Evidence map›Paper›PMID 35846218›Full record

ArticleEJHaem2022

Second primary malignancies in chronic lymphocytic leukaemia: Skin, solid organ, haematological and Richter's syndrome.

Yandong Shen, Luke Coyle, Ian Kerridge, William Stevenson, Christopher Arthur, Naomi McKinlay, Keith Fay, Christopher Ward, Matthew Greenwood, Oliver Giles Best and 4 more

Open access · diamondAbstract read
In one paragraph

Article in EJHaem, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.4field-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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  9. Risk of Incident Melanoma Among Individuals With Low-Count Monoclonal B-Cell Lymphocytosis.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
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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

14 authors at 3 institutions in 2 countries.

Yandong ShenDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.ORCID https://orcid.org/0000-0002-1344-5143
Luke CoyleDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.
Ian KerridgeDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.
William StevensonDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.
Christopher ArthurDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.
Naomi McKinlayDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.
Keith FayDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.
Christopher WardDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.
Matthew GreenwoodDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.
Oliver Giles BestCollege of Medicine and Public Health Flinders University Bedford Park South Australia Australia.ORCID https://orcid.org/0000-0003-2685-3880
Ann SolterbeckStatistical Revelations Pty Ltd Ocean Grove Victoria Australia.
Alexander GuminskiDepartment of Medical Oncology Royal North Shore Hospital St Leonards New South Wales Australia.
Stephen ShumackDepartment of Dermatology Royal North Shore Hospital St Leonards New South Wales Australia.
Stephen P MulliganDepartment of Haematology Royal North Shore Hospital St Leonards New South Wales Australia.
Royal North Shore Hospital · AUFlinders University · AUStatistical Research (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic lymphocytic leukaemia (CLL) is invariably accompanied by some degree of immune failure, and CLL patients have a high rate of second primary malignancy (SPM) compared to the general population. We comprehensively documented the incidence of all forms of SPM including skin cancer (SC), solid organ malignancy (SOM), second haematological malignancy (SHM) and separately Richter's syndrome (RS) across all therapy eras. Among the 517 CLL/small lymphocytic lymphoma (SLL) patients, the overall incidence of SPMs with competing risks was SC 31.07%, SOM 25.99%, SHM 5.19% and RS 7.55%. Of the 216 treated patients, 106 (49.1%) had at least one form of SPM, and 63 of 106 (29.2% of treated patients) developed an SPM 1.5 years (median) after treatment for their CLL. Melanoma accounted for 30.3% of SC. Squamous cell carcinoma (SCC), including eight metastatic SCCs, was 1.8 times more than basal cell carcinoma (BCC), a reversal of the typical BCC:SCC ratio. The most common SOMs were prostate (6.4%) and breast (4.5%). SHM included seven acute myeloid leukaemia (AML) and five myelodysplasia (MDS) of which eight (four AML, four MDS) were therapy-related. Any SPM occurred in 32.1% of 53 Monoclonal B-lymphocytosis (MBL) patients. Age-adjusted standardised rates of SPM (per 100,000) for CLL, MBL and the general Australian population were 2648, 1855 and 486.9, respectively. SPMs are a major health burden with 44.9% of CLL patients with having at least one SPM, and apart from SC, associated with significantly reduced overall survival. Dramatic improvements in CLL treatment and survival have occurred with immunochemotherapy and targeted therapies, but mitigating SPM burden will be important to sustain further progress.

Indexed as

chronic lymphocytic leukaemiaRichter's syndromesecond malignanciesskin cancer

Identifiers

PMID35846218
PMCPMC9175984
OpenAlexW4226249788

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.