All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a Healthcare Professional. If you are a patient or carer, please visit Know ALL.
Introducing
Now you can personalise
your ALL Hub experience!
Bookmark content to read later
Select your specific areas of interest
View content recommended for you
Find out moreThe ALL Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the ALL Hub cannot guarantee the accuracy of translated content. The ALL Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.
The ALL Hub is an independent medical education platform, sponsored by Jazz Pharmaceuticals, Amgen, and Pfizer. The funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders.
Bookmark this article
Adult patients with acute lymphoblastic leukemia (ALL) have a poor prognosis, and 5-year overall survival (OS) in adults aged >50 years is 20%. Blinatumomab has shown efficacy in patients with relapsed/refractory B-cell ALL (B-ALL) and has achieved minimal residual negativity; however, there are limited data on the impact of pretransplant blinatumomab in adults.
Here, we summarize a retrospective study on the effect of blinatumomab prior to allogeneic stem cell transplantation (allo-HSCT) in adult patients with B-ALL, published by Sayyed et al.1 in Transplantation and Cellular Therapy.
Table 1. Patient baseline characteristics*
Characteristic, % |
Overall |
Blinatumomab |
No blinatumomab |
p value |
Diagnosis |
|
|
|
p = 0.01 |
Ph-negative |
57.3 |
77.4 |
50 |
|
Ph-positive |
42.7 |
22.6 |
50 |
|
Disease-risk index |
|
|
|
p < 0.001 |
Intermediate |
68.4 |
35.5 |
80.2 |
|
High |
30.8 |
61.3 |
19.8 |
|
Very high |
0.8 |
3.2 |
0 |
|
Indication for transplant |
|
|
|
p < 0.001 |
Relapse |
29.9 |
54.8 |
20.9 |
|
Primary induction failure |
16.2 |
41.9 |
7.0 |
|
Chemotherapy intolerance |
2.7 |
0 |
3.5 |
|
High-risk features |
39.3 |
0 |
53.5 |
|
Therapy-related |
8.5 |
3.2 |
10.5 |
|
MRD positivity after chemotherapy |
3.4 |
0 |
4.7 |
|
Dual T-cell depletion |
|
|
|
p = 0.005 |
Yes |
39.3 |
61.3 |
31.4 |
|
No |
60.7 |
38.7 |
68.6 |
|
PTCy-based GVHD prophylaxis |
|
|
|
p < 0.001 |
Yes |
45.3 |
80.6 |
32.6 |
|
No |
54.7 |
19.4 |
67.4 |
|
Lines of treatment before transplant |
|
|
|
p < 0.001 |
1 |
49.6 |
0 |
67.4 |
|
2 |
41.0 |
64.5 |
32.6 |
|
3 |
7.7 |
29.0 |
0 |
|
4 |
1.7 |
6.5 |
0 |
|
Year of transplant |
|
|
|
p < 0.001 |
2010–2015 |
72 |
57 |
95 |
|
2016–2021 |
15 |
22 |
5 |
|
GvHD, graft-versus-host disease; MRD, minimal residual disease; Ph, Philadelphia chromosome; PTCy, post-transplant cyclophosphamide *Adapted from Sayyed, et al.1 |
Figure 1. 2-year outcomes in blinatumomab treated vs no blinatumomab groups*
aGvHD, acute graft-versus-host disease; CIR, cumulative incidence of relapse; GRFS, GvHD-free and relapse-free survival; NRM, non-relapse mortality; OS, overall survival
*Data from Sayyed, et al.1
Key learnings |
|
Your opinion matters
Subscribe to get the best content related to ALL delivered to your inbox