Rath G K, Sharma D N, Mallick S, Gandhi A K, Joshi N P, Haresh K P, Gupta S, Julka P K
Department of Radiation Oncology, Dr. B.R.A. IRCH, All India Institute of Medical Sciences, New Delhi, India.
Indian J Cancer. 2015 Oct-Dec;52(4):599-603. doi: 10.4103/0019-509X.178407.
The prognosis of primary gliosarcoma (PGS) remains dismal with current treatment modalities. We analyzed the outcome of PGS patients treated with concurrent and adjuvant temozolomide (TMZ).
Retrospective single institutional analysis.
We retrospectively evaluated 27 patients of PGS treated with radiotherapy (RT) and TMZ during 2007-2012.
Overall survival (OS) was estimated by the use of Kaplan Meier method and toxicities were evaluate using common terminology criteria for adverse events version 2.0 (National Cancer Institute, USA).
Median age at presentation and Karnofsky performance status was 45 years and 90 respectively and male: female ratio was 20:7. Patients received adjuvant RT to a total dose of 60 Gy at 2 Gy/fraction. All patients except 5 received adjuvant TMZ to a median number of 6 cycles. Grade 2 and 3 hematological toxicity was seen in 8% and 4% of patients respectively during concurrent RT. During adjuvant chemotherapy, 13.6% had Grade 3 thrombocytopenia and 9.5% had Grade 3 neutropenia. Median OS was 16.7 months (1 year and 2 year actuarial OS was 70.8% and 32.6% respectively). Adjuvant TMZ was associated with a better survival (median survival 21.21 vs. 11.93 months; P = 0.0046) on univariate analysis and also on multivariate analysis (hazard ratio 1.82, 95% confidence interval: 1.503-25.58; P = 0.012).
The results of our study, largest series of patients with PGS treated with concurrent and adjuvant TMZ shows an impressive survival with acceptable toxicity. We suggest TMZ be included in the "standard of care" for this tumor.
原发性胶质肉瘤(PGS)采用当前的治疗方式,预后依然很差。我们分析了接受同步和辅助替莫唑胺(TMZ)治疗的PGS患者的结局。
回顾性单机构分析。
我们回顾性评估了2007年至2012年间接受放疗(RT)和TMZ治疗的27例PGS患者。
采用Kaplan Meier法估计总生存期(OS),并使用美国国立癌症研究所不良事件通用术语标准2.0版评估毒性。
患者就诊时的中位年龄和卡氏评分分别为45岁和90,男女比例为20:7。患者接受辅助放疗,总剂量为60 Gy,每次2 Gy。除5例患者外,所有患者均接受辅助TMZ治疗,中位疗程为6个周期。同步放疗期间,分别有8%和4%的患者出现2级和3级血液学毒性。辅助化疗期间,13.6%的患者出现3级血小板减少,9.5%的患者出现3级中性粒细胞减少。中位OS为16.7个月(1年和2年实际OS分别为70.8%和32.6%)。单因素分析及多因素分析均显示,辅助TMZ与更好的生存期相关(中位生存期21.21个月对11.93个月;P = 0.0046)(多因素分析风险比1.82,95%置信区间:1.503 - 25.58;P = 0.012)。
我们的研究结果是最大系列接受同步和辅助TMZ治疗的PGS患者,显示出令人印象深刻的生存期且毒性可接受。我们建议将TMZ纳入该肿瘤的“标准治疗”。