基于真实世界的研究——646例肿瘤患者使用免疫检查点抑制剂相关不良反应的临床特征
作者:
作者单位:

上海交通大学医学院附属仁济医院,上海,200127

作者简介:

叶淑芳,女,护师,研究方向:肿瘤护理。

通讯作者:

仇晓霞,女,硕士,主任护师,研究方向:肿瘤护理、护理管理。

中图分类号:

R730.51


A real world research: the clinical characteristics of immune-related adverse events in 646 cases
Author:
Affiliation:

Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, 200127, China

  • 摘要
  • | |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • | | |
  • 文章评论
    摘要:

    目的 探讨免疫检查点抑制剂(ICI)在临床应用中的免疫相关不良事件(irAE)发生情况及临床特征。方法 回顾性分析2020年5月—2022年6月接受PD-1和PD-L1治疗的晚期恶性肿瘤患者646例,观察并记录治疗期间irAEs的发生情况,包括发生率、发生时间、分级等。结果 646例患者中,259例患者共发生370次irAEs,发生率为40.1%。1、2级不良反应266次(71.9%),3级以上不良反应104次(28.1%)。irAEs可累及全身各个器官系统,其中以皮肤毒性(15.6%)最常见。61例(23.6%)患者发生多系统irAEs。年龄≤65岁,联合用药,使用卡瑞利珠单抗、信迪利单抗、帕博利珠单抗的患者更易发生多系统irAEs。血液系统毒性、肝脏毒性、心血管毒性发生在早期,平均发生时间为治疗3个疗程内。年龄>65岁、合并自身免疫性疾病的患者行ICIs治疗可获得同等临床效益,具有良好的安全性。irAEs发生情况与患者的性别、年龄、合并症、用药方案、肿瘤类型、ICIs种类、免疫药物类型无关(P>0.05),与用药疗程有关(P<0.05)。结论 ICIs临床应用广泛,严重不良反应发生率低,有一定的安全性,但不良反应可累及全身各个器官系统,应做好各类irAEs的早期识别、诊断及治疗。

    Abstract:

    Objective To investigate the incidence and clinical characteristics of immune-related adverse events (irAE) in the clinical application of immune checkpoint inhibitors (ICIs).Methods 646 patients with advanced malignant tumors who were treated by PD-1 and PD-L1 inhibitors between May 2020 and June 2022 were retrospectively analyzed in this study. The occurrence of their irAEs during treatment was observed and recorded, including the incidence rate, occurrence time, grade, etc.Results A total of 370 irAEs occurred in 259 of 646 patients, with an incidence rate of 40.1%. There were 266 (71.9%) irAEs of grade 1 and 2, and 104 (28.1%) irAEs of grade 3 or higher grade. The irAEs could involve all organs and systems, among which skin toxicities (15.6%) were the most common. 61 (23.6%) patients experienced multisystem irAEs. Patients with ≤65 years of age, drug combination, camrelizumab, sintilimab, or pembrolizumab were more likely to have multisystem irAEs. Hematological toxicities, hepatic toxicities, and cardiotoxicity occurred in the early time, averagely within 3 courses of treatment. Patients >65 years old and complicated with autoimmune diseases could also achieve clinical benefits with a good safety. Though incidence of irAEs was not associated with gender, age, complications, therapeutic regimens, tumor types, types of ICIs, and types of immune drugs (P>0.05), it was associated with the course of treatment (P<0.05).Conclusion ICIs are widely used in clinical practice, with a low incidence rate of serious adverse events and a relative safety. However, their adverse reactions can involve various organs and systems throughout the body, so it is important to get early identification, diagnosis and treatment of irAEs for these patients.

    参考文献
    [1] 王月华, 胡志远. PD-1/PD-L1在肿瘤免疫逃逸中的作用机制及其临床应用[J]. 中国肿瘤生物治疗杂志, 2017, 24(7): 784-790. DOI: 10.3872/j.issn.1007-385X.2017.07.015.
    [2] BAGCHI S, YUAN R, ENGLEMAN E G. Immune checkpoint inhibitors for the treatment of cancer: clinical impact and mechanisms of response and resistance [J]. Annu Rev Pathol, 2021, 16: 223-249. DOI: 10.1146/annurev-pathol-042020-042741.
    [3] FIALA O, SOREJS O, SUSTR J, et al. Immune-related adverse effects and outcome of patients with cancer treated with immune checkpoint inhibitors [J]. Anticancer Res, 2020, 40(3): 1219-1227. DOI: 10.21873/anticanres.14063.
    [4] WANG Y C, ZHOU S H, YANG F, et al. Treatment-related adverse events of PD-1 and PD-L1 inhibitors in clinical trials: a systematic review and meta-analysis [J]. JAMA Oncol, 2019, 5(7): 1008-1019. DOI: 10.1001/jamaoncol.2019.0393.
    [5] LOMAX A J, LIM J, CHENG R, et al. Immune toxicity with checkpoint inhibition for metastatic melanoma: case series and clinical management [J]. J Skin Cancer, 2018, 2018: 9602540. DOI: 10.1155/2018/9602540.
    [6] BISHAY K, TANDON P, BOURASSA-BLANCHETTE S, et al. The risk of diarrhea and colitis in patients with lung cancer treated with immune checkpoint inhibitors: a systematic review and meta-analysis [J]. Curr Oncol, 2020, 27(5): e486-e494. DOI: 10.3747/co.27.6251.
    [7] KENNEDY L B, SALAMA A K S. A review of cancer immunotherapy toxicity [J]. CA Cancer J Clin, 2020, 70(2): 86-104. DOI: 10.3322/caac.21596.
    [8] LI Z C, SUN Y T, LAI M Y, et al. Efficacy and safety of PD-1 inhibitors combined with chemotherapy as first-line therapy for advanced esophageal cancer: a systematic review and network meta-analysis [J]. Int Immunopharmacol, 2022, 109: 108790. DOI: 10.1016/j.intimp.2022.108790.
    [9] CHOI J, ANDERSON R, BLIDNER A, et al. Multinational Association of Supportive Care in Cancer (MASCC) 2020 clinical practice recommendations for the management of severe dermatological toxicities from checkpoint inhibitors [J]. Support Care Cancer, 2020, 28(12): 6119-6128. DOI: 10.1007/s00520-020-05706-4.
    [10] BUKAMUR H, KATZ H, ALSHAREDI M, et al. Immune checkpoint inhibitor-related pulmonary toxicity: focus on nivolumab [J]. South Med J, 2020, 113(11): 600-605. DOI: 10.14423/SMJ.0000000000001166.
    [11] 赵静, 苏春霞. 《CSCO免疫检查点抑制剂相关的毒性管理指南》解读: 对比NCCN免疫治疗相关毒性管理指南[J]. 实用肿瘤杂志, 2020, 35(1): 11-15. DOI: 10.13267/j.cnki.syzlzz.2020.01.002.
    [12] REYNOLDS K L, GUIDON A C. Diagnosis and management of immune checkpoint inhibitor-associated neurologic toxicity: illustrative case and review of the literature [J]. Oncologist, 2019, 24(4): 435-443. DOI: 10.1634/theoncologist.2018-0359.
    [13] SEETHAPATHY H, HERRMANN S M, SISE M E. Immune checkpoint inhibitors and kidney toxicity: advances in diagnosis and management [J]. Kidney Med, 2021, 3(6): 1074-1081. DOI: 10.1016/j.xkme.2021.08.008.
    [14] MALATY M M, AMARASEKERA A T, LI C, et al. Incidence of immune checkpoint inhibitor mediated cardiovascular toxicity: a systematic review and meta-analysis [J]. Eur J Clin Invest, 2022, 52(12): e13831. DOI: 10.1111/eci.13831.
    [15] CAPPELLI L C, GUTIERREZ A K, BINGHAM C O3rd, et al. Rheumatic and musculoskeletal immune-related adverse events due to immune checkpoint inhibitors: a systematic review of the literature [J]. Arthritis Care Res, 2017, 69(11): 1751-1763. DOI: 10.1002/acr.23177.
    [16] GHOSH N, TIONGSON M D, STEWART C, et al. Checkpoint inhibitor-associated arthritis: a systematic review of case reports and case series [J]. J Clin Rheumatol, 2021, 27(8): e317-e322. DOI: 10.1097/RHU.0000000000001370.
    [17] MUNTYANU A, NETCHIPOROUK E, GERSTEIN W, et al. Cutaneous immune-related adverse events (irAEs) to immune checkpoint inhibitors: a dermatology perspective on management [formula: see text] [J]. J Cutan Med Surg, 2021, 25(1): 59-76. DOI: 10.1177/1203475420943260.
    [18] LIU X Y, SHI Y Q, ZHANG D M, et al. Risk factors for immune-related adverse events: what have we learned and what lies ahead? [J]. Biomark Res, 2021, 9(1): 79. DOI: 10.1186/s40364-021-00314-8.
    [19] CONFORTI F, PALA L, BAGNARDI V, et al. Cancer immunotherapy efficacy and patients’ sex: a systematic review and meta-analysis [J]. Lancet Oncol, 2018, 19(6): 737-746. DOI: 10.1016/S1470-2045(18)30261-4.
    [20] CORTELLINI A, BUTI S, SANTINI D, et al. Clinical outcomes of patients with advanced cancer and pre-existing autoimmune diseases treated with anti-programmed death-1 immunotherapy: a real-world transverse study [J]. Oncologist, 2019, 24(6): e327-e337. DOI: 10.1634/theoncologist.2018-0618.
    [21] WALLIS C J D, BUTANEY M, SATKUNASIVAM R, et al. Association of patient sex with efficacy of immune checkpoint inhibitors and overall survival in advanced cancers [J]. JAMA Oncol, 2019, 5(4): 529. DOI: 10.1001/jamaoncol.2018.5904.
    [22] SAITO Z, FUJITA K, OKAMURA M, et al. Efficacy and safety of immune checkpoint inhibitors in patients with non-small cell lung cancer aged 80 years or older [J]. Cancer Rep, 2021, 4(6): e1405. DOI: 10.1002/cnr2.1405.
    [23] NEBHAN C A, CORTELLINI A, MA W J, et al. Clinical outcomes and toxic effects of single-agent immune checkpoint inhibitors among patients aged 80 years or older with cancer [J]. JAMA Oncol, 2021, 7(12): 1856. DOI: 10.1001/jamaoncol.2021.4960.
    [24] 中国临床肿瘤学会免疫治疗专家委员会. 免疫检查点抑制剂特殊人群应用专家共识[J]. 临床肿瘤学杂志, 2022, 27(5): 442-454. DOI: 10.3969/j.issn.1009-0460.2022.05.009.
    [25] MARTINEZ CHANZA N, XIE W L, ISSA M, et al. Safety and efficacy of immune checkpoint inhibitors in advanced urological cancers with pre-existing autoimmune disorders: a retrospective international multicenter study [J]. J Immunother Cancer, 2020, 8(1): e000538. DOI: 10.1136/jitc-2020-000538.
    [26] THOMPSON J A, SCHNEIDER B J, BRAHMER J, et al. NCCN guidelines insights: management of immunotherapy-related toxicities, version 1.2020 [J]. J Natl Compr Canc Netw, 2020, 18(3): 230-241. DOI: 10.6004/jnccn.2020.0012.
    引证文献
    网友评论
    网友评论
    分享到微博
    发 布
引用本文

叶淑芳,刘苗兰,仇晓霞.基于真实世界的研究——646例肿瘤患者使用免疫检查点抑制剂相关不良反应的临床特征[J].肿瘤药学,2024,14(1):72-79 ( in Chinese)

复制
分享
文章指标
  • 点击次数:271
  • 下载次数: 898
  • HTML阅读次数: 140
  • 引用次数: 0
历史
  • 在线发布日期: 2024-04-08
我要投稿 杂志简介 杂志简介 二维码
TOP
×
《肿瘤药学》
《肿瘤药学》编辑部打假维权声明