Evidence map›Paper›PMID 27766477›Full record

ArticleTargeted oncology2017

Risk of Second Primary Malignancies in Lung Cancer Survivors - The Influence of Different Treatments.

Vincent Yi-Fong Su, Chia-Jen Liu, Yuh-Min Chen, Teh-Ying Chou, Tzeng-Ji Chen, Sang-Hue Yen, Tzeon-Jye Chiou, Jin-Hwang Liu, Yu-Wen Hu

Abstract read
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In one paragraph

Article in Targeted oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Vincent Yi-Fong SuDepartment of Critical Care Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Chia-Jen LiuFaculty of Medicine, National Yang-Ming University, Taipei, Taiwan.
Yuh-Min ChenFaculty of Medicine, National Yang-Ming University, Taipei, Taiwan.
Teh-Ying ChouInstitute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan.
Tzeng-Ji ChenFaculty of Medicine, National Yang-Ming University, Taipei, Taiwan.
Sang-Hue YenFaculty of Medicine, National Yang-Ming University, Taipei, Taiwan.
Tzeon-Jye ChiouFaculty of Medicine, National Yang-Ming University, Taipei, Taiwan.
Jin-Hwang LiuFaculty of Medicine, National Yang-Ming University, Taipei, Taiwan.
Yu-Wen HuFaculty of Medicine, National Yang-Ming University, Taipei, Taiwan. mimicx@gmail.com.
National Yang Ming Chiao Tung University · TWNational Yang Ming Chiao Tung University · TWNational Yang Ming University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurrently, no large study addressing the relationship between lung cancer patients with different therapies and second primary malignancies (SPMs) is available.

methodsUsing the Taiwan National Health Insurance Research Database, we conducted a population-based cohort study. Patients with newly diagnosed lung cancer between 1997 and 2005 were enrolled and followed up until Dec. 31, 2011. The endpoint of the study was SPM occurrence. Standardized incidence ratios (SIRs) of cancers were calculated to compare the cancer incidence of the study cohort to that of the general population.

resultsWe identified 52,639 patients with lung cancer and excluded 34,267 patients who had expired within one year after diagnosis. The study included 18,372 subjects with a median follow-up period of 2.24 years. 590 patients developed an SPM. The overall cancer risk was significantly increased (SIR 1.33, 95% confidence interval [CI]: 1.22-1.44, p < 0.001), and there was a significant increase in the incidences of head and neck (SIR 1.60, 95% CI 1.21-2.07, p = 0.001), bone and soft tissue (SIR 2.65, 95% CI 1.27-4.87, p = 0.011), genitourinary (SIR 1.50, 95% CI 1.27-1.76, p < 0.001), and thyroid (SIR 3.85, 95% CI 2.28-6.08, p < 0.001) cancers. Importantly, after multivariate adjustment, the use of tyrosine kinase inhibitors (TKIs) statistically significantly reduced SPM incidence (HR, 0.41; 95% CI, 0.21-0.79; p = 0.008).

conclusionsOur study indicates that lung cancer may be a risk factor for SPM. TKI use was associated with a significantly lower risk of SPM development. However, because patients with epidermal growth factor receptor mutant lung adenocarcinoma (associated with non-smokers) tend to receive TKI treatment, they might have fewer smoking-related SPMs.

Indexed as

AdultAgedAged, 80 and overFemaleHumansLung NeoplasmsMaleMiddle AgedNeoplasms, Second PrimaryRisk FactorsYoung Adult

Identifiers

PMID27766477
OpenAlexW2533591317

What OpenQuestion holds

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Registered trials

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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.