Background: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is pivotal for treating blood disorders but is complicated by graft-versus-host disease (GVHD), infections, and transplant-associated thrombotic microangiopathy (TA-TMA). This case series evaluates the clinical utility of novel agents (Iptacopan, Vedolizumab, Ruxolitinib) in managing these complications.

Case Summaries Methods -Interventions: Novel agents combined with standard therapies (immunosuppressants, antivirals).

-Monitoring: Serial blood counts, liver/kidney function, viral load (CMV/EBV DNA), and coagulation profiles.

Results

  • Symptom Improvement:

    • GVHD: Reduced diarrhea frequency (Case 2) and abdominal pain severity (Case 3) with vedolizumab.

    • TA-TMA: Stabilized blood pressure and improved renal function using Iptacopan.

  • Lab Trends:

    • Blood Counts: Platelet recovery in Case 2 (19→44×10⁹/L).

    • Liver Function: Declined ALT/AST (Case 3: ALT 35→25 U/L).

    • Viral Load: EBV DNA turned negative in Cases 2 and 3.

  • Safety:

    • Infections: EBV/Enterococcus faecium reactivation (Case 3).

    • Organ Toxicity: Transient liver enzyme elevation (Case 1).

Discussion - Efficacy: Novel agents demonstrated targeted efficacy in GVHD/TA-TMA with improved lab parameters.

  • Safety: Increased infection risk and transient organ toxicity necessitate vigilant monitoring.

  • Personalization: Tailored dosing based on genetic/clinical factors may optimize outcomes.

Conclusion: Iptacopan, Vedolizumab and Ruxolitinib show promise in managing post-allo-HSCT complications. Balancing efficacy with safety through personalized regimens and long-term follow-up is critical.

Keywords: Allo-HSCT, GVHD, TA-TMA, Novel agents, Iptacopan, Vedolizumab, Ruxolitinib

Table: Baseline Characteristics vs. Post-Treatment Lab Trends

Case
Diagnosis
Complications
Key Novel Agents Used
1
 
Severe Aplastic Anemia (SAA)
 
Intestinal GVHD, TA-TMA, Cytomegalovirus (CMV) viremia
 
Iptacopan, Vedolizumab
 
2
 
Myelodysplastic Syndrome (MDS)-EB-2
 
Intestinal GVHD, TA-TMA, Epstein-Barr Virus (EBV) infection
 
Iptacopan
 
3
 
MDS-LB
 
Liver/Intestinal GVHD, TA-TMA, EBV viremia
 
Iptacopan, Vedolizumab, Ruxolitinib
 
Case
Diagnosis
Complications
Key Novel Agents Used
1
 
Severe Aplastic Anemia (SAA)
 
Intestinal GVHD, TA-TMA, Cytomegalovirus (CMV) viremia
 
Iptacopan, Vedolizumab
 
2
 
Myelodysplastic Syndrome (MDS)-EB-2
 
Intestinal GVHD, TA-TMA, Epstein-Barr Virus (EBV) infection
 
Iptacopan
 
3
 
MDS-LB
 
Liver/Intestinal GVHD, TA-TMA, EBV viremia
 
Iptacopan, Vedolizumab, Ruxolitinib
 
Parameter
Case I (41F, SAA)
Case II (53F, MDS-EB-2)
Case III (28M, MDS-LB)
Baseline Characteristics
 
Diagnosis
 
Severe Aplastic Anemia (SAA)
 
Myelodysplastic Syndrome with Excess Blasts-2 (MDS-EB-2)
 
Myelodysplastic Syndrome-Low Blast (MDS-LB)
 
Pre-Treatment Labs
 
- WBC: ↓ (2.13×10⁹/L)

- HGB: 65g/L↓

- PLT: 4×10⁹/L↓↓

- ALT/AST: ↑ (44.56/50.96 U/L)
 
- WBC: ↓ (3.73×10⁹/L)

- HGB: 44g/L↓↓

- PLT: 19×10⁹/L↓

- PT/INR: ↑ (24.8s/2.17)
 
- WBC: ↑ (15.42×10⁹/L)

- HGB: 105g/L↓

- ALT/AST: ↑ (35.49/47.32 U/L)

- D-dimer: 3.56 mg/L↑
 
Complications
 
CMV viremia, TA-TMA, intestinal GVHD, heart failure
 
EBV infection, TA-TMA, intestinal GVHD
 
EBV viremia, liver GVHD, intestinal GVHD, TA-TMA
 
New Drugs Used
 
Iptacopan, Vedolizumab
 
Iptacopan
 
Iptacopan, Vedolizumab, Ruxolitinib
 
Post-Treatment Trends
 
Blood Routine
 
- WBC/HGB/PLT: Continued fluctuations (no stabilization)
 
- PLT: ↑ (improvement)

- WBC/HGB: Partial stabilization
 
- WBC: Stabilized

- HGB/PLT: Gradual improvement
 
Liver Function
 
- ALT/AST: Persistent fluctuations (disease/drug-related)
 
- Bilirubin: Improved with supportive care
 
- ALT/AST: ↓ (improved with ruxolitinib)

- Bilirubin: Stabilized
 
Kidney Function
 
- Creatinine: Fluctuations
 
- Urea/Creatinine: Partial improvement
 
- Creatinine: Stabilized
 
Coagulation
 
- PT/INR/D-dimer: Persistent abnormalities
 
- PT/INR: Partial improvement
 
- D-dimer: ↓ (3.56 → lower)

- Fibrinogen: Remained low
 
Viral Load
 
- CMV DNA: Controlled (↓ with ganciclovir/foscarnet)
 
- EBV DNA: Turned negative
 
- EBV DNA: Significant ↓
 
Other
 
- Heart failure: Improved with cardiac drugs
 
- Brain lesions: Stabilized with adjusted treatment
 
-Hypokalemia/Hyponatremia: Corrected
 
Parameter
Case I (41F, SAA)
Case II (53F, MDS-EB-2)
Case III (28M, MDS-LB)
Baseline Characteristics
 
Diagnosis
 
Severe Aplastic Anemia (SAA)
 
Myelodysplastic Syndrome with Excess Blasts-2 (MDS-EB-2)
 
Myelodysplastic Syndrome-Low Blast (MDS-LB)
 
Pre-Treatment Labs
 
- WBC: ↓ (2.13×10⁹/L)

- HGB: 65g/L↓

- PLT: 4×10⁹/L↓↓

- ALT/AST: ↑ (44.56/50.96 U/L)
 
- WBC: ↓ (3.73×10⁹/L)

- HGB: 44g/L↓↓

- PLT: 19×10⁹/L↓

- PT/INR: ↑ (24.8s/2.17)
 
- WBC: ↑ (15.42×10⁹/L)

- HGB: 105g/L↓

- ALT/AST: ↑ (35.49/47.32 U/L)

- D-dimer: 3.56 mg/L↑
 
Complications
 
CMV viremia, TA-TMA, intestinal GVHD, heart failure
 
EBV infection, TA-TMA, intestinal GVHD
 
EBV viremia, liver GVHD, intestinal GVHD, TA-TMA
 
New Drugs Used
 
Iptacopan, Vedolizumab
 
Iptacopan
 
Iptacopan, Vedolizumab, Ruxolitinib
 
Post-Treatment Trends
 
Blood Routine
 
- WBC/HGB/PLT: Continued fluctuations (no stabilization)
 
- PLT: ↑ (improvement)

- WBC/HGB: Partial stabilization
 
- WBC: Stabilized

- HGB/PLT: Gradual improvement
 
Liver Function
 
- ALT/AST: Persistent fluctuations (disease/drug-related)
 
- Bilirubin: Improved with supportive care
 
- ALT/AST: ↓ (improved with ruxolitinib)

- Bilirubin: Stabilized
 
Kidney Function
 
- Creatinine: Fluctuations
 
- Urea/Creatinine: Partial improvement
 
- Creatinine: Stabilized
 
Coagulation
 
- PT/INR/D-dimer: Persistent abnormalities
 
- PT/INR: Partial improvement
 
- D-dimer: ↓ (3.56 → lower)

- Fibrinogen: Remained low
 
Viral Load
 
- CMV DNA: Controlled (↓ with ganciclovir/foscarnet)
 
- EBV DNA: Turned negative
 
- EBV DNA: Significant ↓
 
Other
 
- Heart failure: Improved with cardiac drugs
 
- Brain lesions: Stabilized with adjusted treatment
 
-Hypokalemia/Hyponatremia: Corrected
 

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