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Disease-Specific Indications and Outcomes

  • AML - Adult
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  • Myeloproliferative Neoplasms
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Myeloproliferative Neoplasms

Myeloproliferative Neoplasms  

Myeloproliferative neoplasms (MPN) are a group of rare disorders, including BCR-ABL-negative myeloproliferative neoplasms, polycythemia vera, and essential thrombocytosis, where diagnosis usually occurs at a young age with a prognosis that depends on disease progression and effectiveness of conservative treatments. MPNs have been treated with conservative strategies over the years, but autologous HCT is an option that can prolong survival. [1-3]

Outcomes  

Data in this section have been prepared by the CIBMTR® (Center for International Blood and Marrow Transplant Research®). The CIBMTR is a research collaboration between the National Marrow Donor Program® (NMDP)/Be The Match® and the Medical College of Wisconsin. 

Figure 1. Trends in MPN Survival, Allogeneic HCT 

Figure 1. Trends in MPN Survival, Allogeneic HCT

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Figure 2. MPN Survival, Matched Related and Matched Unrelated Allogeneic HCT 

Figure 2. MPN Survival, Matched Related and Matched Unrelated Allogeneic HCT

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Figure 3. MPN Survival, Haploidentical and Mismatched Unrelated Allogeneic HCT 

Figure 3. MPN Survival, Haploidentical and Mismatched Unrelated Allogeneic HCT

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HCT Consultation Timing Guidelines 

The National Marrow Donor Program® (NMDP)/Be The Match® and the American Society for Transplantation and Cellular Therapy (ASTCT) have jointly developed guidelines for transplant consultation and referral timing based on disease characteristics. [4] The National Comprehensive Cancer Network Clinical Practice Guidelines (NCCN Guidelines®) were consulted in developing these guidelines and are a valuable tool in determining risk stratification. [5] 

Our guidelines highlight disease categories that include patients at risk for disease progression and who should be referred for a consultation for autologous or allogeneic transplantation. [4]

Transplant Consultation Guidelines: Myeloproliferative neoplasms (MPN) 

(Including BCR-ABL-negative MPNs and later stages of polycythemia vera and essential thrombocytosis)

High-resolution HLA typing is recommended at diagnosis for all patients

Intermediate- or high-risk disease, including: 

  • High-risk cytogenetics 
  • Poor initial response or at progression 

Download as a slide 

View complete HCT Consultation Timing Guidelines

Clinical Trials Search and Support 

The NMDP/Be The Match offers the Be The Match® Jason Carter Clinical Trials Search and Support (CTSS) program, which can provide clinical trial navigation to your patients. The CTSS Program was created to help people with blood cancers or blood disorders and their families find and join clinical trials.

For more information, visit Clinical Trials Search and Support.  

References 

  1. Tefferi A. How I treat myelofibrosis. Blood. 2011; 117(13): 3494-3504. Access
  2. Kröger NM, et al. Indication and management of allogeneic stem cell transplantation in primary myelofibrosis: a consensus process by an EBMT/ELN international working group. Leukemia. 2015; 29(11): 2126-2133. Access
  3. Deeg HJ, et al. Hematopoietic cell transplantation as curative therapy for patients with myelofibrosis: Long-term success in all age groups. Biol Blood Marrow Transplant. 2015; 21(11): 1883-1887. Access
  4. NMDP/Be The Match and ASTCT Recommended Timing for Transplant Consultation. Download (PDF)
  5. National Comprehensive Cancer Network. Myeloproliferative Neoplasms. (Version 3.2022). Access 

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Transplant Indications and Outcomes

  • HLA Today
  • Disease-Specific Indications and Outcomes
  • Additional Outcomes
  • Eligibility
  • Referral Timing Guidelines
  • Order Kits
  • HLA Typing for Family Members

Transplant Therapy and Donor Matching

  • Cell Sources
  • HLA Typing and Matching
  • Donor or Cord Blood Search Process
  • Jason Carter Clinical Trials Program

Resources

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  • Obstetrician Resources
  • Technique Videos
  • Umbilical Cord Blood Collection Training for Public Donation
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