Evidence map›Paper›PMID 41619253›Full record

ArticleThe American journal of case reports2026

Chemotherapy-Free Achievement of Minimal Residual Disease in a Jehovah's Witness Patient With Ph-Negative B-ALL.

Sarina Koilpillai, Rida Altaf, Alejandro El Barche Palmera, Hatem Hassanein, Stephen J Carlan

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Article in The American journal of case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sarina KoilpillaiDepartment of Medical Oncology and Hematology, Orlando Regional Medical Center, Orlando, FL, USA.
Rida AltafDepartment of Internal Medicine, Orlando Regional Medical Center, Orlando, FL, USA.
Alejandro El Barche PalmeraDepartment of Medical Oncology and Hematology, Orlando Regional Medical Center, Orlando, FL, USA.
Hatem HassaneinDepartment of Pathology, Orlando Regional Medical Center, Orlando, FL, USA.
Stephen J CarlanDepartment of Academic Affairs and Research, Orlando Regional Medical Center, Orlando, FL, USA.ORCID 0000-0001-9867-8538

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Philadelphia chromosome (Ph)-negative B-cell acute lymphoblastic leukemia (B-ALL) is usually treated with intensive chemotherapy, presenting challenges for Jehovah's Witness patients who refuse blood products due to religious beliefs. These regimens often lead to severe cytopenias that require transfusion support. New targeted therapies (eg, inotuzumab ozogamicin and blinatumomab) have become effective options with lower toxicity, particularly for older or frail patients; these benefits may extend to the Jehovah's Witness population. CASE REPORT A 44-year-old Jehovah's Witness man was diagnosed with Ph-negative B-ALL. His comorbidities included hypertension, atrial fibrillation, and a newly identified reduced ejection fraction of 30% to 35%, which precluded the use of anthracyclines. Due to his refusal of blood products and cardiac limitations, he was treated with a chemotherapy-free regimen consisting of inotuzumab induction followed by blinatumomab consolidation. Supportive care included epoetin alfa, romiplostim, iron, and vitamin supplementation. The patient tolerated induction well, with minimal cytopenias and no serious adverse effects. After 2 cycles of inotuzumab, he achieved complete morphologic remission and minimal residual disease (MRD) negativity according to ClonoSEQ. He is currently receiving consolidation with blinatumomab. CONCLUSIONS This is the first known reported case that demonstrates the feasibility and effectiveness of a chemotherapy-free induction strategy using inotuzumab and blinatumomab for frontline treatment of Ph-negative B-ALL in Jehovah's Witness patients. It shows that MRD negativity can be safely achieved without cytotoxic chemotherapy or transfusion support and supports the use of the ALLIANCE A041703 trial regimen as a treatment model for this unique and underserved patient group.

Indexed as

Antibodies, BispecificJehovah's WitnessesPrecursor B-Cell Lymphoblastic Leukemia-LymphomaPrecursor Cell Lymphoblastic Leukemia-LymphomaAdultHumansInotuzumab OzogamicinMaleNeoplasm, ResidualPhiladelphia ChromosomeTreatment RefusalAntibodies, BispecificblinatumomabInotuzumab Ozogamicin

Identifiers

PMID41619253
PMCPMC12870160

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.