Evidence map›Paper›PMID 26706949›Full record

Trial reportZhongguo fei ai za zhi = Chinese journal of lung cancer2015

[Clinical Observation of Icotinib Hydrochloride for Advanced Non-small Cell Lung Cancer Patients with EGFR Status Identified].

Xi Li, Na Qin, Jinghui Wang, Xinjie Yang, Xinyong Zhang, Jialin Lv, Yuhua Wu, Hui Zhang, Jingying Nong, Quan Zhang and 1 more

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Zhongguo fei ai za zhi = Chinese journal of lung cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 2 syntheses or guidelines pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Survival difference betweenChinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2017
    Article
  4. Article
  5. 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

11 authors at 1 institution in 1 country.

Xi LiDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Na QinDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Jinghui WangDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Xinjie YangDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Xinyong ZhangDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Jialin LvDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Yuhua WuDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Hui ZhangDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Jingying NongDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Quan ZhangDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Shucai ZhangDepartment of Medical Oncology, Beijing Chest Hospital, Capital Medical University, Beijing 101149, China.
Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIcotinib is the first self-developed small molecular drug in China for targeted therapy of lung cancer. Compared to the other two commercially available epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors, gefitinib and erlotinib, icotinib is similar to them in chemical structure, mechanism of activity and therapeutic effects. To explore the efficacy and side effects of icotinib hydrochloride in the treatment of the advanced non-small cell lung cancer (NSCLC) patients with EGFR mutation and wild-type.

methodsPatients with advanced NSCLC who were treated with icotinib hydrochloride in Beijing Chest Hospital were retrospective analyzed from March 2009 to December 2014.

resultsThe clinical data of 124 patients (99 with EGFR mutation and 25 with wild type) with advanced NSCLC were enrolled in this study. The patients' overall objective response rate (ORR) was 51.6 % and the disease control rate (DCR) was 79.8%; The patients with EGFR mutation, ORR was 63.6%, DCR was 93.9%. The ORR was 4.0% and the DCR was 24.0% in the wild-type patients. Median progression-free survival (PFS) with icotinib treatment in EGFR mutation patients was 10.5 months and 1.0 month in wild-type patients. The major adverse events were mild skin rash (30.6%) and diarrhea (16.1%).

conclusionsMonotherapy with icotinib hydrochloride is effective and tolerable for the advanced NSCLC EGFR mutation patients.

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsCarcinoma, Non-Small-Cell LungChinaCrown EthersDisease-Free SurvivalErbB ReceptorsFemaleHumansLung NeoplasmsMaleMiddle AgedMutationQuinazolinesAntineoplastic AgentsCrown EthersEGFR protein, humanErbB ReceptorsicotinibQuinazolines

Identifiers

PMID26706949
PMCPMC6015183
OpenAlexW2220085643

What OpenQuestion holds

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LicenceCC BY
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.