Risberg Karianne, Fodstad Oystein, Andersson Yvonne
Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway.
Ochsner J. 2010 Fall;10(3):193-9.
The incidence of melanoma is rising in the Western population, and melanoma is the most aggressive form of skin cancer with a very poor prognosis once it has progressed to metastatic stages. Patients with stage IV melanoma (metastases to distant lymph nodes and other areas of the body) are treated with the chemotherapeutic drug dacarbazine (DTIC). However, fewer than 5% of the patients treated with DTIC sustain long-term complete responses; hence, DTIC is administered with palliative purposes. New therapy is urgently needed. We are developing another therapeutic strategy, specifically targeting melanoma cells with the 9.2.27PE immunotoxin (IT). ITs bind to antigens overexpressed on cancer cells and are therefore tumor selective. This targeted approach may potentially cause fewer side effects in a clinical situation compared to conventional approaches like chemotherapy and radiotherapy.
在西方人群中,黑色素瘤的发病率正在上升,并且黑色素瘤是皮肤癌中最具侵袭性的形式,一旦发展到转移阶段,预后非常差。IV期黑色素瘤患者(转移至远处淋巴结和身体其他部位)接受化疗药物达卡巴嗪(DTIC)治疗。然而,接受DTIC治疗的患者中只有不到5%能维持长期完全缓解;因此,使用DTIC是出于姑息治疗目的。迫切需要新的治疗方法。我们正在开发另一种治疗策略,即使用9.2.27PE免疫毒素(IT)特异性靶向黑色素瘤细胞。免疫毒素与癌细胞上过度表达的抗原结合,因此具有肿瘤选择性。与化疗和放疗等传统方法相比,这种靶向方法在临床情况下可能产生更少的副作用。