紫杉醇和西妥昔单抗在超选择性动脉内化疗后复发/转移性口腔癌病例中的疗效:回顾性队列研究

Cancer diagnosis & prognosis Pub Date : 2024-11-03 eCollection Date: 2024-11-01 DOI:10.21873/cdp.10394
Kaname Sakuma, Tomoyuki Kii, Toko Machida, Yosuke Kikuchi, Masaki Yoda, Shuji Toya, Akira Tanaka
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引用次数: 0

摘要

背景/目的:研究紫杉醇(PTX)+西妥昔单抗(Cmab)联合方案对口腔癌超选择性动脉内放化疗(SSIACRT)后复发或转移患者的疗效,并对其安全性进行回顾性研究:自2012年12月至2022年12月的10年间,所有入组的晚期口腔癌患者或拒绝手术的患者均接受了为期6至9周的SSIACRT治疗[顺铂(CDDP):总量160-630 mg/m2,放疗:总量50-70 Gy]。九例患者(舌癌、上颌骨牙龈癌和下颌骨牙龈癌,各三例)接受了 PTX + Cmab 治疗。治疗开始后六个月内出现复发或转移,使挽救手术的进行变得复杂。Cmab(第一次剂量:400毫克/平方米,第二次及以后剂量:250毫克/平方米)和PTX(80毫克/平方米)每周给药一次:总反应率为44.4%(9例中的4例),疾病控制率为88.9%(9例中的8例),中位无进展生存期为7个月,总生存期为11个月。3-4级不良反应为33.3%的病例出现中性粒细胞减少,55.6%的病例出现白细胞减少,22.2%的病例出现贫血,22.2%的病例出现痤疮样皮疹。综上所述,PTX+Cmab疗法治疗SSIACRT后的复发和转移病例的效果与其他二线疗法相当,并能应对骨髓抑制的副作用:结论:PTX+Cmab疗法可能是对CDDP耐药的SSIACRT治疗后复发或转移性头颈癌的一种有效治疗模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Paclitaxel and Cetuximab in Recurrent/Metastatic Oral Cancer Cases Following Superselective Intraarterial Chemoradiotherapy: A Retrospective Cohort Study.

Background/aim: The therapeutic efficacy of the paclitaxel (PTX) + cetuximab (Cmab) combination regimen was investigated in patients with recurrence or metastasis after superselective intraarterial chemoradiotherapy (SSIACRT) for oral cancer, and the safety was retrospectively examined.

Patients and methods: All enrolled patients with advanced oral cancer or who had refused surgery over 10 years from December 2012 to December 2022 underwent SSIACRT for 6 to 9 weeks [cisplatin (CDDP): total 160-630 mg/m2 and radiotherapy: total 50-70 Gy]. Nine cases (tongue cancer, maxillary gingival cancer, and mandibular gingival cancer; three cases each) were subjected to PTX + Cmab therapy. Recurrence or metastases were observed within six months after the onset of treatment, complicating the conduct of salvage surgery. Cmab (first dose: 400 mg/m2 and second and following doses: 250 mg/m2) and PTX (80 mg/m2) were administered weekly.

Results: The overall response rate was 44.4% (four of nine cases), and the disease control rate was 88.9% (eight of nine cases), whereas the median progression-free survival was seven months, and the overall survival was 11 months. Grade 3-4 adverse events were neutropenia in 33.3% of the cases, leukopenia in 55.6%, anemia in 22.2%, and acneiform skin rash in 22.2%. Based on the above, PTX + Cmab therapy for recurrent and metastatic cases after SSIACRT had comparable results to other second-line modalities and enabled to cope with the side effects of myelosuppression.

Conclusion: PTX + Cmab therapy may be an effective treatment mode for recurrent or metastatic head and neck cancer resistant to CDDP after SSIACRT treatment.

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