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
相关论文
共 30 条
[21]   A randomized phase II study of SRL172 (Mycobacterium vaccae) combined with chemotherapy in patients with advanced inoperable non-small-cell lung cancer and mesothelioma [J].
O'Brien, MER ;
Saini, A ;
Smith, IE ;
Webb, A ;
Gregory, K ;
Mendes, R ;
Ryan, C ;
Priest, K ;
Bromelow, KV ;
Palmer, RD ;
Tuckwell, N ;
Kennard, DA ;
Souberbielle, BE .
BRITISH JOURNAL OF CANCER, 2000, 83 (07) :853-857
[22]   Chemotherapy in malignant pleural mesothelioma: A review [J].
Ong, ST ;
Vogelzang, NJ .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (03) :1007-1017
[23]   CONTINUING INCREASE IN MESOTHELIOMA MORTALITY IN BRITAIN [J].
PETO, J ;
HODGSON, JT ;
MATTHEWS, FE ;
JONES, JR .
LANCET, 1995, 345 (8949) :535-539
[24]  
RODIER JM, 1996, P AN M AM SOC CLIN, V15, P390
[25]   Combined systemic chemoimmunotherapy in advanced diffuse malignant mesothelioma: Report of a phase I-II study of weekly cisplatin interferon alfa-2a [J].
Soulie, P ;
Ruffie, P ;
Trandafir, L ;
Monnet, I ;
Tardivon, A ;
Terrier, P ;
Cvitkovic, E ;
LeChevalier, T ;
Armand, JP .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (03) :878-885
[26]   Phase II study of vinorelbine in patients with malignant pleural mesothelioma [J].
Steele, JPC ;
Shamash, J ;
Evans, MT ;
Gower, NH ;
Tischkowitz, MD ;
Rudd, RM .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (23) :3912-3917
[27]  
Therasse P, 2000, J NATL CANCER I, V92, P205, DOI 10.1093/jnci/92.3.205
[28]  
Thödtmann R, 1999, SEMIN ONCOL, V26, P89
[29]   Higher doses of alpha-interferon do not increase the activity of the weekly cisplatin-interferon combination in advanced malignant mesothelioma [J].
Trandafir, L ;
Ruffie, P ;
Borel, C ;
Monnet, I ;
Soulie, P ;
Adams, D ;
Cvitkovic, E ;
Armand, JP .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (11) :1900-1902
[30]  
VOROBIOF DA, 2000, P AM SOC CLIN ONCOL, V19