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P781: EVALUATION OF PEGCETACOPLAN TREATMENT SUCCESS IN PAROXYSMAL NOCTURNAL HEMOGLOBINURIA WITH AND WITHOUT BONE MARROW FAILURE: A MOVE TOWARDS INDIVIDUALIZED PATIENT TREATMENT

2023· article· en· W4385955625 on OpenAlexaff
Jeff Szer, Jens Panse, Austin Kulasekararaj, Monika Oliver, Bruno Fattizzo, Jun‐ichi Nishimura, Johan Szamosi, Regina Horneff, Régis Peffault de Latour

Bibliographic record

VenueHemaSphere · 2023
Typearticle
Languageen
FieldImmunology and Microbiology
TopicComplement system in diseases
Canadian institutionsUniversity of Alberta Hospital
Fundersnot available
KeywordsParoxysmal nocturnal hemoglobinuriaMedicineEculizumabBone marrow failureInternal medicineMyelodysplastic syndromesHemoglobinuriaBone marrowAplastic anemiaGastroenterologyAnemiaImmunologyComplement systemAntibodyHaematopoiesis

Abstract

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Topic: 12. Bone marrow failure syndromes incl. PNH - Clinical Background: Paroxysmal nocturnal hemoglobinuria (PNH) is a rare and potentially life-threatening hematological disease characterized by chronic complement-mediated hemolysis with multiple clinical consequences all of which impair quality of life. PNH patients are highly variable, as is their hematologic response to standard treatment, and the association of underlying bone marrow failure (BMF) syndromes is likely to limit the ability to achieve normalization of hematologic parameters in all patients. Pegcetacoplan (PEG), the first proximal complement inhibitor approved by FDA/EMA for the treatment of adults with PNH, has demonstrated broad control of both intravascular and extravascular hemolysis through complement factor 3 inhibition in several clinical trials. Aims: This post-hoc analysis assessed hematologic and clinical response in PNH patients with BMF treated with PEG or eculizumab (ECU) and examined a new set of parameters to evaluate treatment success in these patients. Methods: The post-hoc analysis included adult patients with PNH from the PEGASUS (NCT03500549) study. PNH patients (Hb <10.5 g/dL despite prior stable ECU) were randomized 1:1 to PEG, or ECU, for 16 weeks. Hematologic and clinical responses were assessed in patients with or without active BMF (aBMF) defined by at least two of the following criteria: Hb <10 g/dL, platelet count <50×109/L, neutrophil count <1.5×109/L at baseline, and those with or without a history of aplastic anemia or myelodysplastic syndrome (AA/MDS): Hemoglobin (Hb) (males: ≥13.6 g/dL; females: ≥12.0 g/dL), Hb ≥12 g/dL, lactate dehydrogenase (LDH) (≤upper limit of normal [ULN]: 226 U/L), and Functional Assessment of Chronic Illness Therapy (FACIT)-Fatigue score (≥population norm: 43.6). Treatment success was subsequently evaluated against a new set of parameters: Hb (change from baseline [CFB] ≥2 g/dL); LDH (≤1.5x ULN: 339 U/L); FACIT-Fatigue (CFB ≥5 points). Results: In total, 80 patients (PEG, n=41; ECU, n=39) were evaluated from PEGASUS. Overall, a greater proportion of PEG-treated patients with BMF syndromes experienced improvement in hematologic parameters and fatigue when compared to ECU treatment (Table 1). In general, the number of patients with BMF syndromes reaching assessed levels of relevant hematologic parameters was comparably lower than non-BMF patients. With PEG treatment, 11% of AA/MDS and 20% of aBMF patients achieved gender specific Hb normalization, compared to 41% of non-AA/MDS and 36% of non-aBMF patients. Similarly, PEG led to Hb ≥12 g/dL being reached in 33% and 20% of AA/MDS and aBMF patients, respectively, compared to 41% of non-AA/MDS and 42% of non-aBMF patients. The proportion of AA/MDS and aBMF patients treated with PEG achieving a ≥2 g/dL increase in Hb was 56% and 40%, respectively. No ECU treated patients with or without AA/MDS or aBMF achieved any of the Hb response parameters assessed. The proportion of AA/MDS, and aBMF PEG-treated patients achieving LDH normalization was 78% and 60%, compared to 69% and 72% of non-AA/MDS and non-aBMF patients, respectively. PEG-treatment led to LDH levels ≤1.5x ULN in all AA/MDS, and 60% of aBMF patients, and 78% and 86% of non-AA/MDS and non-aBMF patients, respectively. Summary/Conclusion: Not all PNH patients may be able to achieve normalization of hematologic parameters due to various reasons such as underlying BMF. Nevertheless, patients with BMF syndromes showed benefit in hematologic and clinical outcomes in response to PEG treatment. Treatment success may best be evaluated against individually set treatment targets.Keywords: Aplastic anemia, Paroxysmal nocturnal hemoglobinuria (PNH), Complement, Bone marrow failure

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How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.110
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
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 head0.031
GPT teacher head0.293
Teacher spread0.262 · 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 teacher head, not a consensus.

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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Citations1
Published2023
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