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首页> 外文期刊>OncoTargets and therapy >Intensity-modulated radiotherapy plus nimotuzumab with or without concurrent chemotherapy for patients with locally advanced nasopharyngeal carcinoma
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Intensity-modulated radiotherapy plus nimotuzumab with or without concurrent chemotherapy for patients with locally advanced nasopharyngeal carcinoma

机译:局部晚期鼻咽癌患者调强放疗加尼莫妥单抗联合或不联合化疗

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Objective: This study aimed to evaluate the safety and efficacy of intensity-modulated radiotherapy (IMRT) plus nimotuzumab with or without concurrent chemotherapy (CCT) for patients with locally advanced nasopharyngeal carcinoma (LA-NPC). Patients and methods: A total of 50 newly diagnosed patients with LA-NPC treated at the Affiliated Hospital of Jiangnan University between November 2011 and January 2017 were retrospectively analyzed. All patients received the combined treatment modality of nimotuzumab plus IMRT. Nimotuzumab was administered concurrently with IMRT at a weekly dose of 200 mg. Neoadjuvant, concurrent or adjuvant chemotherapy with the doublet regimen of taxanes (docetaxel or paclitaxel) plus platinum (cisplatin or nedaplatin) were administered. Among the 50 patients, 43 (86.0%) received ≥6 cycles of nimotuzumab (median 7 cycles, range 2–14 cycles) and 29 (58.0%) received two cycles of CCT with docetaxel plus nedaplatin. Results: With a median follow-up of 28.0 months, the 2-year progression-free survival (PFS) and overall survival were 83.29% (95% confidence interval [CI]: 67.93%–91.72%) and 97.67% (95% CI: 84.62%–99.67%), respectively. Both univariate and multivariate analyses revealed that cycles of nimotuzumab were significantly associated with PFS. Patients who received?≥6?cycles of nimotuzumab showed a better PFS than those receiving <6 cycles ( P =0.006), whereas the addition of CCT failed to improve PFS. Oral mucositis was the most common adverse event, which was recorded as grade 3–4 in 18 (36.0%) patients. Besides, two (4.0%) patients experienced nimotuzumab-related anaphylaxis, and no skin rash was found in any patient. Subgroup analysis revealed that the patients who received CCT had more grade 3–4 adverse events as compared to those who did not receive CCT (62.1% vs 33.3%, P =0.045). Conclusion: The regime of nimotuzumab plus IMRT for the treatment of LA-NPC was well tolerated, with encouraging survival data, and it could be an effective treatment alternative for patients with LA-NPC. Further clinical trials are needed to confirm these findings.
机译:目的:本研究旨在评估调强放疗(IMRT)加尼莫妥单抗联合或不联合化疗(CCT)对局部晚期鼻咽癌(LA-NPC)患者的安全性和有效性。患者与方法:回顾性分析2011年11月至2017年1月在江南大学附属医院治疗的50例新诊断的LA-NPC患者。所有患者均接受了尼莫妥珠单抗联合IMRT的联合治疗方式。 Nimotuzumab与IMRT并用,每周200 mg。给予新辅助,同时或辅助化疗联合紫杉烷类药物(多西他赛或紫杉醇)加铂类药物(顺铂或奈达铂)。在50例患者中,有43例(86.0%)接受了≥6个周期的尼莫妥珠单抗(中位数为7个周期,范围为2-14个周期),而29例(58.0%)接受了两个周期的多西他赛联合奈达铂的CCT治疗。结果:中位随访28.0个月,两年无进展生存率(PFS)和总生存率分别为83.29%(95%置信区间[CI]:67.93%–91.72%)和97.67%(95%) CI:84.62%–99.67%)。单变量和多变量分析均显示尼莫妥单抗的周期与PFS显着相关。接受尼莫妥珠单抗≥6个周期的患者比接受小于6个周期的患者表现出更好的PFS(P = 0.006),而添加CCT不能改善PFS。口腔粘膜炎是最常见的不良事件,在18名(36.0%)患者中记录为3–4级。此外,有2名(4.0%)患者经历了尼莫妥单抗相关的过敏反应,并且在任何患者中均未发现皮疹。亚组分析显示,与未接受CCT的患者相比,接受CCT的患者发生3-4级不良事件的发生率更高(62.1%vs 33.3%,P = 0.045)。结论:尼莫妥珠单抗联合IMRT治疗LA-NPC的方案耐受性好,生存数据令人鼓舞,可以作为LA-NPC患者的有效替代治疗方法。需要进一步的临床试验以证实这些发现。

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