Dawson Laura A, Ringash Jolie, Fairchild Alysa, Stos Paul, Dennis Kristopher, Mahmud Aamer, Stuckless Teri Lynn, Vincent Francois, Roberge David, Follwell Matthew, Wong Raimond K W, Jonker Derek J, Knox Jennifer J, Zimmermann Camilla, Wong Philip, Barry Aisling S, Gaudet Marc, Wong Rebecca K S, Purdie Thomas G, Tu Dongsheng, O'Callaghan Christopher J
University Health Network-Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.
University Health Network-Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.
Lancet Oncol. 2024 Oct;25(10):1337-1346. doi: 10.1016/S1470-2045(24)00438-8. Epub 2024 Sep 5.
Palliative treatment options for painful hepatic cancer can be restricted due to patients eventually becoming refractory to standard treatment. The aim of this study was to determine whether radiotherapy improves hepatic pain from cancer.
In this open-label, randomised, controlled, phase 3 trial (CCTG HE1) done in nine cancer centres across Canada, we included patients aged 18 years or older with hepatocellular carcinoma or liver metastases, who were refractory to standard treatment, with an Eastern Cooperative Oncology Group performance status of 0-3, with life expectancy of more than 3 months, and pain or discomfort at its worst in the past 24 hours on the Brief Pain Inventory (BPI) of at least 4 out of 10, which was stable for up to 7 days before randomisation. Patients were randomly assigned (1:1), via a minimisation method after stratification by centre and type of cancer (hepatocellular carcinoma vs liver metastases), to single-fraction radiotherapy (8 Gy) to the liver with 8 mg ondansetron (or equivalent) orally and 4 mg dexamethasone orally given 1-2 h before radiotherapy plus best supportive care (including non-opioid or opioid analgesia, or dexamethasone, or a combination of these) or best supportive care alone. The primary endpoint was improvement in patient-reported liver cancer pain or discomfort of at least 2 points on worst pain intensity on the BPI at 1 month after randomisation. All patients with both baseline and 1-month assessments were included in the primary endpoint analysis. Safety was assessed in all patients randomly assigned to treatment. This trial is registered with ClinicalTrials.gov, NCT02511522, and is complete.
Between July 25, 2015, and June 2, 2022, 66 patients were screened and randomly assigned to radiotherapy plus best supportive care (n=33) or best supportive care (n=33). Median age was 65 years (IQR 57-72), 37 (56%) of 66 patients were male, 29 (44%) were female, 43 (65%) had liver metastases, and 23 (35%) had hepatocellular carcinoma (data on race and ethnicity were not collected). As of data cutoff (Sept 8, 2022), median follow-up was 3·2 months (95% CI 3·0-3·4). 24 (73%) of 33 in the radiotherapy plus best supportive care group and 18 (55%) of 33 in the best supportive care only group completed baseline and 1-month assessments. An improvement in hepatic pain of at least 2 points in worst pain intensity on the BPI at 1 month was seen in 16 (67%) of 24 patients in the radiotherapy plus best supportive care group versus four (22%) of 18 patients in the best supportive care group (p=0·0042). The most common grade 3-4 adverse events within 1 month after randomisation were abdominal pain (three [9%] of 33 in the radiotherapy group vs one [3%] of 33 in best supportive care group) and ascites (two [6%] vs one [3%]). No serious adverse events or treatment-related deaths were observed.
Single-fraction radiotherapy plus best supportive care improved pain compared with best supportive care alone in patients with liver cancer, and could be considered a standard palliative treatment.
Canadian Cancer Society.
由于患者最终可能对标准治疗产生耐药性,肝癌疼痛的姑息治疗选择可能会受到限制。本研究的目的是确定放射治疗是否能改善肝癌引起的肝区疼痛。
在加拿大9个癌症中心进行的这项开放标签、随机、对照、3期试验(CCTG HE1)中,我们纳入了年龄在18岁及以上、患有肝细胞癌或肝转移、对标准治疗耐药、东部肿瘤协作组体能状态为0 - 3、预期寿命超过3个月,且在过去24小时内根据简明疼痛量表(BPI)评估的最严重疼痛或不适至少为4分(满分10分)且在随机分组前至少7天稳定的患者。患者通过中心和癌症类型(肝细胞癌与肝转移)分层后的最小化法,以1:1的比例随机分配,接受单次肝脏放射治疗(8 Gy),同时在放疗前1 - 2小时口服8 mg昂丹司琼(或等效药物)和4 mg地塞米松,再加上最佳支持治疗(包括非阿片类或阿片类镇痛、地塞米松或这些药物的组合),或仅接受最佳支持治疗。主要终点是随机分组后1个月时患者报告的肝癌疼痛或不适在BPI最严重疼痛强度上至少改善2分。所有有基线和1个月评估的患者均纳入主要终点分析。对所有随机分配接受治疗的患者进行安全性评估。本试验已在ClinicalTrials.gov注册,注册号为NCT02511522,现已完成。
在2015年7月25日至2022年6月2日期间,66例患者被筛选并随机分配至放射治疗加最佳支持治疗组(n = 33)或最佳支持治疗组(n = 33)。中位年龄为65岁(四分位间距为57 - 72岁),66例患者中37例(56%)为男性,29例(44%)为女性,43例(65%)有肝转移,23例(35%)有肝细胞癌(未收集种族和民族数据)。截至数据截止日期(2022年9月8日),中位随访时间为3.2个月(95%置信区间3.0 - 3.4)。放射治疗加最佳支持治疗组33例中有24例(73%)、仅最佳支持治疗组33例中有18例(55%)完成了基线和1个月评估。放射治疗加最佳支持治疗组24例患者中有16例(67%)在1个月时BPI最严重疼痛强度上肝区疼痛改善至少2分,而最佳支持治疗组18例患者中有4例(22%)改善(p = 0.0042)。随机分组后1个月内最常见的3 - 4级不良事件是腹痛(放射治疗组33例中有3例[9%],最佳支持治疗组33例中有1例[3%])和腹水(2例[6%]对1例[3%])。未观察到严重不良事件或与治疗相关的死亡。
与单纯最佳支持治疗相比,单次放射治疗加最佳支持治疗可改善肝癌患者的疼痛,可被视为一种标准的姑息治疗方法。
加拿大癌症协会。