Department of Radiation Oncology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
Institute of Radiation Medicine, Medical Research Center, Seoul National University, Seoul, Korea.
Cancer Res Treat. 2021 Oct;53(4):983-990. doi: 10.4143/crt.2020.1052. Epub 2021 Jan 13.
We aimed to refine the radiotherapy (RT) volume and dose for intracranial germinoma considering recurrences and long-term toxicities.
Total 189 patients with intracranial germinoma were treated with RT alone (n=50) and RT with upfront chemotherapy (CRT) (n=139). All cases were confirmed histologically. RT fields comprised the extended-field and involved-field only for primary site. The extended-field, including craniospinal, whole brain (WB), and whole ventricle (WV) for cranial field, is followed by involved-field boost. The median follow-up duration was 115 months.
The relapses developed in 13 patients (6.9%). For the extended-field, cranial RT dose down to 18 Gy exhibited no cranial recurrence in 34 patients. In CRT, 74 patients (56.5%) showed complete response to chemotherapy and no involved-field recurrence with low-dose RT of 30 Gy. WV RT with chemotherapy for the basal ganglia or thalamus germinoma showed no recurrence. Secondary malignancy developed in 10 patients (5.3%) with a latency of 20 years (range, 4 to 26 years) and caused mortalities in six. WB or craniospinal field rather than WV or involved-field significantly increased the rate of hormone deficiencies, and secondary malignancy. RT dose for extended-field correlated significantly with the rate of hormone deficiencies, secondary malignancy, and neurocognitive dysfunction.
De-intensifying extended-field rather than involved-field or total scheme of RT will be critical to decrease the late toxicities. Upfront chemotherapy could be beneficial for the patients with complete response to minimize the RT dose down to 30 Gy. Prospective trials focused on de-intensification of the extended-field RT are warranted.
考虑到复发和长期毒性,我们旨在细化颅内生殖细胞瘤的放疗(RT)体积和剂量。
共有 189 例颅内生殖细胞瘤患者接受单纯放疗(n=50)和放化疗(CRT)(n=139)治疗。所有病例均经组织学证实。放疗野包括原发部位的扩展野和累及野。扩展野包括颅脊髓、全脑(WB)和全脑室(WV),随后进行累及野加量。中位随访时间为 115 个月。
13 例(6.9%)患者出现复发。对于扩展野,34 例患者颅部 RT 剂量降至 18 Gy 时无颅部复发。在 CRT 中,74 例(56.5%)患者对化疗完全缓解,且低剂量 RT 30 Gy 无累及野复发。伴有化疗的基底节或丘脑生殖细胞瘤的 WV RT 无复发。10 例(5.3%)患者发生继发性恶性肿瘤,潜伏期为 20 年(范围 4 至 26 年),其中 6 例死亡。WB 或颅脊髓野而非 WV 或累及野显著增加了激素缺乏和继发性恶性肿瘤的发生率。扩展野的 RT 剂量与激素缺乏、继发性恶性肿瘤和神经认知功能障碍的发生率显著相关。
与降低累及野或全方案 RT 相比,降低扩展野 RT 的强度对于降低迟发性毒性至关重要。对于完全缓解的患者,化疗前治疗可能有助于将 RT 剂量降至 30 Gy 以下。需要进行前瞻性试验,重点关注降低扩展野 RT 的强度。