Pasquariello Stefano, Clavarezza Matteo, Piredda Sabrina, Foppiani Luca, Pesce Giampaola, Antonucci Giancarlo, De Censi Andrea, Mattioli Francesca
Department of Internal Medicine, Clinical Pharmacology and Toxicology Unit, University of Genoa, I-16132 Genoa, Italy.
Clinical Pharmacology Unit, E.O. Ospedali Galliera, I-16128 Genoa, Italy.
Oncol Lett. 2023 Jul 28;26(3):398. doi: 10.3892/ol.2023.13984. eCollection 2023 Sep.
Drug-induced thrombocytopenia is an adverse reaction characterized by accelerated platelet destruction. The present study described a case of thrombocytopenia that occurred during treatment with panitumumab. A female patient aged 49 years with metastatic rectal adenocarcinoma was treated with 9 out of 12 cycles of therapy with the standard of care, 5-fluorouacil (5-FU), oxaliplatin and folic acid, in association with panitumumab. During cycle 10, the patient developed severe thrombocytopenia, so the therapy was adjusted to a lower dosage; however, during cycle 11, after administration of panitumumab and before administration of 5-FU or oxaliplatin, the patient again presented with severe thrombocytopenia, with a platelet count <2×10/l. Immunology test results were negative apart from anti-nucleus antibodies (titration, 1:160). Naranjo's algorithm was used to establish the relationship between the use of panitumumab and thrombocytopenia onset and a score of 6 ('probable') was found. The temporal link between the onset of symptoms and administration of therapy, the relapse of thrombocytopenia after re-administration of the drug during cycle 11 (positive rechallenge) and Naranjo score of 6 ('probable') are crucial elements for establishing the causal relationship and the probability that thrombocytopenia was related to the administration of panitumumab. The patient then underwent two cycles of therapy with 5-FU, folic acid and irinotecan, in association with bevacizumab, experiencing again the same adverse event. Treatment with monoclonal antibodies was suspended altogether in favor of a switch to trifluridine/tipiracil. No other serious adverse events were reported.
药物性血小板减少症是一种以血小板加速破坏为特征的不良反应。本研究描述了一例在帕尼单抗治疗期间发生的血小板减少症病例。一名49岁的转移性直肠腺癌女性患者接受了12个周期治疗中的9个周期,采用标准治疗方案,即5-氟尿嘧啶(5-FU)、奥沙利铂和叶酸,并联合帕尼单抗。在第10周期,患者出现严重血小板减少症,因此将治疗调整为较低剂量;然而,在第11周期,在给予帕尼单抗后、给予5-FU或奥沙利铂之前,患者再次出现严重血小板减少症,血小板计数<2×10⁹/L。免疫检测结果除抗核抗体外均为阴性(滴度,1:160)。使用Naranjo算法确定帕尼单抗的使用与血小板减少症发作之间的关系,结果发现评分为6分(“可能”)。症状发作与治疗给药之间的时间联系、第11周期再次给药后血小板减少症的复发(阳性再激发)以及Naranjo评分为6分(“可能”)是确定因果关系以及血小板减少症与帕尼单抗给药相关可能性的关键因素。该患者随后接受了两个周期的5-FU、叶酸和伊立替康联合贝伐单抗的治疗,再次出现相同的不良事件。完全暂停单克隆抗体治疗,转而使用曲氟尿苷/替匹嘧啶。未报告其他严重不良事件。