Exploring the toxicity and clinical outcomes of doxorubicin, cyclophosphamide, and taxane-based chemotherapies in women with breast cancer in Bangladesh.

IF 0.9 4区 医学 Q4 ONCOLOGY
Md Shalahuddin Millat, Md Saddam Hussain, Arafat Miah, Md Abdul Barek, Mohammad Sarowar Uddin, Mahmuda Ferdous, Md Abdul Aziz, Md Mahmudul Hoque, Md Saiful Islam, Mohammad Safiqul Islam
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引用次数: 0

Abstract

BackgroundIndividuals receiving chemotherapy for breast cancer frequently experience severe drug reactions, which exacerbates safety issues such as decreased quality of life, prolonged treatment, and reinforcement of negative emotions associated with therapy. The emergence of these issues is especially devastating in developing countries like Bangladesh, where the medication's safety profile is inadequate. The goal of the current study was to assess the real-time toxicological and clinical outcomes of doxorubicin, cyclophosphamide, and taxanes treated breast cancer patients in Bangladesh.MethodsAbout 151 breast cancer patients were recruited from the National Institute of Cancer Research and Hospital (NICRH), Dhaka, Bangladesh, where 132 and 19 patients received doxorubicin-cyclophosphamide-paclitaxel and doxorubicin-cyclophosphamide-docetaxel chemotherapy regimen, respectively. Clinical responses were evaluated using Response Evaluation Criteria in Solid Tumors (RECIST), whereas chemotherapy-associated toxicities were graded according to the Common Terminology Criteria for Adverse Events version 5.0 (CTCAE v5.0).ResultsThe most common non-hematological adverse events reported across the both treatment regimens were nausea, vomiting, diarrhea, and fatigue, along with several other symptoms. Anemia (61.93%) emerged as the most common hematological toxicity, followed by conditions like neutropenia (21.8%), leukocytosis (19.87%), and lymphocytosis (18.54%). Patients also experienced various organ and tissue specific toxicities, with liver, kidney, and heart complications being notable. These side effects contributed to significant health challenges during the course of treatment. Unfortunately, a number of patients passed away, with most of the deaths occurring within five years of their cancer diagnosis.ConclusionsIn conclusion, breast cancer patients in Bangladesh are experiencing numerous non-haematological and haematological side effects, which impacting overall patient wellbeing that contributed to notable challenges including death. Personalized treatment approach could therefore be helpful to mitigate side effects and improve overall patient's experience.

探讨孟加拉国乳腺癌妇女使用阿霉素、环磷酰胺和紫杉烷为基础的化疗的毒性和临床结果。
背景:接受乳腺癌化疗的个体经常经历严重的药物反应,这加剧了安全问题,如生活质量下降,治疗时间延长,以及与治疗相关的负面情绪的强化。这些问题的出现在孟加拉国等发展中国家尤其具有破坏性,在这些国家,药物的安全性不足。当前研究的目的是评估孟加拉国阿霉素、环磷酰胺和紫杉烷治疗乳腺癌患者的实时毒理学和临床结果。方法从孟加拉国达卡国立癌症研究所和医院(NICRH)招募约151例乳腺癌患者,其中132例和19例分别接受阿霉素-环磷酰胺-紫杉醇和阿霉素-环磷酰胺-多西他赛化疗方案。使用实体瘤反应评价标准(RECIST)评估临床反应,而化疗相关毒性根据不良事件通用术语标准5.0 (CTCAE v5.0)分级。结果两种治疗方案中最常见的非血液学不良事件是恶心、呕吐、腹泻和疲劳,以及其他一些症状。贫血(61.93%)是最常见的血液学毒性,其次是中性粒细胞减少(21.8%)、白细胞增多(19.87%)和淋巴细胞增多(18.54%)。患者还经历了各种器官和组织特异性毒性,肝、肾和心脏并发症是显著的。这些副作用在治疗过程中对健康构成重大挑战。不幸的是,许多患者去世了,其中大多数死亡发生在癌症诊断后的五年内。总之,孟加拉国的乳腺癌患者正在经历许多非血液学和血液学副作用,这影响了患者的整体健康,导致了包括死亡在内的重大挑战。因此,个性化的治疗方法可能有助于减轻副作用并改善患者的整体体验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.70
自引率
7.70%
发文量
276
期刊介绍: Journal of Oncology Pharmacy Practice is a peer-reviewed scholarly journal dedicated to educating health professionals about providing pharmaceutical care to patients with cancer. It is the official publication of the International Society for Oncology Pharmacy Practitioners (ISOPP). Publishing pertinent case reports and consensus guidelines...
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