以多西他赛为基础的可手术乳腺癌辅助治疗方案的患者概况和当前护理模式评估

M. Hai, P. Akhter, Q. Chowdhury, P. Banu, M. Hossain, K. Pervin
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引用次数: 0

摘要

背景:早期癌症通常可以通过手术治愈,尽管有复发和生存率下降的机会。以多西他赛为基础的辅助多化疗方案可以提高可手术乳腺癌症患者的无病生存率和总生存率。目的:本研究旨在评估癌症手术患者多烯紫杉醇辅助方案的患者概况和目前的护理模式,包括临床实践的治疗结果。材料和方法:这项前瞻性、观察性、非对比性研究计划纳入术后复发风险高的新诊断的可手术乳腺癌癌症患者。基于多西他赛的治疗策略和治疗剂量的选择由个体肿瘤学家根据常规临床实践自行决定。在纳入期间、每个治疗周期以及纳入后1年(+/-1个月)的随访中记录患者数据。结果:2008年8月至2011年7月,共有85名中位年龄为53岁(23-73岁)的患者入选,53名(62.4%)患者为绝经后患者。导管癌是癌症最常见的类型,在73例(85.9%)患者中发现。雌激素、孕激素或Her2/neu/erbB2受体状态阳性的患者分别为65.9%、47.1%和5.8%。76名(89.4%)患有当前疾病的患者进行了部分或全部乳房切除术。56例患者平均切除了8个(范围:2-15)淋巴结(LN),其中大部分位于腋窝,平均4个淋巴结(范围:1-11)呈阳性。前哨淋巴结阴性,4例患者切除。平均肿瘤大小为5.5厘米,大多数(82.4%)患者被诊断为II期疾病,包括一些I期和III期患者(7.1%,10.6%)。多西他赛(Taxotere®)与环磷酰胺单独或与阿霉素、表阿霉素、5-FU和曲妥珠单抗联合或序贯治疗。63.5%的患者计划使用紫杉醇与阿霉素和环磷酰胺联合用药。曲妥珠单抗作为序贯疗法只能由1名患者提供。没有记录有关放射治疗或激素治疗的数据。在四个周期结束时,83.5%的患者没有疾病,5.9%的患者局部复发。1年时,71例(93.4%)患者存活,63例(88.7%)无复发,8例(11.2%)局部复发。恶心、呕吐、腹泻、脱发、贫血和中性粒细胞减少症是最常见的1级或2级不良事件。5名患者报告3级中性粒细胞减少症,2名患者报告4级中性粒病毒减少症。1例患者报告3级腹泻。结论:多西他赛辅助化疗可使93.4%(71/76)的患者存活一年,88.7%(63/71)的患者无病。以多西他赛为基础的方案的安全性是预期的,并且是可控的。德尔塔医学杂志2019年1月7(1):4-10
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the Patient Profile and Current Pattern of Care with Docetaxel Based Adjuvant Regimen in Operable Breast Cancer
Background: Early stage breast cancer can often be cured with surgery alone though there are chances of recurrent disease and decrease in survival. Adjuvant poly-chemotherapy with docetaxel-based regimens can improve both disease-free and overall survival in patients with operable breast cancer. Objective: This study was designed to evaluate the patient profile and current pattern of care with docetaxel based adjuvant regimen in operable breast cancer patients including the treatment outcome from clinical practice. Materials and method: This prospective, observational, non-comparative study planned to enroll newly diagnosed operable breast cancer patients with high risk of recurrence after surgery. Selection of docetaxel-based treatment strategy and dosage of therapy was at the discretion of individual oncologists as per routine clinical practice. Patient data were recorded during inclusion, each cycle of therapy, and follow-up at 1 year (+/- 1 month) after inclusion. Results: Between August 2008 and July 2011 a total of 85 patients with median age of 53 years (23-73 years) were enrolled and 53 (62.4%) patients were postmenopausal. Ductal carcinoma, the most common cancer type,was found in 73 (85.9%) patients. Receptor status was positive for estrogen, progesterone or Her2/neu/erbB2 in 65.9%, 47.1% and 5.8% patients, respectively. Mastectomy either partial or total was performed in 76 (89.4%) patients for the current disease. An average of 8 (range: 2-15) lymph nodes (LN) mostly in axilla were excised in 56 patients and average of 4 (range: 1-11) LN nodes were positive. Sentinel LNs were negative, excised in 4 patients. The mean tumor size was 5.5 cm and most (82.4%) patients were diagnosed at Stage II disease including some at Stage I and III (7.1%, 10.6%). Docetaxel (Taxotere®) was combined with cyclophosphamide alone or in addition with doxorubicin, epirubicin, 5 FU and trastuzumab either in combination or sequential regimen. Taxotere in combination with adriamycin and cyclophosphamide was planned for 63.5% patients. Trastuzumab as sequential therapy could be afforded by 1 patient only. Data regarding radiotherapy or hormone therapy was not recorded. At the end of four cycles, 83.5% of patients were found disease free and 5.9% had loco regional relapse. At 1 year 71 (93.4%) patients were alive, 63 (88.7%) were relapse-free and 8 (11.2%) had loco regional relapse. Nausea, vomiting, diarrhea, alopecia, anemia and neutropenia were most commonly reported adverse events classified as Grade 1 or Grade 2. Grade 3 neutropenia was reported in 5 patients and 2 patients reported grade 4 neutropenia. Grade 3 diarrhea was reported in 1 patient. Conclusion: Docetaxel as adjuvant chemotherapy offered one year survival in 93.4% (71/76) of the patients and 88.7% (63/71 patients) were disease-free. The safety profile of docetaxel based regimens was expected and manageable. Delta Med Col J. Jan 2019 7(1): 4-10
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