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妊娠危及生命的血液系统恶性肿瘤的免疫化疗:文献系统评价和临床试验资格的横断面分析。

Immunochemotherapy for life-threatening haematological malignancies in pregnancy: a systematic review of the literature and cross-sectional analysis of clinical trial eligibility.

机构信息

Department of Haematology, Northern Beaches Hospital, Frenchs Forest, NSW, Australia; Faculty of Medicine and Health, University of New South Wales, Sydney, NSW, Australia; Faculty of Medicine, Macquarie University, North Ryde, NSW, Australia.

Department of Haematology and Bone Marrow Transplant, St Vincent's Hospital, Darlinghurst, NSW, Australia.

出版信息

Lancet Haematol. 2023 Jun;10(6):e458-e467. doi: 10.1016/S2352-3026(23)00059-5.

Abstract

The management of potentially life-threatening malignancies in pregnancy is complicated by a lack of robust safety and efficacy evidence. This data shortage stems from a historical exclusion of women of childbearing potential from prospective clinical trials due to concerns around potential teratogenicity and toxicity of investigational agents. We conducted a systematic review of published data on immunochemotherapeutic treatment of life-threatening haematological malignancies in pregnancy between 2010 and 2022, and the maternal and neonatal outcomes. We then performed a cross-sectional observational study of clinical trial protocols on ClinicalTrials.gov, between 2016 and 2022, recruiting women of childbearing potential with potentially life-threatening haematological malignancies, collecting trial demographic data, and documenting whether pregnant or lactating women were explicitly excluded, along with the type and duration of contraception required for women of childbearing potential. We included 17 studies for analysis in our systematic review. A total of 595 women were treated with immunochemotherapy during pregnancy, with a median age of 29 years (range 14-48). Of these, 81 women (14%) were treated in the first trimester, and 514 (86%) were treated in the second and third trimesters collectively. In total, 68 trials for acute myeloid leukaemia, acute lymphocytic leukaemia, high-grade non-Hodgkin lymphoma, and Hodgkin lymphoma (40%, 26%, 21%, and 13%, respectively) were included in our ClinicalTrials.gov analysis. Most protocols (66 [97%]) explicitly excluded pregnant women, with 40 (69%) not providing a rationale for exclusion. The potential harm to the fetus from anti-cancer therapy has historically been given greater moral precedence than a pregnant woman's autonomy. This pattern is reflected in the lack of rigorous evidence for immunochemotherapy in pregnancy and a universal exclusion of pregnant and lactating women from clinical trial protocols in this study. Nonetheless, the administration of systemic chemotherapy in the second and third trimesters was not associated with an increased rate of congenital malformations or perinatal mortality in our systematic review cohort, with maternal outcomes broadly comparable to those of the non-pregnant population.

摘要

在怀孕期间,对潜在危及生命的恶性肿瘤的管理因缺乏强有力的安全性和疗效证据而变得复杂。这种数据短缺源于历史上由于对潜在致畸性和受试药物毒性的担忧,将有生育能力的女性排除在前瞻性临床试验之外。我们对 2010 年至 2022 年期间发表的关于免疫化学治疗危及生命的血液系统恶性肿瘤的研究数据进行了系统评价,并对母婴结局进行了分析。然后,我们对 2016 年至 2022 年期间 ClinicalTrials.gov 上的临床试验方案进行了横断面观察性研究,这些方案招募了患有潜在危及生命的血液系统恶性肿瘤的有生育能力的女性,收集了试验人口统计学数据,并记录了是否明确排除了孕妇或哺乳期妇女,以及有生育能力的女性所需的避孕类型和持续时间。我们将 17 项研究纳入系统评价进行分析。共有 595 名女性在怀孕期间接受了免疫化学治疗,中位年龄为 29 岁(范围 14-48 岁)。其中,81 名女性(14%)在孕早期接受治疗,514 名女性(86%)在孕中期和孕晚期联合接受治疗。共有 68 项针对急性髓系白血病、急性淋巴细胞白血病、高级别非霍奇金淋巴瘤和霍奇金淋巴瘤的临床试验(分别占 40%、26%、21%和 13%)被纳入我们的 ClinicalTrials.gov 分析。大多数方案(66 [97%])明确排除了孕妇,其中 40 项(69%)未提供排除的理由。从历史上看,抗癌治疗对胎儿的潜在危害比孕妇的自主权更具道德优先权。这种模式反映在妊娠期间免疫化学治疗缺乏严格的证据,以及本研究中普遍将孕妇和哺乳期妇女排除在临床试验方案之外。尽管如此,在我们的系统评价队列中,在妊娠中期和晚期使用全身化疗与先天性畸形或围产期死亡率增加无关,母婴结局与非孕妇人群大致相当。

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