Immunotherapy for lung cancer

被引:59
作者
Bradbury, Penelope A.
Shepherd, Frances A. [1 ]
机构
[1] Univ Toronto, Princess Margaret Hosp, Dept Hematol & Oncol,Univ Hlth Network, Div Med Oncol,Scott Taylor Chair Lung Canc Res, Toronto, ON M5G 2M9, Canada
关键词
immunotherapy; lung cancer; cellular immune system; vaccines;
D O I
10.1097/JTO.0b013e318174e9a7
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Reports of turner regression after infection date back as far as 1550 BC. In the twentieth century, Dr. William Coley, witnessing regression of a malignant tumor in one of his patients after a bacterial infection, developed the first cancer treatment vaccine derived from killed bacteria, with some reported success. However, despite decades of research, no specific, active tumor vaccine has been approved for the treatment of cancer. In lung cancer, initial attempts to modulate the immune system with nonspecific therapies were unsuccessful. However, more sophisticated specific vaccines have now been developed, and an increasing number are being evaluated in randomized phase 3 trials, raising hopes that vaccines may be an additional novel therapy for patients with lung cancer. This article reviews the following seven vaccines, which have entered randomized trials: L-BLP25 (Stimuvax), BEC-2, 1E10, PF-3512676 (Promune), melanoma-associated antigen A3 immunotherapeutic, granulocyte-macrophage colony-stimulating factor-transduced allogeneic cancer cellular immunotherapy, and belagenpumatucel-L (Lucanix).
引用
收藏
页码:S164 / S170
页数:7
相关论文
共 54 条
[1]
Rapid induction of primary human CD4+ and CD8+ T cell responses against cancer-associated MUC1 peptide epitopes [J].
Agrawal, B ;
Krantz, MJ ;
Reddish, MA ;
Longenecker, BM .
INTERNATIONAL IMMUNOLOGY, 1998, 10 (12) :1907-1916
[2]
Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[3]
COMPLEX GANGLIOSIDES MODULATE THE INTEGRIN-MEDIATED ADHESION IN A RAT HEPATOMA-CELL LINE [J].
BARLETTA, E ;
MUGNAI, G ;
RUGGIERI, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 192 (01) :214-222
[4]
A THEORY OF SELF-NONSELF DISCRIMINATION [J].
BRETSCHER, P ;
COHN, M .
SCIENCE, 1970, 169 (3950) :1042-+
[5]
Randomized phase IIB trial of BLP25 liposome vaccine in stage IIIB and IV non-small-cell lung cancer [J].
Butts, C ;
Murray, N ;
Maksymiuk, A ;
Goss, G ;
Marshall, E ;
Soulières, D ;
Cormier, Y ;
Ellis, P ;
Price, A ;
Sawhney, R ;
Davis, M ;
Mansi, J ;
Smith, C ;
Vergidis, D ;
Ellis, P ;
MacNeil, M ;
Palmer, M .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (27) :6674-6681
[6]
BUTTS CM, 2007, J THORAC ONCOL S, V2
[7]
Toll-like receptors in inflammation, infection and cancer [J].
Chen, Keqiang ;
Huang, Jian ;
Gong, Wanghua ;
Iribarren, Pablo ;
Dunlop, Nancy M. ;
Wang, Ji Ming .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2007, 7 (10) :1271-1285
[8]
DANIOTTI JL, 1994, J NEUROCHEM, V62, P1131
[9]
VACCINATION WITH IRRADIATED TUMOR-CELLS ENGINEERED TO SECRETE MURINE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR STIMULATES POTENT, SPECIFIC, AND LONG-LASTING ANTITUMOR IMMUNITY [J].
DRANOFF, G ;
JAFFEE, E ;
LAZENBY, A ;
GOLUMBEK, P ;
LEVITSKY, H ;
BROSE, K ;
JACKSON, V ;
HAMADA, H ;
PARDOLL, D ;
MULLIGAN, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3539-3543
[10]
T cell memory: Heterogeneity and mechanisms [J].
Farber, DL .
CLINICAL IMMUNOLOGY, 2000, 95 (03) :173-181