Evidence map›Paper›PMID 32196388›Full record

ArticleJCO global oncology2020

Real-World Evidence: Multicenter Efficacy and Toxicity Analysis of Nintedanib With Docetaxel as Second-Line Treatment in Mexican Patients With Advanced Lung Adenocarcinoma.

Jeronimo Rafael Rodríguez-Cid, Saul Campos-Gomez, Vanessa García-Montes, Manuel Magallanes-Maciel, Rodrigo Rafael Flores-Mariñelarena, Valeria Michelle Fernández-Garibay, Iván Romarico González-Espinoza, Juan Paulo Ceja-García, Juan Carlos Cázarez-Price, Luis Martínez-Barrera and 18 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in JCO global oncology, 2020. 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
0.1field-weighted citation impact, top 51% 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. 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

28 authors at 12 institutions in 1 country.

Jeronimo Rafael Rodríguez-CidDepartment of Oncology, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, Mexico.
Saul Campos-GomezDepartment of Oncology, Centro Oncológico Estatal ISSEMYM, State of Mexico, Toluca de Lerdo, Mexico.
Vanessa García-MontesDepartment of Oncology, Hospital Español, Mexico City, Mexico.
Manuel Magallanes-MacielDepartment of Oncology, Hospital Central Militar, Mexico City, Mexico.
Rodrigo Rafael Flores-MariñelarenaDepartment of Internal Medicine, Fundación Clínica Médica Sur, Mexico City, Mexico.
Valeria Michelle Fernández-GaribaySchool of Medicine, Monterrey Institute of Technology and Higher Education, Mexico City, Mexico.
Iván Romarico González-EspinozaDepartment of Oncology, Hospital Ángeles Puebla, Puebla, Mexico.
Juan Paulo Ceja-GarcíaDepartment of Oncology, Hospital General ISSSTE La Paz, Baja California Sur, Mexico.
Juan Carlos Cázarez-PriceDepartment of Oncology, American British Cowdray Medical Center, Mexico City, Mexico.
Luis Martínez-BarreraDepartment of Oncology, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, Mexico.
Leopoldo Barriguete-ParraDepartment of Oncology, Centro Oncológico de Chihuahua, Chihuahua, Mexico.
Carlos Jose Zuloaga-FernandezDepartment of Oncology, Oncología Privada Integral, Guadalajara, Mexico.
Roberto Kuri-ExsomeDepartment of Oncology, Hospital Aranda de la Parra, Guanajuato, Mexico.
David Suárez-GarcíaDepartment of Oncology, Seguro Popular, León, Mexico.
Jorge Ignacio Gonzalez-VillanuevaDepartment of Oncology, Oncare Treatment Center, Monterrey, Mexico.
Noé Flores-AnayaDepartment of Oncology, Medionco, Mexico City, Mexico.
Jose Antonio Acevedo-DelgadoDepartment of Oncology, Unidad de Cancerología, Jalisco, Mexico.
Alma Magdalena Astorga-RamosDepartment of Oncology, Sanatorio San José, Monterrey, Mexico.
Raquel Gerson-CwilichDepartment of Oncology, American British Cowdray Medical Center, Mexico City, Mexico.
Alberto Villalobos-PrietoDepartment of Oncology, American British Cowdray Medical Center, Mexico City, Mexico.
Claudia Rodríguez-SilvaDepartment of Oncology, Hospital Universitario Dr. José Eleuterio González, Monterrey, Mexico.
Maria Fernanda Noriega-IriondoDepartment of Oncology, Centro Médico Hospital San José, Monterrey, Mexico.
Leticia Vázquez-CortésDepartment of Oncology, Clínica Médica ARCOS, Morelia, Mexico.
Eusebio Perales-RodríguezDepartment of Oncology, Servicio de Salud Pemex, Reynosa, Mexico.
Alicia Acosta-EspinozaDepartment of Oncology, Hospital ISSSTE Mexicali, Baja California, Mexico.
Yareni Perez-LozanoDepartment of Oncology, Hospital Puebla, Puebla, Mexico.
Daniel Capdeville-GarcíaDepartment of Oncology, Hospital Aranda de la Parra, Guanajuato, Mexico.
Jorge Arturo Alatorre-AlexanderDepartment of Oncology, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, Mexico.
Centro Médico ABC · MXInstituto Nacional de Enfermedades Respiratorias · MXTecnológico de Monterrey · MXInstitute for Social Security and Services for State Workers · MXClínica Ruiz · MXHospital Central Militar · MXHospital Español · MXHospital Médica Sur · MXHospital Universitario Dr José Eleuterio Gonzalez · MXInstituto de Salud del Estado de México · MXPemex (Mexico) · MXUniversidad de Puebla · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe LUME-Lung 1 study has brought consistent evidence of the effective use of nintedanib in lung adenocarcinoma as a second line of treatment; however, differences among ethnicities have been found in some studies.

methodsThis was a retrospective review among 21 medical centers of 150 patients with a confirmed diagnosis of lung adenocarcinoma, included in a compassionate use program of nintedanib from March 2014 to September 2015. The current study aimed to analyze the effectiveness of nintedanib in combination with docetaxel in the Mexican population, using progression-free survival rate and the best objective response to treatment by RECIST 1.1 as a surrogate of effectiveness. In addition, we examined the toxicity profile of our study population as a secondary end point.

resultsAfter exclusion criteria, only 99 patients met the criteria for enrollment in the current study. From the total study population, 53 patients (53.5%) were male and 46 (46.5%) were female, with an average age of 60 years and stage IV as the most prevalent clinical stage at the beginning of the compassionate use program. A total of 48 patients (48.5%) had partial response; 26 (26.3%), stable disease; 4 (4%), complete response; and 16 (16.2%), progression; and 5 (5%) were nonevaluable. We found a median progression-free survival of 5 months (95% CI, 4.3 to 5.7 months). The most common grade 3 or 4 adverse reactions were fatigue (14%) and diarrhea (13%).

conclusionNintedanib, as part of a chemotherapy regimen, is an effective option with an acceptable toxicity profile for advanced lung adenocarcinoma after first-line treatment progression.

Indexed as

Adenocarcinoma of LungCarcinoma, Non-Small-Cell LungLung NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsDocetaxelFemaleHumansIndolesLungMaleMiddle AgedRetrospective StudiesTaxoidsTreatment OutcomeDocetaxelIndolesnintedanibTaxoids

Identifiers

PMID32196388
PMCPMC7113104
OpenAlexW3010957310

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Registered trials

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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.