多西他赛对进展期胃癌术后化疗疗效影响的倾向评分匹配分析

Effects of docetaxel for postoperative chemotherapy of advanced gastric cancer based on propensity score matching

  • 摘要: 目的:探讨多西他赛对进展期胃癌术后化疗疗效的影响。
    方法:采用倾向评分匹配及回顾性队列研究方法。收集2013年1月至2018年12月兰州大学第二医院收治的311例进展期胃癌术后化疗患者的临床病理资料;男224例,女87例;中位年龄为58岁,年龄范围为26~82岁。311例患者中,204例行FOLFOX方案(奥沙利铂、亚叶酸钙、5-氟尿嘧啶)化疗,设为FOLFOX组;107例行FLOT方案(多西他赛、奥沙利铂、亚叶酸钙、5-氟尿嘧啶)化疗,设为FLOT组。观察指标:(1)倾向评分匹配情况及匹配后两组患者一般资料比较。(2)随访情况。(3)生存因素分析。(4)亚组分析。(5)不良反应情况。采用门诊、住院复查和电话相结合的方式进行随访,了解患者化疗情况、术后生存、肿瘤复发和转移情况,随访时间截至2019年2月。倾向评分匹配按1:1最近邻匹配法匹配,卡钳值设定为0.02。正态分布的计量资料以±s表示,组间比较采用t检验。偏态分布的计量资料以M(范围)表示。计数资料以绝对数或百分比表示,组间比较采用x2检验或Fisher确切概率法。等级资料比较采用非参数秩和检验。采用Kaplan-Meier法计算生存率和绘制生存曲线。采用 Log-rank检验进行生存情况分析。单因素及多因素分析采用COX回归模型。亚组分析采用交互作用检验。
    结果:(1)倾向评分匹配情况及匹配后两组患者一般资料比较:311例患者中,198例(FOLFOX组和FLOT组各99例)匹配成功。倾向评分匹配前FOLFOX组患者肿瘤分化程度(分化差、分化好),CA19-9 (<27 U/mL、≥27 U/mL),CA125(<35 U/mL、≥35 U/mL)分别为109、95例,156、48例,186、18例,FLOT组上述指标分别为42、65例,93、14例,104、3例。两组患者上述指标比较,差异均有统计学意义(x2=5.649,4.798,4.039,P<0.05);经倾向评分匹配后FOLFOX组患者上述指标分别为44、55例,85、14例,96、3例,FLOT组上述指标分别为42、57例,85、14例,96、3例,两组患者上述指标比较,差异均无统计学意义(x2=0.082,0.000,0.000,P>0.05)。(2)随访情况:倾向评分匹配后198例患者均获得随访,随访时间为2~ 69个月,中位随访时间为38个月。随访期间,92例患者无瘤生存,2例出现肿瘤复发或转移,104例死亡(103例为肿瘤相关性死亡,1例为非肿瘤相关性死亡)。FOLFOX组与FLOT组患者化疗疗程分别为(5.6±0.7)个与(5.4±0.8)个,两组患者比较,差异无统计学意义(t=1.651,P>0.05)。FOLFOX组患者1、3、5年累计生存率分别为72.2%、31.5%、27.7%;FLOT组上述指标分别为83.2%、42.8%、38.2%。FOLFOX组与FLOT组患者中位总体生存时间分别为21个月和34个月,两组患者生存情况比较,差异有统计学意义 (x2=4.473,P<0.05)。(3)生存因素分析:单因素分析结果显示FLOT方案、Lauren分型弥漫型、Lauren分型混合型、肿瘤分化程度好、肿瘤长径≥5 cm、CA19-9≥27 U/mL、癌胚抗原≥3.4 μg/L、T4分期、N2分期、N3分期、远端胃切除及全胃切除是影响患者术后生存的相关因素(相对危险度为 0.659,1.617,1.798,0.672,1.726,1.655,1.942,2.036,2.536,4.085,1.810,2.310;95%可信区间为 0.444~0.978,1.024~2.556,1.105~2.926,0.457~0.990,1.159~2.569,1.006~2.723,1.295~2.912,1.190~3.484,1.409~4.564,2.491~6.697,1.020~3.211,1.261~4.233,P<0.05)。多因素分析结果显示FLOT方案、癌胚抗原≥3.4 μg/L、N2分期、N3分期是影响患者术后生存的独立危险因素(相对危险度为0.622,1.732,2.217,4.039;95%可信区间为0.418~0.926,1.124~2.670,1.200~4.097,2.448~6.662,P<0.05)。(4)亚组分析:亚组分析结果显示性别、年龄、Lauren分型、肿瘤分化程度、肿瘤位置、肿瘤长径、肿瘤标志物、肿瘤T分期、肿瘤N分期及手术方式亚组中,FOLFOX组与FLOT组的疗效比较,差异均无统计学意义(交互P>0.05)。(5)不良反应情况:FOLFOX组患者白细胞减少症、贫血、血小板减少、恶心、呕吐、肝肾功能受损Ⅲ~Ⅳ级不良反应发生率分别为11.1%(11/99)、2.0%(2/99)、3.0%(3/99)、12.1%(12/99)、4.0%(4/99)、1.0%(1/99),FLOT组患者上述指标分别为34.3%(34/99)、1.0%(1/99)、9.1%(9/99)、24.2%(24/99)、4.0%(4/99)、0。两组患者白细胞减少症发生率、恶心发生率比较,差异均有统计学意义(x2=15.213,4.889,P<0.05);两组患者血小板减少发生率比较,差异无统计学意义(x2=3.194,P>0.05);两组患者其余指标比较,差异均无统计学意义(P>0.05)。两组均无患者因为不能耐受毒性反应退出化疗疗程,所有患者化疗期间行糖皮质激素、质子泵抑制剂和五羟色胺受体拮抗剂治疗,白细胞减少症患者行粒细胞刺激因子治疗。
    结论:与FOLFOX方案比较,FLOT方案增加多西他赛明显延长进展期胃癌术后化疗患者的中位生存时间,但也增加了Ⅲ~Ⅳ级白细胞减少症与恶心的发生率。

     

    Abstract: Objective:To investigate the effects of docetaxel for postoperative chemotherapy of advanced gastric cancer.
    Methods:The propensity score matching and retrospective cohort study was conducted. The clinicopathological data of 311 patients with advanced gastric cancer who were admitted to Lanzhou University Second Hospital from January 2013 to December 2018 were collected. There were 224 males and 87 females, aged from 26 to 82 years, with a median age of 58 years. Of 311 patients, 204 cases undergoing chemotherapy with the FOLFOX regimen (oxaliplatin, calcium folinate, 5-fluorouracil) were allocated into the FOLFOX group, and 107 cases undergoing chemotherapy with the FLOT regimen (docetaxel, oxaliplatin, calcium folinate, 5-fluorouracil) were allocated into the FLOT group. Observation indicators: (1) the propensity score matching conditions and comparison of general data between the two groups of patients after matching; (2) follow-up; (3) analysis of survival factors; (4) subgroup analysis; (5) adverse reactions. Follow-up was performed using a combination of outpatient examination, hospitalization review and telephone interview to detect situations of patients chemotherapy, postoperative survival, tumor recurrence and metastasis up to February 2019. The propensity score matching was realized using the nearest neighbor method with 1:1 ratio and caliper setting as 0.02. Measurement data with normal distribution were represented as Mean±SD, and comparison between groups was analyzed using the t test. Count data were described as absolute numbers or percentages, and comparison between groups was analyzed using the chi-square test or Fisher exact probability method. Rank data was analyzed using non parametric Rank sum test. The survival curve and rate were respectively drawn and calculated using the Kaplan-Meier method. The survival analysis was done using the Log-rank test. Univariate analysis and multivariate analysis were conducted using the COX regression model. Subgroup analysis was done using interaction test.
    Results:(1) The propensity score matching conditions and comparison of general data between the two groups of patients after matching: 198 of 311 patients had successful matching, including 99 in each group. Cases with tumor differentiated as poorly differentiation or well differentiation, cases with CA19-9 <27 U/mL or ≥27 U/mL, cases with CA125 <35 U/mL or ≥35 U/mL before propensity score matching were 109, 95, 156, 48, 186, 18 in the FOLFOX group, and 42, 65, 93, 14, 104, 3 in the FLOT group, respectively, showing significant differences in the above indicators between the two groups (x2=5.649, 4.798, 4.039, P<0.05). After propensity score matching, the above indicators were 44, 55, 85, 14, 96, 3 in the FOLFOX group, and 42, 57, 85, 14, 96, 3 in the FLOT group, respectively, showing no significant difference in the above indicators between the two groups (x2=0.082, 0.000, 0.000, P>0.05). (2) Follow-up: 198 patients of the two groups after matching were followed up for 2 to 69 months, with a median follow-up time of 38 months. During the follow-up, 92 cases survived without tumor, 2 cases underwent tumor recurrence or metastasis, and 104 cases died including 103 with tumor related death and 1 case with non-tumor related death. The courses of chemotherapy were 5.6±0.7 and 5.4±0.8 for the FOLFOX group and FLOT group, respectively, showing no significant difference between the two groups (t=1.651, P>0.05). The 1, 3, and 5-year cumulative survival rates of patients were 72.2%, 31.5%, 27.7% and 83.2%, 42.8%, 38.2% for the FOLFOX group and FLOT group, respectively. The median overall survival time were 21 months and 34 months for the FOLFOX group and FLOT group, respectively, showing significant difference between the two groups (x2=4.473, P<0.05). (3) Analysis of survival factors: results of univariate analysis showed that cases undergoing chemotherapy with the FLOT regimen, cases with tumor as diffuse type of Lauren classification, cases with tumor as mixed type of Lauren classification, cases with tumor differentiated as well differentiation, cases with tumor diameter≥5 cm, cases with CA19-9≥27 U/mL, cases with carcinoembryonic antigen (CEA)≥3.4 μg/L, cases with tumor as T4 stage of T staging, cases with tumor as N2 stage of N staging, cases with tumor as N3 stage of N staging, cases undergoing distal gastrectomy and cases undergoing total gastrectomy were related factors influencing postoperative survival of patients (hazard ratio=0.659, 1.617, 1.798, 0.672, 1.726, 1.655, 1.942, 2.036, 2.536, 4.085, 1.810, 2.310, 95% confidence interval: 0.444-0.978, 1.024-2.556, 1.105-2.926, 0.457-0.990, 1.159-2.569, 1.006-2.723, 1.295-2.912, 1.190-3.484, 1.409-4.564, 2.491-6.697, 1.020-3.211, 1.261-4.233, P<0.05). Results of multivariate analysis showed that cases undergoing chemotherapy with the FLOT regimen, cases with CEA≥ 3.4 μg/L, cases with tumor as N2 stage of N staging and cases with tumor as N3 stage of N staging were independent risk factors influencing postoperative survival of patients (hazard ratio=0.622, 1.732, 2.217, 4.039, 95% confidence interval: 0.418-0.926, 1.124-2.670, 1.200-4.097, 2.448-6.662, P<0.05). (4) Subgroup analysis: results of subgroup analysis showed that of the different subgroups using gender, age, tumor Lauren classification, tumor differentiation degree, tumor location, tumor diameter, tumor markers, tumor T staging, tumor N staging and surgical procedures as subgrouping index, the efficacy difference between the FLOT group and the FOLFOX group was the same (interaction P>0.05). (5) Adverse reactions: the incidence of grade Ⅲ-Ⅳ adverse reactions of leukopenia, anemia, thrombocytopenia, nausea, vomiting and liver and kidney dysfunction were 11.1%(11/99), 2.0% (2/99), 3.0%(3/99), 12.1%(12/99), 4.0%(4/99), 1.0%(1/99) and 34.3%(34/99), 1.0%(1/99), 9.1%(9/99), 24.2%(24/99), 4.0%(4/99), 0 in the FOLFOX group and the FLOT group, respectively. There were significant differences of the incidence of leukopenia and nausea between the two groups (x2=15.213, 4.889, P<0.05). There was no significant difference of the incidence of thrombocytopenia between the two groups (x2=3.194, P>0.05) and there was no significant difference of the incidence of anemia, vomiting and liver and kidney dysfunction between the two groups (P>0.05). There was no patient in the two group withdrawal from chemotherapy as no tolerance to toxic reactions. All patients were treated with glucocorticoids, proton pump inhibitors and serotonin receptor antagonists during chemotherapy. Patients undergoing leukopenia were treated with granulocyte stimulating factor.
    Conclusions:Compared with FOLFOX regimen, FLOT regimen which adds docetaxel significantly prolongs the postoperative median overall survival time of patients with advanced gastric cancer. However, FLOT regimen increases the incidence of grade Ⅲ-Ⅳ adverse reactions of leukopenia and nausea.

     

/

返回文章
返回