Response Assessment of ^sup 68^Ga-DOTA-E-[c(RGDfK)]^sup 2^ PET/CT in Lung Adenocarcinoma Patients Treated with Nintedanib Plus Docetaxel

Nintedanib is an oral angiokinase inhibitor used as second-line treatment for non-small cell lung cancer. New radiotracers, such as 68Ga-DOTA-E-[c(RGDfK)]2, that target avβ3 integrin might have an impact as a noninvasive method for assessing angiogenesis inhibitors. Methods: From July 2011 through O...

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Veröffentlicht in:The Journal of nuclear medicine (1978) 2018-03, Vol.59 (3), p.403
Hauptverfasser: Arrieta, Oscar, Garcia-Perez, Francisco O, Michel-Tello, David, Ramírez-Tirado, Laura-Alejandra, Pitalua-Cortes, Quetzali, Cruz-Rico, Graciela, Macedo-Pérez, Eleazar-Omar, Cardona, Andrés F, de la Garza-Salazar, Jaime
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container_issue 3
container_start_page 403
container_title The Journal of nuclear medicine (1978)
container_volume 59
creator Arrieta, Oscar
Garcia-Perez, Francisco O
Michel-Tello, David
Ramírez-Tirado, Laura-Alejandra
Pitalua-Cortes, Quetzali
Cruz-Rico, Graciela
Macedo-Pérez, Eleazar-Omar
Cardona, Andrés F
de la Garza-Salazar, Jaime
description Nintedanib is an oral angiokinase inhibitor used as second-line treatment for non-small cell lung cancer. New radiotracers, such as 68Ga-DOTA-E-[c(RGDfK)]2, that target avβ3 integrin might have an impact as a noninvasive method for assessing angiogenesis inhibitors. Methods: From July 2011 through October 2015, 38 patients received second-line nintedanib plus docetaxel. All patients underwent PET/CT with 68Ga-DOTA-E-[c(RGDfK)]2 radiotracer and blood-sample tests to quantify angiogenesis factors (fibroblast growth factor, vascular endothelial growth factor, and platelet-derived growth factor AB) before and after completing 2 therapy cycles. Results: Of the 38 patients, 31 had available baseline and follow-up PET/CT. Baseline lung tumor volume addressed with 68Ga-DOTA-E-[c(RGDfK)]2 PET/CT correlated with serum vascular endothelial growth factor levels, whereas baseline lung/liver SUVmax index correlated with platelet-derived growth factor AB. After treatment, the overall response rate and disease control rate were 7.9% and 47.3%, respectively. A greater decrease in lung tumor volume (-37.2% vs. -27.6%) was associated with a better disease control rate in patients (P = 0.005). Median progression-free survival was 3.7 mo. Nonsmokers and patients with a higher baseline lung tumor volume were more likely to have a higher progression-free survival (6.4 vs. 3.74 [P = 0.023] and 6.4 vs. 2.1 [P = 0.003], respectively). Overall survival was not reached. Patients with a greater decrease in lung SUVmax (not reached vs. 7.1 mo; P = 0.016) and a greater decrease in the lung/spleen SUVmax index (not reached vs. 7.1; P = 0.043) were more likely to have a longer overall survival. Conclusion: 68Ga-DOTA-E-[c(RGDfK)]2 PET/CT is a potentially useful tool for assessing responses to angiogenesis inhibitors. Further analysis and novel studies are warranted to identify patients who might benefit from this therapy.
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New radiotracers, such as 68Ga-DOTA-E-[c(RGDfK)]2, that target avβ3 integrin might have an impact as a noninvasive method for assessing angiogenesis inhibitors. Methods: From July 2011 through October 2015, 38 patients received second-line nintedanib plus docetaxel. All patients underwent PET/CT with 68Ga-DOTA-E-[c(RGDfK)]2 radiotracer and blood-sample tests to quantify angiogenesis factors (fibroblast growth factor, vascular endothelial growth factor, and platelet-derived growth factor AB) before and after completing 2 therapy cycles. Results: Of the 38 patients, 31 had available baseline and follow-up PET/CT. Baseline lung tumor volume addressed with 68Ga-DOTA-E-[c(RGDfK)]2 PET/CT correlated with serum vascular endothelial growth factor levels, whereas baseline lung/liver SUVmax index correlated with platelet-derived growth factor AB. After treatment, the overall response rate and disease control rate were 7.9% and 47.3%, respectively. A greater decrease in lung tumor volume (-37.2% vs. -27.6%) was associated with a better disease control rate in patients (P = 0.005). Median progression-free survival was 3.7 mo. Nonsmokers and patients with a higher baseline lung tumor volume were more likely to have a higher progression-free survival (6.4 vs. 3.74 [P = 0.023] and 6.4 vs. 2.1 [P = 0.003], respectively). Overall survival was not reached. Patients with a greater decrease in lung SUVmax (not reached vs. 7.1 mo; P = 0.016) and a greater decrease in the lung/spleen SUVmax index (not reached vs. 7.1; P = 0.043) were more likely to have a longer overall survival. Conclusion: 68Ga-DOTA-E-[c(RGDfK)]2 PET/CT is a potentially useful tool for assessing responses to angiogenesis inhibitors. Further analysis and novel studies are warranted to identify patients who might benefit from this therapy.</description><identifier>ISSN: 0161-5505</identifier><identifier>EISSN: 1535-5667</identifier><language>eng</language><publisher>New York: Society of Nuclear Medicine</publisher><subject>Adenocarcinoma ; Angiogenesis ; Angiogenesis inhibitors ; Cancer therapies ; Disease control ; Drugs ; Fibroblast growth factors ; Inhibitors ; Liver ; Lung cancer ; Medical treatment ; Non-small cell lung carcinoma ; Patient assessment ; Patients ; Platelet-derived growth factor ; Positron emission tomography ; Spleen ; Studies ; Survival ; Therapy ; Tumors ; Vascular endothelial growth factor</subject><ispartof>The Journal of nuclear medicine (1978), 2018-03, Vol.59 (3), p.403</ispartof><rights>Copyright Society of Nuclear Medicine Mar 1, 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Arrieta, Oscar</creatorcontrib><creatorcontrib>Garcia-Perez, Francisco O</creatorcontrib><creatorcontrib>Michel-Tello, David</creatorcontrib><creatorcontrib>Ramírez-Tirado, Laura-Alejandra</creatorcontrib><creatorcontrib>Pitalua-Cortes, Quetzali</creatorcontrib><creatorcontrib>Cruz-Rico, Graciela</creatorcontrib><creatorcontrib>Macedo-Pérez, Eleazar-Omar</creatorcontrib><creatorcontrib>Cardona, Andrés F</creatorcontrib><creatorcontrib>de la Garza-Salazar, Jaime</creatorcontrib><title>Response Assessment of ^sup 68^Ga-DOTA-E-[c(RGDfK)]^sup 2^ PET/CT in Lung Adenocarcinoma Patients Treated with Nintedanib Plus Docetaxel</title><title>The Journal of nuclear medicine (1978)</title><description>Nintedanib is an oral angiokinase inhibitor used as second-line treatment for non-small cell lung cancer. New radiotracers, such as 68Ga-DOTA-E-[c(RGDfK)]2, that target avβ3 integrin might have an impact as a noninvasive method for assessing angiogenesis inhibitors. Methods: From July 2011 through October 2015, 38 patients received second-line nintedanib plus docetaxel. All patients underwent PET/CT with 68Ga-DOTA-E-[c(RGDfK)]2 radiotracer and blood-sample tests to quantify angiogenesis factors (fibroblast growth factor, vascular endothelial growth factor, and platelet-derived growth factor AB) before and after completing 2 therapy cycles. Results: Of the 38 patients, 31 had available baseline and follow-up PET/CT. Baseline lung tumor volume addressed with 68Ga-DOTA-E-[c(RGDfK)]2 PET/CT correlated with serum vascular endothelial growth factor levels, whereas baseline lung/liver SUVmax index correlated with platelet-derived growth factor AB. After treatment, the overall response rate and disease control rate were 7.9% and 47.3%, respectively. A greater decrease in lung tumor volume (-37.2% vs. -27.6%) was associated with a better disease control rate in patients (P = 0.005). Median progression-free survival was 3.7 mo. Nonsmokers and patients with a higher baseline lung tumor volume were more likely to have a higher progression-free survival (6.4 vs. 3.74 [P = 0.023] and 6.4 vs. 2.1 [P = 0.003], respectively). Overall survival was not reached. Patients with a greater decrease in lung SUVmax (not reached vs. 7.1 mo; P = 0.016) and a greater decrease in the lung/spleen SUVmax index (not reached vs. 7.1; P = 0.043) were more likely to have a longer overall survival. Conclusion: 68Ga-DOTA-E-[c(RGDfK)]2 PET/CT is a potentially useful tool for assessing responses to angiogenesis inhibitors. Further analysis and novel studies are warranted to identify patients who might benefit from this therapy.</description><subject>Adenocarcinoma</subject><subject>Angiogenesis</subject><subject>Angiogenesis inhibitors</subject><subject>Cancer therapies</subject><subject>Disease control</subject><subject>Drugs</subject><subject>Fibroblast growth factors</subject><subject>Inhibitors</subject><subject>Liver</subject><subject>Lung cancer</subject><subject>Medical treatment</subject><subject>Non-small cell lung carcinoma</subject><subject>Patient assessment</subject><subject>Patients</subject><subject>Platelet-derived growth factor</subject><subject>Positron emission tomography</subject><subject>Spleen</subject><subject>Studies</subject><subject>Survival</subject><subject>Therapy</subject><subject>Tumors</subject><subject>Vascular endothelial growth factor</subject><issn>0161-5505</issn><issn>1535-5667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqNjNFKwzAUhoMoWKfvcMAbvQimrcnqZVnrBIeWkTuxI3anmtEltSdlPoKPbREfwKvvh-_nO2JRLFPJpVLzYxaJWMVcSiFP2RnRTgihsiyL2PcaqfeOEHIiJNqjC-BbqGnsQWX10vDiWee85C_N1XpZtI_Xr78uqaEq9c1Cg3WwGt075Ft0vjFDY53fG6hMsFOMQA9oAm7hYMMHPFk3bePsG1TdSFD4BoP5wu6cnbSmI7z444xd3pd68cD7wX-OSGGz8-PgJrVJRHKn0tt4nqX_e_0ADTJR6g</recordid><startdate>20180301</startdate><enddate>20180301</enddate><creator>Arrieta, Oscar</creator><creator>Garcia-Perez, Francisco O</creator><creator>Michel-Tello, David</creator><creator>Ramírez-Tirado, Laura-Alejandra</creator><creator>Pitalua-Cortes, Quetzali</creator><creator>Cruz-Rico, Graciela</creator><creator>Macedo-Pérez, Eleazar-Omar</creator><creator>Cardona, Andrés F</creator><creator>de la Garza-Salazar, Jaime</creator><general>Society of Nuclear Medicine</general><scope>4T-</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>NAPCQ</scope><scope>P64</scope></search><sort><creationdate>20180301</creationdate><title>Response Assessment of ^sup 68^Ga-DOTA-E-[c(RGDfK)]^sup 2^ PET/CT in Lung Adenocarcinoma Patients Treated with Nintedanib Plus Docetaxel</title><author>Arrieta, Oscar ; Garcia-Perez, Francisco O ; Michel-Tello, David ; Ramírez-Tirado, Laura-Alejandra ; Pitalua-Cortes, Quetzali ; Cruz-Rico, Graciela ; Macedo-Pérez, Eleazar-Omar ; Cardona, Andrés F ; de la Garza-Salazar, Jaime</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_20296341783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adenocarcinoma</topic><topic>Angiogenesis</topic><topic>Angiogenesis inhibitors</topic><topic>Cancer therapies</topic><topic>Disease control</topic><topic>Drugs</topic><topic>Fibroblast growth factors</topic><topic>Inhibitors</topic><topic>Liver</topic><topic>Lung cancer</topic><topic>Medical treatment</topic><topic>Non-small cell lung carcinoma</topic><topic>Patient assessment</topic><topic>Patients</topic><topic>Platelet-derived growth factor</topic><topic>Positron emission tomography</topic><topic>Spleen</topic><topic>Studies</topic><topic>Survival</topic><topic>Therapy</topic><topic>Tumors</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arrieta, Oscar</creatorcontrib><creatorcontrib>Garcia-Perez, Francisco O</creatorcontrib><creatorcontrib>Michel-Tello, David</creatorcontrib><creatorcontrib>Ramírez-Tirado, Laura-Alejandra</creatorcontrib><creatorcontrib>Pitalua-Cortes, Quetzali</creatorcontrib><creatorcontrib>Cruz-Rico, Graciela</creatorcontrib><creatorcontrib>Macedo-Pérez, Eleazar-Omar</creatorcontrib><creatorcontrib>Cardona, Andrés F</creatorcontrib><creatorcontrib>de la Garza-Salazar, Jaime</creatorcontrib><collection>Docstoc</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>The Journal of nuclear medicine (1978)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arrieta, Oscar</au><au>Garcia-Perez, Francisco O</au><au>Michel-Tello, David</au><au>Ramírez-Tirado, Laura-Alejandra</au><au>Pitalua-Cortes, Quetzali</au><au>Cruz-Rico, Graciela</au><au>Macedo-Pérez, Eleazar-Omar</au><au>Cardona, Andrés F</au><au>de la Garza-Salazar, Jaime</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Response Assessment of ^sup 68^Ga-DOTA-E-[c(RGDfK)]^sup 2^ PET/CT in Lung Adenocarcinoma Patients Treated with Nintedanib Plus Docetaxel</atitle><jtitle>The Journal of nuclear medicine (1978)</jtitle><date>2018-03-01</date><risdate>2018</risdate><volume>59</volume><issue>3</issue><spage>403</spage><pages>403-</pages><issn>0161-5505</issn><eissn>1535-5667</eissn><abstract>Nintedanib is an oral angiokinase inhibitor used as second-line treatment for non-small cell lung cancer. New radiotracers, such as 68Ga-DOTA-E-[c(RGDfK)]2, that target avβ3 integrin might have an impact as a noninvasive method for assessing angiogenesis inhibitors. Methods: From July 2011 through October 2015, 38 patients received second-line nintedanib plus docetaxel. All patients underwent PET/CT with 68Ga-DOTA-E-[c(RGDfK)]2 radiotracer and blood-sample tests to quantify angiogenesis factors (fibroblast growth factor, vascular endothelial growth factor, and platelet-derived growth factor AB) before and after completing 2 therapy cycles. Results: Of the 38 patients, 31 had available baseline and follow-up PET/CT. Baseline lung tumor volume addressed with 68Ga-DOTA-E-[c(RGDfK)]2 PET/CT correlated with serum vascular endothelial growth factor levels, whereas baseline lung/liver SUVmax index correlated with platelet-derived growth factor AB. After treatment, the overall response rate and disease control rate were 7.9% and 47.3%, respectively. A greater decrease in lung tumor volume (-37.2% vs. -27.6%) was associated with a better disease control rate in patients (P = 0.005). Median progression-free survival was 3.7 mo. Nonsmokers and patients with a higher baseline lung tumor volume were more likely to have a higher progression-free survival (6.4 vs. 3.74 [P = 0.023] and 6.4 vs. 2.1 [P = 0.003], respectively). Overall survival was not reached. Patients with a greater decrease in lung SUVmax (not reached vs. 7.1 mo; P = 0.016) and a greater decrease in the lung/spleen SUVmax index (not reached vs. 7.1; P = 0.043) were more likely to have a longer overall survival. Conclusion: 68Ga-DOTA-E-[c(RGDfK)]2 PET/CT is a potentially useful tool for assessing responses to angiogenesis inhibitors. Further analysis and novel studies are warranted to identify patients who might benefit from this therapy.</abstract><cop>New York</cop><pub>Society of Nuclear Medicine</pub></addata></record>
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subjects Adenocarcinoma
Angiogenesis
Angiogenesis inhibitors
Cancer therapies
Disease control
Drugs
Fibroblast growth factors
Inhibitors
Liver
Lung cancer
Medical treatment
Non-small cell lung carcinoma
Patient assessment
Patients
Platelet-derived growth factor
Positron emission tomography
Spleen
Studies
Survival
Therapy
Tumors
Vascular endothelial growth factor
title Response Assessment of ^sup 68^Ga-DOTA-E-[c(RGDfK)]^sup 2^ PET/CT in Lung Adenocarcinoma Patients Treated with Nintedanib Plus Docetaxel
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