Hersey P, Halliday G M, Farrelly M L, DeSilva C, Lett M, Menzies S W
Oncology and Immunology Unit, Room 443, David Maddison Clinical Sciences Building, Cnr. King & Watt Streets, Newcastle, NSW 2300, Australia.
Cancer Immunol Immunother. 2008 Jul;57(7):1039-51. doi: 10.1007/s00262-007-0435-8.
In the present study, we have examined whether treatment of patients with metastatic melanoma with matured dendritic cell (DC) vaccines with or without low dose IL-2 may improve treatment outcomes.
Sixteen patients received DC vaccines (DCs) sensitized with autologous melanoma lysates and 18 patients received DCs sensitized with peptides from gp100, MART-1, tyrosinase, MAGE-3.A2, MAGE-A10 and NA17. IL-2 was given subcutaneously (sc) at 1 MU/m2 on the second day after each injection for 5-14 days in half of each group. DCs were given by intranodal injection.
There were 2 partial responses (PR) and 3 with stable disease (SD) in the nine patients receiving DCs + peptides + IL-2, and 1 PR and 1 SD in nine patients treated with DCs + peptides without IL-2. There were only two patients with SD in the group receiving DCs + autologous lysates and no IL-2. Median overall survival for all patients was very good at 18.5 months but this was most probably due to selection of a favourable group of patients for the study. There was no significant difference in survival between the groups by log rank analysis. Treatment was not associated with significant side effects. The quality and yield of the DCs in the preparations were generally good.
We conclude that mature DC preparations may be superior to immature DC preparations for presentation of melanoma peptides and that IL-2 may increase clinical responses to the DCs plus peptides. However, in our view the low response rates do not justify the cost and complexity of this treatment approach.
在本研究中,我们检测了使用或不使用低剂量白细胞介素-2的成熟树突状细胞(DC)疫苗治疗转移性黑色素瘤患者是否能改善治疗效果。
16例患者接受了用自体黑色素瘤裂解物致敏的DC疫苗,18例患者接受了用来自gp100、MART-1、酪氨酸酶、MAGE-3.A2、MAGE-A10和NA17的肽致敏的DC。每组中的一半患者在每次注射后的第二天皮下注射1 MU/m²的IL-2,持续5 - 14天。DC通过结内注射给药。
在接受DC + 肽 + IL-2的9例患者中,有2例部分缓解(PR)和3例病情稳定(SD),在接受DC + 肽但未使用IL-2治疗的9例患者中,有1例PR和1例SD。在接受DC + 自体裂解物且未使用IL-2的组中,只有2例患者病情稳定。所有患者的中位总生存期非常好,为18.5个月,但这很可能是由于为该研究选择了一组有利的患者。通过对数秩分析,各组之间的生存率无显著差异。治疗未伴有明显的副作用。制剂中DC的质量和产量总体良好。
我们得出结论,成熟的DC制剂在呈递黑色素瘤肽方面可能优于未成熟的DC制剂,并且IL-2可能会增加对DC加肽的临床反应。然而,在我们看来,低反应率并不能证明这种治疗方法的成本和复杂性是合理的。