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 |
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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. |
doi_str_mv | 10.1097/JTO.0000000000000481 |
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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.</description><identifier>ISSN: 1556-0864</identifier><identifier>EISSN: 1556-1380</identifier><identifier>DOI: 10.1097/JTO.0000000000000481</identifier><identifier>PMID: 25634006</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>Journal of thoracic oncology, 2015-05, Vol.10 (5), p.838-843</ispartof><rights>2015 International Association for the Study of Lung Cancer</rights><rights>Copyright © 2015 by the International Association for the Study of Lung Cancer</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5741-ab767650b6a93919a409395766d1a0ff152cb1dee461c3a0a69ea34b493b9d133</citedby><cites>FETCH-LOGICAL-c5741-ab767650b6a93919a409395766d1a0ff152cb1dee461c3a0a69ea34b493b9d133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25634006$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arrieta, Oscar</creatorcontrib><creatorcontrib>Cardona, Andrés F.</creatorcontrib><creatorcontrib>Martín, Claudio</creatorcontrib><creatorcontrib>Más-López, Luis</creatorcontrib><creatorcontrib>Corrales-Rodríguez, Luis</creatorcontrib><creatorcontrib>Bramuglia, Guillermo</creatorcontrib><creatorcontrib>Castillo-Fernandez, Omar</creatorcontrib><creatorcontrib>Meyerson, Matthew</creatorcontrib><creatorcontrib>Amieva-Rivera, Eduardo</creatorcontrib><creatorcontrib>Campos-Parra, Alma Delia</creatorcontrib><creatorcontrib>Carranza, Hernán</creatorcontrib><creatorcontrib>Gómez de la Torre, Juan Carlos</creatorcontrib><creatorcontrib>Powazniak, Yanina</creatorcontrib><creatorcontrib>Aldaco-Sarvide, Fernando</creatorcontrib><creatorcontrib>Vargas, Carlos</creatorcontrib><creatorcontrib>Trigo, Mariana</creatorcontrib><creatorcontrib>Magallanes-Maciel, Manuel</creatorcontrib><creatorcontrib>Otero, Jorge</creatorcontrib><creatorcontrib>Sánchez-Reyes, Roberto</creatorcontrib><creatorcontrib>Cuello, Mauricio</creatorcontrib><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><title>Journal of thoracic oncology</title><addtitle>J Thorac Oncol</addtitle><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.</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 & 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 ; 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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5741-ab767650b6a93919a409395766d1a0ff152cb1dee461c3a0a69ea34b493b9d133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - pathology</topic><topic>Aged</topic><topic>American Native Continental Ancestry Group - genetics</topic><topic>Anaplastic lymphoma kinase</topic><topic>Argentina</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - genetics</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Colombia</topic><topic>Costa Rica</topic><topic>Disease-Free Survival</topic><topic>Epidermal growth factor</topic><topic>ErbB Receptors - antagonists & inhibitors</topic><topic>ErbB Receptors - genetics</topic><topic>European Continental Ancestry Group - genetics</topic><topic>Female</topic><topic>Frequency</topic><topic>Genetic Heterogeneity</topic><topic>Humans</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Mexico</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Mutation Rate</topic><topic>Non small-cell lung cancer</topic><topic>Panama</topic><topic>Peru</topic><topic>Protein Kinase Inhibitors - therapeutic use</topic><topic>Proto-Oncogene Proteins p21(ras) - genetics</topic><topic>Sex Factors</topic><topic>Smoking - genetics</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arrieta, Oscar</creatorcontrib><creatorcontrib>Cardona, Andrés F.</creatorcontrib><creatorcontrib>Martín, Claudio</creatorcontrib><creatorcontrib>Más-López, Luis</creatorcontrib><creatorcontrib>Corrales-Rodríguez, Luis</creatorcontrib><creatorcontrib>Bramuglia, Guillermo</creatorcontrib><creatorcontrib>Castillo-Fernandez, Omar</creatorcontrib><creatorcontrib>Meyerson, Matthew</creatorcontrib><creatorcontrib>Amieva-Rivera, Eduardo</creatorcontrib><creatorcontrib>Campos-Parra, Alma Delia</creatorcontrib><creatorcontrib>Carranza, Hernán</creatorcontrib><creatorcontrib>Gómez de la Torre, Juan Carlos</creatorcontrib><creatorcontrib>Powazniak, Yanina</creatorcontrib><creatorcontrib>Aldaco-Sarvide, Fernando</creatorcontrib><creatorcontrib>Vargas, Carlos</creatorcontrib><creatorcontrib>Trigo, Mariana</creatorcontrib><creatorcontrib>Magallanes-Maciel, Manuel</creatorcontrib><creatorcontrib>Otero, Jorge</creatorcontrib><creatorcontrib>Sánchez-Reyes, Roberto</creatorcontrib><creatorcontrib>Cuello, Mauricio</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of thoracic oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arrieta, Oscar</au><au>Cardona, Andrés F.</au><au>Martín, Claudio</au><au>Más-López, Luis</au><au>Corrales-Rodríguez, Luis</au><au>Bramuglia, Guillermo</au><au>Castillo-Fernandez, Omar</au><au>Meyerson, Matthew</au><au>Amieva-Rivera, Eduardo</au><au>Campos-Parra, Alma Delia</au><au>Carranza, Hernán</au><au>Gómez de la Torre, Juan Carlos</au><au>Powazniak, Yanina</au><au>Aldaco-Sarvide, Fernando</au><au>Vargas, Carlos</au><au>Trigo, Mariana</au><au>Magallanes-Maciel, Manuel</au><au>Otero, Jorge</au><au>Sánchez-Reyes, Roberto</au><au>Cuello, Mauricio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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)</atitle><jtitle>Journal of thoracic oncology</jtitle><addtitle>J Thorac Oncol</addtitle><date>2015-05</date><risdate>2015</risdate><volume>10</volume><issue>5</issue><spage>838</spage><epage>843</epage><pages>838-843</pages><issn>1556-0864</issn><eissn>1556-1380</eissn><abstract>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.</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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