Polyzos Aristides, Tsavaris Nikolas, Gogas Hellen, Souglakos John, Vambakas Lambros, Vardakas Nikolaos, Polyzos Kostas, Tsigris Christos, Mantas Demetrios, Papachristodoulou Antonios, Nikiteas Nikolas, Karavokyros John G, Felekouras Evangelos, Griniatsos John, Giannopoulos Athanasios, Kouraklis Gregory
Medical Oncology Unit, Laiko General Hospital, Athens University School of Medicine, Athens, Greece.
Oncology. 2009;76(1):36-41. doi: 10.1159/000178163. Epub 2008 Nov 26.
Oxaliplatin has become one of the major cytotoxic agents for the treatment of gastrointestinal tumors. As a result, several cases of the so-called oxaliplatin-associated hypersensitivity reaction have been documented.
We have retrospectively evaluated and characterized these reactions in our patient group by reviewing the files of 1,224 patients exposed to an oxaliplatin-containing regimen in order to provide useful clinical information for diagnosis and management.
Three hundred and eight (308) patients who have never been exposed to platinum compounds developed symptoms compatible with a reaction to oxaliplatin that was verified by manifestation of at least similar symptoms on rechallenging. The reactions occurred after the first 5 courses, with a median course number of 9 (range 1-24). These reactions could be distinguished as (1) mild reactions occurring in 195 (63%) patients manifesting with itching and small area erythema either during treatment or within the next hours, and (2) severe reactions occurring in 113 (37%) patients within minutes of drug infusion manifesting with diffuse erythroderma, facial swelling, chest tightness, bronchospasm and changes in blood pressure. Oxaliplatin withdrawal was not required in patients with a mild reaction. Forty-eight (42%) patients having a severe reaction with appropriate premedication and prolongation of the infusion duration could tolerate 2-4 subsequent courses. For the remaining 65 (58%) patients, oxaliplatin withdrawal was inevitable because of the very severe reactions occurring on rechallenging. In addition, 3 patients presented with thrombocytopenia and 3 others with hemolytic anemia, all reversible upon oxaliplatin discontinuation.
Hypersensitivity reactions to oxaliplatin are underestimated. Although the reactions are not frequent during first courses, in extensively pretreated patients, they may become a serious problem. In the majority of patients, drug discontinuation might not be necessary. In patients manifesting a severe reaction, re-exposure to oxaliplatin should be considered only if the patient can tolerate the reaction and there has been clinical benefit from this therapy. Physicians and nursing staff should be aware of the risk and be well prepared.
奥沙利铂已成为治疗胃肠道肿瘤的主要细胞毒性药物之一。因此,已有数例所谓的奥沙利铂相关过敏反应的病例记录在案。
我们通过回顾1224例接受含奥沙利铂方案治疗的患者病历,对我们患者组中的这些反应进行了回顾性评估和特征分析,以便为诊断和管理提供有用的临床信息。
308例从未接触过铂类化合物的患者出现了与奥沙利铂反应相符的症状,再次给药时至少出现类似症状证实了这一点。这些反应发生在最初5个疗程之后,中位疗程数为9(范围1 - 24)。这些反应可分为两类:(1)195例(63%)患者出现轻度反应,表现为治疗期间或之后数小时内瘙痒和小面积红斑;(2)113例(37%)患者在药物输注数分钟内出现严重反应,表现为弥漫性红皮病、面部肿胀、胸闷、支气管痉挛和血压变化。轻度反应患者无需停用奥沙利铂。48例(42%)严重反应患者经适当预处理并延长输注时间后能够耐受后续2 - 4个疗程。其余65例(58%)患者因再次给药时出现非常严重的反应而不可避免地停用了奥沙利铂。此外,3例患者出现血小板减少,3例出现溶血性贫血,停用奥沙利铂后均可逆。
对奥沙利铂的过敏反应被低估了。虽然这些反应在最初疗程中并不常见,但在接受过广泛预处理的患者中,可能会成为一个严重问题。在大多数患者中,可能无需停药。对于出现严重反应的患者,仅当患者能够耐受该反应且该治疗已带来临床益处时,才应考虑再次使用奥沙利铂。医生和护理人员应意识到风险并做好充分准备。