About the 2026 EHA Annual Meeting

The 31st European Hematology Association (EHA) Annual Meeting was held in Stockholm, Sweden from June 11–14, 2026, in a hybrid format combining in-person and online participation. The congress brought together leading hematologists and researchers from around the world to discuss the pathogenesis, precision diagnostics, cutting-edge therapies, and patient management in blood disorders.

Invited by the scientific committee, Dr. Xiao Juan (Director) and Dr. Chen Jiao (Director) from Prof. Sun Yuan's team presented their research as poster presentations, delivering the "Jingdu Voice" of Chinese pediatric hematology to the world.

EHA 2026 Annual Meeting - Jingdu team

Prof. Sun Yuan's team at the 31st EHA Annual Meeting, Stockholm, June 2026

Poster 1: HSCT for CNS-HLH in Children

Allogeneic Hematopoietic Stem Cell Transplantation in Primary Hemophagocytic Lymphohistiocytosis with Central Nervous System Involvement in Children

Juan Xiao, Shifen Fan, Zhouyang Liu, Fan Jiang, Jiao Chen, Yuan Sun*
Department of Hematology, Beijing Jingdu Children's Hospital, Beijing, China

Background

Primary hemophagocytic lymphohistiocytosis (PHLH) is a life-threatening immune disorder. When the central nervous system (CNS) is involved (CNS-HLH), the prognosis is particularly poor, and data on transplant outcomes in this subgroup are limited.

Methods

A retrospective analysis was performed on 74 pediatric patients with PHLH who underwent allogeneic HSCT at Beijing Jingdu Children's Hospital between January 2018 and June 2025. Of these, 18 had CNS involvement.

74
Total PHLH Patients
18
CNS-HLH Cases
3.6 yrs
Median Age
28.6 mo
Median Follow-up

Key Findings

EHA 2026 Poster - CNS-HLH HSCT Outcomes

Poster: Allogeneic HSCT in primary HLH with CNS involvement — EHA 2026, Stockholm

  • Gene mutations: FHL-2 (PRF1) n=6, FHL-3 (UNC13D) n=6, XLP1 (SH2D1A) n=3, FHL-4 (STX11) n=2, CHS (LYST) n=1
  • Transplant types: Haploidentical HSCT n=10, Unrelated donor HSCT n=6, Sibling-matched HSCT n=2
  • Pre-transplant status: Complete remission (CR) n=8, Partial remission (PR) n=6, Active disease (AD) n=4
  • Conditioning: VP-16 / Busulfan / Fludarabine / Cyclophosphamide / ATG

Outcomes

73.5%
5-Year Overall Survival
67.2%
5-Year Event-Free Survival
13/18
Patients Alive
9/13
Survivors with Normal Neurodevelopment
Conclusion: Allo-HSCT is an effective treatment for primary HLH with CNS involvement. Achieving disease remission before transplantation leads to better survival. Once PHLH is diagnosed, HSCT should be performed as soon as possible.

Poster 2: HSCT for Shwachman-Diamond Syndrome (SDS) — 116 Cases

Clinical Characteristics and Hematopoietic Stem Cell Transplantation Prognosis in Shwachman-Diamond Syndrome: A Report of 116 Cases from a Single Chinese Center

Jiao Chen, Zhouyang Liu, Zhende Hou, Xiaoda Li, Shifen Fan, Fan Jiang, Yuan Sun*
Beijing Jingdu Children's Hospital, Beijing, China

Background

Shwachman-Diamond syndrome (SDS) is a rare inherited bone marrow failure syndrome characterized by pancreatic exocrine insufficiency, bone marrow dysfunction, and skeletal abnormalities. Severe cases can progress to myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML). This study represents the largest single-center case series of SDS transplant outcomes reported internationally to date.

Patient Cohort (N=116)

116
Total SDS Patients
64 M / 52 F
Male / Female
<1 mo
Median Age at Onset
14 mo
Median Age at Diagnosis

Key Clinical Findings

  • Genetic mutations: SBDS compound heterozygous n=92, SBDS homozygous n=23, EFL1 compound heterozygous n=1
  • Chronic diarrhea: 86.2%
  • Cytopenia: 97.4%
  • Liver dysfunction: 86.2%
  • Neurological abnormalities: 50%
  • Dental abnormalities: 41.4%
  • Skeletal abnormalities: 37.9%
  • Cardiac abnormalities: 36.0%
  • Progressed to AML: 1 case (0.9%); progressed to MDS: 11 cases (9.5%)

Transplant Outcomes (28 Transplanted Patients)

28
Transplanted Cases
26.5 mo
Median Age at HSCT
92.9%
Overall Survival
89.3%
Event-Free Survival
EHA 2026 Poster - SDS 116 Cases

Poster: Clinical Characteristics and HSCT Prognosis in Shwachman-Diamond Syndrome — 116 Cases — EHA 2026, Stockholm

  • Donor sources: Unrelated cord blood (UCB) n=16, Mismatched related donor (MMRD) n=7, Unrelated donor (UD) n=6
  • Engraftment success: 27/28 (96.3%) after primary transplant; 1 UCB failure salvaged by haploidentical HSCT
  • Neutrophil engraftment: UCB group median 14 days; UD/MMRD group median 11 days
  • Acute GVHD (grade II–IV): UCB 0/15, MMRD 3/7, UD 2/6
  • Chronic GVHD: No moderate or severe cases in any group
  • Ovarian tissue cryopreservation: performed in 7 female patients prior to HSCT
Conclusion: When SDS is complicated by severe cytopenia, MDS, or AML, allo-HSCT is a safe and effective treatment. Compared with MMRD and UD transplants, UCB transplantation is associated with a significantly lower incidence of GVHD. Patients with complex karyotypic abnormalities combined with TP53 mutations have an extremely poor prognosis.

Impact & Significance

These two presentations represent important contributions from China to the global pediatric hematology community:

  • The CNS-HLH study provides the first systematic analysis of HSCT outcomes in this high-risk subgroup, offering evidence-based guidance for international clinical practice.
  • The SDS study is the largest single-center transplant case series ever reported for this ultra-rare disease, providing invaluable real-world data for global rare disease management.
  • Both studies showcase the clinical excellence and research capabilities of Prof. Sun Yuan's team at Beijing Jingdu Children's Hospital, Asia's largest pediatric HSCT center.

About the Hematology & Oncology Center

Under the leadership of Prof. Sun Yuan (President of Beijing Jingdu Children's Hospital), the Hematology & Oncology Center has completed nearly 1,000 hematopoietic stem cell transplants, covering PHLH, Shwachman-Diamond syndrome, primary immunodeficiency diseases, and thalassemia. Multiple research achievements have been presented at top international academic conferences including ASH and EHA.

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