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本文引用的文献

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Therapeutic vaccination for the treatment of malignant melanoma.用于治疗恶性黑色素瘤的治疗性疫苗接种。
Recent Results Cancer Res. 2007;176:219-27. doi: 10.1007/978-3-540-46091-6_19.
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Bcl-2 antisense (oblimersen sodium) plus dacarbazine in patients with advanced melanoma: the Oblimersen Melanoma Study Group.Bcl-2反义核酸(奥布利默森钠)联合达卡巴嗪治疗晚期黑色素瘤患者:奥布利默森黑色素瘤研究组
J Clin Oncol. 2006 Oct 10;24(29):4738-45. doi: 10.1200/JCO.2006.06.0483. Epub 2006 Sep 11.
3
Dacarbazine (DTIC) versus vaccination with autologous peptide-pulsed dendritic cells (DC) in first-line treatment of patients with metastatic melanoma: a randomized phase III trial of the DC study group of the DeCOG.达卡巴嗪(DTIC)与自体肽脉冲树突状细胞(DC)疫苗用于转移性黑色素瘤患者一线治疗的比较:DeCOG DC研究组的一项随机III期试验
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Melanoma vaccines: prospects for the treatment of melanoma.
Expert Opin Investig Drugs. 1997 Mar;6(3):267-27. doi: 10.1517/13543784.6.3.267.
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Phase I/II study of immunotherapy with T-cell peptide epitopes in patients with stage IV melanoma.IV期黑色素瘤患者使用T细胞肽表位进行免疫治疗的I/II期研究。
Cancer Immunol Immunother. 2005 Mar;54(3):208-18. doi: 10.1007/s00262-004-0587-8. Epub 2004 Sep 21.
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Maturation of dendritic cells is a prerequisite for inducing immune responses in advanced melanoma patients.树突状细胞的成熟是在晚期黑色素瘤患者中诱导免疫反应的先决条件。
Clin Cancer Res. 2003 Nov 1;9(14):5091-100.
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Phase I/II study of treatment with dendritic cell vaccines in patients with disseminated melanoma.树突状细胞疫苗治疗播散性黑色素瘤患者的I/II期研究。
Cancer Immunol Immunother. 2004 Feb;53(2):125-34. doi: 10.1007/s00262-003-0429-0. Epub 2003 Nov 5.
8
Clinical and immunologic results of a randomized phase II trial of vaccination using four melanoma peptides either administered in granulocyte-macrophage colony-stimulating factor in adjuvant or pulsed on dendritic cells.一项随机II期试验的临床和免疫学结果,该试验采用四种黑色素瘤肽进行疫苗接种,这些肽要么与粒细胞-巨噬细胞集落刺激因子联合作为佐剂给药,要么负载于树突状细胞上。
J Clin Oncol. 2003 Nov 1;21(21):4016-26. doi: 10.1200/JCO.2003.10.005.
9
Results of a phase I clinical study using autologous tumour lysate-pulsed monocyte-derived mature dendritic cell vaccinations for stage IV malignant melanoma patients combined with low dose interleukin-2.一项针对IV期恶性黑色素瘤患者,使用自体肿瘤裂解物脉冲单核细胞衍生的成熟树突状细胞疫苗联合低剂量白细胞介素-2的I期临床研究结果。
Melanoma Res. 2003 Oct;13(5):521-30. doi: 10.1097/00008390-200310000-00011.
10
Differentiation of CD8+ T cells from tumor-invaded and tumor-free lymph nodes of melanoma patients: role of common gamma-chain cytokines.黑色素瘤患者肿瘤浸润及未受肿瘤侵犯淋巴结中CD8 + T细胞的分化:常见γ链细胞因子的作用
J Immunol. 2003 Aug 15;171(4):2134-41. doi: 10.4049/jimmunol.171.4.2134.

采用成熟树突状细胞联合或不联合低剂量白细胞介素-2治疗播散性黑色素瘤患者的I/II期研究。

Phase I/II study of treatment with matured dendritic cells with or without low dose IL-2 in patients with disseminated melanoma.

作者信息

Hersey P, Halliday G M, Farrelly M L, DeSilva C, Lett M, Menzies S W

机构信息

Oncology and Immunology Unit, Room 443, David Maddison Clinical Sciences Building, Cnr. King & Watt Streets, Newcastle, NSW 2300, Australia.

出版信息

Cancer Immunol Immunother. 2008 Jul;57(7):1039-51. doi: 10.1007/s00262-007-0435-8.

DOI:10.1007/s00262-007-0435-8
PMID:18157724
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11030839/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。