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Record W4417020225 · doi:10.1182/blood-2025-3462

Thioguanine and decitabine can overcome hypomethylating agent resistance in patients with advanced myeloid malignancies

2025· article· en· W4417020225 on OpenAlexaff
Sunil Iyer, Joseph G. Jurcic, Daniel J. Lee, Mark G. Frattini, Monica Kasbekar, Alina Varabyeva, Azra Raza, Yi Chen, Sebastian Fernando, Stefan Petkov, Simon Fredriksson, Aaron D. Viny, Todd Rosenblat

Bibliographic record

VenueBlood · 2025
Typearticle
Languageen
FieldMedicine
TopicAcute Myeloid Leukemia Research
Canadian institutionsForming Technologies (Canada)
Fundersnot available
KeywordsDecitabineHypomethylating agentAzacitidineRegimenMyeloid leukemiaMyeloidVenetoclaxBone marrowProgressive disease

Abstract

fetched live from OpenAlex

Abstract BACKGROUND Despite active therapies such as hypomethylating agents (HMA) and venetoclax advanced myeloid malignancies, outcomes in relapsed/refractory (R/R) disease or secondary acute myeloid leukemia (AML) remain poor. We previously showed that combination thioguanine (6TG) and decitabine (DEC) restores therapeutic efficacy in vitro in R/R AML (O'Dwyer K et al. Blood 2010;114:2657). Building on these observations, we completed a Phase I dose-escalation study of 6TG with DEC in advanced myeloid malignancies followed by a retrospective analysis of 42 patients treated with this regimen at our institution (Cicero KI et al. Blood 2019;134:3899). In this cohort, which included patients on- and off-study, responses were seen in 33% of patients, without a significant difference between patients who had or had not received prior HMA. This suggested that combination therapy with 6TG and DEC could overcome HMA resistance. We now present updated clinical and mechanistic data from an expanded cohort, including insights into regimen-specific effects on malignant clones and immune constitution. METHODS A retrospective chart review was performed of all adult patients at our institution with advanced myeloid malignancies who received at least 1 cycle of 6TG and DEC between 2013-2025 with formal disease assessment evaluable by bone marrow biopsy or blood. The regimen utilized the maximum tolerated dose of 6TG identified in the phase I trial. Up to 2 cycles of induction with oral 6TG 80 mg/m2/day in 2 divided doses was given on Days 1-12. Decitabine 20 mg/m2 IV was given on Days 3-12. Following this, maintenance cycles consisted of 6TG on Days 1-7 and decitabine on Days 3-7 at the same doses. Treatment continued until the time of hematopoietic stem cell transplant (HSCT), disease progression, or toxicity. The primary objective of this retrospective analysis was to determine the overall response rate (ORR). Secondary objectives were to evaluate progression-free survival (PFS) and overall survival (OS) in this population. RESULTS Sixty-seven patients were identified, 53% of whom were female, with a median age of 68 years (range, 23-86 years). Thirty-four patients (51%) had secondary AML, 26 (39%) had de novo AML, 5 (7%) had higher-risk MDS, and 2 (3%) had chronic myelomonocytic leukemia (CMML). By ELN2022 risk stratification among AML patients, 40 (60%), 6 (9%), 6 (9%), and 8 (12%) had adverse, intermediate, favorable, and unknown risk disease, respectively. Patients received a median of 2 cycles of therapy (range, 1-10). Eight (12%) patients achieved complete remission (CR), 7 (10.5%) obtained a CR with incomplete count recovery (CRi), and 5 (7.5%) had morphologic leukemia-free state (MLFS), for an ORR of 30% (CR+CRi+MLFS). Nine of 20 responders (45%) had prior HMA exposure; 3 of these patients had exposure to prior HMA plus venetoclax. For the responders, the median PFS was 24 weeks (range, 7-NR), while the median OS was 50 weeks (range, 7-NR). For responders achieving composite CR (CRc: CR + CRi), median PFS was 35 weeks and median OS was 54 weeks. Two notable patients, one with CMML and another with relapsed AML, were bridged to allogeneic HSCT and are currently alive and in remission over 10 years after treatment. To elucidate response mechanisms, we performed methylome-aware whole-genome long-read sequencing and Pixelgen single-cell proteomic analysis. Pre-treatment samples from non-responders showed elevated CD44 co-localized with HLA and β2-microglobulin, while responders exhibited low CD44, uniform HLA/β2M expression, and expanded effector T-cell pools, suggesting immune activation as a key therapeutic axis. Post-treatment samples revealed persistent CD44 in non-responders, while responders expressed unexpectedly high CD36 expression in the context of re-emergence of normal stem cell marker expression. CONCLUSIONS: 6TG/DEC is a clinically active regimen in high-risk and R/R AML with a 30% ORR and favorable survival outcomes compared to historical controls. Single-cell proteomic data reveal immune-modulatory mechanisms that may underlie therapeutic response, offering a novel lens into resistance biology. Taken together, this combination remains a viable therapeutic option for elderly and unfit patients with high-risk and R/R AML who cannot tolerate intensive chemotherapy. A phase II study of 6TG and decitabine-cedazuridine as an entirely oral regimen for R/R AML irrespective of molecular phenotype is in preparation.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.002

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.007
GPT teacher head0.243
Teacher spread0.236 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2025
Admission routes1
Has abstractyes

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