Cuitlahuac Arroyo-Rodríguez, Arturo E Espinosa-Picos, Lorena Ledesma-Lopez, Marian Rodriguez-Contreras, Maxwell Avilés-Rodríguez, Jorge R Urias-Rocha, Siria M Carvajal-Lohr, Pamela Báez-Islas, Cynthia Rojas-Camarena, Hassan Brau-Figueroa, Sergio López-Portugal, Francisco E Ramirez-Montoya, German T Cabada-Cota, Julio C Abitia-Castro, América Avila-Ariyoshi, Enrique Avila-Monteverde
{"title":"癌症患者的心血管风险:来自墨西哥心脏肿瘤诊所的初步经验。","authors":"Cuitlahuac Arroyo-Rodríguez, Arturo E Espinosa-Picos, Lorena Ledesma-Lopez, Marian Rodriguez-Contreras, Maxwell Avilés-Rodríguez, Jorge R Urias-Rocha, Siria M Carvajal-Lohr, Pamela Báez-Islas, Cynthia Rojas-Camarena, Hassan Brau-Figueroa, Sergio López-Portugal, Francisco E Ramirez-Montoya, German T Cabada-Cota, Julio C Abitia-Castro, América Avila-Ariyoshi, Enrique Avila-Monteverde","doi":"10.24875/ACM.24000080","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To describe the cardiovascular risk from Mexican patients scheduled to initiate cancer treatment and to compare the risk between oncological and hematological malignancies.</p><p><strong>Methods: </strong>We enrolled patients referred for echocardiography before initiating cancer therapies. Left ventricular ejection fraction (LVEF) and global longitudinal strain (GLS) was evaluated. To estimate the risk for developing cancer therapy-related cardiovascular toxicity (CTR-CVT) we used the Heart Failure Association-International Cardio-Oncology Society risk score (HFA-ICOS).</p><p><strong>Results: </strong>106 patients were studied, 83% (n = 88) had an oncological, and 17% (n = 18) a hematological malignancy. Breast cancer represented 89.8% (n = 79) of the oncological and lymphoma 61.1% (n = 11) of the hematological malignancies. Patients with oncological malignancies were older (55 ± 11 vs. 46 ± 14 years; p = 0.020) and more frequently female (95.5 vs. 44.4%; p < 0.001). Metastasis was more prevalent in patients with hematological malignancies (38.9 vs. 13.6%; p = 0.011). Mean LVEF was 59.42 ± 6.36 and mean GLS was 20.26 ± 4.89. Prevalence of borderline (50-54%) and reduced LVEF (< 50%) was 4.7 and 3.8%, respectively. Abnormal GLS (< 18%) was identified in 10.4%. HFA-ICOS classified 14.7% of oncological and 10.2% of hematological malignancies in the high and very high-risk categories for developing CTR-CVT (p = 0.68).</p><p><strong>Conclusions: </strong>A high risk for developing CTR-CVT was identified in 14.2% of our population. This risk was comparable among oncological and hematological malignancies.</p>","PeriodicalId":93885,"journal":{"name":"Archivos de cardiologia de Mexico","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cardiovascular risk in cancer patients: initial experience from a cardio-oncology clinic in Mexico.\",\"authors\":\"Cuitlahuac Arroyo-Rodríguez, Arturo E Espinosa-Picos, Lorena Ledesma-Lopez, Marian Rodriguez-Contreras, Maxwell Avilés-Rodríguez, Jorge R Urias-Rocha, Siria M Carvajal-Lohr, Pamela Báez-Islas, Cynthia Rojas-Camarena, Hassan Brau-Figueroa, Sergio López-Portugal, Francisco E Ramirez-Montoya, German T Cabada-Cota, Julio C Abitia-Castro, América Avila-Ariyoshi, Enrique Avila-Monteverde\",\"doi\":\"10.24875/ACM.24000080\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To describe the cardiovascular risk from Mexican patients scheduled to initiate cancer treatment and to compare the risk between oncological and hematological malignancies.</p><p><strong>Methods: </strong>We enrolled patients referred for echocardiography before initiating cancer therapies. Left ventricular ejection fraction (LVEF) and global longitudinal strain (GLS) was evaluated. To estimate the risk for developing cancer therapy-related cardiovascular toxicity (CTR-CVT) we used the Heart Failure Association-International Cardio-Oncology Society risk score (HFA-ICOS).</p><p><strong>Results: </strong>106 patients were studied, 83% (n = 88) had an oncological, and 17% (n = 18) a hematological malignancy. Breast cancer represented 89.8% (n = 79) of the oncological and lymphoma 61.1% (n = 11) of the hematological malignancies. Patients with oncological malignancies were older (55 ± 11 vs. 46 ± 14 years; p = 0.020) and more frequently female (95.5 vs. 44.4%; p < 0.001). Metastasis was more prevalent in patients with hematological malignancies (38.9 vs. 13.6%; p = 0.011). Mean LVEF was 59.42 ± 6.36 and mean GLS was 20.26 ± 4.89. Prevalence of borderline (50-54%) and reduced LVEF (< 50%) was 4.7 and 3.8%, respectively. Abnormal GLS (< 18%) was identified in 10.4%. HFA-ICOS classified 14.7% of oncological and 10.2% of hematological malignancies in the high and very high-risk categories for developing CTR-CVT (p = 0.68).</p><p><strong>Conclusions: </strong>A high risk for developing CTR-CVT was identified in 14.2% of our population. 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Cardiovascular risk in cancer patients: initial experience from a cardio-oncology clinic in Mexico.
Objective: To describe the cardiovascular risk from Mexican patients scheduled to initiate cancer treatment and to compare the risk between oncological and hematological malignancies.
Methods: We enrolled patients referred for echocardiography before initiating cancer therapies. Left ventricular ejection fraction (LVEF) and global longitudinal strain (GLS) was evaluated. To estimate the risk for developing cancer therapy-related cardiovascular toxicity (CTR-CVT) we used the Heart Failure Association-International Cardio-Oncology Society risk score (HFA-ICOS).
Results: 106 patients were studied, 83% (n = 88) had an oncological, and 17% (n = 18) a hematological malignancy. Breast cancer represented 89.8% (n = 79) of the oncological and lymphoma 61.1% (n = 11) of the hematological malignancies. Patients with oncological malignancies were older (55 ± 11 vs. 46 ± 14 years; p = 0.020) and more frequently female (95.5 vs. 44.4%; p < 0.001). Metastasis was more prevalent in patients with hematological malignancies (38.9 vs. 13.6%; p = 0.011). Mean LVEF was 59.42 ± 6.36 and mean GLS was 20.26 ± 4.89. Prevalence of borderline (50-54%) and reduced LVEF (< 50%) was 4.7 and 3.8%, respectively. Abnormal GLS (< 18%) was identified in 10.4%. HFA-ICOS classified 14.7% of oncological and 10.2% of hematological malignancies in the high and very high-risk categories for developing CTR-CVT (p = 0.68).
Conclusions: A high risk for developing CTR-CVT was identified in 14.2% of our population. This risk was comparable among oncological and hematological malignancies.