Patient-Derived Xenografts for Individualized Care in Advanced Sarcoma

被引:143
作者
Stebbing, Justin [1 ,2 ]
Paz, Keren [3 ]
Schwartz, Gary K. [4 ]
Wexler, Leonard H. [4 ]
Maki, Robert [5 ]
Pollock, Raphael E. [6 ]
Morris, Ronnie [3 ]
Cohen, Richard [7 ]
Shankar, Arjun [7 ]
Blackman, Glen [8 ]
Harding, Victoria [1 ,2 ]
Vasquez, David [3 ]
Krell, Jonathan [1 ,2 ]
Ciznadija, Daniel [3 ]
Katz, Amanda [3 ]
Sidransky, David [9 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Oncol, London W12 0NN, England
[2] Hammersmith Hosp, Imperial Healthcare Natl Hlth Serv Trust, London, England
[3] Champ Oncol, Dept Oncol, Baltimore, MD USA
[4] Mem Sloan Kettering Canc Ctr, Dept Oncol, New York, NY 10021 USA
[5] Mt Sinai Sch Med, Dept Oncol, New York, NY USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Oncol, Houston, TX 77030 USA
[7] Univ Coll London Hosp, Dept Surg, London, England
[8] Univ Coll London Hosp, Dept Radiotherapy, London, England
[9] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
关键词
sarcoma; prediction; biomarker; response; chemotherapy; trial; mice; TumorGraft; CANCER CELL-LINES; SYNOVIAL SARCOMA; GENE-EXPRESSION; HETEROGENEITY; RESISTANCE; CETUXIMAB; EVOLUTION; INSIGHTS; DISEASE; TUMORS;
D O I
10.1002/cncr.28696
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Patients with advanced, metastatic sarcoma have a poor prognosis, and the overall benefit from the few standard-of-care therapeutics available is small. The rarity of this tumor, combined with the wide range of subtypes, leads to difficulties in conducting clinical trials. The authors previously reported the outcome of patients with a variety of common solid tumors who received treatment with drug regimens that were first tested in patient-derived xenografts using a proprietary method ("TumorGrafts"). METHODS: Tumors resected from 29 patients with sarcoma were implanted into immunodeficient mice to identify drug targets and drugs for clinical use. The results of drug sensitivity testing in the TumorGrafts were used to personalize cancer treatment. RESULTS: Of 29 implanted tumors, 22 (76%) successfully engrafted, permitting the identification of treatment regimens for these patients. Although 6 patients died before the completion of TumorGraft testing, a correlation between TumorGraft results and clinical outcome was observed in 13 of 16 (81%) of the remaining individuals. No patients progressed during the TumorGraft-predicted therapy. CONCLUSIONS: The current data support the use of the personalized TumorGraft model as an investigational platform for therapeutic decision-making that can guide treatment for rare tumors such as sarcomas. A randomized phase 3 trial versus physician's choice is warranted. (C) 2014 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society.
引用
收藏
页码:2006 / 2015
页数:10
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