Evidence map›Paper›PMID 25581025›Full record

ArticleAmerican journal of hematology2015

Hodgkin transformation of chronic lymphocytic leukemia: Incidence, outcomes, and comparison to de novo Hodgkin lymphoma.

Sameer A Parikh, Thomas M Habermann, Kari G Chaffee, Timothy G Call, Wei Ding, Jose F Leis, William R Macon, Susan M Schwager, Kay M Ristow, Luis F Porrata and 3 more

Abstract readComparative Study
In one paragraph

Article in American journal of hematology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Trial
  2. Pembrolizumab in relapsed or refractory Richter syndrome.British journal of haematology · 2020
    Trial
  3. Article
  4. Article
  5. Article
  6. Increased Frequency of the Chemokine Receptor CCR2 on Circulating CD19+CD5+ Lymphocytes in Therapy-Naïve CLL Patients With the Detectable EBV DNA and High-Avidity Antibodies Against the EBV Capsid Antigen.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Richter's Transformation.Current oncology reports · 2022
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  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

13 authors.

Sameer A ParikhDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Thomas M Habermann
Kari G Chaffee
Timothy G Call
Wei Ding
Jose F Leis
William R Macon
Susan M Schwager
Kay M Ristow
Luis F Porrata
Neil E Kay
Susan L Slager
Tait D Shanafelt

Funding

Combination Therapy in B-Chronic Lymphocytic LeukemiaR01CA095241 · NCI · MAYO CLINIC ROCHESTER · PI KAY, NEIL E · 2002 to 2012
$5.7M
Targeting Akt Activation in CLLK23CA160345 · NCI · MAYO CLINIC ROCHESTER · PI DING, WEI · 2011 to 2015
$837k
NCI NIH HHS CA95241NCI NIH HHS K23 CA160345NCI NIH HHS K23CA160345NCI NIH HHS R01 CA095241
6 · The paper itself

Abstract

Although transformation to Hodgkin lymphoma (HL) is a recognized complication in patients with chronic lymphocytic leukemia (CLL), its incidence, clinical characteristics and outcomes are not well defined. We used the Mayo Clinic CLL and Lymphoma Databases to identify CLL patients who developed biopsy-proven HL (CLL/HL) on follow-up, as well as cases of de novo HL (i.e., without prior CLL). Among 3887 CLL patients seen at Mayo Clinic from January 1995 through August 2011, 26 (0.7%) developed HL. In a nested cohort of 2,465 newly diagnosed CLL patients followed prospectively, the incidence of HL was 0.05%/year (10 year risk = 0.5%). The median overall survival (OS) from date of HL diagnosis in patients with CLL/HL was 3.9 years compared to not reached for de novo HL patients (n = 709) seen during the same time interval (P < 0.001). The shorter OS of CLL/HL patients persisted after adjusting for differences in age and Ann Arbor stage of disease. The International Prognostic score (IPS) developed for de novo HL stratified prognosis among CLL/HL patients with median survival of not reached, 6.2, 2.4, and 0.3 years (P = 0.006) for those with IPS scores of ≤2, 3, 4, and ≥5, respectively. In summary, approximately 1 of every 200 CLL patients will develop HL within 10 years. Survival after HL diagnosis in patients with CLL is shorter than de novo HL patients. The IPS for de novo HL may be useful for stratifying survival in CLL/HL patients.

Indexed as

AgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsCell Transformation, NeoplasticDatabases, FactualDisease-Free SurvivalFemaleHodgkin DiseaseHumansIncidenceLeukemia, Lymphocytic, Chronic, B-CellMaleMiddle AgedProspective StudiesRisk Factors

Identifiers

PMID25581025
PMCPMC4438308

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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.