B-Cell Acute Lymphoblastic LeukaemiaNCT07117136
Blinatumomab Consolidation in Real World
An observational study of B-Cell Acute Lymphoblastic Leukaemia, run by Medical College of Wisconsin at 5 sites in United States.
Trial summary
This will be a multi-center registry for patients with B-ALL. Patient data will be collected both retrospectively and prospectively. The data forms and surveys will be built and managed through REDCap, a secure web application managed by the Clinical \& Translational Science Institute. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- B-Cell Acute Lymphoblastic Leukaemia
- How many people
- 200 participants
- Where
- 5 sitesUnited States
- Study dates
- 28 Aug 2025to 14 May 2029
- Phase
- Observational
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Patients with B-ALL diagnosed during or after December 2022
Who may be able to join
- 1) aged 18 years or older 2) diagnosed with B-ALL on or after December 1st 2022 3) Not received blinatumomab in an interventional clinical trial setting 4) Willing and able to give informed consent (or retrospective data for deceased patients
Who cannot join
- N/A
Trial locations and contacts
5 sites in 1 country. Contact the study team or a site near you to ask about taking part.
5 sites in 1 country
United States5 sites, 5 recruiting
- Recruiting
Northwestern University
Chicago, Illinois, 60611
Shira Dinner, MD, 312-695-3101, cancer@northwestern.edu
Shira Dinner, MD
- Recruiting
The University of Chicago
Chicago, Illinois, 60637
Anand Patel, MD, 773-702-1577, cancerclinicaltrials@bsd.uchicago.edu
Anand Patel, MD
- Recruiting
Mayo Clinic Cancer Center
Jacksonville, Florida, 32224
Talha Badar, MD, 904-953-7556, Badar.Talha@mayo.edu
Talha Badar, MD
- Recruiting
Medical College of Wisconsin
Milwaukee, Wisconsin, 53226
Arielle Program Manager, 414-805-8745, abaim@mcw.edu
Ehab Atallah, MD
- Recruiting
University of Pennsylvania
Philadelphia, Pennsylvania, 19104
Camila Ludlow, MPH, 908-930-0704, camila.ludlow@pennmedicine.upenn.edu
Selina Luger, MD
About this study
Official title: Real World Outcomes of Blinatumomab Consolidation in Patients With B-cell Acute Lymphoblastic Leukemia
This will be a multi-center registry for patients with B-ALL. Patient data will be collected both retrospectively and prospectively. The data forms and surveys will be built and managed through REDCap, a secure web application managed by the Clinical \& Translational Science Institute.
Read the detailed description
B-cell Acute lymphoblastic leukemia (B-ALL) is a potentially curable malignancy in the pediatric population. In contrast, the outcomes of adults with B-ALL have remained historically poor due to risk of relapse after frontline therapy. Novel agents in the current era have changed the treatment landscape of adults with relapsed/refractory B-ALL with improved tolerability and better outcomes [1]. Currently, blinatumomab (CD3-CD19 bispecific molecule) and inotuzumab (CD22 antibody drug conjugate) are approved for the management of patients with relapsed/refractory B-ALL. With the superior efficacy of these agents, recent clinical trials have focused on incorporating them in the management of newly diagnosed B-ALL.
A phase 3 randomized clinical trial (E1910) has recently demonstrated the superiority of adding blinatumomab during consolidation for patients who have achieved MRD negative CR [2]. Patients between the ages of 30 and 70 with newly diagnosed BCR-ABL1 negative B-ALL were enrolled and initially received 2.5 months of combination induction chemo utilizing a BFM-like regimen adapted from the E2993/UKALLXII clinical trial with extended remission induction, addition of pegasparginase for patients <55 years of age and addition of rituximab for CD20 positive patients. Subsequently, their remission and MRD status were determined centrally by 6-color flow cytometry with MRD negativity defined as <0.01%. All patients were then randomized to receive an additional four cycles of consolidation chemo or two cycles of blin for 28 days each cycle followed by 3 cycles of consolidation chemo, another 4-week cycle of blinatumomab (3rd cycle of blinatumomab) followed by an additional cycle of chemo and then a 4th cycle of blinatumomab. Two hundred and twenty-four MRD negative patients were randomized, 112 pts to each arm. Among the MRD negative patients, superior overall survival was seen in patients who received blinatumomab (median OS: not reached vs. 71.4 months; Hazard ratio 0.42, 95% CI: 0.24 - 0.75; two-sided p=0.003) with a median follow-up of 43 months.
While the results are encouraging and practice changing to consider adding blinatumomab to MRD negative CR patients, the backbone chemotherapy regimen used in E1910 study is not a commonly used regimen in clinical practice. Due to the unmet need, physicians are often considering combining blinatumomab consolidation with several other commonly used chemotherapy regimens. However, the outcome in this setting remains unknown. Our goal in this study is to evaluate the real-world utilization of blinatumomab in the frontline setting for management of B-ALL in the United States.
- Conditions
- B-Cell Acute Lymphoblastic Leukaemia
- Medical subject headings
- Burkitt Lymphoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Patients who received Blinatumomab Therapy | Not described | |
| Patients who did not receive Blinatumomab Therapy | Not described |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of participants with complete remission
Complete remission as defined by patients having no lymphoblasts in the marrow or blood
Measured: 5 years or e.g., 1 year after closure of study
Secondary outcomes (1)
Overall Survival
Percentage of participants overall survival (OS). OS will be calculated from the time of diagnosis of to death from any cause, and patients will be censored if they were alive at the last follow-up
Measured: 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Aug 2025
- Study start28 Aug 2025
- Primary completion14 May 2029 (estimated)
- Study completion14 May 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for B-Cell Acute Lymphoblastic LeukaemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Medical College of Wisconsin
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ehab L Atallah, Medical College of Wisconsin
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07117136
- Sponsor's protocol ID
- PRO00054269
- Status last verified
- Sep 2026
- First submitted
- 5 Aug 2025
- Last updated
- 1 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No