首页|舒尼替尼联合卡培他滨治疗三阴性乳腺癌的临床疗效

舒尼替尼联合卡培他滨治疗三阴性乳腺癌的临床疗效

扫码查看
目的 探讨舒尼替尼联合卡培他滨治疗三阴性乳腺癌(TNBC)的临床疗效。方法 选取2020年3月至2022年3月河北中石油中心医院收治的TNBC患者为研究对象,采用随机数字表法将其分为对照组和研究组。对照组应用卡培他滨治疗,研究组加用舒尼替尼治疗,均治疗3个周期。对两组患者疗效、免疫功能和血清糖类抗原153(CA153)、特异性组织多肽抗原(TPS)、胸苷激酶1(TK1)水平,以及患者的生活质量、不良反应发生情况进行评价。结果 共纳入60例患者,对照组和研究组各30例。治疗3个周期后,两组患者的客观缓解率比较,差异无统计学意义(P>0。05);研究组的疾病控制率高于对照组(86。67%比60。00%),CD3+、CD4+、CD4+/CD8+水平及乳腺癌生命质量测定量表、社会适应性问卷评分高于对照组[(49。26±3。11)比(41。02±3。46)、(42。55±5。11)比(35。16±4。18)、(1。98±0。22)比(1。66±0。36)、(85。12±1。65)分比(72。65±1。48)分、(143。65±2。78)分比(135。26±3。16)分],CD8+、血清CA153、TPS、TK1水平及医院焦虑抑郁量表评分低于对照组[(16。56±1。87)比(21。34±2。15)、(20。45±3。79)U/mL比(24。22±4。12)U/mL、(5。45±1。46)ng/mL比(7。11±2。01)ng/mL、(1。56±0。26)pmol/L比(1。91±0。23)pmol/L、(10。33±1。08)分比(12。22±1。02)分],差异均有统计学意义(P<0。05)。随访发现,研究组患者的疾病控制时间[8。85(6。11,9。26)个月]和无进展生存期[5。16(4。87,6。78)个月]均长于对照组[7。11(5。26,8。78)个月和4。89(3。98,5。65)个月](P<0。05);两组发热、贫血、恶心、呕吐等不良反应发生率比较,差异均无统计学意义(P>0。05)。结论 舒尼替尼联合卡培他滨治疗TNBC疗效较好,能显著提高患者的疾病控制率,改善其免疫功能和生活质量,降低血清CA153、TPS、TK1水平,安全性较高。
Clinical efficacy study of sunitinib combined with capecitabine in the treatment of triple-negative breast cancer
Objective To investigate the clinical efficacy of sunitinib combined with capecitabine in the treatment of tri-ple-negative breast cancer(TNBC).Methods TNBC patients treated at Hebei Petro China Central Hospital from March 2020 to March 2022 were selected for this study.Patients were divided into the control group and the study group using the a ran-dom number table method.The control group received capecitabine treatment,while the study group received additional suni-tinib treatment,with both groups undergoing three treatment cycles.The therapeutic effects,immune function,serum CA153,TPS,TK1 levels,patient quality of life,and adverse reactions were evaluated for both groups.Results A total of 60 patients were included,with 30 cases in the control group and 30 cases in the study group.After three treatment cycles,no significant difference in the objective response rate was observed between the two groups(P>0.05).However,the disease control rate in the study group was higher than that of the control group(86.67%vs 60.00%).The levels of CD3+,CD4+,CD4+/CD8+,FACT-B,and SAQ scores were higher than those of the control group[(49.26±3.11)vs(41.02±3.46),(42.55±5.11)vs(35.16±4.18),(1.98±0.22)vs(1.66±0.36),(85.12±1.65)points vs(72.65±1.48)points,(143.65±2.78)points vs(135.26±3.16)points],CD8+,serum CA153,TPS,TK1 levels,and HADS scores were lower than those of the control group[(16.56±1.87)vs(21.34±2.15),(20.45±3.79)U/mL vs(24.22±4.12)U/mL,(5.45±1.46)ng/mL vs(7.11±2.01)ng/mL,(1.56±0.26)pmol/L vs(1.91±0.23)pmol/L,(10.33±1.08)points vs(12.22±1.02)points],the differences were statisti-cally significant(P<0.05).Follow-up showed that the study group had longer disease control time[8.85(6.11,9.26)months]and progression-free survival[5.16(4.87,6.78)months]than those of the control group[7.11(5.26,8.78)months and 4.89(3.98,5.65)months](P<0.05).The incidence rates of adverse reactions such as fever,anemia,nausea and vomiting were similar between the two groups(P>0.05).Conclusion Sunitinib combined with capecitabine treatment for TNBC shows promising efficacy,significantly improving disease control rates,enhancing immune function and quality of life,reducing serum CA153,TPS,TK1 levels,and maintaining high safety.

sunitinibcapecitabinetriple-negative breast cancerimmune functionclinical efficacy

杨娜、李国明、李建红、吕建男、王久洁

展开 >

河北中石油中心医院 乳腺外科,河北 廊坊 065000

舒尼替尼 卡培他滨 三阴性乳腺癌 免疫功能 临床疗效

河北省廊坊市科学技术研究与发展计划

2021013042

2024

临床药物治疗杂志
北京药学会

临床药物治疗杂志

CSTPCD
影响因子:1.07
ISSN:1672-3384
年,卷(期):2024.22(5)
  • 23