Evidence map›Paper›PMID 33679141›Full record

ArticleCancer management and research2021

Real-World Data on Osimertinib in Chinese Patients with Pretreated, EGFR T790M Mutation Positive, Advanced Non-Small Cell Lung Cancer: A Retrospective Study.

Da Peng, Dongfeng Shan, Chengcheng Dai, Jie Li, Zifan Wang, Ziyi Huang, Rui Peng, Peng Zhao, Xuezhen Ma

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 11 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.

Da PengDepartment of Oncology, Affiliated Qingdao Central Hospital, Qingdao University, Qingdao, Shandong, People's Republic of China.
Dongfeng ShanThe Affiliated Hospital of Qingdao University, Qingdao, Shandong, People's Republic of China.
Chengcheng DaiDepartment of Oncology, Affiliated Qingdao Central Hospital, Qingdao University, Qingdao, Shandong, People's Republic of China.
Jie LiDepartment of Oncology, Jiaozhou Central Hospital, Jiaozhou, People's Republic of China.
Zifan WangDepartment of Oncology, Affiliated Qingdao Central Hospital, Qingdao University, Qingdao, Shandong, People's Republic of China.
Ziyi HuangDepartment of Oncology, Affiliated Qingdao Central Hospital, Qingdao University, Qingdao, Shandong, People's Republic of China.
Rui PengDepartment of Oncology, Affiliated Qingdao Central Hospital, Qingdao University, Qingdao, Shandong, People's Republic of China.
Peng ZhaoBiotherapy Center, Affiliated Qingdao Central Hospital, Qingdao University, Qingdao, Shandong, People's Republic of China.
Xuezhen MaDepartment of Oncology, Affiliated Qingdao Central Hospital, Qingdao University, Qingdao, Shandong, People's Republic of China.
Affiliated Hospital of Qingdao University · CNQingdao University · CNShuozhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAs a third-generation EGFR TKI has been taken orally, Osimertinib effectively inhibits mutant EGFR, including T790M EGFR resistance mutations. Here, we examined real-world efficacy and tolerability of Osimertinib among Chinese patients with advanced EGFR T790M-mutant NSCLC. PATIENTS AND

methodsA total of 106 advanced NSCLC patients who were taking Osimertinib following disease progression after EGFR-TKIs or other treatments were retrospectively recruited in this study. The PFS and OS after Osimertinib treatment were analyzed as the primary endpoints.

resultsOsimertinib was used as a second line and ≥3rd line treatment in 22.6% and 77.4% of the patients, respectively. DCR and ORR were 93.4% and 57.5%, respectively. Median PFS was 12.4 12 (95% CI, 10.5-13.5) months. The PFS was 11 (8.0, 14.0) and 12 (10.3,13.7) months (

conclusionOsimertinib can effectively treat advanced NSCLC with T790M mutations independently of previous treatment lines.

Indexed as

EGFR-activating mutationsnon-small cell lung cancerosimertinibT790M EGFR mutationtyrosine-kinase inhibitors

Identifiers

PMID33679141
PMCPMC7926038
OpenAlexW3131413306

What OpenQuestion holds

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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.