Liang Liping, Chen Lingchao, Ni Chunxia, Shi Wenyin, Zhou Zhirui, Chen Shu, Zhu Wenjia, Liu Jiabing, Qiu Xianxin, Lin Wanzun, Zhang Junyan, Qin Zhiyong, Wang Yang
Department of Radiation Oncology Center, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Chin Neurosurg J. 2025 Mar 7;11(1):5. doi: 10.1186/s41016-025-00391-w.
Tumor-treating fields (TTFields) therapy and radiotherapy may have synergistic anti-glioma effect based on preclinical studies. The combination of chemoradiation therapy (CRT) with TTFields therapy has noticeably attracted clinicians' attention. This study aimed to provide insights into the clinical outcomes of patients with newly diagnosed glioblastoma who received either concurrent CRT and TTFields therapy or adjuvant TTFields therapy following CRT. The findings were based on a cohort of patients who were treated at Huashan Hospital (Shanghai, China).
This retrospective study analyzed ndGBM patients' clinical outcomes who were treated at Huashan Hospital and received TTFields therapy. Patients were categorized into two groups: one group received adjuvant TTFields therapy after completing CRT (referred to as the A-TTF group), while the other received TTFields therapy concurrently with CRT and continued TTFields after treatment (referred to as the CA-TTF group). The study evaluated treatment efficacy and toxicities, comparing outcomes between the two groups. Overall survival (OS) and progression-free survival (PFS) were analyzed using the Kaplan-Meier method. To mitigate confounding factors, efficacy was assessed using the Cox proportional hazards regression model, propensity score matching, and inverse probability of treatment weighting (IPTW) based on the propensity score.
A total of 72 patients with ndGBM were included in the study. Among them, 41 patients received concurrent and adjuvant TTFields therapy in combination with CRT (CA-TTF group), and 31 patients received adjuvant TTFields therapy with temozolomide (A-TTF group). The median follow-up time was 18.0 months. No significant differences were observed in median PFS (14.2 vs. 15.0 months, P = 0.92) or OS (20.8 vs. 20.0 months, P = 0.92) between the CA-TTF and A-TTF groups. Skin toxicity was common, while manageable, with no significant difference between the two groups. Following IPTW adjustment, the hazard ratios for PFS and OS indicated a potential advantage for the CA-TTF group, although this difference was not statistically significant.
Concurrent CRT and TTFields therapy emerged safe for newly diagnosed GBM patients. Although no significant survival differences were found between the CA-TTF and A-TTF groups, the potential benefit of concurrent TTFields warrants further investigation through large-scale clinical trials.
基于临床前研究,肿瘤电场(TTFields)疗法与放射疗法可能具有协同抗胶质瘤作用。放化疗(CRT)联合TTFields疗法已显著引起临床医生的关注。本研究旨在深入了解新诊断的胶质母细胞瘤患者接受同步CRT与TTFields疗法或CRT后辅助TTFields疗法的临床结局。研究结果基于在华山医院(中国上海)接受治疗的一组患者。
这项回顾性研究分析了在华山医院接受TTFields疗法的新诊断胶质母细胞瘤患者的临床结局。患者分为两组:一组在完成CRT后接受辅助TTFields疗法(称为A-TTF组),另一组在CRT期间接受TTFields疗法并在治疗后继续接受TTFields疗法(称为CA-TTF组)。该研究评估了治疗效果和毒性,比较了两组之间的结局。采用Kaplan-Meier方法分析总生存期(OS)和无进展生存期(PFS)。为了减轻混杂因素的影响,基于倾向评分,使用Cox比例风险回归模型、倾向评分匹配和治疗权重逆概率(IPTW)评估疗效。
该研究共纳入72例新诊断胶质母细胞瘤患者。其中,41例患者接受同步和辅助TTFields疗法联合CRT(CA-TTF组),31例患者接受替莫唑胺辅助TTFields疗法(A-TTF组)。中位随访时间为18.0个月。CA-TTF组和A-TTF组之间在中位PFS(14.2对15.0个月,P = 0.92)或OS(20.8对20.0个月,P = 0.92)方面未观察到显著差异。皮肤毒性常见但可控,两组之间无显著差异。经过IPTW调整后,PFS和OS的风险比表明CA-TTF组具有潜在优势,尽管这种差异无统计学意义。
同步CRT和TTFields疗法对新诊断的胶质母细胞瘤患者是安全的。虽然CA-TTF组和A-TTF组之间未发现显著的生存差异,但同步TTFields疗法的潜在益处值得通过大规模临床试验进一步研究。