Evidence map›Paper›PMID 28776311›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2018

Continued EGFR-TKI with concurrent radiotherapy to improve time to progression (TTP) in patients with locally progressive non-small cell lung cancer (NSCLC) after front-line EGFR-TKI treatment.

Y Wang, Y Li, L Xia, K Niu, X Chen, D Lu, R Kong, Z Chen, J Sun

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
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 2 institutions in 1 country.

Y WangDepartment of Oncology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Y LiDepartment of Gastroenterology, First People's Hospital of Liangjiang New District, Chongqing, 400020, China.
L XiaDepartment of Oncology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
K NiuDepartment of Oncology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
X ChenMedical English Department, College of Basic Medicine, Third Military Medical University, Chongqing, 400038, China.
D LuMedical English Department, College of Basic Medicine, Third Military Medical University, Chongqing, 400038, China.
R KongDepartment of Oncology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China.
Z ChenDepartment of Oncology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China. czt05@163.com.
J SunDepartment of Oncology, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China. sunjg09@aliyun.com.ORCID http://orcid.org/0000-0002-1792-5689
Army Medical University · CNFirst People's Hospital of Chongqing · CN

Funding

Third Military Medical University No. yclkt-201408
6 · The paper itself

Abstract

backgroundEpidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) is the optimal treatment for EGFR-mutant advanced non-small cell lung cancer (NSCLC). However, most patients developed systemic or local progression due to acquired EGFR-TKI resistance. This retrospective study aimed to evaluate the feasibility of continued EGFR-TKI with concurrent radiotherapy (CTCRT) in patients with local progression after front-line EGFR-TKI treatment.

methodsAdvanced NSCLC patients with active EGFR mutation who received EGFR-TKI were treated with CTCRT after local progression. Medical data were analyzed for time to progression (TTP), progression-free survival (PFS), tumor response rate, overall survival (OS) and adverse events.

resultsA total of 50 irradiated lesions from 44 patients were included. Median TTP and PFS of measurable lesions (n = 31) were both significantly prolonged after local radiotherapy (TTP1 + TTP2 vs. TTP1: 21.7 vs. 16.0 months, P = 0.010; PFS1 + PFS2 vs. PFS1: 21.3 vs. 16.0 months, P = 0.027). For all lesions (n = 50), objective response rate (ORR) and local tumor control rate (LCR) were 54.0 and 84.0%, respectively. Median OS was 26.6 months. There were no serious adverse events before or after radiotherapy.

conclusionsThe treatment modality of CTCRT is considerable and effective for EGFR-mutant NSCLC patients even with local failure from front-line EGFR-TKI treatment.

Indexed as

AdultAgedCarcinoma, Non-Small-Cell LungChemoradiotherapyCrown EthersDisease-Free SurvivalDisease ProgressionErbB ReceptorsErlotinib HydrochlorideFemaleGefitinibHumansKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedCrown EthersEGFR protein, humanErbB ReceptorsErlotinib HydrochlorideGefitinibicotinibProtein Kinase InhibitorsQuinazolinesAdvanced NSCLCContinued EGFR-TKIEGFR active mutationLocal progressionRadiation therapy

Identifiers

PMID28776311
OpenAlexW2743332049

What OpenQuestion holds

Textmetadata
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.