Fogh Shannon E, Boreta Lauren, Nakamura Jean L, Johnson Derek R, Chi Andrew S, Kurz Sylvia C
Department of Radiation Oncology, University of California, San Francisco, CA, USA.
Department of Radiology, Mayo Clinic, Rochester, MN, USA.
Neurooncol Pract. 2020 Jun 27;8(1):11-17. doi: 10.1093/nop/npaa037. eCollection 2021 Feb.
Advances in treatment of oligodendroglioma represent arguably the most significant recent development in the treatment of brain tumors, with multiple clinical trials demonstrating that median survival is approximately doubled in patients with World Health Organization grade II and III 1p/19q codeleted gliomas (ie, oligodendrogliomas) treated with procarbazine, lomustine, vincristine chemotherapy and radiation vs radiation alone. However, chemoradiotherapy itself is not without morbidity, including both short-term toxicities primarily related to chemotherapy and longer-term cognitive issues likely due to radiation. Patients and physicians both desire maximally effective therapy with minimal toxicity, and it remains unclear whether some patients with macroscopic residual disease after surgery can safely delay therapy, to avoid or delay toxicity, while simultaneously preserving the full benefits of treatment. In this article, experts in the field discuss the rationale for the approaches of up-front treatment with chemoradiotherapy and initial observation, respectively.
少突胶质细胞瘤治疗方面的进展可以说是近期脑肿瘤治疗领域最重大的发展,多项临床试验表明,对于世界卫生组织二级和三级1p/19q共缺失型胶质瘤(即少突胶质细胞瘤)患者,接受丙卡巴肼、洛莫司汀、长春新碱化疗及放疗的患者中位生存期较单纯接受放疗的患者延长了约一倍。然而,放化疗本身并非没有不良反应,包括主要与化疗相关的短期毒性以及可能由放疗导致的长期认知问题。患者和医生都希望采用毒性最小而疗效最佳的治疗方法,目前尚不清楚部分术后有肉眼可见残留病灶的患者能否安全地推迟治疗,以避免或延缓毒性反应,同时又能保留治疗的全部益处。在本文中,该领域的专家分别讨论了放化疗 upfront 治疗和初始观察这两种方法的理论依据。