Clinical Studies With Anti-CTLA-4 Antibodies in Non-melanoma Indications

被引:47
作者
Calabro, Luana [1 ]
Danielli, Riccardo [1 ,2 ]
Sigalotti, Luca [2 ]
Maio, Michele [1 ,2 ]
机构
[1] Univ Hosp Siena, Div Med Oncol & Immunotherapy, Dept Oncol, Ist Toscano Tumori, I-53100 Siena, Italy
[2] Ist Ricovero & Cura Carattere Sci, Canc Bioimmunotherapy Unit, Dept Med Oncol, Ctr Riferimento Oncol, Aviano, Italy
关键词
PHASE-II; CTLA-4; BLOCKADE; CANCER; TREMELIMUMAB; COMBINATION; MODULATION; THERAPY; TRIAL;
D O I
10.1053/j.seminoncol.2010.09.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Available medical treatments have limited impact on the survival of patients with advanced cancer; therefore, new therapeutic strategies able to generate more effective host's immune responses against neoplastic cells are being actively pursued. Among these, a recent approach involves targeting of cytotoxic T-lymphocyte antigen-4 (CTLA-4), a key immune checkpoint molecule, by monoclonal antibodies (mAbs). Ipilimumab and tremelimumab represent the prototypes of this new class of immunomodulating mAb and have been extensively tested in metastatic melanoma with highly promising results. The clinical activity observed in melanoma has served as a model to exploit the therapeutic potential of CTLA-4 blockade in a variety of human malignancies. Along this line, early-phase trials with anti-CTLA-4 mAbs have been completed or are ongoing in tumors of different histotype. Results are demonstrating the feasibility, safety, and activity of these agents, thus suggesting a promising therapeutic role to be further investigated in phase II/III trials in a wide range of tumors. This review summarizes the main trials with ipilimumab and tremelimumab in tumors of different histotypes, excluding cutaneous melanoma, which is extensively described in other chapters of this issue of Seminars in Oncology. Semin Oncol 37:460-467 (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:460 / 467
页数:8
相关论文
共 35 条
  • [21] Gerritsen W, 2006, J CLIN ONCOL, V24, p100S
  • [22] GORDON MS, 2009, J CLIN ONCOL S, V27, pNI436
  • [23] Harzstark AL, 2010, J CLIN ONCOL, V28
  • [24] Overall survival (OS) analysis of a phase I trial of a vector-based vaccine (PSA-TRICOM) and ipilimumab (lpi) in the treatment of metastatic castration-resistant prostate cancer (mCRPC)
    Madan, R. A.
    Mohebtash, M.
    Arlen, P. M.
    Vergati, M.
    Steinberg, S. M.
    Tsang, K. Y.
    Dahut, W. L.
    Schlom, J.
    Gulley, J. L.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
  • [25] Integrated Positron Emission Tomography/Computed Tomography May Render Bone Scintigraphy Unnecessary to Investigate Suspected Metastatic Breast Cancer
    Morris, Patrick G.
    Lynch, Colleen
    Feeney, John N.
    Patil, Sujata
    Howard, Jane
    Larson, Steven M.
    Dickler, Maura
    Hudis, Clifford A.
    Jochelson, Maxine
    McArthur, Heather L.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (19) : 3154 - 3159
  • [26] Modulation of Lymphocyte Regulation for Cancer Therapy: A Phase II Trial of Tremelimumab in Advanced Gastric and Esophageal Adenocarcinoma
    Ralph, Christy
    Elkord, Eyad
    Burt, Deborah J.
    O'Dwyer, Jackie F.
    Austin, Eric B.
    Stern, Peter L.
    Hawkins, Robert E.
    Thistlethwaite, Fiona C.
    [J]. CLINICAL CANCER RESEARCH, 2010, 16 (05) : 1662 - 1672
  • [27] Do We Need a Different Set of Response Assessment Criteria for Tumor Immunotherapy?
    Ribas, Antoni
    Chmielowski, Bartosz
    Glaspy, John A.
    [J]. CLINICAL CANCER RESEARCH, 2009, 15 (23) : 7116 - 7118
  • [28] ROSAI J, 2004, ROSAIACKERMANS SURG, V1
  • [29] Slovin SF, 2009, J CLIN ONCOL, V27
  • [30] Small E, 2006, J CLIN ONCOL, V24, p243S