Evidence map›Paper›PMID 42117759›Full record

SynthesisBJU international2026

Secondary leukaemia after testicular germ cell tumour treatment: a systematic review and meta-analysis.

Ahmad Mousa, Ali Amiri, Sanchit Kaushal, Emma Wilson, Isabelle Tan, Robert J Hamilton

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in BJU international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Ahmad MousaDivision of Urology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0001-9119-8048
Ali AmiriDivision of Urology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Sanchit KaushalDivision of Urology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Emma WilsonLibrary Services, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Isabelle TanDivision of Urology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Robert J HamiltonDivision of Urology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTesticular germ cell tumours (TGCTs) are the most common malignancy in men aged 15-35 years. Management options for men with TGCTs include surgery, radiation and/or chemotherapy, depending on stage. Given TGCTs' excellent survival, most patients live long enough to experience delayed treatment toxicities, warranting careful consideration of therapeutic decisions. An important outcome of interest is the development of secondary leukaemia.

methodsA systematic literature search was conducted through a combination of database searches (MEDLINE, EMBASE, and Cochrane library) and manual review. Studies evaluating the incidence of secondary malignant neoplasms in patients following treatment for TGCTs were identified. Our primary outcome was the diagnosis of any leukaemia following treatment, compared to the general population. Meta-analyses were performed using random-effects models, with outcomes reported as standardised incidence ratios (SIRs). Strength of evidence was evaluated using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework.

resultsSix studies including 57 365 patients with 163 secondary leukaemias were included. The weighted-mean follow-up was 12.8 years. The incidence of leukaemia following definitive treatment of TGCTs varied by treatment modality. Chemotherapy was associated with an increase in risk (SIR 5.77, 95% confidence interval [CI] 1.35-24.62; P = 0.03), whereas radiation showed no statistically significant association (SIR 2.55, 95% CI 0.70-9.32; P = 0.11). The certainty of evidence was graded as moderate using the GRADE framework.

conclusionsChemotherapy is associated with an increase in the relative risk of secondary leukaemias after treatment of TGCTs, although the absolute risk remains small.

Indexed as

LeukemiaNeoplasms, Germ Cell and EmbryonalNeoplasms, Second PrimaryTesticular NeoplasmsHumansMaleleukaemianon‐seminomasecondary leukaemiasecondary malignancysecondary malignant neoplasmsecond primary malignancysecond primary neoplasmtesticular cancertesticular germ cell tumours

Identifiers

PMID42117759
PMCPMC13458650

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.