Miolo GianMaria, Baldo Paolo, Bidoli Ettore, Lombardi Davide, Scalone Simona, Sorio Roberto, Veronesi Andrea
Division of Medical Oncology C, Centro di Riferimento Oncologico, National Cancer Institute, Aviano, Italy.
Tumori. 2009 Nov-Dec;95(6):687-90. doi: 10.1177/030089160909500608.
Association between pegylated liposomal doxorubicin-based regimens and palmar-plantar erythrodysesthesia have just been emphasized, whereas the relationship between previous treatment and palmar-plantar erythrodysesthesia is still a matter of discussion. We evaluate the relationship between previous chemotherapy treatments and the development of palmar-plantar erythrodysesthesia in patients receiving pegylated liposomal doxorubicin-based regimens.
Between January 2005 and November 2006, 92 patients received regimens including pegylated liposomal doxorubicin. Patients were divided into three groups based on pegylated liposomal doxorubicin dosing interval length, different dose chosen, and previous chemotherapy.
Among pretreated patients receiving regimens including 30 mg/m2 of pegylated liposomal doxorubicin repeated every three weeks, the incidence of palmar-plantar erythrodysesthesia was not significantly higher than in unpretreated patients receiving the same weekly schedule (P = 0.4). There was no difference in the incidence of palmar-plantar erythrodysesthesia between pretreated patients with regimens including 30 mg/m2 of pegylated liposomal doxorubicin every three weeks and pretreated patients receiving 20 mg/m2 of pegylated liposomal doxorubicin every two weeks (P = 0.8). The prevalence of palmar-plantar erythrodysesthesia observed in the unpretreated group exposed to 30 mg/m2 every three weeks was comparable to that of the pretreated group receiving 20 mg/m2 biweekly (P = 0.3). However, excluding all the patients who developed grade 1 palmar-plantar erythrodysesthesia, the incidence of grade 2 and 3 palmar-plantar erythrodysesthesia observed in pretreated patients receiving regimens including 20 mg/m2 of pegylated liposomal doxorubicin biweekly was significantly higher than in unpretreated patients receiving 30 mg/m2 of pegylated liposomal doxorubicin every three weeks (P = 0.001).
Our findings indicate that the pretreatment is not involved in the increased incidence of any grade palmar-plantar erythrodysesthesia. On the contrary, the study could suggest that the type of previous treatment may be an important factor in the development of more severe forms of palmar-plantar erythrodysesthesia.
基于聚乙二醇化脂质体阿霉素的治疗方案与手足红斑性感觉异常之间的关联刚刚得到强调,而既往治疗与手足红斑性感觉异常之间的关系仍存在争议。我们评估接受基于聚乙二醇化脂质体阿霉素治疗方案的患者既往化疗治疗与手足红斑性感觉异常发生之间的关系。
2005年1月至2006年11月期间,92例患者接受了包含聚乙二醇化脂质体阿霉素的治疗方案。根据聚乙二醇化脂质体阿霉素给药间隔时长、所选不同剂量以及既往化疗情况,将患者分为三组。
在接受每三周重复一次30mg/m²聚乙二醇化脂质体阿霉素治疗方案的预处理患者中,手足红斑性感觉异常的发生率并不显著高于接受相同每周给药方案的未预处理患者(P = 0.4)。每三周接受30mg/m²聚乙二醇化脂质体阿霉素治疗方案的预处理患者与每两周接受20mg/m²聚乙二醇化脂质体阿霉素治疗方案的预处理患者之间,手足红斑性感觉异常的发生率无差异(P = 0.8)。每三周接受30mg/m²的未预处理组中观察到的手足红斑性感觉异常患病率与每两周接受20mg/m²的预处理组相当(P = 0.3)。然而,排除所有发生1级手足红斑性感觉异常的患者后,每两周接受20mg/m²聚乙二醇化脂质体阿霉素治疗方案的预处理患者中观察到的2级和3级手足红斑性感觉异常的发生率显著高于每三周接受30mg/m²聚乙二醇化脂质体阿霉素的未预处理患者(P = 0.001)。
我们的研究结果表明,预处理与任何级别的手足红斑性感觉异常发生率增加无关。相反,该研究可能提示既往治疗类型可能是更严重形式的手足红斑性感觉异常发生的一个重要因素。