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Mifamurtide in metastatic and recurrent osteosarcoma: a patient access study with pharmacokinetic, pharmacodynamic, and safety assessments.转移性和复发性骨肉瘤中的米伐木肽:一项具有药代动力学、药效学和安全性评估的患者准入研究。
Pediatr Blood Cancer. 2014 Feb;61(2):238-44. doi: 10.1002/pbc.24686. Epub 2013 Aug 31.
2
Breast cancer metastasis: issues for the personalization of its prevention and treatment.乳腺癌转移:个性化预防和治疗的问题。
Am J Pathol. 2013 Oct;183(4):1084-1095. doi: 10.1016/j.ajpath.2013.06.012. Epub 2013 Jul 26.
3
A review of targeted therapies evaluated by the pediatric preclinical testing program for osteosarcoma.骨肉瘤儿科临床前检测计划评估的靶向治疗综述。
Front Oncol. 2013 May 31;3:132. doi: 10.3389/fonc.2013.00132. eCollection 2013.
4
Biomarker-driven trial in metastatic pancreas cancer: feasibility in a multicenter study of saracatinib, an oral Src inhibitor, in previously treated pancreatic cancer.生物标志物驱动的转移性胰腺癌试验:在先前治疗的胰腺癌中,口服Src 抑制剂 saracatinib 的多中心研究中的可行性。
Cancer Med. 2012 Oct;1(2):207-17. doi: 10.1002/cam4.27. Epub 2012 Aug 16.
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Pathways of metastasizing intestinal cancer cells revealed: how will fighting metastases at the site of cancer cell arrest affect drug development?揭示了转移性肠癌细胞的转移途径:在癌细胞停滞部位对抗转移将如何影响药物开发?
Future Oncol. 2013 Jan;9(1):1-4. doi: 10.2217/fon.12.163.
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Genetically engineered mouse models and human osteosarcoma.基因工程小鼠模型与人类骨肉瘤
Clin Sarcoma Res. 2012 Oct 4;2(1):19. doi: 10.1186/2045-3329-2-19.
7
Perspective: The right trials.观点:正确的试验。
Nature. 2012 May 30;485(7400):S58-9. doi: 10.1038/485S58a.
8
Metastasis: The rude awakening.转移:如梦初醒。
Nature. 2012 May 30;485(7400):S55-7. doi: 10.1038/485S55a.
9
The translational landscape of mTOR signalling steers cancer initiation and metastasis.mTOR 信号转导的翻译景观指导癌症的发生和转移。
Nature. 2012 Feb 22;485(7396):55-61. doi: 10.1038/nature10912.
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Cancer dormancy: a model of early dissemination and late cancer recurrence.癌症休眠:早期播散和晚期癌症复发的模型。
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走向一条针对骨肉瘤转移进展的药物研发之路。

Toward a drug development path that targets metastatic progression in osteosarcoma.

作者信息

Khanna Chand, Fan Timothy M, Gorlick Richard, Helman Lee J, Kleinerman Eugenie S, Adamson Peter C, Houghton Peter J, Tap William D, Welch Danny R, Steeg Patricia S, Merlino Glenn, Sorensen Poul H B, Meltzer Paul, Kirsch David G, Janeway Katherine A, Weigel Brenda, Randall Lor, Withrow Stephen J, Paoloni Melissa, Kaplan Rosandra, Teicher Beverly A, Seibel Nita L, Smith Malcolm, Uren Aykut, Patel Shreyaskumar R, Trent Jeffrey, Savage Sharon A, Mirabello Lisa, Reinke Denise, Barkaukas Donald A, Krailo Mark, Bernstein Mark

机构信息

Molecular Oncology Section, Metastasis Biology; Center for Cancer Research; National Cancer Institute, NIH, Bethesda, Maryland;

Department of Veterinary Clinical Medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois;

出版信息

Clin Cancer Res. 2014 Aug 15;20(16):4200-9. doi: 10.1158/1078-0432.CCR-13-2574. Epub 2014 May 6.

DOI:10.1158/1078-0432.CCR-13-2574
PMID:24803583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4134738/
Abstract

Despite successful primary tumor treatment, the development of pulmonary metastasis continues to be the most common cause of mortality in patients with osteosarcoma. A conventional drug development path requiring drugs to induce regression of established lesions has not led to improvements for patients with osteosarcoma in more than 30 years. On the basis of our growing understanding of metastasis biology, it is now reasonable and essential that we focus on developing therapeutics that target metastatic progression. To advance this agenda, a meeting of key opinion leaders and experts in the metastasis and osteosarcoma communities was convened in Bethesda, Maryland. The goal of this meeting was to provide a "Perspective" that would establish a preclinical translational path that could support the early evaluation of potential therapeutic agents that uniquely target the metastatic phenotype. Although focused on osteosarcoma, the need for this perspective is shared among many cancer types. The consensus achieved from the meeting included the following: the biology of metastatic progression is associated with metastasis-specific targets/processes that may not influence grossly detectable lesions; targeting of metastasis-specific processes is feasible; rigorous preclinical data are needed to support translation of metastasis-specific agents into human trials where regression of measurable disease is not an expected outcome; preclinical data should include an understanding of mechanism of action, validation of pharmacodynamic markers of effective exposure and response, the use of several murine models of effectiveness, and where feasible the inclusion of the dog with naturally occurring osteosarcoma to define the activity of new drugs in the micrometastatic disease setting.

摘要

尽管原发性肿瘤治疗取得成功,但肺转移的发生仍然是骨肉瘤患者最常见的死亡原因。传统的药物研发路径要求药物诱导已形成的病灶消退,然而30多年来,这一路径并未给骨肉瘤患者带来改善。基于我们对转移生物学认识的不断加深,现在我们合理且有必要专注于开发针对转移进展的治疗方法。为推动这一议程,在马里兰州贝塞斯达召开了一次由转移和骨肉瘤领域的关键意见领袖及专家参加的会议。本次会议的目标是提供一种“视角”,确立一条临床前转化路径,以支持对独特靶向转移表型的潜在治疗药物进行早期评估。尽管该视角聚焦于骨肉瘤,但许多癌症类型都有这样的需求。会议达成的共识包括:转移进展的生物学与转移特异性靶点/过程相关,这些靶点/过程可能不会影响可明显检测到的病灶;靶向转移特异性过程是可行的;需要严格的临床前数据来支持将转移特异性药物转化为人体试验,在人体试验中,可测量疾病的消退并非预期结果;临床前数据应包括对作用机制的理解、有效暴露和反应的药效学标志物的验证、使用多种有效的小鼠模型,以及在可行的情况下纳入患有自然发生骨肉瘤的犬只,以确定新药在微转移疾病环境中的活性。