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顺铂和氟尿嘧啶作为头颈癌新辅助治疗的初步报告

Cisplatin and fluorouracil as neoadjuvant therapy in head and neck cancer. A preliminary report.

作者信息

Toohill R J, Anderson T, Byhardt R W, Cox J D, Duncavage J A, Grossman T W, Haas C D, Haas J S, Hartz A J, Libnoch J A

出版信息

Arch Otolaryngol Head Neck Surg. 1987 Jul;113(7):758-61. doi: 10.1001/archotol.1987.01860070072019.

Abstract

A randomized, prospective trial utilizing cisplatin and fluorouracil as neoadjuvant chemotherapy in the treatment of advanced squamous cell carcinomas of the upper aerodigestive tract was initiated in January 1983. Sixty patients were stratified by site (oral cavity, 19; larynx, 14; hypopharynx, 14; oropharynx, 11; nasopharynx, one; and paranasal sinuses, one) and by stage (III, 19; IV, 41), and then randomized to receive either standard treatment (defined as preoperative irradiation followed by radical excision or irradiation alone) or adjuvant chemotherapy followed by standard treatment. An additional three patients were entered into the study, but withdrew. Chemotherapy consisted of three cycles for those patients in whom an objective tumor response was observed; nonresponders received standard treatment. Response to chemotherapy was complete in five and partial (greater than 50%) in 18 patients, for an overall response rate of 85%. The follow-up for surviving patients was a minimum of 24 months and a maximum of 44 months. Survival was compared for patients in both treatment groups according to the method of Lee and Desu. Despite excellent tumor response, actuarial survival was 70% in the standard treatment group as opposed to 56% in the experimental group. It was therefore evident that the high response rates reported in previous pilot studies do not necessarily result in improved survival in these cancers.

摘要

1983年1月开展了一项随机前瞻性试验,该试验采用顺铂和氟尿嘧啶作为新辅助化疗药物,用于治疗上消化道晚期鳞状细胞癌。60例患者按部位(口腔19例、喉14例、下咽14例、口咽11例、鼻咽1例、鼻窦1例)和分期(III期19例、IV期41例)进行分层,然后随机分为接受标准治疗组(定义为术前放疗后行根治性切除或单纯放疗)或辅助化疗后行标准治疗组。另有3例患者进入研究,但随后退出。对观察到有客观肿瘤反应的患者,化疗进行三个周期;无反应者接受标准治疗。18例患者化疗反应为完全缓解,5例为部分缓解(缓解率大于50%),总缓解率为85%。存活患者的随访时间最短为24个月,最长为44个月。根据Lee和Desu的方法对两个治疗组患者的生存率进行比较。尽管肿瘤反应良好,但标准治疗组的精算生存率为70%,而试验组为56%。因此很明显,先前初步研究报告的高缓解率不一定能改善这些癌症患者的生存率。

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