Evidence map›Paper›PMID 32072746›Full record

ArticleThoracic cancer2020

Response rate of patients with baseline brain metastases from recently diagnosed non-small cell lung cancer receiving radiotherapy according to EGFR, ALK and KRAS mutation status.

Oscar Arrieta, Laura-Alejandra Ramírez-Tirado, Enrique Caballé-Perez, Alberto Mejia-Perez, Zyanya Lucia Zatarain-Barrón, Andrés F Cardona, Francisco Lozano-Ruíz, Manuel Segura-González, Graciela Cruz-Rico, Federico Maldonado and 1 more

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

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  15. Longitudinal Monitoring ofFrontiers in oncology · 2020
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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

11 authors at 2 institutions in 2 countries.

Oscar ArrietaThoracic Oncology Unit, National Cancer Institute (INCan), México City, Mexico.ORCID 0000-0002-1164-3779
Laura-Alejandra Ramírez-TiradoThoracic Oncology Unit, National Cancer Institute (INCan), México City, Mexico.
Enrique Caballé-PerezThoracic Oncology Unit, National Cancer Institute (INCan), México City, Mexico.
Alberto Mejia-PerezDepartment of Imagenology, National Cancer Institute (INCan), Mexico City, Mexico.
Zyanya Lucia Zatarain-BarrónThoracic Oncology Unit, National Cancer Institute (INCan), México City, Mexico.
Andrés F CardonaClinical and Translational Oncology Group, Institute of Oncology, Clínica del Country, Bogotá, Colombia.ORCID 0000-0003-3525-4126
Francisco Lozano-RuízThoracic Oncology Unit, National Cancer Institute (INCan), México City, Mexico.
Manuel Segura-GonzálezThoracic Oncology Unit, National Cancer Institute (INCan), México City, Mexico.
Graciela Cruz-RicoExperimental Oncology Laboratory, National Cancer Institute (INCan), Mexico City, Mexico.
Federico MaldonadoThoracic Oncology Unit, National Cancer Institute (INCan), México City, Mexico.
Rafael RosellPersonalized Medicine Program, Catalan Institute of Oncology-ICO, Barcelona, Spain.
Instituto Nacional de Cancerología · MXInstitut Català d'Ornitologia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies have identified that patients with EGFR mutations tend to have better responses to targeted therapy, as well as chemotherapy; however, the effect of genetic alterations in terms of radiotherapy (RT)-related outcomes has not been fully assessed. We studied the impact of common non-small cell lung cancer (NSCLC) genetic alterations (EGFR, ALK and KRAS) in relation to objective response rate (ORR) to RT in patients with brain metastases.

methodsFrom 2009-2015, 153 patients with an available genotyping status were treated with whole-brain irradiation (WBI) before receiving systemic therapy. Primary outcome was ORR; secondary outcomes included intracranial progression-free survival (IPFS) and overall survival (OS).

resultsOverall, ORR was 47.1%. ORR to RT varied significantly according to molecular status: EGFR (64.5%) ALK (54.5%) KRAS (20%) and WT (35.4%) (P = 0.001). EGFR mutation was the only independently associated factor for response to WBI (RR 3.52 [95% CI 1.6-7.7]; P = 0.002). Median IPFS was 10.8 months [95% CI 8.2-13.5] overall; however, IPFS also varied significantly according to molecular status: EGFR (18.2 months), ALK (18.4 months), KRAS (6.0 months) and WT (8.7 months) (P < 0.0001). OS for EGFR, ALK, KRAS and WT patients was 36.6, 32.2, 15.5 and 22.4 months, respectively (P = 0.014). Intracranial-ORR (HR 0.4 [95% CI 0.2-0.6], P < 0.001) and mutation status (HR 0.7 [95% CI 0.6-0.9], P < 0.042) were independently associated with a higher OS.

conclusionsRT response varies as per tumor molecular status. The presence of EGFR mutations favors the organ-specific response to RT, and is associated with longer OS in patients with NSCLC and BM. KEY POINTS: This study addressed for the first time the difference in radiotherapy-related outcomes in patients with different genotypes of non-small cell lung cancer (NSCLC) before they received systemic therapy. Results show that response to radiotherapy varies as per tumor molecular status, particularly EGFR-mutated tumors, have a favorable response to radiotherapy, contrary to KRAS-mutated tumors.

Indexed as

MutationAdenocarcinoma of LungAgedAged, 80 and overAnaplastic Lymphoma KinaseBiomarkers, TumorBrain NeoplasmsCarcinoma, Non-Small-Cell LungErbB ReceptorsFemaleFollow-Up StudiesGene Expression Regulation, NeoplasticGene RearrangementHumansLung NeoplasmsMaleALK protein, humanAnaplastic Lymphoma KinaseBiomarkers, TumorEGFR protein, humanErbB ReceptorsKRAS protein, humanProto-Oncogene Proteins p21(ras)EGFRKRASradiosensitivityradiotherapyresponse rate

Identifiers

PMID32072746
PMCPMC7113051
OpenAlexW3007861895

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.