Yeoh Hui-Ling, Shingles Helen, Paul Eldho, Levvey Bronwyn J, Schwarz Max, Voskoboynik Mark, Haydon Andrew M, Shackleton Mark, Snell Gregory I, Andrews Miles C
Department of Medical Oncology, Alfred Health, Melbourne, Victoria, Australia.
Lung Transplant Service, Alfred Health, Melbourne, Victoria, Australia.
JHLT Open. 2024 Apr 4;4:100094. doi: 10.1016/j.jhlto.2024.100094. eCollection 2024 May.
Malignancy is a long-term complication of lung transplantation (LTx); however, contemporary Australian data and detailed evaluation of nonreportable cancers are lacking.
Retrospective review of LTx recipients' medical records and registry data linkage were performed to identify histologically proven malignancies. Baseline clinico-demographic variables were collected, and cancer incidence was compared with reported data for the general Australian population.
There were 1,715 LTx in 1,631 patients between 1989 and 2021, with a follow-up of 9,696 person-years. Eight hundred and ninety-three (54.8%) patients were male, and the median age at first LTx was 54.7 years. There were 886 deaths with a median overall survival of 7.5 years (95% confidence intervals (CI) 6.8-8.3 years). One thousand seven hundred and seventy-four separate invasive cancer events occurred across 407 patients, of which, 1,588 (89.5%) were nonmelanoma skin cancers (NMSCs). This translated to a 9-fold increased incidence of NMSCs and a 4-fold increased incidence of other cancers compared with the general population. Cancer mortality reached parity with chronic lung allograft dysfunction 10 years postfirst transplant and was independently associated with age (hazard ratios (HR) per year increase in age 1.02 [95% CI 1.01-1.03], = 0.001), Epstein-Barr virus primary mismatch (HR 3.24 [95% CI 1.68-6.25], vs nonmismatch, = 0.002), and cancer count (HR per cancer event 1.19 [95% CI 1.13-1.24], < 0.0001), but was not associated with a pretransplant malignancy history.
Our 31-year single-center experience demonstrates that malignancies are a significant mortality burden to long-term LTx survivors, dominated by NMSCs that are poorly reported in cancer datasets. A history of pretransplant malignancy was associated with a shorter time to post-transplant malignancy but was not associated with cancer death.
恶性肿瘤是肺移植(LTx)的一种长期并发症;然而,目前缺乏澳大利亚的相关数据以及对不可报告癌症的详细评估。
对肺移植受者的病历进行回顾性分析,并将登记数据进行关联,以确定经组织学证实的恶性肿瘤。收集基线临床人口统计学变量,并将癌症发病率与澳大利亚普通人群的报告数据进行比较。
1989年至2021年间,1631例患者接受了1715次肺移植,随访时间为9696人年。893例(54.8%)患者为男性,首次肺移植的中位年龄为54.7岁。共有886例死亡,中位总生存期为7.5年(95%置信区间[CI]6.8 - 8.3年)。407例患者共发生1774起独立的侵袭性癌症事件,其中1588例(89.5%)为非黑色素瘤皮肤癌(NMSC)。这意味着与普通人群相比,NMSC的发病率增加了9倍,其他癌症的发病率增加了4倍。首次移植后10年,癌症死亡率与慢性肺移植功能障碍相当,且与年龄(年龄每增加一岁的风险比[HR]为1.02[95%CI 1.01 - 1.03],P = 0.001)、爱泼斯坦 - 巴尔病毒初次错配(HR 3.24[95%CI 1.68 - 6.25],与非错配相比,P = 0.002)以及癌症数量(每起癌症事件的HR为1.19[95%CI 1.13 - 1.24],P < 0.0001)独立相关,但与移植前恶性肿瘤病史无关。
我们31年的单中心经验表明,恶性肿瘤是长期肺移植幸存者的重大死亡负担,以癌症数据集中报告不足的非黑色素瘤皮肤癌为主。移植前恶性肿瘤病史与移植后发生恶性肿瘤的时间较短有关,但与癌症死亡无关。