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贝伐珠单抗联合帕博利珠单抗治疗转移性宫颈癌致严重血尿 1 例报告

Severe hematuria in a patient receiving bevacizumab and pembrolizumab for metastatic cervical cancer: a case report.

机构信息

Department of Pharmacy, West China Second University Hospital, Sichuan University, 610041, Chengdu, Sichuan, China.

Evidence-based Pharmacy Center, West China Second University Hospital, Sichuan University, Chengdu, China.

出版信息

BMC Nephrol. 2023 Mar 10;24(1):51. doi: 10.1186/s12882-023-03101-9.

Abstract

BACKGROUND

Bevacizumab is a monoclonal antibody drug targeting Vascular Endothelial Growth Factor (VEGF), which binds to VEGF receptors to inhibit vascular endothelial cell proliferation and angiogenesis, thus inhibiting tumorigenesis. Pembrolizumab is a monoclonal antibody that can bind to the programmed death-1 (PD-1) receptor, which can block the binding of the PD-1 receptor to its ligands PD-L1 and PD-L2, and release PD-1 pathway-mediated suppression of immune responses. By blocking the activity of PD-1, the purpose of inhibiting tumor growth is achieved.

CASE PRESENTATION

We report a severe hematuria of bevacizumab plus pembrolizumab, in a 58-year-old woman with metastatic cervical cancer. After three cycles every three weeks of consolidation chemotherapy (carboplatin, paclitaxel, bevacizumab) and following three cycles consolidation chemotherapy (carboplatin, paclitaxel, bevacizumab, pembrolizumab), the patient presented a worsening state. Manifested as massive gross hematuria with blood clots. After stopping chemotherapy, cefoxitin, tranexamic acid and hemocoagulase atrox therapy was administered resulting in rapid clinical improvement. The patient was a cervical cancer with bladder metastasis that increases the risk of development of hematuria. Inhibition of VEGF, which has anti-apoptotic, anti-inflammatory, and pro-survival influences on endothelial cells, weakens their regenerative capacity and increases expression of proinflammatory genes leading to weakened supporting layers of blood vessels and, hence, to damaged vascular integrity. In our patient, the development of hematuria may result from the anti-VEGF effect of bevacizumab. In addition, pembrolizumab may also cause bleeding, and the mechanism of bleeding caused by pembrolizumab is currently unclear, which may be related to immune mediation.

CONCLUSION

To our knowledge, this is the first case reporting on the development of severe hematuria during bevacizumab plus pembrolizumab treatment, which should alert the clinicians in case of bleeding adverse events onset in older patients under bevacizumab plus pembrolizumab therapy.

摘要

背景

贝伐珠单抗是一种靶向血管内皮生长因子(VEGF)的单克隆抗体药物,它与 VEGF 受体结合,抑制血管内皮细胞增殖和血管生成,从而抑制肿瘤发生。帕博利珠单抗是一种单克隆抗体,可与程序性死亡受体-1(PD-1)结合,从而阻断 PD-1 受体与其配体 PD-L1 和 PD-L2 的结合,并释放 PD-1 通路介导的免疫反应抑制。通过阻断 PD-1 的活性,达到抑制肿瘤生长的目的。

病例介绍

我们报告了一例 58 岁转移性宫颈癌患者使用贝伐珠单抗联合帕博利珠单抗后出现严重血尿。在每 3 周进行 3 个周期的巩固化疗(卡铂、紫杉醇、贝伐珠单抗)后,又进行了 3 个周期的巩固化疗(卡铂、紫杉醇、贝伐珠单抗、帕博利珠单抗)后,患者病情恶化。表现为大量肉眼血尿伴血块。停止化疗后,给予头孢西丁、氨甲环酸和巴曲酶治疗,临床症状迅速改善。该患者患有宫颈癌伴膀胱转移,增加了血尿发生的风险。VEGF 的抑制作用对内皮细胞具有抗凋亡、抗炎和促生存的影响,削弱了它们的再生能力,并增加了促炎基因的表达,导致血管支持层减弱,从而导致血管完整性受损。在我们的患者中,血尿的发生可能是由于贝伐珠单抗的抗 VEGF 作用。此外,帕博利珠单抗也可能导致出血,帕博利珠单抗引起出血的机制目前尚不清楚,可能与免疫介导有关。

结论

据我们所知,这是首例报道贝伐珠单抗联合帕博利珠单抗治疗后发生严重血尿的病例,在贝伐珠单抗联合帕博利珠单抗治疗的老年患者出现出血不良事件时,应引起临床医生的警惕。

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Pembrolizumab for Persistent, Recurrent, or Metastatic Cervical Cancer.派姆单抗治疗持续性、复发性或转移性宫颈癌。
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