Carr T Hedley, Adelman Carrie, Barnicle Alan, Kozarewa Iwanka, Luke Sally, Lai Zhongwu, Hollis Sally, Dougherty Brian, Harrington Elizabeth A, Kang Jinyu, Saad Fred, Sala Nuria, Thiery-Vuillemin Antoine, Clarke Noel W, Hodgson Darren, Barrett J Carl
AstraZeneca, Cambridge CB4 0WG, UK.
AstraZeneca, Boston, MA 43183, USA.
Cancers (Basel). 2021 Nov 20;13(22):5830. doi: 10.3390/cancers13225830.
Phase III randomized trial data have confirmed the activity for olaparib in homologous recombination repair (HRR) mutated metastatic castration-resistant prostate cancer (mCRPC) post next-generation hormonal agent (NHA) progression. Preclinical data have suggested the potential for a combined effect between olaparib and NHAs irrespective of whether an HRR gene alteration was present. NCT01972217 was a randomised double-blind Phase II study which evaluated olaparib and abiraterone versus placebo and abiraterone in mCRPC patients who had received prior chemotherapy containing docetaxel. The study showed that radiologic progression was significantly delayed by the combination of olaparib and abiraterone regardless of homologous recombination repair mutation (HRRm) status. The study utilized tumour, blood (germline), and circulating tumour DNA (ctDNA) analysis to profile patient HRRm status, but tumour tissue provision was not mandated, leading to relatively low tissue acquisition and DNA sequencing success rates not representative of real-world testing.
Further analysis of germline and ctDNA samples has been performed for the trial to characterize HRRm status more fully and robustly analyse patient response to treatment.
Germline and plasma testing increased the HRRm characterized population from 27% to 68% of 142 randomized patients. Tumour-derived variants were detectable with high confidence in 78% of patients with a baseline plasma sample (71% of randomized patients). There was high concordance across methodologies (plasma vs. tumour; plasma vs. germline). The HR for the exploratory analysis of radiographic progression-free survival was 0.54 (95% CI: 0.32-0.93) in favour of olaparib and abiraterone in the updated HRR wild type (HRRwt) group ( = 73) and 0.62 (95% CI: 0.23-1.65) in the HRRm group ( = 23).
Our results confirm the value of plasma testing for HRRm status when there is insufficient high-quality tissue for multi-gene molecular testing. We show that patients with mCRPC benefit from the combination of olaparib and abiraterone treatment regardless of HRRm status. The combination is currently being further investigated in the Phase III PROpel trial.
III期随机试验数据已证实奥拉帕利在同源重组修复(HRR)突变的转移性去势抵抗性前列腺癌(mCRPC)经新一代激素药物(NHA)治疗进展后的活性。临床前数据表明,无论是否存在HRR基因改变,奥拉帕利与NHA之间都可能存在联合效应。NCT01972217是一项随机双盲II期研究,评估了奥拉帕利和阿比特龙与安慰剂和阿比特龙在接受过含多西他赛化疗的mCRPC患者中的疗效。该研究表明,无论同源重组修复突变(HRRm)状态如何,奥拉帕利和阿比特龙联合使用均能显著延迟影像学进展。该研究利用肿瘤、血液(胚系)和循环肿瘤DNA(ctDNA)分析来确定患者的HRRm状态,但未强制要求提供肿瘤组织,导致组织获取率和DNA测序成功率相对较低,无法代表真实世界的检测情况。
对该试验的胚系和ctDNA样本进行了进一步分析,以更全面、更可靠地分析患者的HRRm状态及对治疗的反应。
胚系和血浆检测使142例随机分组患者中HRRm特征明确的人群比例从27%增加到68%。在78%有基线血浆样本的患者(占随机分组患者的71%)中,可高度可靠地检测到肿瘤衍生变异。各方法之间(血浆与肿瘤;血浆与胚系)具有高度一致性。在更新的HRR野生型(HRRwt)组(n = 73)中,影像学无进展生存期探索性分析的风险比为0.54(95%置信区间:0.32 - 0.93),支持奥拉帕利和阿比特龙联合治疗;在HRRm组(n = 23)中为0.62(95%置信区间:0.23 - 1.65)。
我们的结果证实了在缺乏足够高质量组织进行多基因分子检测时,血浆检测对HRRm状态的价值。我们表明,无论HRRm状态如何,mCRPC患者都能从奥拉帕利和阿比特龙联合治疗中获益。目前正在III期PROpel试验中对该联合治疗进行进一步研究。