Real-world outcomes of adult B-cell acute lymphocytic leukemia patients treated with blinatumomab

Author:

Badar Talha1ORCID,Szabo Aniko1ORCID,Advani Anjali2ORCID,Wadleigh Martha3,Arslan Shukaib4,Khan Muhammad Ali1,Aldoss Ibrahim4,Siebenaller Caitlin2,Schultz Elizabeth3,Hefazi Mehrdad5,Shallis Rory M.6ORCID,Yurkiewicz Ilana7,Podoltsev Nikolai6ORCID,Patel Anand A.8,Curran Emily8,Balasubramanian Suresh9,Yang Jay9,Mattison Ryan J.10,Burkart Madelyn11ORCID,Dinner Shira11,Liedtke Michaela7ORCID,Litzow Mark R.5ORCID,Atallah Ehab1

Affiliation:

1. Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI;

2. Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH;

3. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA;

4. Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA;

5. Division of Hematology, Mayo Clinic, Rochester, MN;

6. Department of Internal Medicine, Section of Hematology, Yale School of Medicine, New Haven, CT;

7. Stanford University Cancer Center, Stanford, CA;

8. Section of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL;

9. Karmanos Cancer Institute, Detroit, MI;

10. Carbone Cancer Center, University of Wisconsin, Madison, WI; and

11. Robert H. Lurie Comprehensive Cancer Center, Northwestern Hospital, Chicago, IL

Abstract

Abstract The availability and use of blinatumomab symbolizes a paradigm shift in the management of B-cell acute lymphoblastic leukemia (ALL). We conducted a retrospective multicenter cohort analysis of 239 ALL patients (227 relapsed refractory [RR], n = 227; minimal residual disease [MRD], n = 12) who received blinatumomab outside of clinical trials to evaluate safety and efficacy in the “real-world” setting. The median age of patients at blinatumomab initiation was 48 years (range, 18-85). Sixty-one (26%) patients had ≥3 prior therapies and 46 (19%) had allogeneic hematopoietic cell transplantation before blinatumomab. The response rate (complete remission/complete remission with incomplete count recovery) in patients with RR disease was 65% (47% MRD−). Among 12 patients who received blinatumomab for MRD, 9 (75%) patients achieved MRD negativity. In patients with RR disease, median relapse-free survival and overall survival (OS) after blinatumomab was 32 months and 12.7 months, respectively. Among patients who received blinatumomab for MRD, median relapse-free survival was not reached (54% MRD− at 2 years) and OS was 34.7 months. Grade ≥3 cytokine release syndrome, neurotoxicity, and hepatotoxicity were observed in 3%, 7%, and 10% of patients, respectively. Among patients who achieved complete remission/complete remission with incomplete count recovery, consolidation therapy with allogeneic hematopoietic cell transplantation retained favorable prognostic significance for OS (hazard ratio, 0.54; 95% confidence interval, 0.30-0.97; P = .04). In this largest “real-world” experience published to date, blinatumomab demonstrated responses comparable to those reported in clinical trials. The optimal sequencing of newer therapies in ALL requires further study.

Publisher

American Society of Hematology

Subject

Hematology

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