Neuroendocrine tumours and pregnancy: Real-world data from an European Neuroendocrine Tumour Centre of Excellence.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-11-06 DOI:10.1111/jne.13465
Gowri M Ratnayake, Kalyan Mansukhbhai Shekhda, Thomas Glover, Yasser Al-Obudi, Aimee Hayes, Panagiotis Armonis, Dalvinder Mandair, Bernard Khoo, TuVinh Luong, Christos Toumpanakis, Ashley Grossman, Martyn Caplin
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Abstract

Neuroendocrine neoplasms (NENs) arise from the diffuse endocrine system and have been considered to be rare. However, the incidence and prevalence of these tumours have increased in recent years, and they are being seen in younger patients including women in the reproductive age group. Due to the paucity of data, diagnostic and therapeutic strategies in managing such tumours during pregnancy can be challenging to both treating physicians and patients. This article describes the experience and outcomes of managing pregnant women with NEN at a European Neuroendocrine Tumour Society (ENETS) Centre of Excellence. In this retrospective analysis, we evaluated a total of 22 pregnancies in 18 pregnant women with concurrent diagnoses of NENs who were managed at Royal Free Hospital ENETS Centre of Excellence throughout their pregnancy. These were identified from our tumour registry of 3500 NEN patients between 2015 and 2023. Cross-sectional imaging (computed tomography (CT)/magnetic resonance imaging (MRI)), pre- and post-pregnancy, for each patient was reviewed by an experienced radiologist. Tumour growth rate (TGR) was calculated using the formula: TGR = 100 × [exp (TG) - 1]; TG. [3 × log (D2/D1)]/time (months), where D1 is the tumour size at date 1; D2 is the tumour size at date 2; and time (months) = (Date 2 - Date 1 + 1)/30.44. Tumour growth rate pre-conception (TGRpc) and tumour growth rate post-partum (TGRpp) were calculated for each patient. In a sub-group of patients, positivity for oestrogen and progesterone receptors were analysed on the tumour tissue to evaluate whether the presence of these receptors affected tumour progression during the pregnancy. We also reviewed the pregnancy outcome in patients treated with somatostatin analogues during pregnancy. We analysed the data of a total 22 pregnancy encounters in 18 women: 15 pregnancies (68%) preceded the diagnosis of the NEN, whereas the diagnosis of NEN was made during pregnancy or in the post-partum period in 5 (23%) and 2 (9%) pregnancies respectively. Eight patients (44%) had a diagnosis of a pancreatic NEN, whereas 5 (28%) were diagnosed with mid-gut NENs, and a further 5 at other sites. The majority of the patients (n = 12, 67%) had evidence of metastatic disease at the time of diagnosis. Most pregnancies had a successful outcome (n = 19, 86%), whereas 3 patients (14%) had miscarriages in the 1st trimester. Five patients in total of 6 pregnancies were treated with somatostatin analogues as monotherapy during the pregnancy, and all of them had stable disease after pregnancy. All of them delivered healthy babies without any side effects or complications due to therapy. The average TGRpc was -0.8% (n = 5) and the average TGRpp was +0.96% (n = 6); 2 patients who did not have suitable targets for calculation of TGRpc developed new lesions suggesting disease progression. Moreover, 2 of the 4 patients who have had both pre-conception and post-pregnancy scans showed an increase in TGRpp compared to TGRpc. The management of NENs during pregnancy should be multidisciplinary with an individualised approach to each patient. Somatostatin analogues appear to be safe during pregnancy, though further robust studies are needed. Pregnancy per se may accelerate tumour progression, and patients should be counselled regarding this possibility.

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神经内分泌肿瘤与妊娠:来自欧洲神经内分泌肿瘤卓越中心的真实世界数据。
神经内分泌肿瘤(NENs)产生于弥漫性内分泌系统,一直被认为是罕见肿瘤。然而,近年来这类肿瘤的发病率和流行率都在上升,而且患者越来越年轻,包括育龄妇女。由于数据匮乏,在妊娠期管理此类肿瘤的诊断和治疗策略对主治医生和患者来说都具有挑战性。本文介绍了欧洲神经内分泌肿瘤协会(ENETS)卓越中心在治疗妊娠合并神经内分泌肿瘤孕妇方面的经验和结果。在这项回顾性分析中,我们评估了皇家自由医院ENETS卓越中心对18名同时诊断为NEN的孕妇的22次妊娠情况。这些孕妇是从 2015 年至 2023 年间 3500 名 NEN 患者的肿瘤登记册中确定的。每位患者怀孕前后的横断面成像(计算机断层扫描(CT)/磁共振成像(MRI))均由经验丰富的放射科医生进行审查。肿瘤生长率(TGR)的计算公式为TGR = 100 × [exp (TG) - 1]; TG.[3 × log (D2/D1)]/时间(月),其中 D1 为日期 1 时的肿瘤大小;D2 为日期 2 时的肿瘤大小;时间(月)= (Date 2 - Date 1 + 1)/30.44。计算每位患者孕前肿瘤生长率(TGRpc)和产后肿瘤生长率(TGRpp)。在一部分患者中,我们分析了肿瘤组织中雌激素和孕激素受体的阳性率,以评估这些受体的存在是否会影响妊娠期间肿瘤的进展。我们还回顾了在怀孕期间接受过体生长激素类似物治疗的患者的妊娠结局。我们分析了 18 名妇女共 22 次妊娠的数据:15 次妊娠(68%)在确诊 NEN 之前,而在妊娠期间或产后确诊 NEN 的分别有 5 次(23%)和 2 次(9%)。8 名患者(44%)被诊断为胰腺 NEN,5 名患者(28%)被诊断为中肠 NEN,另有 5 名患者被诊断为其他部位的 NEN。大多数患者(12 人,67%)在确诊时已有转移性疾病的证据。大多数患者的妊娠结果都很成功(19 人,86%),但有 3 名患者(14%)在妊娠头三个月流产。在 6 次妊娠中,有 5 名患者在妊娠期间接受了体生长抑素类似物单药治疗,所有患者在妊娠后病情均趋于稳定。所有患者都生下了健康的婴儿,没有因治疗而出现任何副作用或并发症。TGRpc的平均值为-0.8%(5例),TGRpp的平均值为+0.96%(6例)。此外,在孕前和孕后扫描的 4 名患者中,有 2 人的 TGRpp 比 TGRpc 有所上升。妊娠期营养不良症的治疗应该是多学科的,并针对每位患者采取个性化的治疗方法。体生长抑素类似物在妊娠期间似乎是安全的,但还需要进一步的可靠研究。妊娠本身可能会加速肿瘤的进展,因此应就这一可能性向患者提供咨询。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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