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本文引用的文献

1
Does sunitinib-induced hypothyroidism play a role in the activity of sunitinib in metastatic renal cell carcinoma?舒尼替尼诱导的甲状腺功能减退症是否在舒尼替尼治疗转移性肾细胞癌的活性中起作用?
Chemotherapy. 2012;58(3):200-5. doi: 10.1159/000337079. Epub 2012 Jun 29.
2
Tyrosine kinase inhibitor-induced hypothyroidism: incidence, etiology, and management.酪氨酸激酶抑制剂引起的甲状腺功能减退症:发病率、病因和治疗。
Target Oncol. 2011 Dec;6(4):217-26. doi: 10.1007/s11523-011-0197-2. Epub 2011 Nov 19.
3
Drug-induced immune thrombocytopenic purpura secondary to sunitinib.药物性免疫性血小板减少性紫癜继发于舒尼替尼。
Curr Oncol. 2008 Jun;15(3):152-4. doi: 10.3747/co.v15i3.233.
4
Sunitinib induced hypertension, thrombotic microangiopathy and reversible posterior leukencephalopathy syndrome.舒尼替尼诱发高血压、血栓性微血管病及可逆性后部白质脑病综合征。
Ann Oncol. 2007 Oct;18(10):1745-7. doi: 10.1093/annonc/mdm454.
5
Drug-induced immune thrombocytopenia.药物性免疫性血小板减少症
N Engl J Med. 2007 Aug 9;357(6):580-7. doi: 10.1056/NEJMra066469.
6
Sunitinib: from rational design to clinical efficacy.舒尼替尼:从合理设计到临床疗效。
J Clin Oncol. 2007 Mar 1;25(7):884-96. doi: 10.1200/JCO.2006.06.3602.
7
Sunitinib versus interferon alfa in metastatic renal-cell carcinoma.舒尼替尼与干扰素α治疗转移性肾细胞癌的对比研究
N Engl J Med. 2007 Jan 11;356(2):115-24. doi: 10.1056/NEJMoa065044.
8
Safety, pharmacokinetic, and antitumor activity of SU11248, a novel oral multitarget tyrosine kinase inhibitor, in patients with cancer.新型口服多靶点酪氨酸激酶抑制剂SU11248在癌症患者中的安全性、药代动力学及抗肿瘤活性
J Clin Oncol. 2006 Jan 1;24(1):25-35. doi: 10.1200/JCO.2005.02.2194. Epub 2005 Nov 28.
9
[A case of renal cell carcinoma associated with idiopathic thrombocytopenic purpura].[一例肾细胞癌合并特发性血小板减少性紫癜]
Hinyokika Kiyo. 2005 Jun;51(6):377-80.
10
Renal cell carcinoma and idiopathic thrombocytopenic purpura.肾细胞癌与特发性血小板减少性紫癜。
Urology. 1984 Mar;23(3):293-6. doi: 10.1016/0090-4295(84)90049-9.

一例转移性肾细胞癌患者因舒尼替尼导致的药物性免疫介导血小板减少症:病例报告

Drug-induced immune-mediated thrombocytopenia secondary to sunitinib in a patient with metastatic renal cell carcinoma: a case report.

作者信息

Ansari Zia, George Mathew K

机构信息

Department of Medical Oncology, Tamworth Rural Referral Hospital, Locked Mail Bag 9783, 2348, Tamworth, NEMSC NSW, Australia.

出版信息

J Med Case Rep. 2013 Feb 26;7:54. doi: 10.1186/1752-1947-7-54.

DOI:10.1186/1752-1947-7-54
PMID:23442444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3599754/
Abstract

INTRODUCTION

Sunitinib is an oral multi-targeted tyrosine kinase inhibitor approved for first line treatment for metastatic renal cell carcinoma and imatinib-resistant metastatic gastrointestinal stromal tumors. Sunitinib administration can cause myelosuppression resulting in neutropenia and thrombocytopenia. Here we present the case of a patient with metastatic renal cell carcinoma who developed sunitinib-induced immune-mediated thrombocytopenia and who was treated with withdrawal of sunitinib and administration of intravenous immunoglobulin and steroids.

CASE PRESENTATION

This case report describes a 70-year-old Aboriginal Australian with a diagnosis of metastatic renal cell carcinoma. Three weeks after the initiation of sunitinib he developed epistaxis and was admitted with thrombocytopenia (platelets 7 × 109/L) which was found to be refractory to platelet transfusion. Sunitinib was stopped and he was treated with intravenous immunoglobulin and steroids. His platelet count rapidly improved and returned to baseline in three weeks. Only two cases of sunitinib-induced immune-mediated thrombocytopenia have been described in the literature.

CONCLUSION

Clinicians should have a high index of suspicion for the potential of immune-mediated thrombocytopenia after the initiation of multi-targeted tyrosine kinase inhibitors such as sunitinib. This is a diagnosis of exclusion and can be safely treated by drug withdrawal.

摘要

引言

舒尼替尼是一种口服多靶点酪氨酸激酶抑制剂,被批准用于转移性肾细胞癌的一线治疗以及对伊马替尼耐药的转移性胃肠道间质瘤的治疗。使用舒尼替尼可导致骨髓抑制,引起中性粒细胞减少和血小板减少。在此,我们报告一例转移性肾细胞癌患者,该患者发生了舒尼替尼诱导的免疫介导性血小板减少症,并通过停用舒尼替尼以及给予静脉注射免疫球蛋白和类固醇进行治疗。

病例介绍

本病例报告描述了一名70岁的澳大利亚原住民,被诊断为转移性肾细胞癌。开始使用舒尼替尼三周后,他出现鼻出血,并因血小板减少症(血小板计数为7×10⁹/L)入院,发现对血小板输注无效。停用舒尼替尼后,他接受了静脉注射免疫球蛋白和类固醇治疗。他的血小板计数迅速改善,并在三周内恢复到基线水平。文献中仅描述了两例舒尼替尼诱导的免疫介导性血小板减少症病例。

结论

临床医生在开始使用舒尼替尼等多靶点酪氨酸激酶抑制剂后,应高度怀疑免疫介导性血小板减少症的可能性。这是一种排除性诊断,通过停药可安全治疗。