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CMV disease and colitis in a kidney transplanted patient under pembrolizumab.一名接受帕博利珠单抗治疗的肾移植患者发生巨细胞病毒病和结肠炎。
Eur J Cancer. 2019 Mar;109:172-174. doi: 10.1016/j.ejca.2018.12.027. Epub 2019 Feb 4.
2
Durable Clinical Benefit With Nivolumab Plus Ipilimumab in DNA Mismatch Repair-Deficient/Microsatellite Instability-High Metastatic Colorectal Cancer.纳武利尤单抗联合伊匹单抗治疗错配修复缺陷/微卫星高度不稳定转移性结直肠癌的持久临床获益。
J Clin Oncol. 2018 Mar 10;36(8):773-779. doi: 10.1200/JCO.2017.76.9901. Epub 2018 Jan 20.
3
Infectious complications associated with the use of immune checkpoint inhibitors in oncology: reactivation of tuberculosis after anti PD-1 treatment.肿瘤学中与使用免疫检查点抑制剂相关的感染并发症:抗PD-1治疗后结核病复发
Clin Microbiol Infect. 2018 Mar;24(3):216-218. doi: 10.1016/j.cmi.2017.12.003. Epub 2017 Dec 18.
4
Cytomegalovirus reactivation in patients with refractory checkpoint inhibitor-induced colitis.难治性检查点抑制剂诱导的结肠炎患者中的巨细胞病毒再激活
Eur J Cancer. 2017 Nov;86:248-256. doi: 10.1016/j.ejca.2017.09.019. Epub 2017 Oct 19.
5
Immune checkpoint blockade in infectious diseases.感染病中的免疫检查点阻断。
Nat Rev Immunol. 2018 Feb;18(2):91-104. doi: 10.1038/nri.2017.112. Epub 2017 Oct 9.
6
Overall Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma.纳武利尤单抗联合伊匹木单抗治疗晚期黑色素瘤的总生存期
N Engl J Med. 2017 Oct 5;377(14):1345-1356. doi: 10.1056/NEJMoa1709684. Epub 2017 Sep 11.
7
Management of toxicities from immunotherapy: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.免疫疗法毒性管理:ESMO诊断、治疗及随访临床实践指南
Ann Oncol. 2017 Jul 1;28(suppl_4):iv119-iv142. doi: 10.1093/annonc/mdx225.
8
Acute hemorrhagic gastritis after nivolumab treatment.纳武单抗治疗后发生的急性出血性胃炎。
Gastrointest Endosc. 2017 Nov;86(5):915-916. doi: 10.1016/j.gie.2017.04.033. Epub 2017 May 3.
9
Severe Esophagitis and Gastritis from Nivolumab Therapy.纳武单抗治疗引起的严重食管炎和胃炎。
ACG Case Rep J. 2017 Apr 12;4:e57. doi: 10.14309/crj.2017.57. eCollection 2017.
10
Indicators of responsiveness to immune checkpoint inhibitors.免疫检查点抑制剂的反应指标。
Sci Rep. 2017 Apr 11;7(1):807. doi: 10.1038/s41598-017-01000-2.

患者黑色素瘤接受帕博利珠单抗治疗后发生严重巨细胞病毒胃炎。

Severe cytomegalovirus gastritis after pembrolizumab in a patient with melanoma.

机构信息

Division of Hematology-Oncology, Department of Medicine.

Department of Pathology and Translational Genomics.

出版信息

Curr Oncol. 2020 Aug;27(4):e436-e439. doi: 10.3747/co.27.6163. Epub 2020 Aug 1.

DOI:10.3747/co.27.6163
PMID:32905211
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7467798/
Abstract

Immunotherapy has emerged as a standard of cancer treatment, with an increasing number of indications. Recently, opportunistic infections have been reported in several cases in which immunotherapy has led to an increased susceptibility to infection. The present case is the first report of cytomegalovirus (cmv) gastritis occurring in a patient with melanoma during immunotherapy without immune-related adverse events (iraes) and without the use of immunosuppressant agents. A 43-year-old woman presented with stage iii malignant melanoma. She underwent wide excision of skin, with lymph node dissection, and she started immunotherapy with a 3-week cycle of pembrolizumab. The patient demonstrated stable disease response, and no iraes were observed during her initial treatment courses. However, after the 9th treatment cycle, she began to experience epigastric pain that worsened significantly, requiring a visit to the emergency centre. Imaging by computed tomography (ct) and integrated positron-emission tomography/ct revealed severe diffuse gastroduodenitis with acute pancreatitis. Esophagogastroduodenoscopy showed diffuse oozing, hemorrhagic, edematous, and exfoliative mucosa involving the entire gastric wall, defined as acute hemorrhagic gastritis. Biopsies of the gastric wall revealed cmv infection. Those findings were consistent with a diagnosis of cmv gastritis, and the patient received antiviral therapy with ganciclovir. After treatment, she recovered enough to resume immunotherapy. This case report presents a rare occurrence of cmv gastritis related to immunotherapy. As more patients are treated with immunotherapy, incidences of cmv infections are expected to increase; a high index of clinical suspicion is therefore needed in symptomatic patients.

摘要

免疫疗法已成为癌症治疗的标准方法,其适应证也在不断增加。最近,有报道称在一些免疫疗法导致感染易感性增加的病例中出现了机会性感染。本病例是首例在免疫治疗期间发生巨细胞病毒(cmv)胃炎的黑色素瘤患者的报告,无免疫相关不良事件(iraes)且未使用免疫抑制药物。一名 43 岁女性患有 iii 期恶性黑色素瘤。她接受了广泛的皮肤切除手术,并进行了淋巴结清扫,随后开始接受派姆单抗免疫治疗,每 3 周为一个周期。患者表现出疾病稳定的反应,在最初的治疗过程中未观察到 iraes。然而,在第 9 个治疗周期后,她开始出现上腹痛,且疼痛明显加重,需要前往急诊中心就诊。计算机断层扫描(ct)和正电子发射断层扫描/ct 成像显示严重弥漫性胃十二指肠炎伴急性胰腺炎。食管胃十二指肠镜检查显示弥漫性渗出、出血、水肿和剥脱性黏膜,累及整个胃壁,定义为急性出血性胃炎。胃壁活检显示 cmv 感染。这些发现与 cmv 胃炎的诊断一致,患者接受了更昔洛韦抗病毒治疗。治疗后,她的病情恢复到足以继续接受免疫治疗。本病例报告了一种罕见的与免疫疗法相关的 cmv 胃炎。随着越来越多的患者接受免疫治疗,cmv 感染的发生率预计会增加;因此,对于有症状的患者,需要高度的临床怀疑。