Kim Michelle M, Camelo-Piragua Sandra, Schipper Matthew, Tao Yebin, Normolle Daniel, Junck Larry, Mammoser Aaron, Betz Bryan L, Cao Yue, Kim Christopher J, Heth Jason, Sagher Oren, Lawrence Theodore S, Tsien Christina I
Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
Department of Pathology, University of Michigan, Ann Arbor, Michigan.
Int J Radiat Oncol Biol Phys. 2016 Feb 1;94(2):305-11. doi: 10.1016/j.ijrobp.2015.10.032. Epub 2015 Nov 10.
To evaluate the tolerability and efficacy of gemcitabine plus radiation therapy (RT) in this phase 1 study of patients with newly diagnosed malignant glioma (HGG).
Between 2004 and 2012, 29 adults with HGG were enrolled. After any extent of resection, RT (60 Gy over 6 weeks) was given concurrent with escalating doses of weekly gemcitabine. Using a time-to-event continual reassessment method, 5 dose levels were evaluated starting at 500 mg/m(2) during the last 2 weeks of RT and advanced stepwise into earlier weeks. The primary objective was to determine the recommended phase 2 dose of gemcitabine plus RT. Secondary objectives included progression-free survival, overall survival (OS), and long-term toxicity.
Median follow-up was 38.1 months (range, 8.9-117.5 months); 24 patients were evaluable for toxicity. After 2005 when standard practice changed, patients with World Health Organization grade 4 tumors were no longer enrolled. Median progression-free survival for 22 patients with grade 3 tumors was 26.0 months (95% confidence interval [CI] 15.6-inestimable), and OS was 48.5 months (95% CI 26.8-inestimable). In 4 IDH mutated, 1p/19q codeleted patients, no failures occurred, with all but 1 alive at time of last follow-up. Seven with IDH mutated, non-codeleted tumors with ATRX loss had intermediate OS of 73.5 months (95% CI 32.8-inestimable). Six nonmutated, non-codeleted patients had a median OS of 26.5 months (95% CI 25.4-inestimable). The recommended phase 2 dose of gemcitabine plus RT was 750 mg/m(2)/wk given the last 4 weeks of RT. Dose reductions were most commonly due to grade 3 neutropenia; no grade 4 or 5 toxicities were seen.
Gemcitabine concurrent with RT is well-tolerated and yields promising outcomes, including in patients with adverse molecular features. It is a candidate for further study, particularly for poor-prognosis patient subgroups with HGG.
在这项针对新诊断的恶性胶质瘤(HGG)患者的1期研究中,评估吉西他滨联合放射治疗(RT)的耐受性和疗效。
2004年至2012年期间,纳入了29例HGG成年患者。在进行任何范围的切除术后,给予RT(6周内60 Gy),同时每周递增剂量的吉西他滨。使用事件发生时间连续重新评估方法,从RT的最后2周开始,以500 mg/m²为起始剂量,分5个剂量水平进行评估,并逐步提前至更早的周次。主要目标是确定吉西他滨联合RT的推荐2期剂量。次要目标包括无进展生存期、总生存期(OS)和长期毒性。
中位随访时间为38.1个月(范围8.9 - 117.5个月);24例患者可评估毒性。2005年标准做法改变后,不再纳入世界卫生组织4级肿瘤患者。22例3级肿瘤患者的中位无进展生存期为26.0个月(95%置信区间[CI] 15.6 - 无法估计),OS为48.5个月(95% CI 26.8 - 无法估计)。在4例异柠檬酸脱氢酶(IDH)突变、1p/19q共缺失的患者中,未发生疾病进展,除1例患者外,其余患者在最后一次随访时均存活。7例IDH突变、无共缺失且伴有ATRX缺失的肿瘤患者的中位OS为73.5个月(95% CI 32.8 - 无法估计)。6例非突变、无共缺失的患者的中位OS为26.5个月(95% CI 25.4 - 无法估计)。吉西他滨联合RT的推荐2期剂量为在RT的最后4周给予750 mg/m²/周。剂量减少最常见的原因是3级中性粒细胞减少;未观察到4级或5级毒性。
吉西他滨与RT联合应用耐受性良好,并产生了有前景的结果,包括在具有不良分子特征的患者中。它是进一步研究的候选药物,特别是对于HGG预后不良的患者亚组。