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新辅助化疗在局部晚期宫颈癌治疗中的作用:一项系统评价

The role of neoadjuvant chemotherapy in the management of locally advanced cervix cancer: a systematic review.

作者信息

Osman Mohammed

机构信息

Oncology Consultant, General Organization of Teaching Hospitals and Institutes , Cairo, Egypt.

出版信息

Oncol Rev. 2014 Sep 23;8(2):250. doi: 10.4081/oncol.2014.250.

Abstract

Cervical cancer is the second most common cancer in women. Neoadjuvant chemotherapy for patients with locally advanced cervix cancer has comparable benefits to concurrent chemoradiotherapy (CCRT), but with fewer side effects. This systematic review aims to provide a comprehensive summary of the benefits of neoadjuvant chemotherapy for the management of locally advanced cervix cancer from stage IB2 (tumor >4.0 cm) to IIIB (tumor extending to the pelvic wall and/or hydronephrosis). Our primary objective was to assess benefits in terms of survival. The data source included the USA national library of medicine, Medline search, and the National Cancer Institute PDQ Clinical Protocols. Inclusion criteria for consideration in the current systematic review included studies published between January 1997 and December 2012. In terms of histology, they had to be focused on squamous cell carcinoma, adenosquamous carcinoma, and/or adenocarcinoma. Patients should be either chemotherapy naïve or cervix cancer chemotherapy naïve, and have a performance status ≤2. The search in the above-mentioned scientific websites led to identify 49 publications, 19 of which were excluded, as they did not meet the inclusion criteria of this systematic review. Therefore only 30 studies were deemed eligible. Data was collected from 1760 patients enrolled in the current systematic review study. The mean age was 45.2 years. The mean tumor size was 4.7 cm. The most commonly used chemotherapies were cisplatin doublets. Paclitaxel was the most commonly used chemotherapeutic agent in the doublets. The mean chemotherapy cycles were 2.7. After chemotherapy, patients underwent surgery after a mean time of 2.5 weeks. The standard operation was radical hysterectomy with pelvic lymphadenectomy. Chemotherapy achieved an objective response rate of 84%. The 5-year progression-free survival and overall survival were 61.9% and 72.8% respectively. The treatment protocol was associated with a mild early toxicity profile. Leucopenia and neutropenia were the most common side effects. Late toxicity was also generally mild and mainly associated with bladder dysfunction and vaginal dehiscence. The quality of the studies was assessed using the Newcastle-Ottawa quality assessment scale. Neoadjuvant chemotherapy achieved comparable survival results to CCRT, and was associated with less toxicity.

摘要

宫颈癌是女性中第二常见的癌症。局部晚期宫颈癌患者的新辅助化疗与同步放化疗(CCRT)具有相当的疗效,但副作用较少。本系统评价旨在全面总结新辅助化疗对IB2期(肿瘤>4.0 cm)至IIIB期(肿瘤延伸至盆腔壁和/或肾积水)局部晚期宫颈癌治疗的益处。我们的主要目标是评估生存方面的益处。数据来源包括美国国立医学图书馆、Medline检索以及美国国立癌症研究所PDQ临床方案。纳入本次系统评价考虑的标准包括1997年1月至2012年12月期间发表的研究。在组织学方面,研究必须聚焦于鳞状细胞癌、腺鳞癌和/或腺癌。患者应为未接受过化疗或未接受过宫颈癌化疗,且体能状态≤2。在上述科学网站进行的检索共识别出49篇出版物,其中19篇因不符合本系统评价的纳入标准而被排除。因此,仅有30项研究被认为符合要求。数据收集自参与本次系统评价研究的1760例患者。平均年龄为45.2岁。平均肿瘤大小为4.7 cm。最常用的化疗方案是顺铂双联化疗。紫杉醇是双联化疗中最常用的化疗药物。平均化疗周期为2.7个。化疗后,患者平均在2.5周后接受手术。标准手术为根治性子宫切除术加盆腔淋巴结清扫术。化疗的客观缓解率为84%。5年无进展生存率和总生存率分别为61.9%和72.8%。该治疗方案的早期毒性较轻。白细胞减少和中性粒细胞减少是最常见的副作用。晚期毒性一般也较轻,主要与膀胱功能障碍和阴道裂开有关。使用纽卡斯尔-渥太华质量评估量表对研究质量进行了评估。新辅助化疗取得了与CCRT相当的生存结果,且毒性较小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5c/4419645/2c10f181e0ca/onco-2014-2-250-g001.jpg

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