bims-hemali Biomed News
on Hematologic malignancies
Issue of 2025–09–21
29 papers selected by
Alexandros Alexandropoulos, Γενικό Νοσοκομείο Αθηνών Λαϊκό



  1. J Assoc Physicians India. 2025 Sep;73(9S): 21-22
      We present the case of a woman in her early 70s with chronic-phase chronic myeloid leukemia (CML-CP), initially diagnosed in 2002. After achieving deep molecular response (DMR) with imatinib for over a decade, the patient discontinued treatment, entering treatment-free remission (TFR) for around 7 years. She later presented with fever, fatigue, and abnormal blood counts. Restarting imatinib led to a near-complete molecular response, emphasizing the potential for late molecular recurrence (LMRec) in TFR, and underscoring the importance of long-term monitoring in CML patients who discontinue tyrosine kinase inhibitor (TKI) therapy.
    DOI:  https://doi.org/10.59556/japi.73.1123
  2. J Cancer Res Clin Oncol. 2025 Sep 19. 151(10): 263
      Chronic myeloid leukemia (CML) is a malignant clonal proliferative disease originating from hematopoietic stem cells. While treatment with tyrosine kinase inhibitors (TKIs) effectively eliminates the majority of leukemia cells in patients, residual leukemia cells can still be detected in those achieving deep molecular remission, ultimately leading to drug resistance or relapse. But the exact mechanism is unclear. In recent years, the immune microenvironment has been a hot research topic in hematologic malignancies. CML patients exhibit abnormalities in antitumor immunity. Myeloid-derived suppressor cells (MDSCs), which possess immune-suppressing functions, inhibit the proliferation and activation of CD4+/CD8+ T cells, Tregs, B cells, and NK cells, and play a central role in the antitumor immune response in a wide range of cancers. Abnormalities in numbers and functions of MDSCs are exhibited in CML patients, which affect the immune status of CML patients through multiple mechanisms. This review summarizes the biological properties of MDSCs, their alterations in CML patients, their roles and specific mechanisms in the development of CML, and how these mechanisms can be leveraged to develop new therapeutic strategies, aiming to provide novel insights and approaches for the treatment of CML.
    Keywords:  Chronic myeloid leukemia; Drug resistance; Immunosuppression; Myeloid-derived suppressor cells
    DOI:  https://doi.org/10.1007/s00432-025-06315-6
  3. Blood. 2025 Sep 19. pii: blood.2025029391. [Epub ahead of print]
      FLAG-IDA with venetoclax shows promise as frontline therapy for pediatric AML. In 12 patients treated at MD Anderson, most achieved remission with good early survival outcomes and many proceeded to transplant. Common toxicities included cytopenias comparable to previous regimens.
    DOI:  https://doi.org/10.1182/blood.2025029391
  4. Ther Adv Med Oncol. 2025 ;17 17588359251370504
       Objective: This study aimed to investigate the correlation between additional cytogenetic abnormalities (ACAs) at diagnosis and their clinical consequences in 337 Chinese chronic myeloid leukemia (CML) patients.
    Design: Retrospective observational cohort study.
    Methods: Response criteria were applied according to the European LeukemiaNet. Event-free survival (EFS) and progression-free survival (PFS) were analyzed. Independent predictors of PFS were assessed using Cox regression analysis.
    Results: At diagnosis, ACAs were identified in 41 patients (12.2%), with 24 exhibiting high-risk ACAs. Patients with high-risk ACAs showed significantly lower molecular response rates than those with low-risk ACAs or non-ACAs. Furthermore, patients with high-risk ACAs demonstrated diminished EFS (45.8% vs 76.5% vs 78.0%, respectively, p = 0.03) and PFS (54.2% vs 94.1% vs 93.9%, p < 0.001) compared with those in the other groups. In the multivariate analysis, both the EUTOS long-term survival (ELTS) score and high-risk ACAs at diagnosis emerged as independent prognostic factors influencing the cumulative major molecular response (MMR) rate and PFS. Moreover, when stratified according to high-risk ACAs and ELTS score, patients with high-risk ACAs alongside an intermediate/high ELTS score exhibited reduced MMR (p < 0.001) and inferior PFS rates (p = 0.0014).
    Conclusion: These findings underscore the importance of integrating cytogenetics-based risk assessments into CML management.
    Keywords:  additional cytogenetic aberrations; at diagnosis; chronic myeloid leukemia; clinical response; prognosis
    DOI:  https://doi.org/10.1177/17588359251370504
  5. bioRxiv. 2025 Sep 05. pii: 2025.09.02.673601. [Epub ahead of print]
      Resistance to Bruton's tyrosine kinase inhibitors (BTKi) remains a major therapeutic challenge in B-cell malignancies, limiting treatment durability. Here, we identify ferroptosis suppression as a central mechanism of BTKi resistance in mantle cell lymphoma (MCL). Aberrant BRG1 activity protects cells from BTKi-induced ferroptosis by restricting reactive oxygen species (ROS) and labile iron. Mechanistically, BRG1 promotes resistance through both BTK-dependent survival signaling and a BTK-independent transcriptional program. The latter is mediated by BRG1-driven induction of MEF2B, which upregulates NDUFA4L2 to inhibit mitochondrial respiration, thereby blocking mitochondria-dependent ferroptosis. Pharmacologic inhibition of BRG1 disrupts these programs, restoring ferroptotic sensitivity and synergizing with BTKi across resistant MCL models. Together, these findings establish BRG1 as a central regulator of therapy resistance and provide a rationale for co-targeting BRG1 and BTK as a therapeutic strategy for B-cell malignancies.
    DOI:  https://doi.org/10.1101/2025.09.02.673601
  6. Blood Cancer Discov. 2025 Sep 16. OF1-OF4
      This commentary explores new challenges in the management of newly diagnosed multiple myeloma and strategies for sustaining improvements in patient outcomes. We highlight the need for risk-adapted approaches, the potential future incorporation of T cell-redirecting immunotherapies in first-line treatment, and the challenge of access to care.
    DOI:  https://doi.org/10.1158/2643-3230.BCD-25-0280
  7. Eur J Haematol. 2025 Sep 16.
      Waldenström macroglobulinemia (WM) is an uncommon indolent B-cell lymphoma driven by MYD88 and CXCR4 mutations. Although serum B-cell maturation antigen (sBCMA) has been shown to be a prognostic and monitoring tool for multiple myeloma patients, it has not been evaluated among those with WM. We assessed sBCMA levels among 50 WM patients: 16 had received prior therapy, while 34 were treatment-naïve (TN), 19 of whom never went on to require therapy (smoldering [S]WM). Levels were higher among WM patients (median, 63.76 ng/mL) than healthy subjects (median, 35.24 ng/mL; p < 0.0001). TNWM patients who required therapy showed higher initial levels (median, 137.71 ng/mL) than those with SWM (median, 50.19 ng/mL; p = 0.0002). sBCMA also correlated with disease status: levels decreased at best response (≥ minimal response; median, 38.36 ng/mL) compared to baseline (median, 117.00 ng/mL; p = 0.0078) and increased among patients who developed progressive disease (median, 79.42 ng/mL; p = 0.0625). Baseline sBCMA levels positively correlated with β2 microglobulin (p = 0.0193) and M-protein (p = 0.0450), and negatively with hemoglobin (p = 0.0090) and albumin (p = 0.0016). Overall, these findings suggest sBCMA may serve as a biomarker for prognosis and monitoring for WM patients.
    Keywords:  B‐cell maturation antigen; Waldenström macroglobulinemia; biomarkers; monitoring disease; prognosis
    DOI:  https://doi.org/10.1111/ejh.70029
  8. Blood. 2025 Sep 19. pii: blood.2025029916. [Epub ahead of print]
      Juvenile myelomonocytic leukemia (JMML) is a rare, aggressive pediatric myeloproliferative neoplasm for which hematopoietic stem cell transplantation (HSCT) is currently the only established curative therapy. However, a watch-and-wait (W&W) approach has shown promise for long-term survival in selected cases. In this real-world study, we analyzed outcomes of JMML patients initially managed with a W&W strategy within a nationwide cohort of 161 genetically characterized cases. W&W was chosen for 35 patients, with increasing adoption over time, reaching 39% in the 2016-2021 period. Most patients carried mutations in CBL (43%), NRAS (34%), or homozygous germline SH2B3 (14%). Over a median follow-up of 6.5 years, 86% (30/35) achieved long-term survival with partial or complete resolution of myeloproliferative symptoms, although clonal hematopoiesis persisted in nearly all survivors (28/30). Disease progression occurred in five patients (CBL: n=3, NRAS: n=1, PTPN11: n=1), mostly within two years post-diagnosis. Overall, in the W&W cohort, the 5-year OS and EFS were 93.1% and 84.5%. In NRAS-mutated cases, age <30 months, normal to slightly elevated fetal hemoglobin, platelet >45x109/L, the absence of additional somatic mutations and low DNA methylation profile were associated with favorable outcomes. In CBL-driven JMML, no predictive factor of adverse evolution was identified. Notably, W&W was effective in all patients with homozygous germline SH2B3, regardless of clinical or biological presentation. These findings support W&W as a viable alternative in up to 30% of JMML patients, potentially sparing them from HSCT-associated risks. Given the persistence of clonal hematopoiesis and the risk of extra-hematological complications, long-term monitoring remains essential.
    DOI:  https://doi.org/10.1182/blood.2025029916
  9. Blood Neoplasia. 2025 Aug;2(3): 100067
      Clarithromycin is a macrolide antibiotic with anti-multiple myeloma (MM) activity when combined with dexamethasone and immunomodulatory agents. This phase 1/2 study of clarithromycin, ixazomib, pomalidomide, and dexamethasone (ClIPd) assessed tolerability and efficacy in relapsed/refractory MM. The primary end points were the maximal tolerated and recommended phase 2 dose. Key secondary end points were the overall response rate (ORR) (≥partial response), disease control rate (DCR) (≥stable disease), progression-free survival (PFS), and overall survival (OS). All 4 medications were given at full dose for 6 cycles. Pomalidomide, ixazomib, and dexamethasone were given at reduced doses with full-dose clarithromycin in subsequent maintenance cycles until unacceptable toxicity or progression. Clarithromycin was withheld during weeks 1 to 2 of cycle 1 to facilitate correlative studies. A total of 28 patients were evaluable for response/survival. The ORR was 75%; DCR was 100%; 56% achieved ≥very good partial response (VGPR), whereas 14% achieved complete response (CR)/stringent CR. High-risk cytogenetics were not associated with ORR (Fisher exact test, P = 1) or ≥VGPR rates (Fisher exact test, P = .42). The median PFS was 22.2 months (95% confidence interval [CI], 13.3 to not reached [NR]). There was no difference in the median PFS between patients with del(17p) (26.8 months; 95% CI, 10.2 to NR) and those without (22.2 months; 95% CI, 13.3 to NR; log rank, P = .4). The median OS was NR. ClIPd combines convenient oral administration, a tolerable side effect profile, and long duration of disease control. This trial was registered at www.clinicaltrials.gov as #NCT02542657.
    DOI:  https://doi.org/10.1016/j.bneo.2025.100067
  10. Blood Adv. 2025 Sep 18. pii: bloodadvances.2025017016. [Epub ahead of print]
      Chronic inflammation may be a key driving force in the development and progression of Philadelphia chromosome-negative myeloproliferative neoplasms (MPNs). Statins, commonly used to lower cholesterol, also possess anti-proliferative, proapoptotic and anti-inflammatory properties, that may be beneficial in the treatment of MPN patients. This retrospective cohort study investigated whether statin use, in addition to standard cytoreductive therapy, shortens the time required to achieve hematological and molecular responses while allowing for lower cytoreductive drug dosages. A total of 129 patients were included, with 53 receiving statins from diagnosis. The study found that statin users achieved complete hematologic response (CHR) significantly faster than non-users (median time: 8 versus 18 months; HR 2.1, 95%CI 1.4-3.1, P = 0.0003). Among patients treated with pegylated interferon-alpha2 (IFN), the CHR rate was 97% in statin users versus 83% in non-users (HR 2.5, 95%CI 1.5-3.9, P = 0.0004), and a higher proportion of statin users sustained CHR throughout follow-up. Additionally, IFN-treated statin users received a significantly lower mean dose of IFN. A dose-response relationship was observed, with higher statin intensity associated with an increase of CHR. Furthermore, statin use was significantly associated with achieving a partial molecular response among IFN-treated patients (HR 2.6, 95%CI: 1.1-6.0, P = 0.029). No significant association was observed in hydroxyurea-treated patients. These findings suggest that statins may enhance the efficacy of IFN in MPN patients, while their benefit in hydroxyurea-treated patients remains unclear. Prospective studies are warranted to further explore the therapeutic potential of statins in MPNs.
    DOI:  https://doi.org/10.1182/bloodadvances.2025017016
  11. Blood Neoplasia. 2025 May;2(2): 100091
      The prognosis for multiple myeloma (MM) has continued to improve with the development of a series of novel molecular targeted drugs over time. However, the prognosis remains poor for cases with high-risk chromosomal abnormalities. Of such abnormalities, t(4;14) is the second most common, occurring in 15% of patients with MM. MM cells carrying t(4;14) strongly express histone methyltransferase with a SET domain, called NSD2, making them resistant to drugs against MM. Therefore, NSD2 is a promising therapeutic target for MM carrying t(4;14). Subsequently, we performed high-throughput screening and identified RK-0080552 (RK-552) as a novel class NSD2 inhibitor. RK-552 was significantly cytotoxic against t(4;14)+ MM compared with t(4;14)- MM cells in vitro and in vivo via transcriptional suppression of the IRF4 gene, coincided with a decrease in histone H3 lysine 36 dimethylation. Moreover, RK-552 acted additively with pomalidomide in vitro and prolonged the survival of recipient mice without side effects. These results suggest that RK-552 may be a clinically relevant NSD2 inhibitor with specific cytotoxicity to MM cells carrying t(4;14). Our study also provides a molecular basis and rationale for the inclusion in current treatment strategies. Therefore, the clinical use of RK-552 may significantly improve the treatment outcome of MM with t(4;14).
    DOI:  https://doi.org/10.1016/j.bneo.2025.100091
  12. Drug Des Devel Ther. 2025 ;19 8161-8180
      Immune thrombocytopenia (ITP), as an autoimmune disease, has various limitations in traditional treatments, and there is a lack of safe and durable targeted therapeutic regimens for refractory patients. Traditional covalent Bruton's tyrosine kinase (BTK) inhibitors are difficult to apply in ITP treatment due to issues such as drug resistance and bleeding risks. As a reversible covalent BTK inhibitor, rilzabrutinib has dual advantages in its molecular design: in terms of evading C481 resistance, it targets the ATP-binding domain of BTK through a non-covalent bond-dominated mode, and maintains highly efficient inhibitory activity in the BTK C481S mutant cell model (with an in vitro IC50 of 1.2 nM), showing significant advantages over traditional covalent inhibitors (eg, ibrutinib, whose IC50 increases to 1 μM); in terms of platelet function protection, in vivo mouse experiments have confirmed that it can reduce venous thrombosis, block the BTK pathway to decrease autoantibody-mediated platelet destruction, and retain the functions of pathways such as G protein-coupled receptors, achieving a balance between abnormal immune suppression and platelet hemostatic function through "on-demand inhibition". Preclinical studies have shown that its binding to human blood BTK is time- and concentration-dependent, and the inhibition of the BTK pathway in B cells and basophils is closely related to the degree of binding, with moderate kinase selectivity. Clinical studies have confirmed that the drug can take effect quickly, with 43% of patients achieving a platelet count ≥50×109/L after 12 weeks of treatment, and the incidence of bleeding events is low. This article systematically analyzes the value of rilzabrutinib from molecular design to clinical translation, and elaborates on its mechanism of overcoming drug resistance and its synergistic regulatory effect on the B cell-macrophage-platelet pathological network. At present, its rapid onset, high safety, and effectiveness in refractory cases have been preliminarily verified, but long-term data from Phase III clinical trials are still needed to support its use as a first-line treatment. It provides a new therapeutic hope for patients with refractory ITP and also offers a paradigmatic reference for the development of kinase inhibitors for autoimmune diseases.
    Keywords:  BTK inhibitor; C481 resistance; dynamic targeted regulation; immune thrombocytopenia; rilzabrutinib
    DOI:  https://doi.org/10.2147/DDDT.S543620
  13. Front Oncol. 2025 ;15 1596270
       Objective: Peripheral T-cell lymphoma (PTCL) is characterized by its significant variability and complexity as malignancy. Treatment outcome is poor with conventional chemotherapy. We sought to exploring the effectiveness and safety profile of chidamide monotherapy as maintenance regimen after chemotherapy.
    Methods: 69 patients for PTCL were included in the study and chidamide was administered as maintenance therapy at a dosage of 15-30 mg twice weekly (biw). The Kaplan-Meier survival analysis was employed to evaluate overall survival (OS) and progression-free survival (PFS).
    Results: The average age of participants was 61 years (17-93). The most prevalent pathologic subtype identified was angioimmunoblastic T-cell lymphoma (AITL, 55.1%), and 43.5% (30/69) of patients were classified as intermediate or high-risk cases. Of the patients, 56.5% (n=39) underwent chidamide maintenance therapy after attaining complete response (CR). Over a median follow-up duration of 43.4 months (21.7-98.4), 47.8% of patients attained CR. The median overall survival (mOS) was not achieved, while the median progression-free survival (mPFS) stood at 54.8 months (95%CI, 21.68-72.78). 20% (6/30) of PR patients exhibited CR after chidamide. Individuals who attained CR at baseline demonstrated superior PFS compared to those in PR group. Baseline effectiveness was recognized as an independent prognostic indicator for PFS. Neutropenia was the most common hematologic TRAE, with a 20.3% rate of grade 3/4 events. Dosage modifications were required for 17 patients owing to adverse events, with no fatalities attributed to the treatment reported.
    Conclusion: In patients with PTCL, chidamide as a single-agent maintenance treatment demonstrates effectiveness and favorable tolerability, while the remission status prior to initiating maintenance therapy is a key factor influencing treatment outcomes. Notably, the depth of response after induction therapy alone cannot determine the long-term efficacy in PTCL. Maintenance therapy can not only bring more significant benefits to CR patients but also improve the prognosis of PR patients and reduce the risk of recurrence and progression, highlighting the core value of the "induction-maintenance" sequential model. Nevertheless, this study is exploratory, and further verification through prospective studies is still required.
    Keywords:  chidamide; effectiveness; maintenance therapy; peripheral T-cell lymphoma; safety
    DOI:  https://doi.org/10.3389/fonc.2025.1596270
  14. Blood. 2025 Sep 12. pii: blood.2025029950. [Epub ahead of print]
      The progression of multiple myeloma (MM), an incurable malignancy of plasma cells, is often associated with the suppression of ferroptosis, a type of cell death driven by iron-dependent lipid peroxidation. The mechanisms underlying this suppression remain largely unknown. Here, we identified STK17B kinase as a critical suppressor of ferroptosis in MM. Elevated levels of STK17B are associated with poor overall survival in MM patients and STK17B expression is significantly higher in relapsed vs newly diagnosed MM cases. We found that inhibiting STK17B in MM cells increased the labile iron pool, enhanced lipid peroxidation, and sensitized cells to conventional anti-MM therapies. Notably, an orally available, in-house-generated STK17B inhibitor induced ferroptosis and significantly reduced tumor growth in MM xenograft mouse models. Mechanistically, proximity labeling assay combined with the phospho-proteomic analysis identified two major regulators of iron uptake and transport as direct targets of STK17B: iron-responsive element binding protein 2 (IREB2) and heat shock protein family B member 1 (HSPB1). We demonstrated that STK17B phosphorylates critical regulatory sites on IREB2 (S157) and HSPB1 (S15), thereby modulating the balance between IREB2 and HSPB1 downstream effectors, pro-ferropototic transferrin receptor and anti-ferroptotic ferritin heavy chain proteins. Furthermore, we demonstrated that STK17B indirectly maintains activating phosphorylation of STAT3, a ferroptosis suppressor and a major driver of MM pathobiology. Our findings uncovered a clinically relevant and targetable STK17B-pIREB2S157/pHSPB1S15 signaling axis that suppresses ferroptosis and contributes to drug resistance in MM.
    DOI:  https://doi.org/10.1182/blood.2025029950
  15. Blood. 2025 Sep 19. pii: blood.2024027496. [Epub ahead of print]
      Glutamine-dependence of cancer cells reduces local glutamine availability, which hinders anti-tumor T-cell functionality and facilitates immune evasion. We thus speculated that glutamine deprivation might be limiting efficacy of CAR T-cell therapies in cancer patients. We have seen that antigen-specific T cells are unable to proliferate or produce IFN-γ in response to antigen stimulation when glutamine concentration is limited. Using multiple myeloma (MM) as a glutamine-dependent disease model, we found that murine CAR-T cells selectively targeting BCMA in MM cells were sensitive to glutamine deprivation. However, CAR-T cells engineered to increase glutamine uptake by expression of the glutamine transporter Asct2 exhibited enhanced proliferation and responsiveness to antigen stimulation, increased production of IFN-γ, and heightened cytotoxic activity, even under conditions of low glutamine concentration. Mechanistically, Asct2 overexpression reprogrammed CART cell metabolic fitness of CART cells by upregulating the mTORC1 gene signature, modifying the Solute Carrier transporter (SLC) repertoire, and improving both basal oxygen consumption rate and glycolytic function thereby enhancing CART cell persistence in vivo. Accordingly, expression of Asct2 increased the efficacy of BCMA-CART cells in syngeneic and genetically-engineered mouse models of MM, which prolonged mouse survival. In patients, reduced expression of Asct2 by MM cells predicted poor outcome to combined immunotherapy and BCMA-CAR T-cell therapy. Our results indicate that reprogramming glutamine metabolism may enhance anti-tumor CAR T-cell functionality in MM. This approach may also be effective for other cancers that depend on glutamine as a key energy source and metabolic hallmark.
    DOI:  https://doi.org/10.1182/blood.2024027496
  16. Am J Cancer Res. 2025 ;15(8): 3417-3433
      ZUMA-24 is a Phase 2, open-label, multicenter study that investigated safety and efficacy of axicabtagene ciloleucel (axi-cel), an autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy, administered in the outpatient setting to patients with relapsed or refractory large B-cell lymphoma (R/R LBCL) with ≥1 prior lines of therapy. Patients underwent leukapheresis and received lymphodepleting chemotherapy, axi-cel infusion (2×106 CAR T cells/kg), and prophylactic steroids. Patients were monitored daily ≥7 days after infusion per institutional outpatient monitoring guidelines. The primary endpoint was incidence and severity of cytokine release syndrome (CRS) and neurologic events (NEs). Median follow-up was 13 months for 30 patients treated with outpatient axi-cel. Grade 1-2 CRS was reported in 90% of patients, with no grade ≥3 CRS. NEs of any grade were reported in 80% of patients (grade ≥3, 23%; no patients died due to NEs). Median time to onset was 4 days for CRS and 7 days for NEs, with a median duration of 5 days and 6 days, respectively. All patients experienced AEs of any grade (grade ≥3, 83%). After axi-cel, 93% of patients were hospitalized, with 4 days median time to first hospitalization (8 days median stay), and 4 patients (13%) were admitted to the ICU (for 2-7 days). Among patients evaluable for efficacy (n=29), the objective response rate was 93% (complete response, 76%), with a median duration of response of 11.4 months. These results support safety and feasibility of outpatient administration of axi-cel. This trial is registered at ClinicalTrials.gov: #NCT05459571.
    Keywords:  CAR-T; Large B-cell lymphoma; chimeric antigen receptor; clinical trial; outpatient; phase 2
    DOI:  https://doi.org/10.62347/GJNN1023
  17. Neoplasma. 2025 Aug;pii: 241028N438. [Epub ahead of print]72(4): 229-241
      This study aimed to evaluate synergistic effects and molecular mechanisms of the histone deacetylase inhibitor chidamide combined with the BCL-2 inhibitor venetoclax in diffuse large B-cell lymphoma (DLBCL) cell lines. Human DLBCL cell lines (U2932, SUDHL-4) were cultured in vitro and treated with chidamide and venetoclax. Cell proliferation inhibition rates were measured using the CCK-8 assay, and IC50 values were calculated. Cells were also treated with a 5:1 combination of chidamide and venetoclax, along with p53 or p21 siRNA. Cell viability, HDAC activity, apoptosis, cell cycle, the amount of p53 and p21 proteins, and BCL-2-BIM binding were analyzed via CCK-8, enzyme activity assays, the Caspase 3/7 Activity Apoptosis Assay Kit, flow cytometry, RT-qPCR, western blot, and co-IP. The binding of p53 and p21 was verified by dual-luciferase reporter assay and chromatin immunoprecipitation. Chidamide and venetoclax exhibited dose- and time-dependent anti-proliferative effects in U2932 and SUDHL-4 cells, with IC50 values of 3.54 μM (chidamide) and 0.67 μM (venetoclax) in the SUDHL-4 cell line and 5.6 μM (chidamide) and 0.91 μM (venetoclax) in the U2932 cell line. Combination treatment significantly enhanced HDAC inhibition, histone H3/H4 acetylation, and p53 expression, leading to increased cell apoptosis. p53 knockdown partially reversed these effects and increased BCL-2/BIM complex formation. The combination also upregulated p53 expression to increase p21 expression, inducing G1/S phase arrest, which was partially reversed by p21 knockdown. To conclude, the chidamide-venetoclax combination synergistically activates the p53-p21 signaling pathway, leading to cell cycle arrest and apoptosis, representing a potential therapeutic strategy for DLBCL.
    DOI:  https://doi.org/10.4149/neo_2025_241028N438
  18. Ann Hematol. 2025 Sep 18.
      T-cell acute lymphoblastic leukemia (T-ALL) in adolescents and young adults (AYA) poses distinct clinical challenges. This study evaluates the effectiveness and tolerability of a pediatric-inspired regimen in this specific age group, focusing on response rates, survival outcomes, and prognostic indicators. We retrospectively analyzed AYA patients (15-29 years) diagnosed with T-ALL between 2010 and 2020 at Aziza Othmana Hospital, Tunis. All patients received treatment per the EORTC 58,951 protocol. Clinical, cytological, and immunophenotypic data were collected, with special attention to treatment response and minimal residual disease (MRD). Survival outcomes were assessed using Kaplan-Meier estimates, and prognostic factors were examined via uni- and multivariate analyses. Thirty-two patients were included (median age: 20 years; male: female ratio 2.3:1). Complete remission after induction was achieved in 84.4% of cases, with MRD negativity (< 10⁻⁴ at day 35) observed in 42% of patients. At a median follow-up of 62 months, the 5-year overall survival (OS), event-free survival (EFS), and relapse-free survival (RFS) were 62.2%, 62.5%, and 70.8%, respectively. Chemotherapy response at day 19 and MRD negativity were associated with better outcomes, although only relapse occurrence remained independently predictive of OS. Induction mortality reached 9.4%. Relapse occurred in 32.1% of patients, underscoring the need for improved risk stratification. Our findings support the efficacy of pediatric-based protocols in treating AYA with T-ALL. However, high relapse rates and early induction mortality highlight the importance of integrating MRD-guided decisions and enhancing supportive care. Future strategies should incorporate targeted and immune-based therapies to improve long-term outcomes in high-risk subgroups.
    Keywords:  Adolescents and young adults; Minimal residual disease; Pediatric-inspired treatment; Relapse; Survival outcomes; T-cell acute lymphoblastic leukemia
    DOI:  https://doi.org/10.1007/s00277-025-06597-3
  19. Ther Drug Monit. 2025 Sep 18.
       BACKGROUND: Therapeutic drug monitoring (TDM) of tyrosine kinase inhibitors may improve treatment outcomes and individualized therapy in patients with cancer. Compared with plasma, the standard TDM matrix, dried blood microsampling is associated with several advantages, including the collection of samples by the patients themselves in their home setting. This study aimed to compare dasatinib and imatinib concentrations in different blood-based matrices and to determine whether dried capillary blood collected via volumetric absorptive microsampling (VAMS) could be used as an alternative to perform TDM in patients with chronic myeloid leukemia.
    METHODS: In addition to venous liquid whole blood, plasma, and VAMS samples (referred to as venous VAMS) prepared thereof, also fingerprick capillary VAMS samples were collected from patients receiving dasatinib or imatinib treatment by skilled personnel in a controlled environment. All samples were analyzed using validated liquid chromatography tandem mass spectrometry methods.
    RESULTS: Fifty-three patients were included in the study: 33 were treated with dasatinib and 20 with imatinib. Although a bias between dasatinib and imatinib venous VAMS and liquid blood concentrations was observed, 94% and 95% of the samples, respectively, fulfilled the 20% difference acceptance criterion. Capillary and venous concentrations were interchangeable and independent of the collection time. Using venous blood-to-plasma ratios from a prior proof-of-concept study, the VAMS results for imatinib, but not dasatinib, could reliably be converted into plasma concentrations.
    CONCLUSIONS: Through a clinical validation study, the authors demonstrated that VAMS is a viable alternative for imatinib monitoring in patients with chronic myeloid leukemia. For dasatinib, VAMS-based analysis may still allow for longitudinal follow-up (ie, provide insight into fluctuations in patients). As a next step, capillary microsampling can be integrated into the home sampling context.
    Keywords:  chronic myeloid leukemia; therapeutic drug monitoring; tyrosine kinase inhibitors; volumetric absorptive microsampling
    DOI:  https://doi.org/10.1097/FTD.0000000000001387
  20. Front Physiol. 2025 ;16 1641323
      Ferroptosis is an iron-dependent programmed cell death that plays an important role in neurodegenerative and neuropsychiatric diseases. In the present study, we have highlighted how different risk factors are involved in the induction of ferroptosis in brain cells. In addition, we also demonstrated how ferroptosis plays an important role in different brain diseases. In our study why we focused and elaborated on the mechanisms of ferroptosis only in brain cells (Neurons, oligodendrocytes, and microglia) because they are particularly vulnerable to such kind of cell death. Additionally, brain cells are more dependent on mitochondrial function, iron regulation, and high levels of polyunsaturated fatty acids (PUFAs) as compared to peripheral body cells. Highlighting ferroptosis is more important because it has demonstrated several important mechanisms of neuronal injury and dysfunction which provides a deep understanding of the etiology of various brain diseases that were not sufficiently described by other programmed cell death pathways. Therefore, it has led to the exploration of new therapeutic strategies against various brain diseases and thus targeting ferroptosis-related proteins opens a new therapeutic window for several incurable brain diseases, and various ferroptosis regulators are now under clinical trials. However, their validation as a preclinical therapeutic agent is needed. Interestingly, here in our study we also summarize the most recent potential therapeutic targets and promising interventions which will provide a beam of light for future therapies against major brain diseases.
    Keywords:  aceruloplasminemia; alzheimer’s disease; ferroptosis; lipid peroxidation; neurodegeneration with brain iron accumulation (NBIA); oxidative stress; parkinson’s disease
    DOI:  https://doi.org/10.3389/fphys.2025.1641323
  21. J Cell Mol Med. 2025 Sep;29(18): e70822
      Rituximab has improved response rates and overall survival in diffuse large B-cell lymphoma (DLBCL). Radiotherapy (RT) is an effective treatment modality for lymphomas. However, significant conceptual challenges, including the application in elderly patients, varying IPI scores and CR patients, remain regarding the current use of RT. We performed a systematic review comparing chemotherapy with RT to chemotherapy alone in patients with DLBCL. We estimated hazard ratios (HR) for OS, PFS and EFS using the proportional hazards model. Five articles involving 1364 patients met inclusion criteria. Patients undergoing consolidative RT had better OS (HR = 0.46, 95% CI 0.31-0.68), PFS (HR = 0.52, 95% CI 0.22-1.25) and EFS (HR = 0.42, 95% CI 0.20-0.90) compared to those who received no RT. But no benefit was shown in patients with achievement of CR. The protective effect of consolidation RT for patients with advanced IPI scores (HR = 0.46, 95% CI 0.31-0.68) and advanced stage (HR = 0.22, 95% CI 0.08-0.59) was shown. The consolidation RT showed a significantly longer PFS (HR = 0.50, 95% CI 0.26-0.94) but no significant benefit on OS in patients with bulky disease. There was also significantly better PFS in RT patients (HR = 0.67, 95% CI 0.49-0.92), but no significant benefit on OS in old age patients. RT act as an efficacious method for DLBCL following a full course of chemotherapy. However, no OS benefit was shown in patients with advanced IPI scores, bulky disease, CR and old age.
    Keywords:  aggressive B cell NHL; consolidation radiotherapy; meta‐analysis; non‐Hodgkin lymphoma; randomised controlled trials
    DOI:  https://doi.org/10.1111/jcmm.70822
  22. JACC CardioOncol. 2025 Sep 12. pii: S2666-0873(25)00293-5. [Epub ahead of print]
      Classic Hodgkin lymphoma is a highly curable lymphoma that affects primarily younger patients. The therapeutic landscape has evolved and generally consists of varying combinations of chemotherapy and immunotherapy as well as radiation in selected cases. Although most patients are cured of their lymphoma, there is a risk for late treatment-related cardiotoxicity that affects long-term survival and quality of life in this population. Careful consideration of baseline cardiac function and risk factors should be undertaken prior to proceeding with anthracycline-based therapies or thoracic radiation, as adjuvant cardiac-focused efforts may serve to mitigate the risk for cardiovascular dysfunction in this population. This review outlines the evidence supporting current recommendations for assessing baseline cardiotoxicity risk, implementing risk reduction strategies and treatment modifications, the role of multidisciplinary evaluation in high-risk patients, and strategies for long-term cardiac monitoring to minimize treatment-related cardiac morbidity and mortality.
    Keywords:  Hodgkin; anthracycline; heart failure; immune checkpoint inhibitor; lymphoma; radiation
    DOI:  https://doi.org/10.1016/j.jaccao.2025.07.011
  23. ACS Appl Mater Interfaces. 2025 Sep 20.
      Laminated perovskite solar cells (L-PSCs), which can be fabricated by independently processing the hole and electron transport sides of the solar cell on separate substrates and then bonding them together, offer unique passivation, transport, and contact-layer combinations. Lamination also facilitates inherent self-encapsulation between two glass substrates, which can be leveraged to improve stability. However, the impacts of this glass-glass encapsulation on the mechanical properties and thermal stresses that arise during operation have not been previously studied. Here, we measured the thermal cycling stability and interfacial toughness of L-PSCs for the first time. L-PSCs withstood thermal cycling (TC50 protocol, -40 to 85 °C) without failure, with all devices exhibiting an increase in power conversion efficiency after cycling. To quantify their mechanical properties, the interfacial toughness values of device stacks were measured, and minimal changes were observed after TC50 cycling. An analytical framework was developed to describe the mechanical failure criterion for the self-encapsulated L-PSC system under thermal cycling, showing that using substrates with the same material properties on both sides makes the device system robust to thermal cycling. This study demonstrates that L-PSCs exhibit strong thermal and mechanical stability without the need for additional encapsulation.
    Keywords:  lamination; mechanics; perovskite; solar cell; thermal cycling; toughness
    DOI:  https://doi.org/10.1021/acsami.5c08406