Evidence map›Paper›PMID 27388008›Full record

ArticleBMC cancer2016

Predictive factors for a long-term response duration in non-squamous cell lung cancer patients treated with pemetrexed.

Sojung Park, Hyun Jung Kim, Chang-Min Choi, Dae Ho Lee, Sang-We Kim, Jung-Shin Lee, Woo Sung Kim, Se Hoon Choi, Jin Kyung Rho, Jae Cheol Lee

Abstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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  13. Analysis of primary tumor metabolic volume during chemoradiotherapy in locally advanced non-small cell lung cancer.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2018
    Article
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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

10 authors.

Sojung ParkDepartment of Pulmonary and Critical Care Medicine, University of Ulsan, College of Medicine, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea.
Hyun Jung KimDepartment of Internal Medicine, Kyungpook National University Hospital, Kyungpook National University School of Medicine, 130 Dongdeok-ro, Jung-gu, Daegu, 41944, South Korea.
Chang-Min ChoiDepartment of Pulmonary and Critical Care Medicine, University of Ulsan, College of Medicine, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea.
Dae Ho LeeDepartment of Oncology, University of Ulsan, College of Medicine, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea.
Sang-We KimDepartment of Oncology, University of Ulsan, College of Medicine, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea.
Jung-Shin LeeDepartment of Oncology, University of Ulsan, College of Medicine, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea.
Woo Sung KimDepartment of Pulmonary and Critical Care Medicine, University of Ulsan, College of Medicine, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea.
Se Hoon ChoiDepartment of Thoracic and Cardiovascular Surgery, University of Ulsan, College of Medicine, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea.
Jin Kyung RhoAsan Institute for Life Sciences, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea.
Jae Cheol LeeDepartment of Oncology, University of Ulsan, College of Medicine, Asan Medical Center, 388-1 Pungnap-Dong, Songpa-gu, Seoul, 05505, South Korea. jclee@amc.seoul.kr.ORCID 0000-0001-5963-0259

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPemetrexed is widely used for the treatment of advanced non-squamous non-small-cell lung cancer (NSCLC). However, factors that can predict the benefits of pemetrexed therapy have not yet been defined.

methodsWe compared the clinical and molecule pathological characteristics of good and poor responders among a cohort of 1,848 non-squamous NSCLC patients who had received at least two cycles of pemetrexed therapy between November 2006 and February 2015. Among these cases, 92 good responders who were the top 5 % in terms of progression-free survival (PFS) and 222 poor responders who had progressive disease after only 2 cycles of therapy were selected for the analysis.

resultsThe median PFS of the good responders was 29.9 months (range; 20.9-90.0) and the median number of cycle was 37 (range; 18-129). Although 53.5 % of patients showed stable disease (SD), this response was sustained (median PFS in SD, 29.6 months). A never-smoking status was related to better survival outcome, whereas EGFR mutation, two or more metastatic sites, and intra-abdominal metastasis were each associated with a poor PFS. ALK translocation showed a tendency for a positive impact on response to pemetrexed, whereas metastatic lesion to liver, adrenal gland or bone showed a tendency for a negative impact despite not reaching our threshold for statistical significance.

conclusionsPredictive factors, such as smoking status, the status of genetic alteration and tumor burden, should be considered when administering pemetrexed therapy for non-squamous NSCLC.

Indexed as

MutationCarcinoma, Non-Small-Cell LungDisease-Free SurvivalErbB ReceptorsFemaleHumansLung NeoplasmsMaleMiddle AgedNeoplasm MetastasisPemetrexedPrognosisRetrospective StudiesRisk AssessmentSmokingSurvival AnalysisEGFR protein, humanErbB ReceptorsPemetrexedAnaplastic lymphoma kinaseEGFRNon-small-cell lung cancerPemetrexedPrognosisProgression-free survival

Identifiers

PMID27388008
PMCPMC4936194

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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.