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采用低剂量个体化化疗方案对无法手术的局部晚期、复发或转移性头颈部鳞状细胞癌患者进行姑息治疗。

Palliative treatment of patients with inoperable locally advanced, recurrent or metastatic head and neck squamous cell cancer, using a low-dose and personalized chemotherapeutic regimen.

作者信息

Bishnoi Rohit, Bennett Jeffery, Reisman David N

机构信息

Division of Hospital Medicine, Department of Medicine, University of Florida, Gainesville, FL 32610, USA.

Department of Radiology, University of Florida, Gainesville, FL 32610, USA.

出版信息

Oncol Lett. 2017 Jun;13(6):4633-4640. doi: 10.3892/ol.2017.6068. Epub 2017 Apr 21.

Abstract

Inoperable or metastatic head and neck squamous cell cancer (HNSCC) is known to be associated with a poor patient prognosis. First line therapies include a Taxol, platinum-based antineoplastic and fluorouracil (FU) treatment regimen (TPF) or a platinum-based antineoplastic, FU and EGFR inhibitor treatment regimen (PFE). The toxicity of these regimens is one of the major limiting factors, particularly for palliative treatment. The present study is a retrospective study of 15 patients with HNSCC, where the treatment goal was palliative. Of the 15 patients, 8 received a TPF, while 7 received a PFE. A total of 129 treatment cycles were administered with a median of 9 cycles (range, 3-14). Chemotherapy began with low doses and was subsequently titrated up based on tolerance and response. Positive responses were noted with the lower doses compared with the conventional doses, and maximal doses were not required. The median dose of cisplatin, paclitaxel and 5-FU administered was 40 mg/m, 80 mg/m and 360 mg/m/day for 5 days, respectively. Cetuximab was used at a standard dose. At the initial follow-up (mean, 64 days; 3 cycles), a 100% disease control rate (DCR) and 80% overall response rate (ORR) was achieved. A positive response, 60% DCR and 60% ORR, was maintained until the late stages of the study (mean, 217 days; 9 cycles). Following termination of chemotherapy after >9 cycles, 4 patients remained disease free for ~1 year. A total of 3 patients exhibited a pathologic complete response despite radiologically exhibiting residual disease. The median progression-free survival time was 10.03 months and the overall survival time was 15.77 months. The only grade 3 hematologic toxicity noted was neutropenia in 3 (20%) patients. Grade 3 vomiting was noted in 1 (6.67%) patient and grade 3 stomatitis was noted in 1 (6.67%) patient. Due to low toxicity patients exhibited improved tolerance to this approach, particularly in terms of palliative care. Furthermore, these results are in contrast to the axiom that increased doses are more effective.

摘要

已知不可切除或转移性头颈部鳞状细胞癌(HNSCC)患者预后较差。一线治疗方案包括紫杉醇、铂类抗肿瘤药和氟尿嘧啶(FU)治疗方案(TPF)或铂类抗肿瘤药、FU和表皮生长因子受体(EGFR)抑制剂治疗方案(PFE)。这些方案的毒性是主要限制因素之一,尤其对于姑息治疗而言。本研究是一项针对15例HNSCC患者的回顾性研究,治疗目标为姑息治疗。15例患者中,8例接受TPF方案,7例接受PFE方案。总共进行了129个治疗周期,中位数为9个周期(范围3 - 14个周期)。化疗从低剂量开始,随后根据耐受性和反应进行剂量滴定。与传统剂量相比,较低剂量时即观察到阳性反应,无需使用最大剂量。顺铂、紫杉醇和5 - FU的中位给药剂量分别为40mg/m²、80mg/m²和360mg/m²/天,持续5天。西妥昔单抗按标准剂量使用。在初始随访时(平均64天;3个周期),疾病控制率(DCR)达到100%,总缓解率(ORR)达到80%。直至研究后期(平均217天;9个周期),仍维持阳性反应,DCR为60%,ORR为60%。在化疗超过9个周期后停药,4例患者疾病无进展约1年。共有3例患者尽管影像学显示有残留病灶,但病理检查显示完全缓解。无进展生存期的中位数为10.03个月,总生存期为15.77个月。仅观察到3例(20%)患者出现3级血液学毒性,为中性粒细胞减少。1例(6.67%)患者出现3级呕吐,1例(6.67%)患者出现3级口腔炎。由于毒性较低,患者对该治疗方法的耐受性有所改善,尤其是在姑息治疗方面。此外,这些结果与“剂量增加更有效”这一公理相悖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/825f/5452905/0827e5953574/ol-13-06-4633-g00.jpg

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