Evidence map›Paper›PMID 37064118›Full record

ArticleFrontiers in oncology2023

Case report: Complete pathological admission in N3 unresectable locally advanced lung adenocarcinoma with a novel INTS10-ALK and EML4-ALK fusion after neoadjuvant crizotinib.

Xiaoqian Zhai, Ting Wang, Yiyun Lin, Jiabi Zhang, Yuqing Wang, Weiya Wang, Qinghua Zhou, Daxing Zhu

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

8 authors at 5 institutions in 2 countries.

Xiaoqian ZhaiLung Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Ting WangLung Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Yiyun LinGraduate School of Biomedical Sciences, MD Anderson Cancer Center UT Health, Houston, TX, United States.
Jiabi ZhangDepartment of Nutrition and Integrative Physiology, College of Health, University of Utah, Salt Lake City, UT, United States.
Yuqing WangGraduate School of Biomedical Sciences, Baylor College of Medicine, Houston, TX, United States.
Weiya WangPathology Department, West China Hospital, Sichuan University, Chengdu, China.
Qinghua ZhouLung Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Daxing ZhuLung Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Sichuan University · CNBaylor College of Medicine · USThe University of Texas MD Anderson Cancer Center · USUniversity of Utah · USWest China Hospital of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Although anaplastic lymphoma kinase tyrosine kinase inhibitors (ALK-TKIs) have impressive response in advanced lung adenocarcinoma with anaplastic lymphoma kinase (ALK) fusion, no guidelines point to the potential benefits of neoadjuvant ALK-TKIs for N3 unresectable locally advanced lung cancer. Current ongoing clinical trials mainly focus on the efficacy of neoadjuvant ALK-TKIs in resectable locally advanced lung cancer and ignore the role of neoadjuvant ALK-TKIs in N3 unresectable locally advanced lung cancer. Materials and methods: We report a lung cancer case with a novel INTS10-ALK and EML4-ALK rearrangement that achieved complete pathologic response to neoadjuvant crizotinib. We conducted molecular pathologic analysis by using next-generation sequencing (NGS). Genomic DNA was extracted from formalin-fixed paraffin-embedded (FFPE) samples and profiled using a capture-based targeted sequencing panel consisting of 56 lung cancer-related genes. Results: Our study reported a patient with stage IIIB-N3 lung adenocarcinoma with an unreported dual ALK rearrangement (INTS10-ALK and EML4-ALK) who received 5 months of crizotinib, followed by R0 right upper lobectomy, achieving complete pathological response (ypT0 ypN0). No recurrence of the tumor was found for 3 years postoperatively. Conclusion: The case supports the strategy of neoadjuvant ALK inhibitors for N3 unresectable locally advanced lung cancer, expanding the spectrum of treatment of stage IIIB-N3 lung cancer.

Indexed as

case reportcomplete pathologic responsecrizotinibINTS10-ALK and EML4-ALKlung cancerneoadjuvantstage IIIB-N3

Identifiers

PMID37064118
PMCPMC10095823
OpenAlexW4361298136

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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.