Kokka Fani, Bryant Andrew, Brockbank Elly, Powell Melanie, Oram David
Women's Health, Birchington Ward, Queen Elizabeth The Queen Mother Hospital, St Peters Road, Kent, UK, CT9 4AN.
Cochrane Database Syst Rev. 2015 Apr 7(4):CD010260. doi: 10.1002/14651858.CD010260.pub2.
Cervical cancer is the second commonest cancer among women up to 65 years of age and is the most frequent cause of death from gynaecological cancers worldwide. Sources suggest that a very high proportion of new cervical cancer cases in developing countries are at an advanced stage (IB2 or more) and more than a half of these may be stage III or IV. Cervical cancer staging is based on findings from clinical examination (FIGO) staging). Standard care in Europe and US for stage IB2 to III is non-surgical treatment (chemoradiation). However in developing countries, where there is limited access to radiotherapy, locally advanced cervical cancer may be treated with a combination of chemotherapy and hysterectomy (surgery to remove the womb and the neck of the womb, with or without the surrounding tissues). It is not certain if this improves survival. Therefore, it is important to systematically assess the value of hysterectomy in addition to radiotherapy or chemotherapy, or both, as an alternative intervention in the treatment of locally advanced cervical cancer (stage IB2 to III).
To determine whether hysterectomy, in addition to standard treatment with radiation or chemotherapy, or both, in women with locally advanced cervical cancer (stage IB2 to III) is safe and effective compared with standard treatment alone.
We searched the Cochrane Gynaecological Cancer Group Trials Register, CENTRAL, MEDLINE, EMBASE and LILACS up to February 2014. We also searched registers of clinical trials, abstracts of scientific meetings and reference lists of included studies.
We searched for randomised controlled trials (RCTs) that compared treatment protocols involving hysterectomy versus radiotherapy or chemotherapy, or both, in women with advanced stage (IB2 to III) cervical cancer presenting for the first time.
We assessed study eligibility independently, extracted data and assessed risk of bias. Where possible, overall and progression or disease-free survival outcomes were synthesised in a meta-analysis using the random-effects model. Adverse events were incompletely reported so results of single trials were described in narrative form.
We included seven RCTs (1217 women) of varying methodological quality in the review; most trials were at moderate or high risk of bias.Three were multi-centre trials, two were single-centre trials, and in two trials it was unclear if they were single or multi-centre. These trials compared the following interventions for women with locally advanced cervical cancer (stages IB2 to III):hysterectomy (simple or radical) with radiotherapy (N = 194) versus radiotherapy alone (N = 180); hysterectomy (simple or radical) with chemoradiotherapy (N = 31) versus chemoradiotherapy alone (N = 30); hysterectomy (radical) with chemoradiotherapy (N = 111) versus internal radiotherapy with chemoradiotherapy (N = 100); hysterectomy (simple or radical) with upfront (neoadjuvant) chemotherapy (N = 298) versus radiotherapy alone (N = 273).One trial (N = 256) found no difference in the risk of death or disease progression between women who received attenuated radiotherapy followed by hysterectomy and those who received radiotherapy (external and internal) alone (hazard ratio (HR) 0.89, 95% confidence interval (CI) 0.61 to 1.29). This trial also reported no difference between the two groups in terms of adverse effects (18/129 grade 3 or 4 adverse effects in the hysterectomy and radiation group and 19 cases in 18/121 women in the radiotherapy alone group). There was no difference in 5-year tumour-free actuarial survival (representation of the probable years of survivorship of a defined population of participants) or severe complications (grade 3) in another trial (N = 118) which reported the same comparison (6/62 versus 6/56 in the radiation with surgery group versus the radiotherapy alone group, respectively). The quality of the evidence was low for all these outcomes.One trial (N = 61) reported no difference (P value > 0.10) in overall and recurrence-free survival at 3 years between chemoradiotherapy and hysterectomy versus chemoradiotherapy alone (low quality evidence). Adverse events and morbidity data were not reported.Similarly, another trial (N = 211) found no difference in the risk of death (HR 0.65, 95% CI 0.35 to 1.21, P value = 0.19, low quality evidence), disease progression (HR 0.70, 95% CI 0.31 to 1.34, P value = 0.24, low quality evidence) or severe late complications (P value = 0.53, low quality evidence) between women who received internal radiotherapy versus hysterectomy after both groups had received external-beam chemoradiotherapy.Meta analysis of three trials of neoadjuvant chemotherapy and hysterectomy versus radiotherapy alone, assessing 571 participants, found that women who received neoadjuvant chemotherapy plus hysterectomy had less risk of death than those who received radiotherapy alone (HR 0.71, 95% CI 0.55 to 0.93, I(2) = 0%, moderate quality evidence). However, a significant number of the participants that received neoadjuvant chemotherapy plus hysterectomy had radiotherapy as well. There was no difference in the proportion of women with disease progression or recurrence between the two groups (RR 0.75, 95% CI 0.53 to 1.05, I(2) = 20%, moderate quality evidence).Results of single trials reported no apparent (P value > 0.05) difference in long-term severe complications, grade 3 acute toxicity and severe late toxicity between the two groups (low quality evidence).Quality of life outcomes were not reported in any of the trials.
AUTHORS' CONCLUSIONS: From the available RCTs, we found insufficient evidence that hysterectomy with radiotherapy, with or without chemotherapy, improves the survival of women with locally advanced cervical cancer who are treated with radiotherapy or chemoradiotherapy alone. The overall quality of the evidence was variable across the different outcomes and was universally downgraded due to concerns about risk of bias. The quality of the evidence for neoadjuvant chemotherapy and radical hysterectomy versus radiotherapy alone for survival outcomes was moderate, with evidence from other comparisons of low quality. This was mainly based on poor reporting and sparseness of data where results were based on single trials. More trials that assess medical management with and without hysterectomy may test the robustness of the findings of this review as further research is likely to have an important impact on our confidence in the estimate of effect.
宫颈癌是65岁以下女性中第二常见的癌症,也是全球妇科癌症最常见的死亡原因。有资料显示,发展中国家很高比例的宫颈癌新发病例处于晚期(IB2期或更晚),其中超过一半可能为III期或IV期。宫颈癌分期基于临床检查结果(国际妇产科联盟(FIGO)分期)。在欧美,IB2期至III期宫颈癌的标准治疗是非手术治疗(放化疗)。然而,在放疗资源有限的发展中国家,局部晚期宫颈癌可能采用化疗联合子宫切除术(切除子宫及子宫颈,可连带或不连带周围组织的手术)进行治疗。尚不确定这种治疗方式能否提高生存率。因此,系统评估子宫切除术作为局部晚期宫颈癌(IB2期至III期)放疗或化疗(或两者)之外的替代干预措施的价值很重要。
确定局部晚期宫颈癌(IB2期至III期)女性在接受放疗或化疗(或两者)标准治疗的基础上,加行子宫切除术与单纯标准治疗相比是否安全有效。
我们检索了截至2014年2月的Cochrane妇科癌症组试验注册库、Cochrane系统评价数据库、医学期刊数据库、荷兰医学文摘数据库和拉丁美洲及加勒比地区卫生科学数据库。我们还检索了临床试验注册库、科学会议摘要以及纳入研究的参考文献列表。
我们检索了随机对照试验(RCT),这些试验比较了首次就诊的晚期(IB2期至III期)宫颈癌女性中,涉及子宫切除术与放疗或化疗(或两者)的治疗方案。
我们独立评估研究的纳入资格,提取数据并评估偏倚风险。在可能的情况下,使用随机效应模型对总体生存率、疾病进展或无病生存率结局进行Meta分析。不良事件报告不完整,因此单个试验结果以叙述形式描述。
我们在综述中纳入了7项方法学质量各异的RCT(1217名女性);大多数试验存在中度或高度偏倚风险。3项为多中心试验,2项为单中心试验,2项试验不清楚是单中心还是多中心。这些试验比较了以下针对局部晚期宫颈癌(IB2期至III期)女性的干预措施:子宫切除术(单纯或根治性)联合放疗(N = 194)与单纯放疗(N = 180);子宫切除术(单纯或根治性)联合放化疗(N = 31)与单纯放化疗(N = 30);根治性子宫切除术联合放化疗(N = 111)与腔内放疗联合放化疗(N = 100);子宫切除术(单纯或根治性)联合新辅助化疗(N = 298)与单纯放疗(N = 273)。一项试验(N = 256)发现,接受减量化放疗后行子宫切除术的女性与单纯接受放疗(外照射和腔内照射)的女性相比,死亡或疾病进展风险无差异(风险比(HR)0.89,95%置信区间(CI)0.61至1.29)。该试验还报告两组在不良反应方面无差异(子宫切除术和放疗组18/129例3级或4级不良反应,单纯放疗组18/121例女性中有19例)。另一项试验(N = 118)报告相同比较时,5年无瘤精算生存率(代表特定参与者群体可能存活年数)或严重并发症(3级)无差异(放疗联合手术组与单纯放疗组分别为6/62和6/56)。所有这些结局的证据质量都很低。一项试验(N = 61)报告,放化疗联合子宫切除术与单纯放化疗相比,3年总生存率和无复发生存率无差异(P值> 0.10,低质量证据)。未报告不良事件和发病率数据。同样,另一项试验(N = 211)发现,两组在接受体外照射放化疗后,接受腔内放疗与子宫切除术的女性在死亡风险(HR 0.65,95% CI 0.35至1.21,P值 = 0.19,低质量证据)、疾病进展风险(HR 0.70,95% CI 0.31至1.34,P值 = 0.24,低质量证据)或严重晚期并发症方面无差异(P值 = 0.53,低质量证据)。对三项新辅助化疗联合子宫切除术与单纯放疗试验的Meta分析,共评估571名参与者,发现接受新辅助化疗加子宫切除术的女性死亡风险低于单纯接受放疗的女性(HR 0.71,95% CI 0.55至0.93,I² = 0%,中度质量证据)。然而,接受新辅助化疗加子宫切除术的参与者中有相当一部分也接受了放疗。两组疾病进展或复发女性的比例无差异(RR 0.75,95% CI 0.53至1.05,I² = 20%,中度质量证据)。单个试验结果报告两组在长期严重并发症、3级急性毒性和严重晚期毒性方面无明显差异(P值> 0.05,低质量证据)。所有试验均未报告生活质量结局。
从现有的RCT中,我们发现没有足够的证据表明,子宫切除术联合放疗(无论是否联合化疗)能提高单纯接受放疗或化疗的局部晚期宫颈癌女性的生存率。不同结局的证据总体质量各不相同,且由于对偏倚风险的担忧,证据质量普遍被下调。新辅助化疗联合根治性子宫切除术与单纯放疗相比,生存结局的证据质量为中度,其他比较的证据质量较低。这主要是基于报告不佳和数据稀少,结果基于单个试验。更多评估有无子宫切除术的医疗管理试验可能会检验本综述结果的稳健性,因为进一步的研究可能会对我们对效应估计的信心产生重要影响。