Pediatric Hematology Oncology Journal

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Pediatric Hematology Oncology Journal

Pediatric Hematology Oncology Journal

@PHOJournal

https://t.co/VdrXEe1Kb2 Official Journal of PHO Chapter of Indian Academy of Pediatrics https://t.co/PZDsoC5jKD

Katılım Haziran 2019
190 Takip Edilen1.8K Takipçiler
Pediatric Hematology Oncology Journal
When one rare tumor wasn’t rare enough, this toddler said 'Let’s make it a case report' Synchronous ERMS + ACC + germline CBL mutation = genetics keeping pediatric oncology on its toes. Moral: If a kid brings two tumors to clinic, always invite genetics to the party #GeneticsWins
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Pediatric Hematology Oncology Journal
This systematic review by Dana Ashkenazi Lustig and colleagues from Israel speaks about the spontaneous resolution of LCH lesions. Proposed mechanisms include biopsy-induced inflammatory system modulation, apoptosis via the Fas/Fas-L pathway, & disruption of the MAPK signalling
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Pediatric Hematology Oncology Journal
These findings highlight the importance of regular monitoring of height & weight during & after therapy.  Future prospective studies incorporating body composition assessments  may provide further insight into sarcopenic obesity & long-term metabolic risks in this population
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Pediatric Hematology Oncology Journal
Krisha Savla and colleagues from Tata Memorial Hospital, Mumbai have described their findings about the nutritional status of children with acute leukemias receiving chemotherapy at their centre. Details of the findings in comments.
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In this cohort, 37.5 % of children classified as malnourished. At end of Rx, 5.3 % were severely & 22.6 %  were moderately malnourished, 8.2 % were overweight & 6.7 % were obese  Improvement in the status could be attributed to effective nutritional interventions, supportive care
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Gargi Das
Gargi Das@drgargidas·
My MD thesis is now published in the Indian Journal of Pediatrics! First prospective research. First lab-based work. A 7-year journey and a very emotional PGI connection. Grateful & proud. 🔗 link.springer.com/article/10.100… @IJPJOURNAL
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Pediatric Hematology Oncology Journal
Read this with a report on triple negative thrombocytosis (apparently group 4) in 2025 issue of PHOJ #thrombocytosis #children #PHOJ
Dr. Chokri Ben Lamine@abouabdrahman0

TNT (Triple-Negative Thrombocytosis) Treatment Algorithm — Proposed by BJHaem, Godfrey et al. — shown at the 3rd Kuwait Hematology Conference 🧬 First question: Clonal or non-clonal? 🔍 Second question: Megakaryocyte atypia or not? ➡️ These 2 answers place every patient into 1 of 4 treatment pathways. ⸻ 🟥 1) Clonal marker + Megakaryocyte atypia Triple-Negative ET with clonal marker (cTNT-ET / ITAM-C) • Age ≥60 or refractory symptoms or cardiovascular RFs → Aspirin if no bleeding risk • Age ≥60, prior vascular event, persistent Plt ≥1500×10⁹/L, or refractory symptoms → Consider cytoreduction • Monitor for evolution toward PMF/MDS/other MPN ⸻ 🟧 2) Non-clonal + Megakaryocyte atypia ITAM (Idiopathic thrombocytosis with atypical megakaryocytes / TN-ET without clonal markers) • Age ≥60, symptoms, or CV risk → Consider aspirin • Age ≥60, prior vascular event, Plt ≥1500×10⁹/L, or multiple CV RFs → Consider cytoreduction • Monitor carefully for transformation; marrow should be repeated if phenotype changes ⸻ 🟦 3) Clonal marker + No megakaryocyte atypia CTUS (Clonal thrombocytosis of undetermined significance) • Age ≥60 or symptoms or CV RFs → Could consider cytoreduction (case-by-case) • Aspirin can be considered depending on risk profile and Plt count • Monitor for evolution to ET/MPN ⸻ 🟩 4) Non-clonal + No megakaryocyte atypia ITUS (Idiopathic thrombocytosis of undetermined significance) • Usually benign course • Annual FBC monitoring • Aspirin only if another indication (e.g., CV risk) • Cytoreduction not recommended ⸻ Key Factors That Determine Treatment 1️⃣ Clonal or non-clonal? 2️⃣ Megakaryocyte atypia present or absent? 3️⃣ Age ≥60? 4️⃣ Symptoms? 5️⃣ Thrombosis history? 6️⃣ Cardiovascular risk factors? 7️⃣ Platelet count? ⸻ #MPN #TNT #TripleNegativeET #ET #CTUS #ITUS #Thrombocytosis #Hematology #NGS #KuwaitHematologyConference #SOHO25 #EmiratesHematologySociety

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Dr. Patrick Hwu
Dr. Patrick Hwu@PatrickHwuMD·
#ScienceSaturday ❓ What controls whether T cells keep fighting or get tired? ➡️ A recent study in Nature Immunology reveals that a protein called SATB1 acts like a “brake” on CD8 T cells, the immune system’s cancer-fighting soldiers. ➡️ During chronic infections or #cancer, T cells can become exhausted over time. This research shows that SATB1 controls how fast T cells multiply and how strongly they attack tumors. When SATB1 levels are high, T cells stay balanced but may hold back their attack. When SATB1 is removed, T cells expand faster and fight harder, especially when combined with immunotherapy, though they may tire sooner. ➡️ Importantly, blocking #SATB1 improved tumor control and boosted the power of checkpoint inhibitors in preclinical models, suggesting a promising new strategy to enhance cancer immunotherapy. 🌟 Congratulations to the study authors at the University of Melbourne, Peter Doherty Institute, University Hospital Bonn, Peter MacCallum Cancer Center, and collaborators for deepening our understanding of T cell biology and uncovering a potential way to make immunotherapies even more effective. @UniMelb @TheDohertyInst @UniklinikBonn @PeterMacCC @NaturePortfolio 🔗 Read more: doi.org/10.1038/s41590…
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Cancer Cell
Cancer Cell@Cancer_Cell·
CHI3L3+ immature neutrophils inhibit anti-tumor immunity and impede immune checkpoint blockade therapy in bone metastases dlvr.it/TNjd8P
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