Proangiogenic Growth Factor Therapy for the Treatment of Refractory Angina: A Meta-analysis
Refractory angina (RFA; limiting angina despite optimal medical therapy) is a growing, global problem, with limited treatment options. Therefore, we conducted a systematic review of randomized controlled trials (RCTs) to evaluate the effect of proangiogenic growth factor therapy (in the form of vasc...
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creator | Weeraman, Deshan Jones, Daniel A. Hussain, Mohsin Beirne, Anne-Marie Hadyanto, Steven Rathod, Krishnaraj S. Whiteford, James R. Reid, Alice E. Bourantas, Christos V. Ylä-Herttuala, Seppo Baumbach, Andreas Gersh, Bernard J. Henry, Timothy D. Mathur, Anthony |
description | Refractory angina (RFA; limiting angina despite optimal medical therapy) is a growing, global problem, with limited treatment options. Therefore, we conducted a systematic review of randomized controlled trials (RCTs) to evaluate the effect of proangiogenic growth factor therapy (in the form of vascular growth factors delivered either as recombinant proteins or gene therapy) in patients with RFA ineligible for revascularization.
We performed a meta-analysis (PROSPERO: CRD42018107283) of RCTs as per the Preferred Reporting Items for Systematic Reviews and Meta-Analyses methodology. A comprehensive search of the PubMed, CENTRAL, Embase, Cochrane, ClinicalTrials.gov and Google Scholar databases, as well as scientific session abstracts, were performed. The pooled outcomes included major adverse cardiac events (MACE), mortality, myocardial perfusion, and indices of angina severity (Canadian Cardiovascular Society angina class [CCS] and exercise tolerance). A prespecified subgroup analysis was performed for delivery method, vector, and protein type. The standardized mean difference (SMD) or odds ratio (OR) was calculated to assess relevant outcomes. We assessed heterogeneity using the χ2 and I2 tests.
We included 16 RCTs involving 1607 patients (1052 received proangiogenic growth factor therapy and 555 received a placebo or optimal medical therapy). Our analysis showed a significant decreased risk of MACE (OR, 0.72; 95% confidence interval [CI], 0.55-0.93) and significantly improved CCS class (SMD, −0.55; 95% CI, −1.10 to 0.00), but not mortality (OR, 0.66; 95% CI, 0.28-1.54) or exercise tolerance (SMD, 0.47; 95% CI, −0.14 to 1.09), in treated patients compared to those in the control group.
Proangiogenic growth factor therapy is a promising treatment option for RFA, with beneficial effects seen on MACE and CCS class. The results of ongoing trials are needed before it can be considered for clinical practice.
[Display omitted]
•Further therapeutic options are needed for the treatment of refractory angina.•Proangiogenic growth factor therapy led to improvements in major adverse cardiac events and Canadian Cardiovascular Society class.•Larger studies are justified to look for a definitive beneficial signal.•The optimal delivery route, delivery vector, and protein type are yet to be identified. |
doi_str_mv | 10.1016/j.jscai.2022.100527 |
format | Article |
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We performed a meta-analysis (PROSPERO: CRD42018107283) of RCTs as per the Preferred Reporting Items for Systematic Reviews and Meta-Analyses methodology. A comprehensive search of the PubMed, CENTRAL, Embase, Cochrane, ClinicalTrials.gov and Google Scholar databases, as well as scientific session abstracts, were performed. The pooled outcomes included major adverse cardiac events (MACE), mortality, myocardial perfusion, and indices of angina severity (Canadian Cardiovascular Society angina class [CCS] and exercise tolerance). A prespecified subgroup analysis was performed for delivery method, vector, and protein type. The standardized mean difference (SMD) or odds ratio (OR) was calculated to assess relevant outcomes. We assessed heterogeneity using the χ2 and I2 tests.
We included 16 RCTs involving 1607 patients (1052 received proangiogenic growth factor therapy and 555 received a placebo or optimal medical therapy). Our analysis showed a significant decreased risk of MACE (OR, 0.72; 95% confidence interval [CI], 0.55-0.93) and significantly improved CCS class (SMD, −0.55; 95% CI, −1.10 to 0.00), but not mortality (OR, 0.66; 95% CI, 0.28-1.54) or exercise tolerance (SMD, 0.47; 95% CI, −0.14 to 1.09), in treated patients compared to those in the control group.
Proangiogenic growth factor therapy is a promising treatment option for RFA, with beneficial effects seen on MACE and CCS class. The results of ongoing trials are needed before it can be considered for clinical practice.
[Display omitted]
•Further therapeutic options are needed for the treatment of refractory angina.•Proangiogenic growth factor therapy led to improvements in major adverse cardiac events and Canadian Cardiovascular Society class.•Larger studies are justified to look for a definitive beneficial signal.•The optimal delivery route, delivery vector, and protein type are yet to be identified.</description><identifier>ISSN: 2772-9303</identifier><identifier>EISSN: 2772-9303</identifier><identifier>DOI: 10.1016/j.jscai.2022.100527</identifier><identifier>PMID: 39132540</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>angiogenesis ; chronic myocardial ischemia ; gene therapy ; meta-analysis ; refractory angina</subject><ispartof>Journal of the Society for Cardiovascular Angiography & Interventions, 2023-01, Vol.2 (1), p.100527, Article 100527</ispartof><rights>2022 The Authors</rights><rights>2022 The Authors.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3197-44005aee07da259a277fb547c596f964c51c7bb1739c9c55b7f0322f0d6f5f573</citedby><cites>FETCH-LOGICAL-c3197-44005aee07da259a277fb547c596f964c51c7bb1739c9c55b7f0322f0d6f5f573</cites><orcidid>0000-0003-1441-0417 ; 0000-0002-8967-7389 ; 0000-0001-7941-9653 ; 0000-0003-4268-5055 ; 0000-0001-7707-2254</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39132540$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Weeraman, Deshan</creatorcontrib><creatorcontrib>Jones, Daniel A.</creatorcontrib><creatorcontrib>Hussain, Mohsin</creatorcontrib><creatorcontrib>Beirne, Anne-Marie</creatorcontrib><creatorcontrib>Hadyanto, Steven</creatorcontrib><creatorcontrib>Rathod, Krishnaraj S.</creatorcontrib><creatorcontrib>Whiteford, James R.</creatorcontrib><creatorcontrib>Reid, Alice E.</creatorcontrib><creatorcontrib>Bourantas, Christos V.</creatorcontrib><creatorcontrib>Ylä-Herttuala, Seppo</creatorcontrib><creatorcontrib>Baumbach, Andreas</creatorcontrib><creatorcontrib>Gersh, Bernard J.</creatorcontrib><creatorcontrib>Henry, Timothy D.</creatorcontrib><creatorcontrib>Mathur, Anthony</creatorcontrib><title>Proangiogenic Growth Factor Therapy for the Treatment of Refractory Angina: A Meta-analysis</title><title>Journal of the Society for Cardiovascular Angiography & Interventions</title><addtitle>J Soc Cardiovasc Angiogr Interv</addtitle><description>Refractory angina (RFA; limiting angina despite optimal medical therapy) is a growing, global problem, with limited treatment options. Therefore, we conducted a systematic review of randomized controlled trials (RCTs) to evaluate the effect of proangiogenic growth factor therapy (in the form of vascular growth factors delivered either as recombinant proteins or gene therapy) in patients with RFA ineligible for revascularization.
We performed a meta-analysis (PROSPERO: CRD42018107283) of RCTs as per the Preferred Reporting Items for Systematic Reviews and Meta-Analyses methodology. A comprehensive search of the PubMed, CENTRAL, Embase, Cochrane, ClinicalTrials.gov and Google Scholar databases, as well as scientific session abstracts, were performed. The pooled outcomes included major adverse cardiac events (MACE), mortality, myocardial perfusion, and indices of angina severity (Canadian Cardiovascular Society angina class [CCS] and exercise tolerance). A prespecified subgroup analysis was performed for delivery method, vector, and protein type. The standardized mean difference (SMD) or odds ratio (OR) was calculated to assess relevant outcomes. We assessed heterogeneity using the χ2 and I2 tests.
We included 16 RCTs involving 1607 patients (1052 received proangiogenic growth factor therapy and 555 received a placebo or optimal medical therapy). Our analysis showed a significant decreased risk of MACE (OR, 0.72; 95% confidence interval [CI], 0.55-0.93) and significantly improved CCS class (SMD, −0.55; 95% CI, −1.10 to 0.00), but not mortality (OR, 0.66; 95% CI, 0.28-1.54) or exercise tolerance (SMD, 0.47; 95% CI, −0.14 to 1.09), in treated patients compared to those in the control group.
Proangiogenic growth factor therapy is a promising treatment option for RFA, with beneficial effects seen on MACE and CCS class. The results of ongoing trials are needed before it can be considered for clinical practice.
[Display omitted]
•Further therapeutic options are needed for the treatment of refractory angina.•Proangiogenic growth factor therapy led to improvements in major adverse cardiac events and Canadian Cardiovascular Society class.•Larger studies are justified to look for a definitive beneficial signal.•The optimal delivery route, delivery vector, and protein type are yet to be identified.</description><subject>angiogenesis</subject><subject>chronic myocardial ischemia</subject><subject>gene therapy</subject><subject>meta-analysis</subject><subject>refractory angina</subject><issn>2772-9303</issn><issn>2772-9303</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kM1OGzEURi1URCLgCZAqL7uZ9Noej3GlLqKoUCQqEAorFpbHc00cJePUnhTl7TEJVF115SvrfPfnEHLBYMKANV-Xk2V2Nkw4cF5-QHJ1RMZcKV5pAeLTP_WInOe8BAB-WaIgT8hIaCa4rGFMnu5TtP1ziM_YB0evU3wZFvTKuiEmOl9gspsd9aUeFkjnCe2wxn6g0dMH9GmP7ei0NOjtNzqlv3Cwle3tapdDPiPH3q4ynr-_p-Tx6sd89rO6vbu-mU1vKyeYVlVdl_UtIqjOcqltWdy3slZO6sbrpnaSOdW2TAnttJOyVR4E5x66xksvlTglXw59Nyn-3mIezDpkh6uV7TFusxGgOTB-2UBBxQF1Keac0JtNCmubdoaBeRNrlmYv1ryJNQexJfX5fcC2XWP3N_OhsQDfDwCWM_8ETCa7gL3DLiR0g-li-O-AV8L-iOc</recordid><startdate>202301</startdate><enddate>202301</enddate><creator>Weeraman, Deshan</creator><creator>Jones, Daniel A.</creator><creator>Hussain, Mohsin</creator><creator>Beirne, Anne-Marie</creator><creator>Hadyanto, Steven</creator><creator>Rathod, Krishnaraj S.</creator><creator>Whiteford, James R.</creator><creator>Reid, Alice E.</creator><creator>Bourantas, Christos V.</creator><creator>Ylä-Herttuala, Seppo</creator><creator>Baumbach, Andreas</creator><creator>Gersh, Bernard J.</creator><creator>Henry, Timothy D.</creator><creator>Mathur, Anthony</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1441-0417</orcidid><orcidid>https://orcid.org/0000-0002-8967-7389</orcidid><orcidid>https://orcid.org/0000-0001-7941-9653</orcidid><orcidid>https://orcid.org/0000-0003-4268-5055</orcidid><orcidid>https://orcid.org/0000-0001-7707-2254</orcidid></search><sort><creationdate>202301</creationdate><title>Proangiogenic Growth Factor Therapy for the Treatment of Refractory Angina: A Meta-analysis</title><author>Weeraman, Deshan ; Jones, Daniel A. ; Hussain, Mohsin ; Beirne, Anne-Marie ; Hadyanto, Steven ; Rathod, Krishnaraj S. ; Whiteford, James R. ; Reid, Alice E. ; Bourantas, Christos V. ; Ylä-Herttuala, Seppo ; Baumbach, Andreas ; Gersh, Bernard J. ; Henry, Timothy D. ; Mathur, Anthony</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3197-44005aee07da259a277fb547c596f964c51c7bb1739c9c55b7f0322f0d6f5f573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>angiogenesis</topic><topic>chronic myocardial ischemia</topic><topic>gene therapy</topic><topic>meta-analysis</topic><topic>refractory angina</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weeraman, Deshan</creatorcontrib><creatorcontrib>Jones, Daniel A.</creatorcontrib><creatorcontrib>Hussain, Mohsin</creatorcontrib><creatorcontrib>Beirne, Anne-Marie</creatorcontrib><creatorcontrib>Hadyanto, Steven</creatorcontrib><creatorcontrib>Rathod, Krishnaraj S.</creatorcontrib><creatorcontrib>Whiteford, James R.</creatorcontrib><creatorcontrib>Reid, Alice E.</creatorcontrib><creatorcontrib>Bourantas, Christos V.</creatorcontrib><creatorcontrib>Ylä-Herttuala, Seppo</creatorcontrib><creatorcontrib>Baumbach, Andreas</creatorcontrib><creatorcontrib>Gersh, Bernard J.</creatorcontrib><creatorcontrib>Henry, Timothy D.</creatorcontrib><creatorcontrib>Mathur, Anthony</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the Society for Cardiovascular Angiography & Interventions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weeraman, Deshan</au><au>Jones, Daniel A.</au><au>Hussain, Mohsin</au><au>Beirne, Anne-Marie</au><au>Hadyanto, Steven</au><au>Rathod, Krishnaraj S.</au><au>Whiteford, James R.</au><au>Reid, Alice E.</au><au>Bourantas, Christos V.</au><au>Ylä-Herttuala, Seppo</au><au>Baumbach, Andreas</au><au>Gersh, Bernard J.</au><au>Henry, Timothy D.</au><au>Mathur, Anthony</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proangiogenic Growth Factor Therapy for the Treatment of Refractory Angina: A Meta-analysis</atitle><jtitle>Journal of the Society for Cardiovascular Angiography & Interventions</jtitle><addtitle>J Soc Cardiovasc Angiogr Interv</addtitle><date>2023-01</date><risdate>2023</risdate><volume>2</volume><issue>1</issue><spage>100527</spage><pages>100527-</pages><artnum>100527</artnum><issn>2772-9303</issn><eissn>2772-9303</eissn><abstract>Refractory angina (RFA; limiting angina despite optimal medical therapy) is a growing, global problem, with limited treatment options. Therefore, we conducted a systematic review of randomized controlled trials (RCTs) to evaluate the effect of proangiogenic growth factor therapy (in the form of vascular growth factors delivered either as recombinant proteins or gene therapy) in patients with RFA ineligible for revascularization.
We performed a meta-analysis (PROSPERO: CRD42018107283) of RCTs as per the Preferred Reporting Items for Systematic Reviews and Meta-Analyses methodology. A comprehensive search of the PubMed, CENTRAL, Embase, Cochrane, ClinicalTrials.gov and Google Scholar databases, as well as scientific session abstracts, were performed. The pooled outcomes included major adverse cardiac events (MACE), mortality, myocardial perfusion, and indices of angina severity (Canadian Cardiovascular Society angina class [CCS] and exercise tolerance). A prespecified subgroup analysis was performed for delivery method, vector, and protein type. The standardized mean difference (SMD) or odds ratio (OR) was calculated to assess relevant outcomes. We assessed heterogeneity using the χ2 and I2 tests.
We included 16 RCTs involving 1607 patients (1052 received proangiogenic growth factor therapy and 555 received a placebo or optimal medical therapy). Our analysis showed a significant decreased risk of MACE (OR, 0.72; 95% confidence interval [CI], 0.55-0.93) and significantly improved CCS class (SMD, −0.55; 95% CI, −1.10 to 0.00), but not mortality (OR, 0.66; 95% CI, 0.28-1.54) or exercise tolerance (SMD, 0.47; 95% CI, −0.14 to 1.09), in treated patients compared to those in the control group.
Proangiogenic growth factor therapy is a promising treatment option for RFA, with beneficial effects seen on MACE and CCS class. The results of ongoing trials are needed before it can be considered for clinical practice.
[Display omitted]
•Further therapeutic options are needed for the treatment of refractory angina.•Proangiogenic growth factor therapy led to improvements in major adverse cardiac events and Canadian Cardiovascular Society class.•Larger studies are justified to look for a definitive beneficial signal.•The optimal delivery route, delivery vector, and protein type are yet to be identified.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39132540</pmid><doi>10.1016/j.jscai.2022.100527</doi><orcidid>https://orcid.org/0000-0003-1441-0417</orcidid><orcidid>https://orcid.org/0000-0002-8967-7389</orcidid><orcidid>https://orcid.org/0000-0001-7941-9653</orcidid><orcidid>https://orcid.org/0000-0003-4268-5055</orcidid><orcidid>https://orcid.org/0000-0001-7707-2254</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | angiogenesis chronic myocardial ischemia gene therapy meta-analysis refractory angina |
title | Proangiogenic Growth Factor Therapy for the Treatment of Refractory Angina: A Meta-analysis |
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