Shields Lisa B E, Kadner Robert, Vitaz Todd W, Spalding Aaron C
Radiat Oncol. 2013 Apr 25;8:101. doi: 10.1186/1748-717X-8-101.
We investigated the pattern of failure in glioblastoma multiforma (GBM) patients treated with concurrent radiation, bevacizumab (BEV), and temozolomide (TMZ). Previous studies demonstrated a predominantly in-field pattern of failure for GBM patients not treated with concurrent BEV.
We reviewed the treatment of 23 patients with GBM who received 30 fractions of simultaneous integrated boost IMRT. PTV60 received 2 Gy daily to the tumor bed or residual tumor while PTV54 received 1.8 Gy daily to the surrounding edema. Concurrent TMZ (75 mg/m^2) daily and BEV (10 mg/kg every 2 weeks) were given during radiation therapy. One month after RT completion, adjuvant TMZ (150 mg/m^2 × 5 days) and BEV were delivered monthly until progression or 12 months total.
With a median follow-up of 12 months, the median disease-free and overall survival were not reached. Four patients discontinued therapy due to toxicity for the following reasons: bone marrow suppression (2), craniotomy wound infection (1), and pulmonary embolus (1). Five patients had grade 2 or 3 hypertension managed by oral medications. Of the 12 patients with tumor recurrence, 7 suffered distant failure with either subependymal (5/12; 41%) or deep white matter (2/12; 17%) spread detected on T2 FLAIR sequences. Five of 12 patients (41%) with a recurrence demonstrated evidence of GAD enhancement. The patterns of failure did not correlate with extent of resection or number of adjuvant cycles.
Treatment of GBM patients with concurrent radiation, BEV, and TMZ was well tolerated in the current study. The majority of patients experienced an out-of-field pattern of failure with radiation, BEV, and TMZ which has not been previously reported. Further investigation is warranted to determine whether BEV alters the underlying tumor biology to improve survival. These data may indicate that the currently used clinical target volume thought to represent microscopic disease for radiation may not be appropriate in combination with TMZ and BEV.
我们研究了接受同步放疗、贝伐单抗(BEV)和替莫唑胺(TMZ)治疗的多形性胶质母细胞瘤(GBM)患者的失败模式。先前的研究表明,未接受同步BEV治疗的GBM患者主要表现为野内失败模式。
我们回顾了23例接受30次同步整合加量调强放疗(IMRT)的GBM患者的治疗情况。计划靶区(PTV)60每天接受2 Gy照射肿瘤床或残留肿瘤,而PTV54每天接受1.8 Gy照射周围水肿区。放疗期间同时给予TMZ(75 mg/m²)和BEV(每2周10 mg/kg)。放疗结束1个月后,给予辅助TMZ(150 mg/m²×5天),BEV每月给药,直至病情进展或共12个月。
中位随访12个月,无病生存期和总生存期的中位数均未达到。4例患者因毒性反应停药,原因如下:骨髓抑制(2例)、开颅伤口感染(1例)和肺栓塞(1例)。5例患者出现2级或3级高血压,通过口服药物控制。在12例肿瘤复发患者中,7例出现远处失败,在T2液体衰减反转恢复(FLAIR)序列上检测到室管膜下(5/12;41%)或深部白质(2/12;17%)扩散。12例复发患者中有5例(41%)显示有钆增强磁共振成像(GAD)强化证据。失败模式与切除范围或辅助周期数无关。
在本研究中GBM患者接受同步放疗、BEV和TMZ治疗耐受性良好。大多数患者出现放疗、BEV和TMZ野外失败模式,这在以前尚未报道。有必要进一步研究以确定BEV是否改变潜在肿瘤生物学特性以提高生存率。这些数据可能表明,目前用于代表放疗微观病变的临床靶区与TMZ和BEV联合使用时可能不合适。