OR27. Novel next generation sequencing based chimerism assay for engraftment monitoring in hematopoietic cell transplantation

2018 ◽  
Vol 79 ◽  
pp. 32
Author(s):  
Medhat Z. Askar ◽  
Amanda Willis ◽  
Jenifer D. Williams ◽  
Leah Pittmon ◽  
Shalini E. Pereira ◽  
...  
2016 ◽  
Vol 54 (2) ◽  
pp. 98-104
Author(s):  
C. Lucan ◽  
Laura-Ancuta Pop ◽  
A. Florian ◽  
Valentina Pileczki ◽  
B. Petrushev ◽  
...  

Abstract From an oncological perspective, the second most common malignancies in children are brain tumors. Despite the recent therapeutic breakthroughs in this field, concerning surgery, radiotherapy and chemotherapy alike, some cases still have poor outcomes in curability. This is especially the case in patients with high-risk histological types of tumors, and those suffering from residual, remitting and disseminated diseases. Due to the unique neuroanatomical emplacement of brain tumors and their aggressive infiltrative behavior, their total removal remains a demanding task. This can be perceived in the high rates of failure treatment and disease recurrence. Furthermore, the adjacent healthy brain tissue is inevitably damaged in the surgical process of effectively removing these tumors. Thus, stem cell transplantation may be a viable solution for the clinical management of these malignancies, as proven by various recent breakthroughs. In the current concise review, we present the role of next generation sequencing in HLA typing for stem cell transplantation in primary CNS pediatric malignancies.


2014 ◽  
Vol 32 (15_suppl) ◽  
pp. 7043-7043 ◽  
Author(s):  
Marlise Rachael Luskin ◽  
Martin Carroll ◽  
Jennifer J. Morrissette ◽  
Robert D Daber ◽  
Noelle V. Frey ◽  
...  

Author(s):  
Astrid Wintering ◽  
Christopher C Dvorak ◽  
Elliot Stieglitz ◽  
Mignon L. Loh

Juvenile myelomonocytic leukemia is an overlapping myeloproliferative and myelodysplastic disorder of early childhood. It is associated with a spectrum of diverse outcomes ranging from spontaneous resolution in rare patients to transformation to acute myeloid leukemia in others that is generally fatal. This unpredictable clinical course, along with initially descriptive diagnostic criteria, led to decades of productive international research. Next generation sequencing now permits more accurate molecular diagnoses in nearly all patients. However, curative treatment is still reliant on allogeneic hematopoietic cell transplantation for most patients, and additional advances will be required to improve risk stratification algorithms that distinguish those that can be observed expectantly from others who require swift hematopoietic cell transplantation.


Sign in / Sign up

Export Citation Format

Share Document