Phase I/IIa trial of autologous formalin-fixed tumor vaccine concomitant with fractionated radiotherapy for newly diagnosed glioblastoma Clinical article

被引:48
作者
Muragaki, Yoshihiro [1 ,2 ]
Maruyama, Takashi [2 ]
Iseki, Hiroshi [2 ]
Tanaka, Masahiko [2 ]
Shinohara, Chie [2 ]
Takakura, Kintomo
Tsuboi, Koji [6 ]
Yamamoto, Tetsuya [7 ]
Matsumura, Akira [7 ]
Matsutani, Masao [9 ]
Karasawa, Katsuyuki [4 ]
Shimada, Katsunori [5 ]
Yamaguchi, Naohito [3 ]
Nakazato, Yoichi [10 ]
Sato, Keiki [8 ]
Uemae, Youji [8 ]
Ohno, Tadao [8 ]
Okada, Yoshikazu [2 ]
Hori, Tomokatsu [2 ]
机构
[1] Tokyo Womens Med Univ, Fac Adv Techno Surg, Grad Sch Med, Shinjuku Ku, Tokyo 1628666, Japan
[2] Tokyo Womens Med Univ, Dept Neurosurg, Tokyo 1628666, Japan
[3] Tokyo Womens Med Univ, Dept Hyg & Publ Hlth 2, Tokyo 1628666, Japan
[4] Komagome Hosp, Dept Radiol, Tokyo Metropolitan Canc & Infect Dis Ctr, Tokyo, Japan
[5] STATZ Inst Inc, Tokyo, Japan
[6] Univ Tsukuba, Grad Sch Comprehens Human Sci, Ibaraki, Japan
[7] Univ Tsukuba, Dept Neurosurg, Ibaraki, Japan
[8] Cell Med Inc, Ibaraki, Japan
[9] Saitama Med Univ, Int Med Ctr, Saitama, Japan
[10] Gumna Univ, Dept Human Pathol, Gunma, Japan
关键词
brain tumor vaccine therapy; glioblastoma; autologous formalin-fixed tumor vaccine; oncology; CYTOTOXIC T-LYMPHOCYTES; RECURSIVE PARTITIONING ANALYSIS; MALIGNANT GLIOMA; ADJUVANT TEMOZOLOMIDE; RANDOMIZED-TRIAL; CELL VACCINE; MULTIFORME; INJECTION; TOXICITY; SECTIONS;
D O I
10.3171/2011.4.JNS10377
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. The objective of the present study was analysis of results of the prospective clinical trial directed toward the evaluation of therapeutic efficacy of the administration of autologous formalin-fixed tumor vaccine (AFTV) concomitant with fractionated radiotherapy in cases of newly diagnosed glioblastoma multiforme. Methods. Twenty-four patients were enrolled into the clinical trial, while 2 cases were excluded from the final analysis of results. The treatment protocol included aggressive tumor resection, fractionated radiotherapy up to a total dose of 60 Gy, and 3 concomitant courses of AFTV administered with an interval of one week at the late stage of irradiation. Two delayed-type hypersensitivity (DTH) tests were done-one 48 hours before the initial course of vaccination (DTH-1) and one 2 weeks after the third (DTH-2). All but one of the patients received salvage therapy at the time of tumor progression. The defined primary end point was overall survival; secondary end points were progression-free survival and safety of concomitant treatment. Results. The median duration of overall survival was 21.4 months (95% CI 13.8-31.3 months). The actuarial 2-year survival rate was 40%. The median duration of progression-free survival was 7.6 months (95% CI 4.3-13.6 months). Overall survival showed a statistically significant association with recursive partitioning analysis class (p < 0.05); progression-free survival showed a statistically significant association with p53 staining index (p < 0.05) and size of DTH-2 response (p < 0.001). AFTV injection concomitant with fractionated radiotherapy was well tolerated by all patients and in no case did treatment-related adverse effects exceed Grade 1 toxicity; adverse effects were limited to local erythema, induration, and swelling at the site of injection. Conclusions. The results of this study demonstrate that AFTV treatment concomitant with fractionated radiotherapy may be effective in patients with newly diagnosed glioblastoma. Further clinical testing is warranted. (DOI: 10.3171/2011.4-JNS10377)
引用
收藏
页码:248 / 255
页数:8
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