Evidence map›Paper›PMID 28390118›Full record

ArticleOncology research2018

Erlotinib-Associated Rash in Advanced Non-Small Cell Lung Cancer: Relation to Clinicopathological Characteristics, Treatment Response, and Survival.

Ilias Kainis, Nikolaos Syrigos, Alexandra Kopitopoulou, Ioannis Gkiozos, Effrosyni Filiou, Vasiliki Nikolaou, Evangelia Papadavid

Open access · hybridAbstract read
In one paragraph

Article in Oncology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Efficacy in patients withFuture oncology (London, England) · 2024
    Trial
  2. Article
  3. Article
  4. Article
  5. Dual contribution of the gut microbiome to immunotherapy efficacy and toxicity: supportive care implications and recommendations.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2022
    Article
  6. Article
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

7 authors at 2 institutions in 1 country.

Ilias Kainis3rd Department of Medicine, Athens Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Nikolaos Syrigos3rd Department of Medicine, Athens Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Alexandra Kopitopoulou3rd Department of Medicine, Athens Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Ioannis Gkiozos3rd Department of Medicine, Athens Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Effrosyni Filiou3rd Department of Medicine, Athens Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Vasiliki Nikolaou3rd Department of Medicine, Athens Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Evangelia Papadavid2nd Department of Dermatology Venereology, Attikon General University Hospital, Athens, Greece.
National and Kapodistrian University of Athens · GRUniversity General Hospital Attikon · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systematic treatment of advanced non-small cell lung cancer (NSCLC) includes targeted treatment with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs). The development of skin rash and its intensity have been associated with EGFR TKI's efficacy. The main purpose of this study was to further investigate the potential value of erlotinib-associated rash as a predictor of prognosis and treatment response in a real-world cohort of patients with advanced NSCLC. The medical records of all NSCLC patients treated with erlotinib at the Oncology Unit of GPP, Sotiria Athens General Hospital between January 1, 2014 and August 31, 2016 were retrospectively reviewed. Seventy-nine patient medical records fulfilled the criteria and were included in the study. Development of erlotinib-associated rash was correlated with clinicopathological characteristics of patients, treatment response, and overall survival (OS) using univariate and multivariate Cox regression analysis. The number of patients with rash was greater in the responders group (90% vs. 46.4%, p = 0.015). In univariate analysis, there was a statistically significant association between rash development and time to progression (TTP) [HR: 0.32 (0.17-0.57), p < 0.001]. With multivariate Cox regression analysis, it was found that PS ≥ 2 (HR: 2.01, 95% CI: 1.12-3.60, p = 0.018) and rash (HR: 0.34, 95% CI: 0.18-0.63, p = 0.001) were independently associated with TTP and also that the duration of treatment with erlotinib (HR: 0.58, 95% CI: 0.42-0.80, p = 0.001) and rash (HR: 0.10, 95% CI: 0.20-0.48, p = 0.004) was an independent predictor of survival. Our results suggest that erlotinib-associated rash may represent a clinically valuable biomarker for the prediction of treatment response and OS in patients with advanced NSCLC.

Indexed as

Drug EruptionsAdultAgedAntineoplastic AgentsCarcinoma, Non-Small-Cell LungDisease-Free SurvivalErlotinib HydrochlorideFemaleHumansKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedPrognosisProportional Hazards ModelsRetrospective StudiesAntineoplastic AgentsErlotinib Hydrochloride

Identifiers

PMID28390118
PMCPMC7844560
OpenAlexW2605375155

What OpenQuestion 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 OpenQuestion graph.