AI Article Synopsis

  • Blinatumomab has shown promise as a key treatment for acute B-cell precursor lymphoblastic leukemia (BCP-ALL) when combined with pre-treatment chemotherapy to minimize side effects and CD19 selection pressure.
  • A recent phase 2 trial involved 35 newly diagnosed patients who received reduced-dose chemotherapy followed by blinatumomab, resulting in a high complete remission rate of 94% after 2 weeks of treatment.
  • With a median follow-up of 11.5 months, the treatment demonstrated excellent long-term outcomes, including a 97.1% one-year overall survival rate, suggesting that a less intensive approach can be both effective and well-tolerated for this leukemia type.

Article Abstract

Blinatumomab has emerged as a promising component of first-line therapy for acute B-cell precursor lymphoblastic leukemia (BCP-ALL), bolstering treatment efficacy. To mitigate CD19 selection pressure and reduce the incidence of blinatumomab-associated toxicities, pre-treatment chemotherapy is recommended before administering blinatumomab. From September 2022 to December 2023, we conducted a single-arm, multicenter, phase 2 trial (NCT05557110) in newly diagnosed Philadelphia chromosome-negative BCP-ALL (Ph-negative BCP-ALL) patients. Participants received induction treatment with reduced-dose chemotherapy (RDC), comprising idarubicin, vindesine, and dexamethasone over 7 days, followed by 2 weeks of blinatumomab. Those failing to achieve composite complete remission (CRc) received an additional 2 weeks of blinatumomab. The primary endpoint was the CRc rate post initial induction treatment. Of the 35 enrolled patients, 33 (94%) achieved CRc after 2 weeks of blinatumomab, with 30 (86%) achieving measurable residual disease (MRD) negativity. Two patients extended blinatumomab to 4 weeks. With either 2 or 4 weeks of blinatumomab treatment, all patients achieved CR (35/35) and 89% (31/35) were MRD negativity. The median time to CR was 22 days. Immune effector cell-associated neurotoxicity syndrome was limited (14%, all grade 1). Non-hematological adverse events of grade 3 or higher included pneumonia (17%), sepsis (6%), and cytokine release syndrome (9%). With a median follow-up of 11.5 months, estimated 1-year overall survival and 1-year progression-free survival rates were 97.1% and 82.2%, respectively. These findings affirm that RDC followed by blinatumomab is an effective and well-tolerated induction regimen for newly diagnosed Ph-negative BCP-ALL, supporting a shift towards less intensive and more targeted therapeutic approaches. Trial registration: https://www.clinicaltrials.Gov . Identifier NCT05557110.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11367979PMC
http://dx.doi.org/10.1186/s13045-024-01597-8DOI Listing

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