吸烟对hpv相关口咽癌联合治疗诱导化疗即刻效果的影响

P. V. Golubev, L. V. Bolotina, A. R. Gevorkov, T. I. Deshkina
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引用次数: 0

摘要

目的。评价吸烟对联合治疗局部晚期口咽部hpv阳性鳞状细胞癌患者诱导化疗的即时有效性(达到客观反应- OR)的影响。患者和方法。68名患者(51名男性和17名女性)患有与乳头瘤病毒相关的口咽局部晚期鳞状细胞癌,该研究于2021年至2023年在P. Hertsen莫斯科肿瘤研究所-国家医学研究放射中心分支,俄罗斯联邦卫生部,莫斯科,俄罗斯联邦和莫斯科卫生部第1市临床肿瘤医院进行。将患者分为两组,在主要特征(吸烟史、分期、组织学类型、肿瘤分化程度)上完全可比。在第一阶段,第一组(主)患者接受逐步降级的诱导化疗:根据TR方案(多西紫杉醇75 mg/m2 +顺铂75 mg/m2), 3个疗程21天;第二组(对照组)采用标准方案(多西他赛75 mg/m2 +顺铂75 mg/m2 + 5-氟尿嘧啶1000 mg/m2)治疗。两组患者均给予预防性粒细胞集落刺激因子治疗。在第二阶段,在卡铂药物放疗的背景下进行标准放化疗。通过计算Spearman系数并进行Bonferroni校正进行相关分析。p <的差异被认为是可靠的;0.05. 结果。在评估治疗的客观反应时,发现第1组有33例(97%)患者达到疾病控制,第2组有34例(100%)患者达到疾病控制。1组3例(8.8%)患者完全缓解,2组4例(11.8%)患者完全缓解;部分回归22例(64.7%)和24例(70.6%);8例(23.5%)和6例(17.6%)的肿瘤进程稳定。进一步分析表明,吸烟与分化反应水平(原发病变、淋巴结改变)之间没有直接或负相关;无论采用何种ICT方案,所有患者(吸烟者和从不吸烟的患者)对第一阶段联合治疗的反应都一样有效。结论。在我们的研究中,无论何种诱导方案,吸烟均未发现对诱导化疗联合治疗局部晚期口咽hpv相关鳞状细胞癌的即时疗效有统计学意义的影响。然而,需要更长的随访期来评估吸烟对长期肿瘤预后的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of smoking on the immediate effectiveness of induction chemotherapy in the combined treatment of HPV-associated oropharyngeal cancer
Purpose. Evaluation of the effect of smoking on the immediate effectiveness (achievement of objective response – OR) of induction chemotherapy in patients receiving combined treatment for locally advanced HPV-positive squamous cell carcinoma of the oropharynx. Patients and methods . Sixty-eight patients (51 men and 17 women) with locally advanced squamous cell cancer of the oropharynx associated with papillomavirus were included in the study, which was carried out from 2021 to 2023 at the P. Hertsen Moscow Oncology Research Institute – Branch of the National Medical Research Radiological Centre, Ministry of Health of the Russian Federation, Moscow, Russian Federation and the Municipal Clinical Oncological Hospital № 1 of the Department of Health of Moscow. The patients were divided into 2 equal groups, fully comparable in terms of the main characteristics (smoking history, stage, histological type, and degree of tumour differentiation). At the first stage, patients of the 1st (main) group received de-escalated induction chemotherapy: three 21-day courses according to the TR scheme (docetaxel in the dose of 75 mg/m2 + cisplatin 75 mg/m2); patients of the 2nd (control) group were treated with standard scheme (docetaxel 75 mg/m2 + cisplatin 75 mg/m2 + 5-fluorouracil 1000 mg/m2). Patients in both groups received prophylactic granulocyte colony-stimulating factor. At the second stage, standard chemoradiotherapy was carried out against the background of drug radiomodification with carboplatin. Correlation analysis was performed by calculating the Spearman coefficient with Bonferroni correction. Differences were considered reliable at p < 0.05. Results. When evaluating the objective response to treatment, it was revealed that disease control was achieved in 33 (97 %) patients from group 1 and in all 34 (100 %) patients from group 2. Complete response was observed in 3 (8.8 %) patients from group 1 and 4 (11.8 %) from group 2; partial regression in 22 (64.7 %) and 24 (70.6 %); stabilisation of the tumour process in 8 (23.5 %) and 6 (17.6 %) respectively. Further analysis showed that there was no direct or inverse correlation between smoking and differentiated level of response (primary lesion, altered lymph nodes); all patients (smokers and those who had never smoked) responded equally effectively to the first stage of combined treatment, regardless of the ICT regimen. Conclusion . In our study, no statistically significant effect of smoking on the immediate effectiveness of induction chemotherapy in the combined treatment of locally advanced HPV-associated squamous cell carcinoma of the oropharynx regardless of the induction regimen was found. However, a longer follow-up period is needed to evaluate the effect of smoking on long-term oncological outcomes.
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