Evidence map›Paper›PMID 31315676›Full record

ArticleBMC cancer2019

Afatinib helped overcome subsequent resistance to osimertinib in a patient with NSCLC having leptomeningeal metastasis baring acquired EGFR L718Q mutation: a case report.

Jing Liu, Bo Jin, Hang Su, Xiujuan Qu, Yunpeng Liu

Abstract readCase Reports
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Acquired multipleOncology letters · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Characterization of Patients withOncoTargets and therapy · 2024
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Acquired Resistance to Osimertinib inInternational journal of molecular sciences · 2022
    Review
  17. Review
  18. Article
  19. Review
  20. 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.

Jing LiuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Bo JinDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Hang SuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China.
Xiujuan QuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China. cmuquxiujuan@163.com.
Yunpeng LiuDepartment of Medical Oncology, The First Hospital of China Medical University, Shenyang, China. ypliu@cmu.edu.cn.ORCID http://orcid.org/0000-0002-9645-7990

Funding

Department of Science and Technology of Liaoning Province 20180551230
6 · The paper itself

Abstract

backgroundThe epidermal growth factor receptor (EGFR)-mutated advanced non-small-cell lung cancer has been successfully treated with tyrosine kinase inhibitors (TKIs). Acquired resistance becomes a tough issue when patients fail to respond to the third-generation TKI osimertinib. This study aimed to report a case baring acquired EGFR L858R/L718Q mutation in the central nervous system induced by osimertinib, which was successfully overcome using afatinib. CASE PRESENTATION: A 65-year-old female patient was diagnosed with stage IV non-small-cell lung adenocarcinoma with synchronic brain metastasis in February 2015. Before and during treatment, 416 tumor-related genes were monitored dynamically by liquid biopsies using next-generation sequencing, and the treatment strategy was decided according to the gene status. At baseline, an EGFR L858R mutation in exon 21 was detected, so treatment with icotinib was started. After 8 months, she experienced disease progression with leptomeningeal metastasis and switched to osimertinib based on an acquired EGFR T790 M mutation. After 9 months, her disease progressed and an EGFR L718Q mutation was found in the cerebrospinal fluid. The patient was then challenged with afatinib, and her disease was under control for 4 months. In January 2017, the patient passed away, with an overall survival time of 23 months, 15 months after leptomeningeal metastasis.

conclusionThe acquired EGFR L718Q mutation in the cerebrospinal fluid resulted in subsequent resistance to osimertinib and could be partly overcome using afatinib, indicating a promising treatment option in the clinic.

Indexed as

MutationAcrylamidesAfatinibAgedAniline CompoundsBrain NeoplasmsCarcinoma, Non-Small-Cell LungCrown EthersDisease ProgressionDrug Resistance, NeoplasmErbB ReceptorsFatal OutcomeFemaleFollow-Up StudiesHumansIndolesAcrylamidesAfatinibAniline CompoundsCrown EthersEGFR protein, humanErbB ReceptorsicotinibIndolesosimertinibProtein Kinase InhibitorsPyrimidinesQuinazolinesAfatinibEGFRL718QLeptomeningeal metastasisNSCLC

Identifiers

PMID31315676
PMCPMC6637526

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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.