Evidence map›Paper›PMID 40374891›Full record

ArticleBJC reports2025

Assessing the risk of second primary lung cancer in women after previous breast cancer.

Yuanhui Huang, Jenny J Lin, Juan P Wisnivesky, Chung Yin Kong, Keith Sigel

Abstract read
In one paragraph

Article in BJC reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Subsequent primary neoplasm risk among survivors of cancer in adolescence and young adulthood: a population-based study from Alberta, Canada.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2026
    Article
  2. Review
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

5 authors.

Yuanhui HuangGraduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA. yuanhui.huang@icahn.mssm.edu.
Jenny J LinDivision of General Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Juan P WisniveskyDivision of General Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Chung Yin KongDivision of General Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Keith SigelDivision of General Internal Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Funding

Optimizing Lung Cancer Screening in Cancer SurvivorsR01CA264995 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KONG, CHUNG YIN, LIN, JENNY J. · 2021 to 2025
$3.4M
NCI NIH HHS R01 CA264995This study is funded through the National Institutes of Health (N.I.H.)/National Cancer Institute (NCI) Cancer Center support grants: R01CA264995 R01CA264995
6 · The paper itself

Abstract

backgroundBreast cancer (BC) survivors may be at increased risk of developing second cancers compared to those without BC diagnosis due to shared risk factors and potential carcinogenic effects of cancer therapy. Lung cancer (LC) is the most common second primary cancer among BC survivors. This study aimed to evaluate the association between BC and the subsequent incidence of LC.

methodsWomen aged 55-74 were identified from the Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial. The risk of incident LC was compared by BC status using a multivariable Cox regression model with BC and smoking exposures incorporated as time-updated variables.

results75,951 females from the PLCO trial were identified, with 5808 diagnosed with BC after enrollment. The unadjusted incidence rate (IR) of the second LC was significantly higher among BC survivors than non-BC participants (231 vs. 172 per 100,000 person-years). The adjusted hazard ratio (HR) for the second primary LC associated with BC diagnosis was 1.24 (95% CI: 1.03-1.49).

conclusionsBC diagnosis was an independent risk factor for the development of second primary LC. Consequently, BC survivors may derive benefits from enhanced LC screening interventions.

Identifiers

PMID40374891
PMCPMC12081664

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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.