Pectasides D, Pectasides M, Psyrri A, Koumarianou A, Xiros N, Pectasides E, Gaglia A, Lianos E, Papaxoinis G, Lampadiari V, Economopoulos Th
2nd Department of Internal Medicine, Propaeduetic, Oncology Section, University of Athens, "Attikon" University Hospital Haidari, 1 Rimini, Athens, Greece.
Cancer Invest. 2006 Dec;24(8):780-5. doi: 10.1080/07357900601062354.
Merkel cell carcinoma (MCC), a rare tumor of the skin with aggressive behavior, is usually fatal when advanced disease is present. The role of chemotherapy (CT) in the treatment of patients with MCC is unclear.
Over 15 years, 9 patients with locally advanced or metastatic disease were treated with carboplatin (CBDCA) (300 mg/m(2) of AUC 5 on Day 1) and etoposide (VP-16) (100 mg/m(2) on Days 1-3) every 3 weeks. As second-line CT, cisplatin (CDDP) (60-100 mg/m(2)), ifosfamide (IFO) (3-5 g/m(2)) and epirubicin (EPI) (30-50 mg/m(2)) were utilized.
Of the 3 patients who received adjuvant therapy, one achieved complete response after 108+ months with second-line chemotherapy and radiotherapy, despite a brief relapse; 2 patients remain disease-free after 84+ and 108+ months. Of the 6 patients with locally advanced or metastatic disease who were treated with first-line chemotherapy, one (16.6 percent) achieved a complete response and 3 (50 percent) achieved partial response, for an overall response rate of 66.6 percent. Two patients (one with complete and one with partial response) received subsequent radiotherapy, following which complete response was achieved. Of the 2 complete responders, one patient remains disease-free after 56+ months. The median overall survival from the time of initial diagnosis for the whole group was 56 months (range 15-114 months); the median overall survival from the initiation of chemotherapy was 18 months (range 6-108+). Local recurrences and soft tissue metastases responded better than visceral metastases. Patients with partial response and no response had rapid disease progression and fatality, despite second-line chemotherapy and/or radiotherapy.
MCC appears to be chemosensitive but can progress rapidly with fatal outcomes. Although the rarity of these tumors precludes randomized trials, a common treatment plan should be utilized by those treating MCC. This may allow some conclusions regarding the optimum treatment of patients with MCC to be drawn in the future.
默克尔细胞癌(MCC)是一种侵袭性皮肤罕见肿瘤,晚期疾病时通常致命。化疗(CT)在MCC患者治疗中的作用尚不清楚。
15年间,9例局部晚期或转移性疾病患者每3周接受卡铂(CBDCA)(第1天300mg/m²,AUC 5)和依托泊苷(VP - 16)(第1 - 3天100mg/m²)治疗。作为二线CT,使用顺铂(CDDP)(60 - 100mg/m²)、异环磷酰胺(IFO)(3 - 5g/m²)和表柔比星(EPI)(30 - 50mg/m²)。
3例接受辅助治疗的患者中,1例在接受二线化疗和放疗后108 +个月达到完全缓解,尽管有短暂复发;2例患者在84 +和108 +个月后仍无疾病进展。6例接受一线化疗的局部晚期或转移性疾病患者中,1例(16.6%)达到完全缓解,3例(50%)达到部分缓解,总缓解率为66.6%。2例患者(1例完全缓解,1例部分缓解)接受后续放疗,之后达到完全缓解。2例完全缓解者中,1例患者在56 +个月后仍无疾病进展。全组从初始诊断时起的中位总生存期为56个月(范围15 - 114个月);从化疗开始起的中位总生存期为18个月(范围6 - 108 +)。局部复发和软组织转移的反应优于内脏转移。部分缓解和无反应的患者尽管接受了二线化疗和/或放疗,疾病仍进展迅速并导致死亡。
MCC似乎对化疗敏感,但可迅速进展并导致致命后果。尽管这些肿瘤罕见,无法进行随机试验,但治疗MCC的人员应采用共同的治疗方案。这可能使未来能够得出关于MCC患者最佳治疗的一些结论。