Genito-Urinary Cancer Research Group, Division of Cancer Sciences, The University of Manchester, Manchester, United Kingdom.
FASTMAN Centre of Excellence, Manchester Cancer Research Centre, Manchester, United Kingdom.
JAMA Oncol. 2021 Apr 1;7(4):555-563. doi: 10.1001/jamaoncol.2020.7857.
Prostate radiotherapy (RT) improves survival in men with low-burden metastatic prostate cancer. However, owing to the dichotomized nature of metastatic burden criteria, it is not clear how this benefit varies with bone metastasis counts and metastatic site.
To evaluate the association of bone metastasis count and location with survival benefit from prostate RT.
DESIGN, SETTING, AND PARTICIPANTS: This exploratory analysis of treatment outcomes based on metastatic site and extent as determined by conventional imaging (computed tomography/magnetic resonance imaging and bone scan) evaluated patients with newly diagnosed metastatic prostate cancer randomized within the STAMPEDE trial's metastasis M1 RT comparison. The association of baseline bone metastasis counts with overall survival (OS) and failure-free survival (FFS) was assessed using a multivariable fractional polynomial interaction procedure. Further analysis was conducted in subgroups.
Patients were randomized to receive either standard of care (androgen deprivation therapy with or without docetaxel) or standard of care and prostate RT.
The primary outcomes were OS and FFS.
A total of 1939 of 2061 men were included (median [interquartile range] age, 68 [63-73] years); 1732 (89%) had bone metastases. Bone metastasis counts were associated with OS and FFS benefit from prostate RT. Survival benefit decreased continuously as the number of bone metastases increased, with benefit most pronounced up to 3 bone metastases. A plot of estimated treatment effect indicated that the upper 95% CI crossed the line of equivalence (hazard ratio [HR], 1) above 3 bone metastases without a detectable change point. Further analysis based on subgroups showed that the magnitude of benefit from the addition of prostate RT was greater in patients with low metastatic burden with only nonregional lymph nodes (M1a) or 3 or fewer bone metastases without visceral metastasis (HR for OS, 0.62; 95% CI, 0.46-0.83; HR for FFS, 0.57; 95% CI, 0.47-0.70) than among patients with 4 or more bone metastases or any visceral/other metastasis (HR for OS, 1.08; 95% CI, 0.91-1.28; interaction P = .003; HR for FFS, 0.87; 95% CI, 0.76-0.99; interaction P = .002).
In this exploratory analysis of a randomized clinical trial, bone metastasis count and metastasis location based on conventional imaging were associated with OS and FFS benefit from prostate RT in M1 disease.
ClinicalTrials.gov Identifier: NCT00268476; ISRCTN.com Identifier: ISRCTN78818544.
前列腺放疗(RT)可改善低负担转移性前列腺癌男性的生存。然而,由于转移性负担标准的二分法性质,尚不清楚这种益处如何随骨转移计数和转移部位而变化。
评估骨转移计数和位置与前列腺 RT 生存获益的关系。
设计、地点和参与者:这项基于转移性部位和程度的治疗结果的探索性分析是根据常规影像学(计算机断层扫描/磁共振成像和骨扫描)确定的,评估了在 STAMPEDE 试验的转移性 M1 RT 比较中随机分组的新发转移性前列腺癌患者。使用多变量分数多项式交互程序评估基线骨转移计数与总生存期(OS)和无失败生存期(FFS)的相关性。进一步在亚组中进行了分析。
患者被随机分配接受标准护理(雄激素剥夺治疗加或不加多西他赛)或标准护理和前列腺 RT。
主要结局是 OS 和 FFS。
共纳入 2061 例男性中的 1939 例(中位[四分位距]年龄,68[63-73]岁);1732 例(89%)有骨转移。骨转移计数与前列腺 RT 的 OS 和 FFS 获益相关。随着骨转移数量的增加,生存获益呈连续下降趋势,最多 3 个骨转移获益最明显。治疗效果的估计图表明,在上限 95%CI 超过 3 个骨转移且无检测到的变化点时,交叉了等效线(危险比[HR],1)。基于亚组的进一步分析表明,在转移性负担较低的患者中,仅存在非区域淋巴结(M1a)或 3 个或更少无内脏转移的骨转移(OS 的 HR,0.62;95%CI,0.46-0.83;FFS 的 HR,0.57;95%CI,0.47-0.70)中,添加前列腺 RT 的获益幅度大于 4 个或更多骨转移或任何内脏/其他转移(OS 的 HR,1.08;95%CI,0.91-1.28;交互 P=0.003;FFS 的 HR,0.87;95%CI,0.76-0.99;交互 P=0.002)。
在这项随机临床试验的探索性分析中,基于常规影像学的骨转移计数和转移部位与 M1 疾病中前列腺 RT 的 OS 和 FFS 获益相关。
ClinicalTrials.gov 标识符:NCT00268476;ISRCTN.com 标识符:ISRCTN78818544。