Steventon Luke, Nicum Shibani, Chambers Pinkie, Man Kenneth, Dodwell David, Wang Zhe, Patel Apini, Pickwell-Smith Ben, Wei Li
Research Department of Practice and Policy, Mezzanine Floor, BMA House, Tavistock Square, UCL School of Pharmacy, London, WC1H 9JP, United Kingdom; University College London Hospital NHS Foundation Trust, 235 Euston Road, London, NW1 2BU, United Kingdom.
University College London Hospital NHS Foundation Trust, 235 Euston Road, London, NW1 2BU, United Kingdom.
Eur J Cancer. 2025 Jun 3;222:115472. doi: 10.1016/j.ejca.2025.115472. Epub 2025 Apr 25.
Poly(ADP-ribose) polymerase inhibitors (PARPi) maintenance therapies are used to treat advanced ovarian cancer in first line and recurrent settings. Because of concerns about associations between PARPi therapy and secondary cancers myelodysplastic syndrome (MDS) and acute myeloid leukaemia (AML), a meta-analysis of clinical trials was conducted, reporting MDS/AML incidence of 0.73 %; however, clinical trial populations are highly selective and may not reflect incidence in the wider population.
This retrospective cohort study calculated incidence of MDS/AML within five years of completing first-line chemotherapy + /- PARPi maintenance for recurrent, advanced-stage ovarian cancer. Absolute and relative risks were calculated and compared to meta-analysis.
Of 11,531 included patients, 1529 received PARPi and 10,002 chemotherapy only. Absolute risk of MDS/AML was 0.3 % (n = 5/1529) for chemotherapy + PARPi maintenance therapy versus 0.1 % (n = 10/10,002) for chemotherapy alone. Relative risk was 2.97 (95 % CI 1.02, 8.68, p = 0.046) in patients receiving PARPi maintenance versus chemotherapy alone.
Relative risk of MDS/AML was greater in patients treated with PARPi; however, absolute risk was low in both treatment groups and lower than in the meta-analysis of trials. This analysis suggests small increased relative risk of MDS/AML associated with PARPi maintenance versus chemotherapy only, but not increased absolute risk.
聚(ADP - 核糖)聚合酶抑制剂(PARPi)维持疗法用于一线治疗晚期卵巢癌以及复发性卵巢癌。由于担心PARPi疗法与继发性癌症骨髓增生异常综合征(MDS)和急性髓细胞白血病(AML)之间的关联,开展了一项临床试验的荟萃分析,报告MDS/AML发病率为0.73%;然而,临床试验人群具有高度选择性,可能无法反映更广泛人群中的发病率。
这项回顾性队列研究计算了复发性晚期卵巢癌患者在完成一线化疗±PARPi维持治疗后的五年内MDS/AML的发病率。计算了绝对风险和相对风险,并与荟萃分析进行比较。
在纳入的11,531例患者中,1529例接受了PARPi治疗,10,002例仅接受了化疗。化疗 + PARPi维持治疗的MDS/AML绝对风险为0.3%(n = 5/1529),而单纯化疗的绝对风险为0.1%(n = 10/10,002)。接受PARPi维持治疗的患者与单纯化疗患者相比,相对风险为2.97(95%CI 1.02, 8.68,p = 0.046)。
接受PARPi治疗的患者发生MDS/AML的相对风险更高;然而,两个治疗组的绝对风险都很低,且低于试验的荟萃分析结果。该分析表明,与单纯化疗相比,PARPi维持治疗与MDS/AML的相对风险略有增加,但绝对风险并未增加。