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保骨髓强度调制放疗同步顺铂治疗 IB-IVA 期宫颈癌的国际多中心 II 期临床试验(INTERTECC-2)。

Bone Marrow-sparing Intensity Modulated Radiation Therapy With Concurrent Cisplatin For Stage IB-IVA Cervical Cancer: An International Multicenter Phase II Clinical Trial (INTERTECC-2).

机构信息

Department of Radiation Medicine and Applied Sciences, University of California, San Diego, La Jolla, California.

Department of Oncology and Radiotherapy, University Hospital, Hradec Kralove, Czech Republic.

出版信息

Int J Radiat Oncol Biol Phys. 2017 Mar 1;97(3):536-545. doi: 10.1016/j.ijrobp.2016.11.027. Epub 2016 Nov 23.

Abstract

PURPOSE

To test the hypothesis that intensity modulated radiation therapy (IMRT) reduces acute hematologic and gastrointestinal (GI) toxicity for patients with locoregionally advanced cervical cancer.

METHODS AND MATERIALS

We enrolled patients with stage IB-IVA cervical carcinoma in a single-arm phase II trial involving 8 centers internationally. All patients received weekly cisplatin concurrently with once-daily IMRT, followed by intracavitary brachytherapy, as indicated. The primary endpoint was the occurrence of either acute grade ≥3 neutropenia or clinically significant GI toxicity within 30 days of completing chemoradiation therapy. A preplanned subgroup analysis tested the hypothesis that positron emission tomography-based image-guided IMRT (IG-IMRT) would lower the risk of acute neutropenia. We also longitudinally assessed patients' changes in quality of life.

RESULTS

From October 2011 to April 2015, 83 patients met the eligibility criteria and initiated protocol therapy. The median follow-up was 26.0 months. The incidence of any primary event was 26.5% (95% confidence interval [CI] 18.2%-36.9%), significantly lower than the 40% incidence hypothesized a priori from historical data (P=.012). The incidence of grade ≥3 neutropenia and clinically significant GI toxicity was 19.3% (95% CI 12.2%-29.0%) and 12.0% (95% CI 6.7%-20.8%), respectively. Compared with patients treated without IG-IMRT (n=48), those treated with IG-IMRT (n=35) had a significantly lower incidence of grade ≥3 neutropenia (8.6% vs 27.1%; 2-sided χP=.035) and nonsignificantly lower incidence of grade ≥3 leukopenia (25.7% vs 41.7%; P=.13) and any grade ≥3 hematologic toxicity (31.4% vs 43.8%; P=.25).

CONCLUSIONS

IMRT reduces acute hematologic and GI toxicity compared with standard treatment, with promising therapeutic outcomes. Positron emission tomography IG-IMRT reduces the incidence of acute neutropenia.

摘要

目的

检验调强放疗(IMRT)可降低局部晚期宫颈癌患者急性血液学和胃肠道(GI)毒性这一假说。

方法和材料

我们在一项涉及 8 个国际中心的单臂 II 期试验中纳入了 IB-IVA 期宫颈癌患者。所有患者均接受每周顺铂同步每日一次 IMRT,视情况给予腔内近距离放疗。主要终点是放化疗结束后 30 天内发生任何急性 3 级以上中性粒细胞减少症或有临床意义的 GI 毒性。一项预先计划的亚组分析检验了基于正电子发射断层扫描的图像引导调强放疗(IG-IMRT)可降低急性中性粒细胞减少症风险的假说。我们还对患者的生活质量变化进行了纵向评估。

结果

从 2011 年 10 月至 2015 年 4 月,符合纳入标准并开始接受方案治疗的患者共 83 例。中位随访时间为 26.0 个月。任何主要事件的发生率为 26.5%(95%置信区间 [CI] 18.2%-36.9%),显著低于从历史数据预先假设的 40%发生率(P=.012)。3 级以上中性粒细胞减少症和有临床意义的 GI 毒性的发生率分别为 19.3%(95% CI 12.2%-29.0%)和 12.0%(95% CI 6.7%-20.8%)。与未接受 IG-IMRT 治疗的患者(n=48)相比,接受 IG-IMRT 治疗的患者(n=35)3 级以上中性粒细胞减少症的发生率显著降低(8.6% vs 27.1%;双侧 χ2 P=.035),3 级以上白细胞减少症(25.7% vs 41.7%;P=.13)和任何等级 3 级以上血液学毒性(31.4% vs 43.8%;P=.25)的发生率均无显著降低。

结论

与标准治疗相比,IMRT 可降低急性血液学和 GI 毒性,具有有前景的治疗结果。正电子发射断层扫描 IG-IMRT 可降低急性中性粒细胞减少症的发生率。

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