Evidence map›Paper›PMID 33680095›Full record

ArticleTherapeutic advances in medical oncology2021

Real-world analysis of the effect of gefitinib as a first-line therapy in patients with advanced non-small cell lung cancer with

Pham Van Luan, Nguyen Dinh Tien, Nguyen Minh Hai, Nguyen Dao Tien, Thi Thi Duyen

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 33% 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, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Healthcare coverage affects survival ofFrontiers in oncology · 2023
    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

5 authors at 1 institution in 1 country.

Pham Van LuanDepartment of Respiratory Medicine, 108 Military Central Hospital, Tran Hung Dao Street, Hai Ba Trung, Hanoi, Vietnam.ORCID https://orcid.org/0000-0002-2291-1054
Nguyen Dinh TienDepartment of Respiratory Medicine, 108 Military Central Hospital, Hai Ba Trung, Hanoi, Vietnam.
Nguyen Minh HaiDepartment of Respiratory Medicine, 108 Military Central Hospital, Hai Ba Trung, Hanoi, Vietnam.
Nguyen Dao TienDepartment of Respiratory Medicine, 108 Military Central Hospital, Hai Ba Trung, Hanoi, Vietnam.
Thi Thi DuyenDepartment of Respiratory Medicine, 108 Military Central Hospital, Hai Ba Trung, Hanoi, Vietnam.
108 Military Central Hospital · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere have been few studies on the efficacy of tyrosine kinase inhibitors in lung carcinomas. The purpose of this study was to evaluate the effect of gefitinib as a first-line therapy in patients with advanced non-small cell lung cancer (NSCLC) who were positive for epidermal growth factor receptor (

methodsThis prospective analysis included 120 patients with advanced NSCLC with

resultsThe ORR and DCR were 59.2% and 95.8%, respectively. The median PFS was 14.5 months and the median OS was 33 months. The longer OS was statistically significant in women and non-smokers, and the patients had a good PS. Adverse events occurred in 59.2% patients, but most of them were grade 1 and 2 events.

conclusionThis study conducted in Vietnam suggests the effectiveness of gefitinib as a first-line treatment option in patients with advanced NSCLC and positive

Indexed as

EGFR mutationsfirst-line treatmentgefitinibnon-small cell lung cancer

Identifiers

PMID33680095
PMCPMC7900790
OpenAlexW3131335352

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.