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化疗联合卡瑞利珠单抗用于不可手术微卫星稳定型结直肠癌的

          临床观察
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          虞伟妃 ,汪笑秋 ,赵丽萍,冯继红,周珏伊(丽水市人民医院肿瘤放化疗科,浙江 丽水 323000)
          中图分类号  R979.1      文献标志码  A      文章编号  1001-0408(2023)10-1242-05
          DOI  10.6039/j.issn.1001-0408.2023.10.17

          摘   要  目的  评价XELOX(奥沙利铂+卡培他滨)化疗联合抗血管生成剂(阿帕替尼)和免疫治疗药物(卡瑞利珠单抗)用于不可
          手术转移性微卫星稳定(MSS)型结直肠癌(CRC)的疗效与安全性。方法  回顾性收集2020年1月-2021年1月丽水市人民医院
          收治的40例不可手术转移性MSS型CRC患者的临床资料。根据治疗方案将患者分为对照组(20例)和观察组(20例)。对照组患
          者接受XELOX+阿帕替尼治疗,观察组患者接受XELOX+阿帕替尼+卡瑞利珠单抗治疗。每3周为1个周期,连续治疗2个周期。
          记录两组患者的客观缓解率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)和不良事件(AEs)发生情况。结果
          观察组患者的ORR和DCR分别为65.0%、85.0%,对照组患者的ORR和DCR分别为35.0%、75.0%,组间比较差异均无统计学意义
         (P>0.05)。观察组和对照组患者的中位PFS分别为16.0、8.0个月,中位OS分别为19.0、12.5个月,组间比较差异均有统计学意义
         (P<0.05)。两组患者均至少发生1次AEs,且观察组患者的反应性皮肤毛细血管增生、甲亢的发生率均显著高于对照组(40.0%
          vs. 0和20% vs. 0,P<0.05),恶心和呕吐的发生率显著低于对照组(10% vs. 90%,P<0.05)。观察组患者发生3级及以上AEs的有
          14例(70.0%),而对照组仅有5例(25.0%),组间比较差异有统计学意义(P<0.05)。但两组患者均未发生不能耐受或致命的严重
          AEs,相关症状经停药或接受治疗后均得以缓解。结论  XELOX化疗联合阿帕替尼和卡瑞利珠单抗用于不可手术转移性MSS型
          CRC患者的效果与XELOX化疗联合阿帕替尼相当,但具有一定的ORR、PFS和OS优势,且安全性可控。
          关键词  不可手术;微卫星稳定型;转移性结直肠癌;化疗;免疫治疗;抗血管生成剂


          Clinical  observation  of  chemotherapy  combined  with  camrelizumab  in  patients  with  inoperable
          microsatellite stable type colorectal cancer
          YU Weifei,WANG Xiaoqiu,ZHAO Liping,FENG Jihong,ZHOU Jueyi(Dept.  of  Chemoradiotherapy,  Lishui
          People’s Hospital, Zhejiang Lishui 323000, China)

          ABSTRACT    OBJECTIVE  To  evaluate  the  clinical  efficacy  and  safety  of  XELOX  chemotherapy (oxaliplatin+capecitabine)
          combined with antiangiogenic agent (apatinib) and immunotherapy (camrelizumab) in patients with inoperable metastatic colorectal
          cancer (CRC)of  microsatellite  stable (MSS)  type.  METHODS  Clinical  medical  records  of  40  patients  with  inoperable  metastatic
          CRC of MSS type treated in Lishui People’s Hospital from January 2020 to January 2021 were retrospectively collected. According
          to the treatment plan, the patients were divided into control group (20 cases) and observation group (20 cases). Control group was
          given XELOX+apatinib regimen, while observation group was given XELOX+apatinib+camrelizumab regimen. Every 3 weeks was
          a  treatment  cycle,  and  the  treatment  lasted  for  2  consecutive  cycles.  The  objective  response  rate (ORR),  disease  control  rate
         (DCR),  progression-free  survival (PFS),  overall  survival (OS)  and  adverse  events (AEs)  were  recorded  for  all  patients.
          RESULTS The ORR and DCR of observation group were 65.0% and 85.0%, respectively; and the ORR and DCR of control group
          were 35.0% and 75.0%, respectively, with no statistical significance between 2 groups (P>0.05). The median PFS of observation
          group and control groups were 16.0 months and 8.0 months, respectively; and the median OS were 19.0 months and 12.5 months,
          respectively,  with  statistical  significance  between  2  groups (P<0.05).  Each  patient  in  both  groups  had  at  least  one AEs,  and  the
          incidences  of  reactive  skin  capillary  hyperplasia  and  hyperthyroidism  in  observation  group (40.0%,  20.0%)  were  significantly
          higher  than  those  in  control  group (both  were  0) (P<0.05).  The  incidence  of  nausea  and  vomiting  in  control  group (90%)  was
          significantly higher than observation group (10%) (P<0.05). There were 14 cases (70.0%) of patients with grade 3 or above AEs
          in  observation  group,  and  only  5  cases (25.0%)  in  control  group,  with  statistical  significance  between  2  groups (P<0.05).
          However,  no  severe  AEs  that  could  not  be  tolerated  or  fatal  occurred  in  the  two  groups,  which  could  be  alleviated  after  drug
          withdrawal  or  treatment.  CONCLUSIONS  The  efficacy  of  XELOX  chemotherapy  combined  with  apatinib  and  camrelizumab  in
          inoperable metastatic CRC patients of MSS type is comparable to that of XELOX chemotherapy combined with apatinib, but it has
                                                              certain  advantages  in  ORR,  PFS  and  OS,  and  controllable
              Δ 基金项目 丽水市科技计划项目(No.2022SJZC032)
                                                              safety.
             *第一作者 主治医师。研究方向:乳腺癌。E-mail:yuweif123@            KEYWORDS    inoperable;  microsatellite  stable  type;  meta-
          163.com                                             static  colorectal  cancer;  chemotherapy;  immunotherapy;
              #  通信作者 副 主 任 医 师 。 研 究 方 向 :临 床 医 学 。 E-mail:  antiangiogenic agent
          waxiaoq1234@163.com


          · 1242 ·    China Pharmacy  2023 Vol. 34  No. 10                            中国药房  2023年第34卷第10期
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