Picard Agathe, Bayart Sophie, Deparis Marianna, De Maricourt Cécile Dumesnil, Haro Sophie, Jourdain Anne, Mallebranche Coralie, Rialland Fanny, Luque Paz Damien, Pastoret Cedric, Gandemer Virginie, Cousin Elie
Pediatric Oncohematology Department, Rennes University Hospital, Rennes, France.
Pediatric Oncohematology Department, Caen-Normandie University Hospital, Caen, France.
Eur J Pediatr. 2025 Feb 4;184(2):173. doi: 10.1007/s00431-025-05993-1.
Polycythemia vera (PV) and essential thrombocythemia (ET) are rare myeloproliferative neoplasms (MPN) in children, adolescents and young adults. No recommendations are available concerning these patients' management. Transposing to children the knowledge established in adult patients is not acceptable. For a better understanding of difficulties encountered by pediatricians and adult hematologists, we conducted a national practice analysis concerning follow-up of patients under 18 diagnosed with ET or PV, in France. Then, we present data from a multicentric, descriptive, retrospective study, including 17 patients with ET or PV, diagnosed under 18, coming from 7 hematopediatric departments in France. Interviewed physicians reported a lack of expertise and theoretical training in the hematological field to diagnose and follow children with MPNs. Data from 17 patients (15 ET, 2 PV) confirmed a high proportion of asymptomatic patients at the time of diagnosis (41%). Proportion of "triple-negative" patients (59%) was higher than in adult cohorts. 60% of patients underwent a bone marrow biopsy and 31% of cases were discussed during a multi-disciplinary staff meeting. 76.5% patients were treated, with a high frequency of antithrombotic and cytoreductive drugs. No complications were observed during the 45 months of median follow-up.
Physicians insisted on the need for training. Only the accumulation of descriptions of MPNs in children will lead to a better management of these diseases. Considering the small proportion of pediatric patients with complications after diagnosis, rapid therapeutic de-escalation seems essential to consider during the follow-up in a close collaboration with adult hematologists.
• Myeloproliferativ neoplams are rare and chronic deseases, most of the time affecting adults but also found in few pediatric patients. • There are no recommendations for the diagnosis, therapeutic management or follow-up of children with polycythemia vera or essential thrombocythemia.
• Find out how adult haematologists and paediatricians feel about the management and follow-up of paediatric patients with myeloproliferative syndrome through a national practice analysis. • Description of the "real life" follow-up of children with polycythemia vera or essential thrombocythemia in France.
真性红细胞增多症(PV)和原发性血小板增多症(ET)是儿童、青少年和青年中罕见的骨髓增殖性肿瘤(MPN)。关于这些患者的管理尚无推荐意见。将成人患者中确立的知识应用于儿童是不可接受的。为了更好地理解儿科医生和成人血液科医生所面临的困难,我们在法国针对18岁以下诊断为ET或PV的患者的随访情况进行了一项全国性实践分析。然后,我们展示了一项多中心、描述性、回顾性研究的数据,该研究纳入了17例18岁以下诊断为ET或PV的患者,他们来自法国7个儿童血液科。接受访谈的医生报告称,在血液学领域缺乏诊断和随访患有MPN的儿童的专业知识和理论培训。17例患者(15例ET,2例PV)的数据证实,诊断时无症状患者的比例较高(41%)。“三阴性”患者的比例(59%)高于成人队列。60%的患者接受了骨髓活检,31%的病例在多学科 staff 会议上进行了讨论。76.5%的患者接受了治疗,抗血栓和细胞减灭药物的使用频率较高。在中位随访的45个月期间未观察到并发症。
医生们强调了培训的必要性。只有积累儿童MPN的描述,才能更好地管理这些疾病。考虑到诊断后出现并发症的儿科患者比例较小,在与成人血液科医生密切合作的随访过程中,快速降低治疗强度似乎至关重要。
• 骨髓增殖性肿瘤是罕见的慢性疾病,大多数情况下影响成人,但也在少数儿科患者中发现。• 对于真性红细胞增多症或原发性血小板增多症患儿的诊断、治疗管理或随访尚无推荐意见。
• 通过全国性实践分析,了解成人血液科医生和儿科医生对儿科骨髓增殖综合征患者的管理和随访的看法。• 描述法国真性红细胞增多症或原发性血小板增多症患儿的“真实生活”随访情况。