Updated Frequency of EGFR and KRAS Mutations in NonSmall-Cell Lung Cancer in Latin America: The Latin-American Consortium for the Investigation of Lung Cancer (CLICaP)

Previously, we reported the frequency of epidermal growth factor receptor (EGFR) and KRAS mutations in nonsmall-cell lung cancer (NSCLC) patients in Latin America. The EGFR mutation frequency was found between Asian (40%) and Caucasian (15%) populations. Here, we report the updated distribution of N...

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Veröffentlicht in:Journal of thoracic oncology 2015-05, Vol.10 (5), p.838-843
Hauptverfasser: Arrieta, Oscar, Cardona, Andrés F., Martín, Claudio, Más-López, Luis, Corrales-Rodríguez, Luis, Bramuglia, Guillermo, Castillo-Fernandez, Omar, Meyerson, Matthew, Amieva-Rivera, Eduardo, Campos-Parra, Alma Delia, Carranza, Hernán, Gómez de la Torre, Juan Carlos, Powazniak, Yanina, Aldaco-Sarvide, Fernando, Vargas, Carlos, Trigo, Mariana, Magallanes-Maciel, Manuel, Otero, Jorge, Sánchez-Reyes, Roberto, Cuello, Mauricio
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container_issue 5
container_start_page 838
container_title Journal of thoracic oncology
container_volume 10
creator Arrieta, Oscar
Cardona, Andrés F.
Martín, Claudio
Más-López, Luis
Corrales-Rodríguez, Luis
Bramuglia, Guillermo
Castillo-Fernandez, Omar
Meyerson, Matthew
Amieva-Rivera, Eduardo
Campos-Parra, Alma Delia
Carranza, Hernán
Gómez de la Torre, Juan Carlos
Powazniak, Yanina
Aldaco-Sarvide, Fernando
Vargas, Carlos
Trigo, Mariana
Magallanes-Maciel, Manuel
Otero, Jorge
Sánchez-Reyes, Roberto
Cuello, Mauricio
description Previously, we reported the frequency of epidermal growth factor receptor (EGFR) and KRAS mutations in nonsmall-cell lung cancer (NSCLC) patients in Latin America. The EGFR mutation frequency was found between Asian (40%) and Caucasian (15%) populations. Here, we report the updated distribution of NSCLC mutations. A total of 5738 samples from NSCLC patients from Argentina (1713), Mexico (1417), Colombia (1939), Peru (393), Panama (174), and Costa Rica (102) were genotyped for EGFR and KRAS. The median patient age was 62.2 ± 12.3 years; 53.5% were women, 46.7% had a history of smoking, and 95.2% had adenocarcinoma histology. The frequency of EGFR mutations was 26.0% (95% confidence interval [CI], 24.9–27.1; Argentina, 14.4% [12.8–15.6]; México, 34.3% [31.9–36.7]; Colombia, 24.7% [22.8–26.6]; Peru, 51.1% [46.2–55.9]; Panamá, 27.3 [20.7–33.9]; and Costa Rica, 31.4% [22.4–40.4]). The frequency of KRAS mutations was 14.0% (9.1–18.9). In patients with adenocarcinoma, EGFR mutations were independently associated with gender (30.7% females vs. 18.4% males; p < 0.001), nonsmoker status (27.4% vs. 17.1%, p < 0.001), ethnicity (mestizo/indigenous, 35.3% vs. Caucasian, 13.7%, p < 0.001), and the absence of KRAS mutation (38.1% vs. 4.7%; p < 0.001). The overall response rate to EGFR tyrosine kinase inhibitors was 60.6% (95% CI, 52–69), with a median progression-free survival and overall survival of 15.9 (95% CI, 12.420.6) and 32 months (95% CI, 26.5–37.6), respectively. Our findings support the genetic heterogeneity of NSCLC in Latin America, confirming that the frequency of EGFR mutations is intermediate between that observed in the Asian and Caucasian populations.
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The EGFR mutation frequency was found between Asian (40%) and Caucasian (15%) populations. Here, we report the updated distribution of NSCLC mutations. A total of 5738 samples from NSCLC patients from Argentina (1713), Mexico (1417), Colombia (1939), Peru (393), Panama (174), and Costa Rica (102) were genotyped for EGFR and KRAS. The median patient age was 62.2 ± 12.3 years; 53.5% were women, 46.7% had a history of smoking, and 95.2% had adenocarcinoma histology. The frequency of EGFR mutations was 26.0% (95% confidence interval [CI], 24.9–27.1; Argentina, 14.4% [12.8–15.6]; México, 34.3% [31.9–36.7]; Colombia, 24.7% [22.8–26.6]; Peru, 51.1% [46.2–55.9]; Panamá, 27.3 [20.7–33.9]; and Costa Rica, 31.4% [22.4–40.4]). The frequency of KRAS mutations was 14.0% (9.1–18.9). In patients with adenocarcinoma, EGFR mutations were independently associated with gender (30.7% females vs. 18.4% males; p &lt; 0.001), nonsmoker status (27.4% vs. 17.1%, p &lt; 0.001), ethnicity (mestizo/indigenous, 35.3% vs. Caucasian, 13.7%, p &lt; 0.001), and the absence of KRAS mutation (38.1% vs. 4.7%; p &lt; 0.001). The overall response rate to EGFR tyrosine kinase inhibitors was 60.6% (95% CI, 52–69), with a median progression-free survival and overall survival of 15.9 (95% CI, 12.420.6) and 32 months (95% CI, 26.5–37.6), respectively. 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In patients with adenocarcinoma, EGFR mutations were independently associated with gender (30.7% females vs. 18.4% males; p &lt; 0.001), nonsmoker status (27.4% vs. 17.1%, p &lt; 0.001), ethnicity (mestizo/indigenous, 35.3% vs. Caucasian, 13.7%, p &lt; 0.001), and the absence of KRAS mutation (38.1% vs. 4.7%; p &lt; 0.001). The overall response rate to EGFR tyrosine kinase inhibitors was 60.6% (95% CI, 52–69), with a median progression-free survival and overall survival of 15.9 (95% CI, 12.420.6) and 32 months (95% CI, 26.5–37.6), respectively. Our findings support the genetic heterogeneity of NSCLC in Latin America, confirming that the frequency of EGFR mutations is intermediate between that observed in the Asian and Caucasian populations.</description><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - pathology</subject><subject>Aged</subject><subject>American Native Continental Ancestry Group - genetics</subject><subject>Anaplastic lymphoma kinase</subject><subject>Argentina</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - genetics</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Colombia</subject><subject>Costa Rica</subject><subject>Disease-Free Survival</subject><subject>Epidermal growth factor</subject><subject>ErbB Receptors - antagonists &amp; inhibitors</subject><subject>ErbB Receptors - genetics</subject><subject>European Continental Ancestry Group - genetics</subject><subject>Female</subject><subject>Frequency</subject><subject>Genetic Heterogeneity</subject><subject>Humans</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Mexico</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Mutation Rate</subject><subject>Non small-cell lung cancer</subject><subject>Panama</subject><subject>Peru</subject><subject>Protein Kinase Inhibitors - therapeutic use</subject><subject>Proto-Oncogene Proteins p21(ras) - genetics</subject><subject>Sex Factors</subject><subject>Smoking - genetics</subject><subject>Survival Rate</subject><issn>1556-0864</issn><issn>1556-1380</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhi0EoqXlDRDysRxS7MZ2NhyQVlG3LIS2ardny3EmXUNiL7bTqk_Ea-IlC6o4UF_GGn__P_L8CL2h5JiSsnj_eXVxTB4fNqPP0D7lXGQ0n5HnuzuZCbaHXoXwLSE8US_R3gkXOSNE7KOfN5tWRWjxwsOPEax-wK7Dp2eLK6xsi79cza_x1zGqaJwN2Fh87uz1oPo-q6DvcT3aW1wpq8FvH-vEWTwfwButPuDVGqZWtmtZXCUb56MZB9w5j2MilvYOQjS3v2dspz82ParqZaUu3x2iF53qA7ze1QN0szhdVZ-y-uJsWc3rTPOC0Uw1hSgEJ41QZV7SUjGSKi-EaKkiXUf5iW5oC8AE1bkiSpSgctawMm_Klub5ATqafDfepX2EKAcTdPqqsuDGIKkoOBVlzkRC2YRq70Lw0MmNN4PyD5ISuY1IpojkvxEl2dvdhLEZoP0r-pNJAmYTcO_6CD5878d78HINqo_rp7w_TlJIK7ozSRW0SaFCazzoKFtn_m_wC_Sfr24</recordid><startdate>201505</startdate><enddate>201505</enddate><creator>Arrieta, Oscar</creator><creator>Cardona, Andrés F.</creator><creator>Martín, Claudio</creator><creator>Más-López, Luis</creator><creator>Corrales-Rodríguez, Luis</creator><creator>Bramuglia, Guillermo</creator><creator>Castillo-Fernandez, Omar</creator><creator>Meyerson, Matthew</creator><creator>Amieva-Rivera, Eduardo</creator><creator>Campos-Parra, Alma Delia</creator><creator>Carranza, Hernán</creator><creator>Gómez de la Torre, Juan Carlos</creator><creator>Powazniak, Yanina</creator><creator>Aldaco-Sarvide, Fernando</creator><creator>Vargas, Carlos</creator><creator>Trigo, Mariana</creator><creator>Magallanes-Maciel, Manuel</creator><creator>Otero, Jorge</creator><creator>Sánchez-Reyes, Roberto</creator><creator>Cuello, Mauricio</creator><general>Elsevier Inc</general><general>Copyright by the International Association for the Study of Lung Cancer</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201505</creationdate><title>Updated Frequency of EGFR and KRAS Mutations in NonSmall-Cell Lung Cancer in Latin America: The Latin-American Consortium for the Investigation of Lung Cancer (CLICaP)</title><author>Arrieta, Oscar ; 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The EGFR mutation frequency was found between Asian (40%) and Caucasian (15%) populations. Here, we report the updated distribution of NSCLC mutations. A total of 5738 samples from NSCLC patients from Argentina (1713), Mexico (1417), Colombia (1939), Peru (393), Panama (174), and Costa Rica (102) were genotyped for EGFR and KRAS. The median patient age was 62.2 ± 12.3 years; 53.5% were women, 46.7% had a history of smoking, and 95.2% had adenocarcinoma histology. The frequency of EGFR mutations was 26.0% (95% confidence interval [CI], 24.9–27.1; Argentina, 14.4% [12.8–15.6]; México, 34.3% [31.9–36.7]; Colombia, 24.7% [22.8–26.6]; Peru, 51.1% [46.2–55.9]; Panamá, 27.3 [20.7–33.9]; and Costa Rica, 31.4% [22.4–40.4]). The frequency of KRAS mutations was 14.0% (9.1–18.9). In patients with adenocarcinoma, EGFR mutations were independently associated with gender (30.7% females vs. 18.4% males; p &lt; 0.001), nonsmoker status (27.4% vs. 17.1%, p &lt; 0.001), ethnicity (mestizo/indigenous, 35.3% vs. Caucasian, 13.7%, p &lt; 0.001), and the absence of KRAS mutation (38.1% vs. 4.7%; p &lt; 0.001). The overall response rate to EGFR tyrosine kinase inhibitors was 60.6% (95% CI, 52–69), with a median progression-free survival and overall survival of 15.9 (95% CI, 12.420.6) and 32 months (95% CI, 26.5–37.6), respectively. Our findings support the genetic heterogeneity of NSCLC in Latin America, confirming that the frequency of EGFR mutations is intermediate between that observed in the Asian and Caucasian populations.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25634006</pmid><doi>10.1097/JTO.0000000000000481</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adenocarcinoma - genetics
Adenocarcinoma - pathology
Aged
American Native Continental Ancestry Group - genetics
Anaplastic lymphoma kinase
Argentina
Carcinoma, Non-Small-Cell Lung - drug therapy
Carcinoma, Non-Small-Cell Lung - genetics
Carcinoma, Non-Small-Cell Lung - pathology
Colombia
Costa Rica
Disease-Free Survival
Epidermal growth factor
ErbB Receptors - antagonists & inhibitors
ErbB Receptors - genetics
European Continental Ancestry Group - genetics
Female
Frequency
Genetic Heterogeneity
Humans
Lung Neoplasms - drug therapy
Lung Neoplasms - genetics
Lung Neoplasms - pathology
Male
Mexico
Middle Aged
Mutation
Mutation Rate
Non small-cell lung cancer
Panama
Peru
Protein Kinase Inhibitors - therapeutic use
Proto-Oncogene Proteins p21(ras) - genetics
Sex Factors
Smoking - genetics
Survival Rate
title Updated Frequency of EGFR and KRAS Mutations in NonSmall-Cell Lung Cancer in Latin America: The Latin-American Consortium for the Investigation of Lung Cancer (CLICaP)
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