Low leukemia burden improves blinatumomab efficacy in patients with relapsed/refractory B-cell acute lymphoblastic leukemia

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Low leukemia burden improves blinatumomab efficacy in patients with relapsed/refractory B-cell acute lymphoblastic leukemia. / Queudeville, Manon; Stein, Anthony S; Locatelli, Franco; Ebinger, Martin; Handgretinger, Rupert; Gökbuget, Nicola; Gore, Lia; Zeng, Yi; Gokani, Priya; Zugmaier, Gerhard; Kantarjian, Hagop M.

In: CANCER-AM CANCER SOC, Vol. 129, No. 9, 01.05.2023, p. 1384-1393.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Queudeville, M, Stein, AS, Locatelli, F, Ebinger, M, Handgretinger, R, Gökbuget, N, Gore, L, Zeng, Y, Gokani, P, Zugmaier, G & Kantarjian, HM 2023, 'Low leukemia burden improves blinatumomab efficacy in patients with relapsed/refractory B-cell acute lymphoblastic leukemia', CANCER-AM CANCER SOC, vol. 129, no. 9, pp. 1384-1393. https://doi.org/10.1002/cncr.34667

APA

Queudeville, M., Stein, A. S., Locatelli, F., Ebinger, M., Handgretinger, R., Gökbuget, N., Gore, L., Zeng, Y., Gokani, P., Zugmaier, G., & Kantarjian, H. M. (2023). Low leukemia burden improves blinatumomab efficacy in patients with relapsed/refractory B-cell acute lymphoblastic leukemia. CANCER-AM CANCER SOC, 129(9), 1384-1393. https://doi.org/10.1002/cncr.34667

Vancouver

Bibtex

@article{c09261003a774968bba9730b379ebafd,
title = "Low leukemia burden improves blinatumomab efficacy in patients with relapsed/refractory B-cell acute lymphoblastic leukemia",
abstract = "BACKGROUND: A lower baseline bone marrow blast percentage (bBMB%) is associated with better outcomes in patients with B-cell acute lymphoblastic leukemia (B-ALL) receiving blinatumomab. The objective of this analysis was to investigate the association between bBMB% and treatment outcomes in relapsed/refractory (R/R) B-ALL.METHODS: Data from five trials of blinatumomab for R/R B-ALL were pooled for analyses. Patients were placed in one of three groups: group 1, ≥50% bBMBs; group 2, ≥25% to <50% bBMBs; group 3, ≥5% to <25% bBMBs. Response and survival outcomes were compared between groups.RESULTS: Data from 683 patients (166 pediatric, 517 adult) were analyzed. Collectively, patients in groups 2 and 3 had significantly higher odds of achieving a complete remission (CR) (odds ratio [OR], 3.50 [95% confidence interval (CI), 2.23-5.48] and 3.93 [95% CI, 2.50-6.18], respectively; p < .001) and minimal/measurable residual disease response (OR, 2.61 and 3.37, respectively; p < .001) when compared with group 1 (reference). Groups 2 and 3 had a 37% and 46% reduction in the risk of death (hazard ratio [HR], 0.63 and 0.54, respectively; p < .001) and a 41% and 43% reduction in the risk of an event (relapse or death) (HR, 0.59 and 0.57, respectively; p < .001) compared with group 1. No significant differences in response or survival outcomes were observed between groups 2 and 3. Seven of nine patients whose bBMB% was lowered to <50% with dexamethasone achieved CR with blinatumomab.CONCLUSION: Any bBMB% <50% was associated with improved efficacy following blinatumomab treatment for R/R B-ALL.",
keywords = "Adult, Humans, Child, Antineoplastic Agents/therapeutic use, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Antibodies, Bispecific/therapeutic use, Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/drug therapy, Recurrence, Lymphoma, B-Cell, Acute Disease",
author = "Manon Queudeville and Stein, {Anthony S} and Franco Locatelli and Martin Ebinger and Rupert Handgretinger and Nicola G{\"o}kbuget and Lia Gore and Yi Zeng and Priya Gokani and Gerhard Zugmaier and Kantarjian, {Hagop M}",
note = "{\textcopyright} 2023 Amgen and The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society.",
year = "2023",
month = may,
day = "1",
doi = "10.1002/cncr.34667",
language = "English",
volume = "129",
pages = "1384--1393",
journal = "CANCER-AM CANCER SOC",
issn = "0008-543X",
publisher = "John Wiley and Sons Inc.",
number = "9",

}

RIS

TY - JOUR

T1 - Low leukemia burden improves blinatumomab efficacy in patients with relapsed/refractory B-cell acute lymphoblastic leukemia

AU - Queudeville, Manon

AU - Stein, Anthony S

AU - Locatelli, Franco

AU - Ebinger, Martin

AU - Handgretinger, Rupert

AU - Gökbuget, Nicola

AU - Gore, Lia

AU - Zeng, Yi

AU - Gokani, Priya

AU - Zugmaier, Gerhard

AU - Kantarjian, Hagop M

N1 - © 2023 Amgen and The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society.

PY - 2023/5/1

Y1 - 2023/5/1

N2 - BACKGROUND: A lower baseline bone marrow blast percentage (bBMB%) is associated with better outcomes in patients with B-cell acute lymphoblastic leukemia (B-ALL) receiving blinatumomab. The objective of this analysis was to investigate the association between bBMB% and treatment outcomes in relapsed/refractory (R/R) B-ALL.METHODS: Data from five trials of blinatumomab for R/R B-ALL were pooled for analyses. Patients were placed in one of three groups: group 1, ≥50% bBMBs; group 2, ≥25% to <50% bBMBs; group 3, ≥5% to <25% bBMBs. Response and survival outcomes were compared between groups.RESULTS: Data from 683 patients (166 pediatric, 517 adult) were analyzed. Collectively, patients in groups 2 and 3 had significantly higher odds of achieving a complete remission (CR) (odds ratio [OR], 3.50 [95% confidence interval (CI), 2.23-5.48] and 3.93 [95% CI, 2.50-6.18], respectively; p < .001) and minimal/measurable residual disease response (OR, 2.61 and 3.37, respectively; p < .001) when compared with group 1 (reference). Groups 2 and 3 had a 37% and 46% reduction in the risk of death (hazard ratio [HR], 0.63 and 0.54, respectively; p < .001) and a 41% and 43% reduction in the risk of an event (relapse or death) (HR, 0.59 and 0.57, respectively; p < .001) compared with group 1. No significant differences in response or survival outcomes were observed between groups 2 and 3. Seven of nine patients whose bBMB% was lowered to <50% with dexamethasone achieved CR with blinatumomab.CONCLUSION: Any bBMB% <50% was associated with improved efficacy following blinatumomab treatment for R/R B-ALL.

AB - BACKGROUND: A lower baseline bone marrow blast percentage (bBMB%) is associated with better outcomes in patients with B-cell acute lymphoblastic leukemia (B-ALL) receiving blinatumomab. The objective of this analysis was to investigate the association between bBMB% and treatment outcomes in relapsed/refractory (R/R) B-ALL.METHODS: Data from five trials of blinatumomab for R/R B-ALL were pooled for analyses. Patients were placed in one of three groups: group 1, ≥50% bBMBs; group 2, ≥25% to <50% bBMBs; group 3, ≥5% to <25% bBMBs. Response and survival outcomes were compared between groups.RESULTS: Data from 683 patients (166 pediatric, 517 adult) were analyzed. Collectively, patients in groups 2 and 3 had significantly higher odds of achieving a complete remission (CR) (odds ratio [OR], 3.50 [95% confidence interval (CI), 2.23-5.48] and 3.93 [95% CI, 2.50-6.18], respectively; p < .001) and minimal/measurable residual disease response (OR, 2.61 and 3.37, respectively; p < .001) when compared with group 1 (reference). Groups 2 and 3 had a 37% and 46% reduction in the risk of death (hazard ratio [HR], 0.63 and 0.54, respectively; p < .001) and a 41% and 43% reduction in the risk of an event (relapse or death) (HR, 0.59 and 0.57, respectively; p < .001) compared with group 1. No significant differences in response or survival outcomes were observed between groups 2 and 3. Seven of nine patients whose bBMB% was lowered to <50% with dexamethasone achieved CR with blinatumomab.CONCLUSION: Any bBMB% <50% was associated with improved efficacy following blinatumomab treatment for R/R B-ALL.

KW - Adult

KW - Humans

KW - Child

KW - Antineoplastic Agents/therapeutic use

KW - Precursor Cell Lymphoblastic Leukemia-Lymphoma

KW - Antibodies, Bispecific/therapeutic use

KW - Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/drug therapy

KW - Recurrence

KW - Lymphoma, B-Cell

KW - Acute Disease

U2 - 10.1002/cncr.34667

DO - 10.1002/cncr.34667

M3 - SCORING: Journal article

C2 - 36829303

VL - 129

SP - 1384

EP - 1393

JO - CANCER-AM CANCER SOC

JF - CANCER-AM CANCER SOC

SN - 0008-543X

IS - 9

ER -