Clinical and immunological assessment of Mycobacterium vaccae (SRL 172) with chemotherapy in patients with malignant mesothelioma

被引:18
作者
Mendes, R
O'Brien, MER
Mitra, A
Norton, A
Gregory, RK
Padhani, AR
Bromelow, KV
Winkley, AR
Ashley, S
Smith, IE
Souberbielle, BE
机构
[1] Royal Marsden Hosp NHS Trust, Dept Haematol, Lung Unit, Sutton SM2 5PT, Surrey, England
[2] Kings Coll London, Rayne Inst, Dept Mol Med, London WC2R 2LS, England
[3] Kent Canc Ctr, Maidstone ME16 9QQ, Kent, England
关键词
intra-pleural; chemotherapy; intradermal; vaccine; immunotherapy;
D O I
10.1038/sj.bjc.6600063
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The objectives of this study were to determine the toxicity of intratumoural/intrapleural SRL172 in addition to intradermal SRL172 and standard chemotherapy (mitomycin-C, vinblastine and cisplatin) in patients with malignant mesothelioma. Patients received chemotherapy (mitomycin-C: 8 mg m(-2), vinblastine: 6 mg m-2. cisplatin 50 mg m(-2)) on a 3-weekly basis for up to six courses. IP SRL172 injections were given 3-weekly prior to chemotherapy and escalated in groups of three patients from 1 mug to 1 mg bacilli in 10-fold increments. Patients were also given ID SRL172 at a dose of 1 mg bacilli 4-weekly. Patients were assessed for toxicity after each course of chemotherapy and for response by CT imaging. Immuno-haematological parameters were analyzed pre-treatment and I month after completion of treatment. There was no dose limiting toxicity with IP SRLI72 although there was greater toxicity at the highest dose (n=13). There were six out of 16 partial responses (37.5%). Haemato-immunological parameters, measured in seven patients pre and post-therapy, revealed that response rate correlated with a decrease in platelet count and there was an increase in activation of natural killer cells and a decrease in the percentage of IL-4 producing T cells in all tested patients post-treatment. SRL172 can be given safely into tumour deposits and the pleural cavity in patients with malignant mesothelioma and we have established the dose for phase II testing.
引用
收藏
页码:336 / 341
页数:6
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