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调强放疗联合碳离子推量治疗涎腺癌:COSMIC 试验的中期分析。

IMRT and carbon ion boost for malignant salivary gland tumors: interim analysis of the COSMIC trial.

机构信息

Department of Radiation Oncology, University of Heidelberg, Heidelberg, Germany.

出版信息

BMC Cancer. 2012 May 2;12:163. doi: 10.1186/1471-2407-12-163.

Abstract

BACKGROUND

The COSMIC trial is designed to evaluate toxicity in dose-escalated treatment with intensity-modulated radiotherapy (IMRT) and carbon ion boost for malignant salivary gland tumors (MSGT) of the head and neck including patients with inoperable/ incompletely resected MSGTs (R2-group) and completely resected tumors plus involved margins or perineural spread (R1-group).

METHODS

COSMIC is a prospective phase II trial of IMRT (25 × 2 Gy) and carbon ion boost (8 × 3 GyE). Primary endpoint is mucositis CTC°III, secondary endpoints are local control, progression-free survival, and toxicity. Evaluation of disease response is carried out according to the Response Evaluation Criteria in Solid Tumors (RECIST); toxicity is assessed using NCI CTC v 3.0.

RESULTS

Twenty-nine patients were recruited from 07/2010 to 04/2011, all patients have at least completed first follow-up. Sixteen patients were treated in the R2-group, 13 in the R1-group. All treatments were completed as planned and well tolerated, mucositis CTC grade III was 25% (R2) and 15.4% (R1), no dysphagia CTC grade III was observed, no feeding tubes were necessary. Side-effects rapidly resolved, only 4 patients (13.8%) reported xerostomia grade II at first follow-up. Overall response rate (complete and partial response) according to RECIST in the R2-group is 68.8% at 6-8 weeks post treatment, all patients within this group showed radiological signs of treatment response.

CONCLUSION

No unexpected toxicity was observed, mucositis rates and other side effects do not differ between patients with visible residual tumor and macroscopically completely resected tumors. Initial treatment response is promising though longer follow-up is needed to assess local control.

TRIAL REGISTRATION

Clinical trial identifier NCT 01154270.

摘要

背景

COSMIC 试验旨在评估头颈部恶性唾液腺肿瘤(MSGT)的调强放疗(IMRT)和碳离子推量递增治疗的毒性,包括无法手术/不完全切除的 MSGT(R2 组)和完全切除肿瘤伴切缘累及或神经周围侵犯(R1 组)的患者。

方法

COSMIC 是一项前瞻性 II 期 IMRT(25×2Gy)和碳离子推量递增(8×3GyE)的试验。主要终点是粘膜炎 CTC°III,次要终点是局部控制、无进展生存期和毒性。根据实体瘤反应评估标准(RECIST)评估疾病反应;使用 NCI CTC v 3.0 评估毒性。

结果

2010 年 7 月至 2011 年 4 月共招募了 29 例患者,所有患者均至少完成了首次随访。16 例患者在 R2 组治疗,13 例在 R1 组治疗。所有治疗均按计划完成,且耐受性良好,粘膜炎 CTC 3 级为 25%(R2)和 15.4%(R1),未见吞咽困难 CTC 3 级,无需置管。副作用迅速缓解,仅有 4 例(13.8%)患者在首次随访时报告口干症 CTC 2 级。根据 RECIST,R2 组在治疗后 6-8 周的总缓解率(完全缓解和部分缓解)为 68.8%,该组所有患者均出现放射治疗反应的影像学征象。

结论

未观察到意外毒性,有肉眼残留肿瘤和肉眼完全切除肿瘤的患者之间的粘膜炎发生率和其他副作用无差异。尽管需要更长时间的随访来评估局部控制,但初始治疗反应很有希望。

试验注册

临床试验标识符 NCT 01154270。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3402/3407497/160aedeb1e9b/1471-2407-12-163-1.jpg

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