Gately Lucy, Drummond Katharine, Dowling Anthony, Bennett Iwan, Freilich Ronnie, Phillips Claire, Ahern Elizabeth, Campbell David, Dumas Megan, Campbell Robert, Harrup Rosemary, Kim Grace Y, Reeves Simone, Collins Ian M, Gibbs Peter
Personalised Oncology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3052, Australia.
Department of Medical Oncology, Alfred Health, Melbourne, VIC 3004, Australia.
Cancers (Basel). 2024 Oct 17;16(20):3514. doi: 10.3390/cancers16203514.
: Grade-2 gliomas (G2-glioma) are uncommon. In 2016, RTOG9802 established the addition of chemotherapy after radiation (CRT) as a new standard of care for patients with high-risk G2-glioma, defined as subtotal resection or age ≥40 yrs. Here, we report current practices using real-world data. : Patients diagnosed with G2-glioma from 1 January 2016 to 31 December 2022 were identified in BRAIN, a prospective clinical registry collecting data on patients with brain tumours. High- and low-risk were defined as per RTOG9802. Two time periods, January 2016-December 2019 (TP1) and January 2020-December 2022 (TP2), were defined. Survival was estimated using the Kaplan-Meier method. : 224 patients were identified. Overall, 38 (17%) were low-risk, with 35 (91%) observed without further treatment. A total of 186 (83%) were high-risk, with 96 (52%) observed, 63 (34%) receiving CRT, and 19 (10%) receiving radiation. Over time, CRT use increased (TP1 vs. TP2: 22% vs. 36%, = 0.004), and the rate of biopsy (TP1 vs. TP2: 35% vs. 20%, = 0.02) and radiotherapy alone (TP1 vs. TP2: 14% vs. 4%, = 0.01) decreased. Median progression-free survival (PFS) was significantly longer in high-risk patients who received CRT (NR) over observation (39 months) (HR 0.49, = 0.007). In high-risk patients who were observed, 59 (61%) were progression-free at 12 months and 10 (10%) at 5 years. OS data remains immature. : Congruent with RTOG9802, real-world BRAIN data shows CRT is associated with improved PFS compared to observation in high-risk G2-glioma. Whilst CRT use has increased over time, observation after surgery remains the most common strategy, with some high-risk patients achieving clinically meaningful PFS. Validated biomarkers are urgently required to better inform patient management.
2级胶质瘤(G2-胶质瘤)并不常见。2016年,放射治疗肿瘤学组(RTOG)9802试验确定了放疗后加用化疗(CRT)作为高危G2-胶质瘤患者的新治疗标准,高危定义为次全切除或年龄≥40岁。在此,我们报告基于真实世界数据的当前治疗实践。
在BRAIN(一个收集脑肿瘤患者数据的前瞻性临床登记系统)中识别出2016年1月1日至2022年12月31日期间诊断为G2-胶质瘤的患者。根据RTOG9802试验定义高风险和低风险。定义了两个时间段,2016年1月至2019年12月(时间段1)和2020年1月至2022年12月(时间段2)。使用Kaplan-Meier方法估计生存率。
共识别出224例患者。总体而言,38例(17%)为低风险,其中35例(91%)未接受进一步治疗。共有186例(83%)为高风险,其中96例(52%)接受观察,63例(34%)接受CRT,19例(10%)接受放疗。随着时间推移,CRT的使用增加(时间段1与时间段2:22%对36%,P = 0.004),活检率(时间段1与时间段2:35%对20%,P = 0.02)和单纯放疗率(时间段1与时间段2:14%对4%,P = 0.01)下降。接受CRT的高危患者的无进展生存期(PFS)中位数(未达到)显著长于接受观察的患者(39个月)(风险比0.49,P = 0.007)。在接受观察的高危患者中,59例(61%)在12个月时无进展,10例(10%)在5年时无进展。总生存期(OS)数据仍不成熟。
与RTOG9802试验一致,BRAIN真实世界数据显示,与高危G2-胶质瘤观察相比,CRT与改善的PFS相关。虽然CRT的使用随时间增加,但手术后观察仍是最常见的策略,一些高危患者实现了具有临床意义的PFS。迫切需要经过验证的生物标志物来更好地指导患者管理。