Bibault Jean-Emmanuel, Fumagalli Ingrid, Ferté Charles, Chargari Cyrus, Soria Jean-Charles, Deutsch Eric
Molecular Radiotherapy Laboratory, INSERM 1030, Faculté de médecine du Kremlin Bicêtre, Université Paris Sud XI, Institut Gustave Roussy, 114 rue Edouard Vaillant, 94805, Villejuif, France.
Cancer Metastasis Rev. 2013 Dec;32(3-4):479-92. doi: 10.1007/s10555-013-9419-7.
Radiosensitivity varies to a great extent across tumor types and also between patients bearing the same type of tumor. Radiation oncology pioneered the field of biomarkers with attempts to correlate tumor response to clonogenic survival, tumor potential doubling time (Tpot), and PaO₂. Biomarkers predicting the clinical outcome after radiotherapy are already available, but their levels of evidence are heterogeneous. In light of these molecular factors, the issue of personalized radiation therapy in combination or as a standalone modality is addressed. Known molecular prognostic and predictive biomarkers and their present or potential respective therapeutic implications are described for six tumor types where radiotherapy is considered to be part of the mainstay: chemoradiation (e.g., gliomas, head and neck, cervical cancer), radiotherapy with or without androgen deprivation (e.g., prostate), neo-adjuvant chemoradiation (e.g., rectum), or adjuvant radiotherapy (e.g., breast).
不同肿瘤类型之间以及患有相同类型肿瘤的患者之间,放射敏感性差异很大。放射肿瘤学开创了生物标志物领域,试图将肿瘤反应与克隆源性存活、肿瘤潜在倍增时间(Tpot)和PaO₂联系起来。预测放疗后临床结果的生物标志物已经存在,但其证据水平参差不齐。鉴于这些分子因素,探讨了个性化放射治疗作为联合治疗手段或单独治疗方式的问题。针对六种被认为放疗是主要治疗手段一部分的肿瘤类型,描述了已知的分子预后和预测生物标志物及其目前或潜在的各自治疗意义:同步放化疗(如胶质瘤、头颈部癌、宫颈癌)、联合或不联合雄激素剥夺的放疗(如前列腺癌)、新辅助同步放化疗(如直肠癌)或辅助放疗(如乳腺癌)。