首页|白蛋白紫杉醇联合卡铂一线治疗晚期肺鳞癌的疗效分析

白蛋白紫杉醇联合卡铂一线治疗晚期肺鳞癌的疗效分析

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目的 观察白蛋白紫杉醇和卡铂联用作为一线治疗方案对晚期肺鳞状细胞癌患者的临床效果及不良反应。方法 选取2020 年 12 月—2022 年 12 月于枣庄市立医院呼吸与危重症医学科接受治疗的 86 例晚期肺鳞状细胞癌(ⅢB/Ⅳ期)患者作为研究对象,根据随机数表法分为NC组(给予白蛋白结合型紫杉醇联合卡铂治疗方案,n=40)与GC 组(给予吉西他滨联合卡铂的治疗方案,n=46)。比较 2 组的临床疗效及不良反应。结果 2 组的客观缓解率和疾病控制率比较,NC组分别为40%(16/40)和72。5%(29/40)。GC组分别为26%(12/46)和 65。2%(30/46)。2 组近期疗效对比表明NC组较GC组客观缓解率提高 14%,但差异无统计学意义(P>0。05)。2组患者无进展生存期分别为 5。10 个月和 4。60 个月,差异无统计学意义(P>0。05)。2 组均出现骨髓抑制、恶心/呕吐、腹泻、周围神经毒性及肌痛/关节痛等症状,其中血小板减少发生率NC组较GC组低,周围神经毒性发生率NC组较GC组高,差异有统计学意义(P<0。05)。2 组其他不良反应发生率比较,差异无统计学意义(P>0。05)。结论 将白蛋白紫杉醇与卡铂联合应用作为治疗晚期肺鳞癌患者的首选方案,在安全和疗效上都得到了正面评价,由此带来的不良反应在可控范围之内,有必要扩充样本规模进行更深入的探讨和验证。
Efficacy of Albumin-Bound Paclitaxel and Carboplatin as a First-Line Treatment for Advanced Lung Squamous Cell Carcinoma
Objective To observe the clinical effects and adverse effects of albumin-bound paclitaxel and carboplatin as a first-line treatment for advanced lung squamous cell carcinoma.Methods A total of 86 patients with advanced lung squamous cell carcinoma(stage ⅢB/Ⅳ)treated in the department of respiratory and critical care medicine,Zaozhuang Municipal Hospital from December 2020 to December 2022 were selected as the study subjects.Patients were divided into experimental and control groups according to the random number table method.The experimental group received albumin-combined paclitaxel with carboplatin(NC experimental group,sample number of 40 patients),and the control group received gemcitabine and carboplatin(GC control group,46 samples).To compare the clinical efficacy and adverse effects.Results The comparison between the objective response rate and the disease control rate.The patients who were treated with nab-Paclitaxel plus carboplatin(group NC)had an objective response rate of 40%(16/40).The disease control rates was 72.5%(29/40).Meanwhile,the patients who were treated with gemcitabine plus carboplatin(group GC)had an objective response rate of 26%(12/46);.The disease control rates(DCR)was 65.2%(30/46).Our results suggested that ORR improved 14%in group NC,compared to that in group GC.However,there was no significant difference in short-term efficacy between two groups(P>0.05).The median progression-free survival(PFS)was 5.10 months in group NC and 4.60 months in group GC.Progression-free survival in two groups showed no significant difference(P>0.05).All the two groups showed myelosuppression,nausea/vomiting,diarrhea,toxicity of peripheral nerve,myalgia/arthralgia,etc.Among them,the incidence of thrombocytopenia in NC group was lower than that of GC group,and the incidence of peripheral neurotoxicity in NC group was higher than that of GC group,with statistically significant differences(P<0.05).Comparison of other adverse effects,no significant difference(P>0.05).Conclusion Administering a combination of albumin-paclitaxel and carboplatin as an initial therapy for individuals with advanced lung squamous cell carcinoma has been proven both safe and efficacious,with tolerable side effects.Additional studies involving more participants are recommended to substantiate these findings.

albumin-bound paclitaxelcarboplatingemcitabineadvanced lung squamous cell carcinomafirst-line chemotherapyadverse effects

陈秀、万国峰、孙丽、李鹏、盛敏、赵绍民

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枣庄市立医院呼吸与危重症医学科,山东枣庄 277100

枣庄市立医院保健科,山东 枣庄 277100

白蛋白结合型紫杉醇 卡铂 吉西他滨 晚期肺鳞状细胞癌 一线化疗 不良反应

2024

中国卫生标准管理
《中国卫生标准管理》杂志社

中国卫生标准管理

影响因子:1.374
ISSN:1674-9316
年,卷(期):2024.15(17)