1 Children's Cancer Research Unit, Kid's Research Institute, The Children's Hospital at Westmead, Westmead, NSW, Australia ; 2 Oncology Department, The Children's Hospital at Westmead, Westmead, NSW, Australia ; 3 Sydney Medical School, University of Sydney, Sydney, NSW, Australia.
Transl Pediatr. 2014 Apr;3(2):156-82. doi: 10.3978/j.issn.2224-4336.2014.02.01.
Four out of five children diagnosed with cancer can be cured with contemporary cancer therapy. This represents a dramatic improvement since 50 years ago when the cure rate of childhood cancer was <25% in the pre-chemotherapy era. Over the past ten years, while improvement in overall survival (OS) has been marginal, progress in pediatric oncology lies with adopting risk-adapted therapeutic approach. This has been made possible through identifying clinical and biologic prognostic factors with rigorous research and stratifying patients using these risk factors, and subsequently modifying therapy according to risk group assignment. This review provides a perspective for eight distinct pediatric malignancies, in which significant advances in treatment were made in the last decade and are leading to changes in standard of care. This includes four hematologic malignancies [acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), non-Hodgkin lymphoma (NHL) and Hodgkin lymphoma (HL)] and four solid tumors [medulloblastoma (MB), low grade glioma (LGG), neuroblastoma (NB) and Ewing sarcoma (ES)]. Together, they comprise 60% of childhood cancer. Improved patient outcome is not limited to better survival, but encompasses reducing both short and long-term treatment-related complications which is as important as cure, given the majority of childhood cancer patients will become long-term survivors. Risk-adapted approach allows treatment intensification in the high-risk cohort while therapy can be de-escalated in the low-risk to minimize toxicity and late sequelae without compromising survival. Advances in medical research technology have also led to a rapid increase in the understanding of the genetics of childhood cancer in the last decade, facilitating identification of molecular targets that can potentially be exploited for therapeutic benefits. As we move into the era of targeted therapeutics, searching for novel agents that target specific genetic lesions becomes a major research focus. We provide an overview of seven novel agents (bevacizumab, bortezomib, vorinostat, sorafenib, tipifarnib, erlotinib and mTOR inhibitors), which have been most frequently pursued in childhood cancers in the last decade, as well as reporting the progress of clinical trials involving these agents.
目前,有五分之四的儿童癌症患者可以通过现代癌症疗法得到治愈。这与 50 年前相比有了显著的改善,当时在化疗前时代,儿童癌症的治愈率<25%。在过去的十年中,尽管总体生存率(OS)的提高微不足道,但儿科肿瘤学的进展在于采用了风险适应的治疗方法。这是通过严格的研究确定临床和生物学预后因素,并对患者进行分层,根据风险因素分配风险组,随后根据风险组分配修改治疗方案来实现的。这篇综述提供了八个不同儿科恶性肿瘤的视角,在过去十年中,这些肿瘤在治疗方面取得了显著进展,并正在改变标准治疗方法。这包括四种血液系统恶性肿瘤[急性淋巴细胞白血病(ALL)、急性髓细胞白血病(AML)、非霍奇金淋巴瘤(NHL)和霍奇金淋巴瘤(HL)]和四种实体瘤[髓母细胞瘤(MB)、低级别胶质瘤(LGG)、神经母细胞瘤(NB)和尤文肉瘤(ES)]。它们共同构成了 60%的儿童癌症。改善患者的预后不仅限于提高生存率,还包括减少短期和长期与治疗相关的并发症,这与治愈一样重要,因为大多数儿童癌症患者将成为长期幸存者。风险适应治疗方法允许高危患者组的治疗强化,同时可以在低危患者组中降低治疗强度,以最小化毒性和长期后遗症,而不影响生存率。医学研究技术的进步也使得过去十年中儿童癌症的遗传学研究迅速增加,有助于确定潜在的分子靶点,从而为治疗带来益处。随着我们进入靶向治疗时代,寻找针对特定遗传病变的新型药物成为主要的研究重点。我们概述了过去十年中在儿童癌症中最常探索的七种新型药物(贝伐单抗、硼替佐米、伏立诺他、索拉非尼、替匹法尼、厄洛替尼和 mTOR 抑制剂),并报告了涉及这些药物的临床试验进展。