紫杉醇、异环磷酰胺和顺铂诱导化疗后同步放化疗治疗不可切除的局部晚期头颈部癌。

I Chitapanarux, E Tharavichitkul, V Lorvidhaya, P Sittitrai, T Pattarasakulchai
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引用次数: 0

摘要

目的:对局部晚期头颈部肿瘤的诱导化疗(IC)和同步放化疗(CCRT)进行了大量的临床研究。本研究旨在确定该组患者的IC联合紫杉醇、异环磷酰胺和顺铂后CCRT联合顺铂的有效率,以及整个治疗对生存和疾病进展时间的影响。方法:采用紫杉醇/异环磷酰胺/顺铂诱导治疗30例晚期不可切除头颈癌患者。如果原发肿瘤有完全或部分缓解,患者再进行2个周期的IC治疗,然后进行70 Gy的放疗加3个周期的顺铂治疗。对于那些没有部分反应或疾病进展的患者,根据医生的判断进行治疗。结果:90%的患者为IV期,40%的患者原发肿瘤位于上颌窦和鼻腔。1例患者(3%)对IC达到完全缓解(CR), 18例患者达到部分缓解(PR)。CCRT提高了缓解率,导致治疗共3例CR(10%)和16例PR(53%)。中位进展时间为11.5个月。中位总生存期为27个月。IC期间最严重的血液学毒性是3-4级中性粒细胞减少(40%)。CCRT期间68%的患者发生3-4级黏膜炎。结论:这种新型的联合治疗方案是有毒性的,但却是可行的,可以用于晚期和不可切除的头颈癌患者。©2010生物医学成像与干预杂志。版权所有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Induction chemotherapy with paclitaxel, ifosfamide, and cisplatin followed by concurrent chemoradiotherapy for unresectable locally advanced head and neck cancer.

Induction chemotherapy with paclitaxel, ifosfamide, and cisplatin followed by concurrent chemoradiotherapy for unresectable locally advanced head and neck cancer.

Induction chemotherapy with paclitaxel, ifosfamide, and cisplatin followed by concurrent chemoradiotherapy for unresectable locally advanced head and neck cancer.

Induction chemotherapy with paclitaxel, ifosfamide, and cisplatin followed by concurrent chemoradiotherapy for unresectable locally advanced head and neck cancer.

Objective: Induction chemotherapy (IC) and concurrent chemoradiotherapy (CCRT) for locally advanced head and neck cancer has been studied in many clinical trials. This study was conducted to determine the response rate of IC with paclitaxel, ifosfamide, and cisplatin followed by CCRT with cisplatin for this group of patients, and the effect of the entire treatment on survival and time to disease progression.

Methods: Thirty patients with advanced and unresectable head and neck cancer were treated with 2 cycles of induction paclitaxel/ ifosfamide/ cisplatin. If the primary tumor had a complete or partial response, patients were treated with 2 more cycles of IC followed by radiotherapy 70 Gy plus 3 cycles of cisplatin. For those with less than partial response or disease progression were treated according to the discretion of the physicians.

Results: Ninety percent of patients had stage IV disease and 40% of them had primary tumor at maxillary sinus and nasal cavity. One patient (3%) achieved complete response (CR) and 18 patients had partial responses (PR) to IC. CCRT enhanced the response rate, resulting in a total of 3 CR (10%) and 16 PR (53%) to treatment. The median time to progression was 11.5 months. The median overall survival was 27 months. The most severe hematologic toxicity occurred during IC was grade3-4 neutropenia (40%). Grade 3-4 mucositis occurred in 68% of patients during CCRT.

Conclusion: This novel combined-modality treatment program, is toxic but feasible, and can be administered for selected patients with advanced and unresectable head and neck cancer. © 2010 Biomedical Imaging and Intervention Journal. All rights reserved.

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