ReviewHematology. American Society of Hematology. Education Program2025
The varieties of therapeutic experience: navigating treatment options for patients with PNH.
Review in Hematology. American Society of Hematology. Education Program, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Beyond Terminal Blockade: A Mechanism-Based Approach to Complement Inhibitor Selection in Paroxysmal Nocturnal Hemoglobinuria.Drug design, development and therapy · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired disorder of complement dysregulation, predisposing patients to complications of intravascular hemolysis, thrombophilia, and marrow failure, with a high risk of mortality without treatment. Allogeneic stem cell transplantation is the only current cure but is typically reserved for marrow failure-predominant disease or when targeted therapies are not available. Terminal complement inhibition with eculizumab has significantly altered management and outcomes for patients with PNH, and the last several years have seen the development and approval of many new complement inhibitors with different molecular targets. Newer inhibitors may also provide options for extended time between doses, for self-administration, and for management of iatrogenic extravascular hemolysis, which can occur secondary to C5 inhibition. This essay reviews the various therapeutic options potentially available to PNH patients, the pros and cons of each treatment, considerations regarding the monitoring of side effects, and the possible complications, as well as breakthrough hemolysis and an approach to shared decision-making.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.