Wannisa Thayarat, Wannaporn Wattanawong, M. Saeteaw
{"title":"Sunpasitthiprasong医院乳腺癌门诊患者使用曲妥珠单抗的心脏毒性不良反应:一项回顾性队列研究","authors":"Wannisa Thayarat, Wannaporn Wattanawong, M. Saeteaw","doi":"10.29090/psa.2023.02.22.327","DOIUrl":null,"url":null,"abstract":"Trastuzumab, a monoclonal antibody, is recommened for agjuvant of non-metastatic and recurrent or stage IV HER2-positive breast cancer. Although the main adverse effect is that greatly reduces the cardiac function, the incidence of cardiac adverse effect has never been systematically evaluated in Sunpasitthiprasong Hospital. To determine the adverse effects and risk factors with trastuzumab-induced cardiotoxicity. A retrospective cohort study with the percentages changes of left ventricular ejection fraction (%LVEF) in the breast cancer patients. The inclusion criterias were the patient who had been followed-up at outpatient oncology clinic, patients who did not have the %LVEF were excluded from the study. The primary endpoint was the incidence of cardiotoxicity. The mean age of 66 patients treated with trastuzumab was 51.98±10.19 years. Of these, 26 patients (39.39%) had the cardiotoxicity. There were mean of %LVEF baseline was 69.64±7.14% and the mean of %LVEF after receiving trastuzumab was 63.09±9.20%. Mean reduction of %LVEF before and after receiving trastuzumab was 6.55 10.80, there was a statistically significant difference ( P <0.001). The mean of %LVEF after receiving trastuzumab was 56.96±7.75% and 38.50±0.50% in patients had a cardiotoxicity and the patients who had a discontinued treatment, respectively. However, the duration of trastuzumab exposure was directly correlated with statistically significant reduction of %LVEF in breast cancer patients ( P =0.021, =0.215, R 2 =0.046). Among breast cancer patients treated with trastuzumab, 39.39% of the patients had cardiac adverse events, most of which were found to have %LVEF reduced greater than 10%. The duration of trastuzumab exposure resulted in an increased of %LVEF reduction.","PeriodicalId":19761,"journal":{"name":"Pharmaceutical Sciences Asia","volume":"3 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cardiotoxic adverse effects of trastuzumab in breast cancer outpatients in Sunpasitthiprasong Hospital, Ubonratchathani: A retrospective cohort study\",\"authors\":\"Wannisa Thayarat, Wannaporn Wattanawong, M. Saeteaw\",\"doi\":\"10.29090/psa.2023.02.22.327\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Trastuzumab, a monoclonal antibody, is recommened for agjuvant of non-metastatic and recurrent or stage IV HER2-positive breast cancer. Although the main adverse effect is that greatly reduces the cardiac function, the incidence of cardiac adverse effect has never been systematically evaluated in Sunpasitthiprasong Hospital. To determine the adverse effects and risk factors with trastuzumab-induced cardiotoxicity. A retrospective cohort study with the percentages changes of left ventricular ejection fraction (%LVEF) in the breast cancer patients. The inclusion criterias were the patient who had been followed-up at outpatient oncology clinic, patients who did not have the %LVEF were excluded from the study. The primary endpoint was the incidence of cardiotoxicity. The mean age of 66 patients treated with trastuzumab was 51.98±10.19 years. Of these, 26 patients (39.39%) had the cardiotoxicity. There were mean of %LVEF baseline was 69.64±7.14% and the mean of %LVEF after receiving trastuzumab was 63.09±9.20%. Mean reduction of %LVEF before and after receiving trastuzumab was 6.55 10.80, there was a statistically significant difference ( P <0.001). The mean of %LVEF after receiving trastuzumab was 56.96±7.75% and 38.50±0.50% in patients had a cardiotoxicity and the patients who had a discontinued treatment, respectively. However, the duration of trastuzumab exposure was directly correlated with statistically significant reduction of %LVEF in breast cancer patients ( P =0.021, =0.215, R 2 =0.046). Among breast cancer patients treated with trastuzumab, 39.39% of the patients had cardiac adverse events, most of which were found to have %LVEF reduced greater than 10%. 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Cardiotoxic adverse effects of trastuzumab in breast cancer outpatients in Sunpasitthiprasong Hospital, Ubonratchathani: A retrospective cohort study
Trastuzumab, a monoclonal antibody, is recommened for agjuvant of non-metastatic and recurrent or stage IV HER2-positive breast cancer. Although the main adverse effect is that greatly reduces the cardiac function, the incidence of cardiac adverse effect has never been systematically evaluated in Sunpasitthiprasong Hospital. To determine the adverse effects and risk factors with trastuzumab-induced cardiotoxicity. A retrospective cohort study with the percentages changes of left ventricular ejection fraction (%LVEF) in the breast cancer patients. The inclusion criterias were the patient who had been followed-up at outpatient oncology clinic, patients who did not have the %LVEF were excluded from the study. The primary endpoint was the incidence of cardiotoxicity. The mean age of 66 patients treated with trastuzumab was 51.98±10.19 years. Of these, 26 patients (39.39%) had the cardiotoxicity. There were mean of %LVEF baseline was 69.64±7.14% and the mean of %LVEF after receiving trastuzumab was 63.09±9.20%. Mean reduction of %LVEF before and after receiving trastuzumab was 6.55 10.80, there was a statistically significant difference ( P <0.001). The mean of %LVEF after receiving trastuzumab was 56.96±7.75% and 38.50±0.50% in patients had a cardiotoxicity and the patients who had a discontinued treatment, respectively. However, the duration of trastuzumab exposure was directly correlated with statistically significant reduction of %LVEF in breast cancer patients ( P =0.021, =0.215, R 2 =0.046). Among breast cancer patients treated with trastuzumab, 39.39% of the patients had cardiac adverse events, most of which were found to have %LVEF reduced greater than 10%. The duration of trastuzumab exposure resulted in an increased of %LVEF reduction.
Pharmaceutical Sciences AsiaPharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
0.90
自引率
0.00%
发文量
59
期刊介绍:
The Pharmaceutical Sciences Asia (PSA) journal is a double-blinded peer-reviewed journal in English published quarterly, by the Faculty of Pharmacy, Mahidol University, Thailand. The PSA journal is formerly known as Mahidol University Journal of Pharmaceutical Sciences and committed to the timely publication of innovative articles and reviews. This journal is available in both printed and electronic formats. The PSA journal aims at establishing a publishing house that is open to all. It aims to disseminate knowledge; provide a learned reference in the field; and establish channels of communication between academic and research expert, policy makers and executives in industry and investment institutions. The journal publishes research articles, review articles, and scientific commentaries on all aspects of the pharmaceutical sciences and multidisciplinary field in health professions and medicine. More specifically, the journal publishes research on all areas of pharmaceutical sciences and related disciplines: Clinical Pharmacy Drug Synthesis and Discovery Targeted-Drug Delivery Pharmaceutics Biopharmaceutical Sciences Phytopharmaceutical Sciences Pharmacology and Toxicology Pharmaceutical Chemistry Nutraceuticals and Functional Foods Natural Products Social, Economic, and Administrative Pharmacy Clinical Drug Evaluation and Drug Policy Making Antimicrobials, Resistance and Infection Control Pharmacokinetics and Pharmacodynamics.