Vivek Subbiah, Megan Othus, Jim Palma, Branko Cuglievan, Razelle Kurzrock
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引用次数: 0
摘要
罕见癌症研究领域正在迅速转变,临床试验和治疗策略取得了重大进展。根据美国国家癌症研究所(National Cancer Institute)的定义,每年每百万人中发生的罕见癌症病例不到150例,但它们在所有癌症诊断中占了很大一部分。由于发病率低,这些癌症给临床试验带来了明显的挑战,包括患者群体有限、地理分散以及普遍缺乏对治疗方案的认识。经济限制进一步使药物开发复杂化,使得《孤儿药法案》等举措对激励研究至关重要。新一代测序(NGS)和精准医学的出现有助于识别可操作的基因改变,同时基因组靶向治疗、免疫治疗和抗体药物偶联物的发展也呈爆炸式增长。临床NGS、精准医学和肿瘤不可知论疗法的进步已经成为罕见癌症研究进展的核心。肿瘤不确定药物的开发和批准,如BRAF、NTRK和RET抑制剂,以及错配修复缺陷/微卫星不稳定高状态癌症的免疫治疗,突出了跨不同癌症类型和跨年龄谱的个性化治疗潜力。来自SWOG DART、ASCO TAPUR、NCI-MATCH、儿科COG-match、DRUP、IMPRESS、创新注册篮子和平台试验(如VE-Basket、ROAR、libreto -001、ARROW)等合作小组的合作试验,以及TRACK等患者倡导小组开展的试验,正在提高临床试验的可及性。此外,人工智能有可能改善审判匹配过程。将这些创新与多个利益攸关方合作结合起来的综合方法对于推进罕见癌症研究至关重要,为改善患者预后和生活质量带来了希望。
Designing Clinical Trials for Patients With Rare Cancers: Connecting the Zebras.
The field of rare cancer research is rapidly transforming, marked by significant progress in clinical trials and treatment strategies. Rare cancers, as defined by the National Cancer Institute, occur in fewer than 150 cases per million people each year, yet they collectively represent a significant portion of all cancer diagnoses. Because of their infrequency, these cancers pose distinct challenges for clinical trials, including limited patient populations, geographical dispersion, and a general lack of awareness of treatment options. Economic limitations further complicate drug development, making initiatives such as the Orphan Drug Act essential for incentivizing research. The advent of next-generation sequencing (NGS) and precision medicine has been instrumental in identifying actionable genetic alterations in parallel with an explosion in the development of genomically targeted therapies, immunotherapies, and antibody drug conjugates. Advances in clinical NGS, precision medicine, and tumor-agnostic therapies have become central to the progress in rare cancer research. The development and approval of tumor-agnostic drugs, such as BRAF, NTRK, and RET inhibitors, and immunotherapy for mismatch repair deficient/microsatellite instability-high status cancers highlight the potential of personalized treatments across diverse cancer types and across the age spectrum. Collaborative trials from cooperative groups including SWOG DART, ASCO TAPUR, NCI-MATCH, pediatric COG-match, DRUP, IMPRESS, and innovative registrational basket and platform trials (eg, VE-Basket, ROAR, LIBRETTO-001, ARROW), along with patient advocacy group-run trials like TRACK, are enhancing access to clinical trials. In addition, artificial intelligence has the potential to improve the trial matching process. An integrated approach, combining these innovations in collaboration with multiple stakeholders, is crucial for advancing rare cancer research, offering hope for better patient outcomes and quality of life.
期刊介绍:
The Ed Book is a National Library of Medicine–indexed collection of articles written by ASCO Annual Meeting faculty and invited leaders in oncology. Ed Book was launched in 1985 to highlight standards of care and inspire future therapeutic possibilities in oncology. Published annually, each volume highlights the most compelling research and developments across the multidisciplinary fields of oncology and serves as an enduring scholarly resource for all members of the cancer care team long after the Meeting concludes. These articles address issues in the following areas, among others: Immuno-oncology, Surgical, radiation, and medical oncology, Clinical informatics and quality of care, Global health, Survivorship.