Evidence map›Paper›PMID 39983071›Full record

ArticleBlood advances2025

Outcomes of the COVID-19 pandemic in chronic lymphocytic leukemia: focus on the very early period and Omicron era.

Pontus Hedberg, Lisa Blixt, Sandra Eketorp Sylvan, Isabela Killander Möller, Hannes Lindahl, Fredrik Kahn, Åsa Nilsdotter-Augustinsson, Mats Fredrikson, Sofia Nyström, Peter Bergman and 5 more

Abstract read
In one paragraph

Article in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Pontus HedbergDepartment of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0003-3153-098X
Lisa BlixtDepartment of Hematology, Karolinska University Hospital, Stockholm, Sweden.
Sandra Eketorp SylvanDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Isabela Killander MöllerDepartment of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-4105-2902
Hannes LindahlDepartment of Clinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0002-4447-9426
Fredrik KahnDepartment of Clinical Sciences, Lund, Section for Infection Medicine, Lund University, Lund, Sweden.ORCID 0000-0001-5566-6350
Åsa Nilsdotter-AugustinssonDivision of Inflammation and Infection, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.ORCID 0000-0001-5719-5601
Mats FredriksonDepartment of Biomedical and Clinical Sciences, Faculty of Medicine, Linköping University, Linköping, Sweden.ORCID 0000-0003-3067-8587
Sofia NyströmDepartment of Biomedical and Clinical Sciences, Faculty of Medicine, Linköping University, Linköping, Sweden.
Peter BergmanDepartment of Clinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0003-3306-3713
Christina CarlanderDepartment of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-9962-5964
Soo AlemanDepartment of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0003-0461-4870
Pontus NauclérDepartment of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.
Anders ÖsterborgDepartment of Hematology, Karolinska University Hospital, Stockholm, Sweden.
Lotta HanssonDepartment of Hematology, Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0001-6614-5737

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractIndividuals with chronic lymphocytic leukemia (CLL) face an increased risk for severe COVID-19. This study from Sweden, a country that only had a few mandatory restrictions at the onset of the pandemic, used 10 nationwide registers to compare the risks for severe COVID-19 outcomes of polymerase chain reaction-verified severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections through February 2023 in individuals with and those without CLL. From a population of 8 275 839 (6653 CLL) individuals born between 1930 and 2003, 2 088 163 first infections (1289 CLL) were included. The 90-day all-cause mortality rate and adjusted relative risk (aRR; 95% confidence interval) for individuals with CLL vs the general population was 24.8% (1.95; 1.58-2.41) during wild-type, 17.2% (2.38; 1.58-3.57) during Alpha, 4.1% (0.71; 0.24-2.08) during Delta, and 12.6% (1.49; 1.24-1.78) during Omicron infections. Their mortality during Omicron was 0.6% (<65 years), 5.4% (65-74 years), and 19.7% (≥75 years). Small molecule inhibitors (1.56; 1.03-2.37) and corticosteroid usage (1.45; 1.04-2.02) was associated with increased mortality. Next, we analyzed the all-cause mortality in the capital (Stockholm), widely affected by SARS-CoV-2 at the onset of the pandemic. Mortality in individuals with CLL increased by 55% during the first 6 months of 2020 vs 2019, and the age- and sex-aRR by 30 June was 1.53 (1.09-2.15) for individuals with CLL (P = .02) and 1.29 (1.25-1.33) for the general population (P < .001). Collectively, a significantly increased risk for severe COVID-19 and death was observed among individuals with CLL in Sweden, particularly at the onset of the pandemic when few national protective measures were introduced and also after Omicron emerged, emphasizing the need for a more pro-active pandemic strategy for CLL.

Indexed as

COVID-19Leukemia, Lymphocytic, Chronic, B-CellSARS-CoV-2AdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPandemicsRegistriesRisk FactorsSweden

Identifiers

PMID39983071
PMCPMC12242415

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.