Phase 1 clinical trials for sarcomas: the cutting edge

被引:30
作者
Subbiah, Vivek [1 ,2 ]
Kurzrock, Razelle [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Pediat, Houston, TX 77030 USA
[2] A Phase I Program, Dept Invest Canc Therapeut, Houston, TX USA
基金
美国国家卫生研究院;
关键词
bone tumors; phase; 1; trials; prognosis; sarcoma; sarcoma therapy; soft tissue sarcoma; targeted therapy; SOFT-TISSUE SARCOMA; IMATINIB; CANCER; TUMORS; NEOADJUVANT; THERAPIES; SELECTION;
D O I
10.1097/CCO.0b013e3283477a94
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review Few standard second-line treatment options exist for advanced sarcoma patients. Some of these patients are offered early-phase clinical trials involving targeted or nontargeted agents. This review outlines recent phase 1 trials involving sarcoma patients, explores current challenges and highlights future opportunities in sarcoma developmental therapeutics. Recent findings New molecularly targeted phase 1 studies have demonstrated efficacy in sarcomas. For instance, insulin-like growth factor-1 receptor (IGF1R) antibodies have produced single agent activity in Ewing's sarcoma. Other promising novel agents include an agonist for the apoptosis ligand 2/tumor necrosis factor-related apoptosis-inducing ligand (Apo2L/TRAIL) for chondrosarcoma, small molecule inhibitor crizotinib for anaplastic lymphoma kinase (ALK)-rearranged inflammatory myofibroblastic tumor, cedarinib for alveolar soft part sarcoma, and rexin-G, a tumor targeted retrovector for osteosarcoma. In addition, different combinations of chemotherapy in combination with newer agents such as trabectedin exhibited efficacy in advanced soft tissue sarcoma. Summary Patients with refractory sarcoma demonstrate benefit from treatment with targeted drugs even in the setting of phase 1 trials. Sarcomas that have a defined translocation and those that express specific activated kinases are particularly promising tumors for targeted therapy. The primary challenge is identifying the biomarkers predictive of response or resistance, matching them with specific patient histology, resulting in successful translation of biology into clinical benefit.
引用
收藏
页码:352 / 360
页数:9
相关论文
共 43 条
[1]   MIFAMURTIDE IN OSTEOSARCOMA-A PRACTICAL REVIEW [J].
Anderson, P. M. ;
Tomaras, M. ;
McConnell, K. .
DRUGS OF TODAY, 2010, 46 (05) :327-337
[2]  
[Anonymous], CONN TISS ONC SOC P
[3]  
[Anonymous], CANC CHEMOTHER PHARM
[4]  
[Anonymous], J CLIN ONCOL S
[5]  
[Anonymous], J CLIN ONCOL S
[6]  
[Anonymous], J CLIN ONCOL S
[7]   Prospective Validation of a Prognostic Score to Improve Patient Selection for Oncology Phase I Trials [J].
Arkenau, Hendrik-Tobias ;
Barriuso, Jorge ;
Olmos, David ;
Ang, Joo Ern ;
de Bono, Johann ;
Judson, Ian ;
Kaye, Stan .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (16) :2692-2696
[8]   Heat shock protein 90 inhibition in imatinib-resistant gastrointestinal stromal tumor [J].
Bauer, Sebastian ;
Yu, Lynn K. ;
Demetri, George D. ;
Fletcher, Jonathan A. .
CANCER RESEARCH, 2006, 66 (18) :9153-9161
[9]   Uncommon tumors and exceptional therapies: paradox or paradigm? [J].
Braiteh, Fadi ;
Kurzrock, Razelle .
MOLECULAR CANCER THERAPEUTICS, 2007, 6 (04) :1175-1179
[10]   Crizotinib in ALK-Rearranged Inflammatory Myofibroblastic Tumor [J].
Butrynski, James E. ;
D'Adamo, David R. ;
Hornick, Jason L. ;
Dal Cin, Paola ;
Antonescu, Cristina R. ;
Jhanwar, Suresh C. ;
Ladanyi, Marc ;
Capelletti, Marzia ;
Rodig, Scott J. ;
Ramaiya, Nikhil ;
Kwak, Eunice L. ;
Clark, Jeffrey W. ;
Wilner, Keith D. ;
Christensen, James G. ;
Jaenne, Pasi A. ;
Maki, Robert G. ;
Demetri, George D. ;
Shapiro, Geoffrey I. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (18) :1727-1733