Efficacy and safety of nanoparticle albumin‑bound paclitaxel compared with solvent‑based paclitaxel in adjuvant therapy for breast cancer: A retrospective study.

IF 2.5 4区 医学 Q3 ONCOLOGY
Huina Lv,Yanyan Hong,Yuting Zhang,Siyu Li,Bingbing Li,Mingjun Zhang
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引用次数: 0

Abstract

The current evidence for the use of nanoparticle albumin-bound paclitaxel (nab-PTX) for adjuvant breast cancer chemotherapy is insufficient. The present study aimed to assess the efficacy and toxicity of nab-PTX in comparison with solvent-based paclitaxel (sb-PTX) in postoperative adjuvant breast cancer treatment. A total of 345 patients were included in the study and separated into nab-PTX (n=289) and sb-PTX (n=56) groups based on the type of taxane used in the adjuvant chemotherapy regimen. The study evaluated the baseline characteristics in both groups and the risk factors for postoperative recurrence of mammary cancer. Furthermore, data concerning disease-free survival (DFS) and adverse effects were obtained and analyzed, and group confounding variables were addressed using 1:2 propensity score matching (PSM). Comparisons before PSM revealed significant differences in baseline characteristics including age, underlying disease, lymph node involvement, vascular invasion, human epidermal growth factor receptor 2 and axillary surgery (P<0.05). Following PSM, there were 90 patients in the nab-PTX group and 56 in the sb-PTX group, with no significant differences in the baseline differences (P>0.05). Before PSM, the 73-month DFS rate was 97.9% in the nab-PTX group compared with 91.1% in the sb-PTX group. However, there were no significant differences between the groups before or after PSM (P=0.15 and P=0.49, respectively). Additionally, Cox regression analysis demonstrated a significantly lower chance of recurrence in patients aged >45 years [hazard ratio (HR), 0.197; 95% confidence interval (CI), 0.052-0.753; P=0.018], whereas underlying disease (HR, 5.352; 95% CI, 1.310-21.854; P=0.019) and lymph node infiltration (HR, 8.930; 95% CI, 1.121-71.161; P=0.039) significantly increased the risk of recurrence. Regarding safety, the sb-PTX group had a significantly greater incidence of anaphylaxis, whereas the nab-PTX group had significantly increased rates of anemia and peripheral neuropathy (P<0.05). In summary, the 73-month DFS rate of the nab-PTX cohort exceeded that of the sb-PTX cohort, but no significant difference was detected between them. Underlying disease, lymph node metastasis and an age of ≤45 years are significant predictors of postoperative recurrence of breast cancer.
纳米颗粒白蛋白结合型紫杉醇与溶剂型紫杉醇在乳腺癌辅助治疗中的疗效和安全性比较:一项回顾性研究。
目前,将纳米颗粒白蛋白结合型紫杉醇(nab-PTX)用于乳腺癌辅助化疗的证据不足。本研究旨在评估 nab-PTX 与溶剂型紫杉醇(sb-PTX)在乳腺癌术后辅助治疗中的疗效和毒性比较。研究共纳入了345名患者,并根据辅助化疗方案中使用的紫杉类药物类型分为nab-PTX组(n=289)和sb-PTX组(n=56)。研究评估了两组患者的基线特征以及乳腺癌术后复发的风险因素。此外,研究还获得并分析了无病生存期(DFS)和不良反应的相关数据,并采用1:2倾向评分匹配法(PSM)解决了组间混杂变量问题。PSM前的比较显示,年龄、基础疾病、淋巴结受累、血管侵犯、人表皮生长因子受体2和腋窝手术等基线特征存在显著差异(P0.05)。在 PSM 前,nab-PTX 组的 73 个月 DFS 率为 97.9%,而 sb-PTX 组为 91.1%。然而,PSM前后两组间无明显差异(分别为P=0.15和P=0.49)。此外,Cox回归分析表明,年龄大于45岁的患者复发几率明显降低[危险比(HR),0.197;95%置信区间(CI),0.052-0.753;P=0.018],而基础疾病(HR,5.352;95% CI,1.310-21.854;P=0.019)和淋巴结浸润(HR,8.930;95% CI,1.121-71.161;P=0.039)会显著增加复发风险。在安全性方面,sb-PTX 组过敏性休克的发生率明显增加,而 nab-PTX 组贫血和周围神经病变的发生率明显增加(P<0.05)。总之,nab-PTX 组的 73 个月 DFS 率高于 sb-PTX 组,但两者之间未发现明显差异。基础疾病、淋巴结转移和年龄≤45岁是乳腺癌术后复发的重要预测因素。
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来源期刊
Oncology Letters
Oncology Letters ONCOLOGY-
CiteScore
5.70
自引率
0.00%
发文量
412
审稿时长
2.0 months
期刊介绍: Oncology Letters is a monthly, peer-reviewed journal, available in print and online, that focuses on all aspects of clinical oncology, as well as in vitro and in vivo experimental model systems relevant to the mechanisms of disease. The principal aim of Oncology Letters is to provide the prompt publication of original studies of high quality that pertain to clinical oncology, chemotherapy, oncogenes, carcinogenesis, metastasis, epidemiology and viral oncology in the form of original research, reviews and case reports.
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