Lechleider Robert J, Arlen Philip M, Tsang Kwong-Yok, Steinberg Seth M, Yokokawa Junko, Cereda Vittore, Camphausen Kevin, Schlom Jeffrey, Dahut William L, Gulley James L
Laboratory of Tumor Immunology and Biology, National Cancer Institute, NIH, Bethesda, Maryland, USA.
Clin Cancer Res. 2008 Aug 15;14(16):5284-91. doi: 10.1158/1078-0432.CCR-07-5162.
We have previously reported on the safety and immunologic response of a poxvirus-based vaccine encoding prostate-specific antigen (PSA) used in combination with radiation therapy in patients with localized prostate cancer. We hypothesized that a "metronomic" dose of interleukin 2 (IL-2) as a biological adjuvant would cause less toxicity while maintaining immunologic response.
Eighteen patients with localized prostate cancer were treated in a single-arm trial using previously established doses of vaccine and radiation therapy. The vaccine used was a recombinant vaccinia virus engineered to encode PSA admixed with a recombinant vaccinia encoding the costimulatory molecule B7.1, followed by booster vaccinations with a recombinant fowlpox vector expressing PSA. Patients received a total of eight planned vaccination cycles, once every 4 weeks, with granulocyte-macrophage colony-stimulating factor given on days 1 to 4 and interleukin 2 (IL-2) at a dose of 0.6 MIU/M2 given from days 8 to 21 after each vaccination. Definitive external beam radiation therapy was initiated after the third vaccination cycle. Patients were evaluated for safety and immunologic response. Toxicity and immunologic activity were compared with the previously reported regimen containing a higher dose of IL-2.
Seventeen of 18 patients received all eight cycles of vaccine with IL-2. Five of eight HLA-A2+ patients evaluated had an increase in PSA-specific T cells of > or =3-fold. Toxicities were generally mild, with only seven vaccination cycles of 140 given resulting in grade 3 toxicities possibly attributable to IL-2.
Metronomic-dose IL-2 in combination with vaccine and radiation therapy is safe, can induce prostate-specific immune responses, and has immunologic activity similar to low-dose IL-2, with markedly reduced toxicities.
我们之前报道了一种基于痘病毒的疫苗(编码前列腺特异性抗原(PSA))与局部前列腺癌患者放射治疗联合使用时的安全性和免疫反应。我们假设,作为生物佐剂的“节拍式”剂量白细胞介素2(IL-2)在维持免疫反应的同时会产生较低的毒性。
18例局部前列腺癌患者在单臂试验中接受了先前确定剂量的疫苗和放射治疗。所用疫苗是一种经基因工程改造以编码PSA的重组痘苗病毒,与编码共刺激分子B7.1的重组痘苗病毒混合,随后用表达PSA的重组禽痘病毒载体进行加强接种。患者共接受8个计划的接种周期,每4周一次,在每次接种后的第1至4天给予粒细胞-巨噬细胞集落刺激因子,在第8至21天给予剂量为0.6 MIU/M2的白细胞介素2(IL-2)。在第三个接种周期后开始确定性外照射放疗。对患者进行安全性和免疫反应评估。将毒性和免疫活性与先前报道的含有较高剂量IL-2的方案进行比较。
18例患者中有17例接受了所有8个含IL-2的疫苗接种周期。在评估的8例HLA-A2+患者中,有5例PSA特异性T细胞增加≥3倍。毒性一般较轻,在140个接种周期中只有7个可能归因于IL-2的3级毒性。
节拍式剂量的IL-2与疫苗和放射治疗联合使用是安全的,可诱导前列腺特异性免疫反应,并且具有与低剂量IL-2相似的免疫活性,毒性明显降低。