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| Indexado |
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| DOI | 10.1200/JCO.2016.71.7629 | ||||
| Año | 2017 | ||||
| Tipo | artículo de investigación |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
The addition of ipilimumab to first-line chemotherapy did not prolong OS compared with chemotherapy alone in patients with advanced squamous NSCLC. The safety profile of chemotherapy plus ipilimumab was consistent with that observed in previous lung and melanoma studies. Ongoing studies are evaluating ipilimumab in combination with nivolumab in this population. (C) 2017 by American Society of Clinical Oncology
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Govindan, Ramaswamy | - |
WASHINGTON UNIV - Estados Unidos
Washington University School of Medicine in St. Louis - Estados Unidos |
| 2 | Szczesna, Aleksandra | Mujer |
Mazowieckie Ctr Leczenia Chorob Pluc & Gruzlicy - Polonia
Mazowieckie Centrum Leczenia Chorób Płuc i Gruźlicy - Polonia |
| 3 | Ahn, Myung Ju | - |
Sungkyunkwan Univ - Corea del Sur
Sungkyunkwan University - Corea del Sur |
| 4 | Schneider, Claus-Peter | Hombre |
Zentralklin Bad Berka - Alemania
Zentralklinik Bad Berka - Alemania |
| 5 | Mella, Pablo | Hombre |
Universidad de Valparaíso - Chile
Fdn Arturo Lopez Perez - Chile |
| 5 | Mella, Pablo Fernando Gonzalez | Hombre |
Universidad de Valparaíso - Chile
Fdn Arturo Lopez Perez - Chile |
| 6 | Barlesi, F. | Hombre |
Aix Marseille Univ - Francia
Aix Marseille Université - Francia |
| 7 | Han, Baohui | - |
Shanghai Jiao Tong Univ - China
Shanghai Chest Hospital - China |
| 8 | Ganea, Doina Elena | Mujer |
Spitalul Judetean Urgenta Suceava - Rumania
Spitalul Judetean De Urgenta Suceava - Rumania |
| 9 | Pawel, Joachim Von | Hombre |
Asklepius Fachkliniken - Alemania
|
| 9 | Von Pawel, Joachim | Hombre |
Asklepius Fachkliniken - Alemania
|
| 10 | Vladimirov, Vladimir | Hombre |
Pyatigorsk Oncol Dispensary - Rusia
State Healthcare Institute - Rusia |
| 11 | Fadeeva, Natalia | Mujer |
Chelyabinsk Reg Oncol Dispensary - Rusia
Chelyabinsk Regional Clinical Oncology Dispensary - Rusia |
| 12 | Lee, Ki Hyeong | - |
Chungbuk Natl Univ Hosp - Corea del Sur
Chungbuk National University Hospital - Corea del Sur |
| 13 | Kurata, Takayasu | Hombre |
Kansai Med Univ - Japón
Kansai Medical University - Japón Kansai Medical University Hospital - Japón |
| 14 | Zhang, Li | - |
Sun Yat Sen Univ - China
Sun Yat-Sen University Cancer Center - China |
| 15 | Tamura, Tomohide | - |
St Lukes Int Hosp - Japón
St. Luke's International Hospital Tokyo - Japón |
| 16 | Postmus, Pieter E. | Hombre |
UNIV LIVERPOOL - Reino Unido
University of Liverpool - Reino Unido |
| 17 | Jassem, Jacek | Hombre |
Med Univ Gdansk - Polonia
Gdanski Uniwersytet Medyczny - Polonia |
| 18 | O'Byrne, Kenneth | Hombre |
Princess Alexandra Hosp - Australia
Queensland Univ Technol - Australia Queensland University of Technology QUT - Australia Queensland University of Technology - Australia |
| 19 | Kopit, Justin | Hombre |
Bristol Myers Squibb - Estados Unidos
Bristol-Myers Squibb - Estados Unidos |
| 20 | Li, Mingshun | - |
Bristol Myers Squibb - Estados Unidos
Bristol-Myers Squibb - Estados Unidos |
| 21 | Tschaika, Marina | Mujer |
Bristol Myers Squibb - Estados Unidos
Bristol-Myers Squibb - Estados Unidos |
| 22 | Reck, Martin | Hombre |
German Ctr Lung Res - Alemania
German Center for Lung Research - Alemania |
| Fuente |
|---|
| European Commission |
| Bristol-Myers Squibb |
| Pfizer |
| AstraZeneca |
| Eli Lilly |
| MethylGene (Inst) |
| GlaxoSmithKline (Inst) |
| Abbvie (Inst) |
| Bayer (Inst) |
| MSD Oncology |
| Chugai Pharma |
| US Code of Federal Regulations |
| Agradecimiento |
|---|
| Bristol-Myers Squibb, Pfizer, Eli Lilly |
| The protocol was approved by each participating center’s ethics committee or institutional review board. The study was run in accordance with Good Clinical Practice (defined by the International Conference on Harmonization) and the ethical principles underlying European Union Directive 2001/20/EC and the US Code of Federal Regulations, Title 21, Part 50 (21CFR50). All patients provided written, informed consent to their participation in the study. An independent data monitoring committee provided study oversight. |