School of Public Health, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, SA, Australia.
The Department of Otolaryngology, Head and Neck Surgery, The University of Adelaide, Adelaide, SA, Australia.
JBI Evid Synth. 2022 Apr 1;20(4):1135-1141. doi: 10.11124/JBIES-21-00159.
The objective of this review is to investigate overall survival in patients with human papillomavirus positive oropharyngeal squamous cell carcinoma (HPV+ OPSCC) comparing standard- versus reduced-dose radiotherapy.
The improved survival of patients with HPV+ compared to HPV-negative OPSCC has raised the question of reducing the total radiation treatment dose delivered to patients with HPV+ OPSCC. A de-escalated radiotherapy protocol may provide equal oncological benefit, with reduced adverse events/toxicity.
We will include any adult patients aged 18years or older who have undergone curative intent treatment for HPV+ OPSCC. These patients can be at any stage at the time treatment is initiated. Exclusion criteria are as follows: pre-clinical or animal studies, patients with non-squamous cell carcinoma lesions of the oropharynx, patients with primary lesions in other head and neck sites, or patients receiving palliative treatment.
A three-step search strategy will be used to identify relevant articles for inclusion through MEDLINE, CINAHL, Embase, Web of Science, Scopus, and gray literature sources. These articles will be assessed against our inclusion and exclusion criteria at the title and abstract level as well as at full-text level. Remaining studies will be critically appraised based on their trial design. Data extraction will occur for all studies and, where possible, will be pooled with statistical meta-analysis.
PROSPERO CRD42021252161.
本综述旨在调查人乳头瘤病毒阳性口咽鳞状细胞癌(HPV+ OPSCC)患者的总生存率,比较标准剂量与降低剂量放疗的效果。
与 HPV 阴性 OPSCC 相比,HPV+患者的生存率提高,这引发了一个问题,即是否可以降低 HPV+ OPSCC 患者接受的总放射治疗剂量。减少放疗方案可能会提供同等的肿瘤学益处,同时减少不良反应/毒性。
我们将纳入任何接受过 HPV+ OPSCC 根治性治疗的 18 岁或以上的成年患者。这些患者在开始治疗时可以处于任何分期。排除标准如下:临床前或动物研究、口咽非鳞状细胞癌病变患者、原发灶位于其他头颈部部位的患者、或接受姑息治疗的患者。
我们将采用三步搜索策略,通过 MEDLINE、CINAHL、Embase、Web of Science、Scopus 和灰色文献来源,确定纳入相关文章。将根据纳入和排除标准在标题和摘要层面以及全文层面评估这些文章。对其余研究将根据其试验设计进行批判性评估。将对所有研究进行数据提取,并在可能的情况下进行统计学荟萃分析。
PROSPERO CRD42021252161。