Thamronganantasakul Komsan, Supakalin Narudom, Kietpeerakool Chumnan, Pattanittum Porjai, Lumbiganon Pisake
Department of Radiology, Khon Kaen University, Faculty of Medicine, Mittraphap Road, Muang, Khon Kaen, Thailand, 40002.
Cochrane Database Syst Rev. 2018 Oct 26;10(10):CD012301. doi: 10.1002/14651858.CD012301.pub2.
The para-aortic lymph nodes (located along the major vessels in the mid and upper abdomen) are a common place for disease recurrence after treatment for locally advanced cervical cancer. The para-aortic area is not covered by standard pelvic radiotherapy fields and so treatment to the pelvis alone is inadequate for women at a high risk of occult cancer within para-aortic lymph nodes. Extended-field radiotherapy (RT) widens the pelvic RT field to include the para-aortic lymph node area. Extended-field RT may improve outcomes in women with locally advanced cervical cancer by treating occult disease in para-aortic nodes not identified at pretreatment imaging. However, RT treatment of the para-aortic area can cause severe adverse effects, so may increase harms.Studies of pelvic chemoradiotherapy (CRT) demonstrated improved survival rates compared to pelvic RT alone. CRT is now the standard of care in the treatment of locally advanced cervical cancer. Studies comparing pelvic RT alone (without concurrent chemotherapy) with extended-field RT should therefore be viewed with caution, since they compare treatments against what is now substandard treatment (pelvic RT alone). This review should therefore be read with this in mind and comparisons with pelvic RT cannot be extrapolated to pelvic CRT.
To evaluate the effectiveness and toxicity of extended-field radiotherapy in women undergoing first-line treatment for locally advanced cervical cancer.
We searched the Cochrane Central Register of Controlled Trials (CENTRAL; 2018, Issue 7), MEDLINE via Ovid (1946 to August week 4, 2018), and Embase via Ovid (1980 to 2018, week 35). We checked registers of clinical trials, grey literature, conference reports, and citation lists of included studies to August 2018.
We included randomised controlled trials (RCTs) evaluating the effectiveness and toxicity of extended-field RT for locally advanced cervical cancer.
Two review authors independently selected potentially relevant RCTs, extracted data, assessed risk of bias, compared results, and made judgements on the quality and certainty of the evidence for each outcome. Any disagreements were resolved by discussion or consultation with a third review author.
Five studies met the inclusion criteria. Three included studies compared extended-field RT versus pelvic RT, one included study compared extended-field RT with pelvic CRT, and one study compared extended-field CRT versus pelvic CRT.Extended-field radiotherapy versus pelvic radiotherapy aloneCompared to pelvic RT, extended-field RT probably reduces the risk of death (hazard ratio (HR) 0.67, 95% confidence interval (CI) 0.48 to 0.94; 1 study; 337 participants; moderate-certainty evidence) and para-aortic lymph node recurrence (risk ratio (RR) 0.36, 95% CI 0.18 to 0.70; 2 studies; 477 participants; moderate-certainty evidence), although there may or may not have been improvement in the risk of disease progression (HR 0.92, 95% CI 0.69 to 1.22; 1 study; 337 participants; moderate-certainty evidence) and severe adverse events (RR 1.05, 95% CI 0.79 to 1.41; 2 studies; 776 participants; moderate-certainty evidence).Extended-field radiotherapy versus pelvic chemoradiotherapyIn a comparison of extended-field RT versus pelvic CRT, women given pelvic CRT probably had a lower risk of death (HR 0.50, 95% CI 0.39 to 0.64; 1 study; 389 participants; moderate-certainty evidence) and disease progression (HR 0.52, 95% CI 0.37 to 0.72; 1 study; 389 participants; moderate-certainty evidence). Participants given extended-field RT may or may not have had a lower risk of para-aortic lymph node recurrence (HR 0.44, 95% CI 0.20 to 0.99; 1 study; 389 participants; low-certainty evidence) and acute severe adverse events (RR 0.05, 95% CI 0.02 to 0.11; 1 study; 388 participants; moderate-certainty evidence). There were no clear differences in terms of late severe adverse events among the comparison groups (RR 1.06, 95% CI 0.69 to 1.62; 1 study; 386 participants; moderate-certainty evidence).Extended-field chemoradiotherapy versus pelvic chemoradiotherapyVery low-certainty evidence obtained from one small study (74 participants) showed that, compared to pelvic CRT, extended-field CRT may or may not have reduced risk of death (HR 0.37, 95% CI 0.14 to 0.96) and disease progression (HR 0.25, 95% CI 0.07 to 0.87). There were no clear differences between the groups in the risks of para-aortic lymph node recurrence (RR 0.19, 95% CI 0.02 to 1.54; very low-certainty evidence) and severe adverse events (acute: RR 0.95, 95% CI 0.20 to 4.39; late: RR 0.95, 95% CI 0.06 to 14.59; very low-certainty evidence).
AUTHORS' CONCLUSIONS: Moderate-certainty evidence shows that, compared with pelvic RT alone, extended-field RT probably improves overall survival and reduces risk of para-aortic lymph node recurrence. However, pelvic RT alone would now be considered substandard treatment, so this result cannot be extrapolated to modern standards of care. Low- to moderate-certainty evidence suggests that pelvic CRT may increase overall and progression-free survival compared to extended-field RT, although there may or may not be a higher rate of para-aortic recurrence and acute adverse events. Extended-field CRT versus pelvic CRT may improve overall or progression-free survival, but these findings should be interpreted with caution due to very low-certainty evidence.High-quality RCTs, comparing modern treatment techniques in CRT, are needed to more fully inform treatment for locally advanced cervical cancer without obvious para-aortic node involvement.
腹主动脉旁淋巴结(位于中上腹部的主要血管旁)是局部晚期宫颈癌治疗后疾病复发的常见部位。腹主动脉旁区域不在标准盆腔放疗野范围内,因此对于腹主动脉旁淋巴结存在隐匿性癌风险较高的女性,仅对盆腔进行治疗是不够的。扩大野放疗(RT)可扩大盆腔放疗野以包括腹主动脉旁淋巴结区域。扩大野放疗可能通过治疗预处理影像学未发现的腹主动脉旁淋巴结隐匿性疾病,改善局部晚期宫颈癌女性的治疗效果。然而,腹主动脉旁区域的放疗会导致严重不良反应,因此可能增加危害。盆腔放化疗(CRT)的研究表明,与单纯盆腔放疗相比,生存率有所提高。CRT目前是局部晚期宫颈癌治疗的标准方案。因此,应谨慎看待比较单纯盆腔放疗(不联合化疗)与扩大野放疗的研究,因为它们是将现有治疗方案与目前的次标准治疗(单纯盆腔放疗)进行比较。因此,本综述应考虑到这一点进行阅读,与盆腔放疗的比较不能外推至盆腔CRT。
评估扩大野放疗对局部晚期宫颈癌一线治疗女性的有效性和毒性。
我们检索了Cochrane对照试验中心注册库(CENTRAL;2018年第7期)、通过Ovid检索的MEDLINE(1946年至2018年8月第4周)以及通过Ovid检索的Embase(1980年至2018年第35周)。我们查阅了临床试验注册库、灰色文献、会议报告以及纳入研究截至2018年8月的参考文献列表。
我们纳入了评估扩大野放疗对局部晚期宫颈癌有效性和毒性的随机对照试验(RCT)。
两位综述作者独立选择潜在相关的RCT,提取数据,评估偏倚风险,比较结果,并对每个结局的证据质量和确定性做出判断。任何分歧都通过讨论或与第三位综述作者协商解决。
五项研究符合纳入标准。三项纳入研究比较了扩大野放疗与盆腔放疗,一项纳入研究比较了扩大野放疗与盆腔CRT,一项研究比较了扩大野CRT与盆腔CRT。
扩大野放疗与单纯盆腔放疗相比
与盆腔放疗相比,扩大野放疗可能降低死亡风险(风险比(HR)0.67,95%置信区间(CI)0.48至0.94;1项研究;337名参与者;中等确定性证据)和腹主动脉旁淋巴结复发风险(风险比(RR)0.36,95%CI 0.18至0.