months vs. not reached p < 0.001). LDT, IGHV mutational status, Beta-2 microglobulin, and Rai clinical stage were independent predictors for time to first treatment in the whole series and in Binet stage A patients. No correlation was observed between LDT and response to chemoimmunotherapy. However, a short LDT along with age ≥65 years, high-risk FISH (del(17p), del(11q)), unmutated IGHV, increased Beta-2 microglobulin, and TP53 mutations predicted short survival. Moreover, the prognostic significance of LDT was independent of the CLL-IPI and the Barcelona/Brno prognostic model. LDT remains an important outcome marker in the modern CLL era and should be incorporated into the clinical assessment and stratification of CLL patients.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsFemaleFollow-Up StudiesHumansImmunotherapyLeukemia, Lymphocytic, Chronic, B-CellLymphocytesMaleMiddle AgedPrognosisRetrospective StudiesSurvival Rate

Identifiers

PMID33542480
OpenAlexW3128153790

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.