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生育力与 CAR-T 细胞:当前实践与未来方向

英文原题:Fertility and CAR T-cells: Current practice and future directions.

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Fertility and CAR T-cells: Current practice and future directions.

PubMed 2022/06/12(内容时间) Transplant Cell Ther Q1 · IF 4.7(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T 细胞有助于克服化疗耐药,已证实对 B 细胞血液系统恶性肿瘤疗效显著。CAR-T 细胞最初用于多线复发/难治性疾病患者;随着治疗时机提前,了解这一新疗法对癌症远期影响的意义将十分重要。

本研究旨在评估 CAR-T 治疗相关生育问题的现有考量框架,并确定教育和未来研究机会。为了解 CAR-T 后生育情况、治疗前后生育指导及生育力保存实践,并确定未来研究方向,研究者于 2021 年 10 月 12 日至 11 月 2 日向美国及国际上约 300 家治疗 CAR-T 患者的国际血液与骨髓移植研究中心(CIBMTR)医疗中心,以电子方式发放关于 CAR-T 生育咨询和结局实践模式的横断面调查;每家机构由一名医疗提供者代表完成调查。共收到 96 份答卷,其中 66 家中心使用 CAR-T 并提供至少部分答复,纳入主要分析。各中心在人口学特征、CAR-T 使用经验及患者构成方面差异较大。18 家中心仅治疗儿童患者,这些中心的患者更可能因 B 急性淋巴细胞白血病接受治疗。6 家中心报告 CAR-T 后妊娠 7 例、活产 5 例(其中 1 家为儿童专科中心)。多数中心尚无 CAR-T 前后生育力保存指南,也未制定 CAR-T 后避免妊娠或使他人受孕的建议。应答中心提出的未来研究方向归纳为三个主题:标准化 CAR-T 前后生育指南、CAR-T 治疗后的长期生育结局、CAR-T 对发育中胎儿的影响,以及评估研究 CAR-T 患者生育问题的必要性。

我们发现,各中心对 CAR-T 后避免妊娠或使他人受孕的指导差异很大,生育力保存转诊实践也广泛不同;后者可能是因为当前接受 CAR-T 的患者多为多线复发/难治性患者。

总之,这是首篇报告 CAR-T 后多例活产的研究,突显进一步研究 CAR-T 治疗和生育问题的重要性,并提出了一系列新研究问题。

展开英文摘要原文

Chimeric antigen receptor (CAR) T-cells serve to overcome chemotherapeutic resistance and have been proven to be highly effective in B-cell hematologic malignancies. Although initial use has been in patients with multiply relapsed/refractory disease, as CAR T-cells are used earlier in the treatment paradigm, it will be important to explore implications of this novel therapy on cancer late-effects.

We sought to assess the current framework for considerations of fertility surrounding CAR T-cell use and identify opportunities for education and future research.

To assess current practice patterns regarding post-CAR T-cell fertility, peri-CAR T-cell fertility guidance, utilization of fertility preservation surrounding CAR T-cell administration and identify future areas of research, a cross-sectional survey assessing practice patterns regarding fertility counseling and outcomes surrounding CAR T-cell therapy was distributed electronically to approximately 300 Center for International Blood and Marrow Transplant Research medical centers treating patients with CAR T-cell therapy in the United States and internationally between October 12 and November 2, 2021.

One medical provider was asked to complete the study survey on behalf of their institution.

We received 96 survey responses, of which 66 centers utilized CAR T-cells and provided at least partial responses that were used for the primary analysis. Centers were varied in demographics, experience in administering CAR T-cells, and aspects of patients receiving CAR T-cells. Eighteen centers exclusively treated pediatric patients, and patients at these centers were more likely to be treated for B-cell acute lymphoblastic leukemia. Seven pregnancies and 5 live births after CAR T-cells were reported from 6 centers (1 pediatric-only).

Most centers had no established guidelines in place regarding fertility preservation in the peri-CAR T-cell period or regarding recommendations for avoiding pregnancy/fathering a child after receiving CAR T-cells.

Areas for future research were elicited from responding centers and categorized into 3 broad themes, including: standardized peri-CAR T-cell fertility guidelines; long-term fertility outcomes after CAR T-cell therapy; impact of CAR T-cells on a developing fetus; and determining the relevance of studying fertility in patients who receive CAR T-cells.

We identified a high degree of variability in peri-CAR T-cell guidance on avoidance of pregnancy/fathering a child, as well as a wide-range of practices surrounding referral for fertility preservation, the latter of which may be likely due to the fact that patients receiving CAR T-cells in the present era are likely multiply relapsed/refractory.

In summary, this is the first report of several live-births following CAR T-cells, which highlights the important need for further research in CAR T-cell therapy and fertility, with a host of novel research questions identified.

论文信息

作者
Ligon JA、Fry A、Maher JY、Foley T、Silbert S、Yates B、Gomez-Lobo V、Wiener L
第一作者单位
Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland; Department of Pediatrics, Division of Hematology/Oncology, University of Florida College of Medicine, Gainesville, Florida. Electronic address: john.ligon@ufl.edu.United States
通讯作者单位
Pediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland. Electronic address: Nirali.Shah@nih.gov.United States
文献类型
美国 NIH 院内研究
期刊
Transplantation and cellular therapy2022 Sep
原文标识
PubMed 35705177 · DOI 10.1016/j.jtct.2022.06.002