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Record W4417004501 · doi:10.1182/blood-2025-1114

Switching between complement inhibitors in patients with PNH: A real-world analysis of strategy, efficacy, and safety.

2025· article· en· W4417004501 on OpenAlexaff
Morag Griffin, Bruno Fattizzo, Jong Wook Lee, Richard J. Kelly, Roochi Trikha, Yasutaka Ueda, J Nishimura, Christopher J. Patriquin, Alexander Röth, Petra Muus, Jens Panse, Miguel Gómez Álvarez, Alexandra Pike, Talha Munir, Shreyans Gandhi, Austin Kulasekararaj

Bibliographic record

VenueBlood · 2025
Typearticle
Languageen
FieldImmunology and Microbiology
TopicComplement system in diseases
Canadian institutionsAssociated Medical Services
Fundersnot available
KeywordsParoxysmal nocturnal hemoglobinuriaHemolysisEculizumabThrombosisClinical trialCohortOff-label use

Abstract

fetched live from OpenAlex

Abstract Complement inhibition (CI) for paroxysmal nocturnal hemoglobinuria (PNH) has transformed patient (pt) care. In 2025, 3 C5 inhibitors (C5i) are approved (eculizumab (ECU), ravulizumab (RAV), crovalimab) & 3 proximal inhibitors (PI) (pegcetacoplan (PEG), ipatacopan (IPTA), danicopan (DAN) plus C5i). Some clinical trial therapies have not continued development (vermicopan (VERM), BCX9930 (BCX), other C5i). PI clinical trials have protocols for changing from terminal to PI, based on drug half-life. Data is not available for changing from PI to alternate approved CI. It's inevitable with increased use of newer CI that some pts will have side effects (SE), inadequate response or clinical status changes that require CI change. We present the first, largest cohort of PNH pts switching across different CI & provide preliminary consensus about switching. Method: PNH pts requiring CI which has included a PI (either to PI or C5i) were included. Anonymised data included demographics, treatment indications and regimen, process of changing CI, hemolysis complications within 14 days of starting the next CI (LDH> 2 x ULN with hemoglobin (Hb) drop; severe: >30g/l, non-severe <30g/l), transfusion requirements & patient outcomes. Results: Sixty-two pts from 8 countries were included with mean age at diagnosis 38.4 years (range 16-79) & mean Hb 87.8 g/L (missing data, n=17). Where reported indications for CI were hemolysis (49/62), hemolysis and thrombosis (5/62), thrombosis (3/62). Mean time on CI was 103.6 months (range 23-276; missing n=3) & mean granulocyte clone 86% (range 31-99; missing n=9). First-line CI were ECU/RAV (50/62), VERM (9/62) & investigational C5i (3/62). Initial treatment response (per Risitano et al. 2019): complete (6/62), good (26/62), partial (19/62), or no response (3/62); 8/62 undefined. There were 129 CI changes in 62 pts, classified as terminal-to-proximal, proximal-to-proximal & proximal-to-terminal. Sixty-four terminal-to-proximal changes were reported, pts switching as per clinical trial guidance. Indications were extravascular hemolysis (55/64), hemolysis (5/64), pt choice (2/64), SE (1/64) & trial termination (1/64). Seven hemolytic events occurred (11%), 5 required transfusion. Proximal-to-proximal switches (35): PEG to IPTA (19); BCX to PEG (1) or IPTA (7); 2 IPTA to PEG; 2 DAN+C5i to IPTA (1) or PEG (2); 1 PEG to DAN+C5i; and 2 VERM to DAN+C5i (1) or IPTA (1). Switch indications: hemolysis (11/35), trial termination (10/35), SE (6/35), pt choice (5/35) & other (3/35). DAN+C5i pts had DAN tapered as per protocol, then commenced the next CI. The VERM to DAN+C5i pt had a C5i dose prior to taper, DAN starting the day after taper. One BCX to PEG pt had a 4-week overlap & one had a 72-hour CI gap (BCX to IPTA). Remaining pts had no CI interruption or overlap. There were 3 hemolytic events (3/35; 8.5%); 2 BCX to IPTA, & 1 IPTA to PEG. Two events were severe, all 3 required transfusion. Twenty six proximal-to-terminal switches occured: 9 VERM to C5i; 9 PEG to C5i; 4 IPTA/ACH228 to C5i; 3 BCX to C5i; and 1 DAN+C5i to C5i alone. Switch indications: trial termination (10/26), hemolysis (8/26), SE (3/26), pt choice (2/26) & other (3/26). Factor D inhibitor pts had treatment taper as per protocol. One pt on PEG had treatment overlap. Excluding those on VERM, remaining pts had no interruption or overlap of CI. Thirteen hemolysis events occurred (13/26; 50%). Ten pts had severe hemolysis, all requiring transfusion. Of the 9 VERM pts, 5 had treatment taper and CI treatment gap of 10-163 days; all 5 hemolysed rapidly off CI. Three were tapered & started C5i on the last day of taper, with 2 hemolysing; 1 pt who started C5i before VERM taper also experienced hemolysis. For the PEG to C5i pts, 3 without overlap had hemolysis. The ACH228 pt (tapered before C5i started), also experienced hemolysis. For the DAN+C5i to C5i alone pt, no taper was done & moderate hemolysis occurred.Discussion: PNH treatment with CI is usually lifelong. With the development of newer CI, 'switching’ treatments is increasingly common. No guidance for changing from one PI to another CI is available. This cohort would suggest pts changing from one CI to another CI should not have CI interrupted due to high risk of hemolysis. Overlapping inhibitors is not required (PI to PI; PI to CI) and tapering of factor D inhibitors is not effective. Pts switching from PI to terminal inhibition are also at risk of hemolysis and clinicians should vigilant in this regard.

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 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 categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.006
Threshold uncertainty score0.482

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

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 head0.011
GPT teacher head0.263
Teacher spread0.252 · 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.

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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