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Record W4417006712 · doi:10.1182/blood-2025-8005

Feasibility assessment of indirect treatment comparison between off-label rituximab and novel treatments in patients with warm autoimmune hemolytic anemia

2025· article· en· W4417006712 on OpenAlexaff
Mahmoud Hashim, Alexa Sibiga, Teige Bourk, Sumeet Singh, Alexander Litvintchouk, Ann Leon

Bibliographic record

VenueBlood · 2025
Typearticle
Languageen
FieldMedicine
TopicBlood groups and transfusion
Canadian institutionsEVERSANA (Canada)
Fundersnot available
KeywordsRituximabAutoimmune hemolytic anemiaClinical trialSystematic reviewMEDLINEAnemia

Abstract

fetched live from OpenAlex

Abstract Introduction: Indirect treatment comparisons (ITCs) provide valuable evidence on comparative efficacy where head-to-head clinical trials do not exist; however, differences in patient and study characteristics may introduce bias [Jansen JP et al., 2011]. Therefore, it is essential to do a systematic and thorough assessment to determine the suitability of different ITC methods. In warm autoimmune hemolytic anemia (wAIHA), rituximab has been widely used off-label, despite lacking regulatory approval for this indication. With several novel targeted therapies now emerging through registrational trials, there will be a critical need for ITCs to contextualize their efficacy relative to the off-label use of rituximab. We provide an illustrative case study in wAIHA where we assess the feasibility of conducting ITCs between studies investigating off-label rituximab and novel treatments. Methods: A systematic literature review was conducted using multiple databases with the Ovid® platform (Embase, Ovid MEDLINE®, and the Cochrane Central Register of Controlled Trials) from January 2013 to December 2024 to retrieve all published interventional studies in wAIHA. We assessed the feasibility of conducting ITCs using standard methods (Bucher ITC or network meta-analysis [NMA]) as well as population-adjusted methods (matching adjusted indirect comparison [MAIC], simulated treatment comparison [STC]) using data from published rituximab trials and existing real-world evidence studies, as well as information available for investigated novel treatments. Results: The electronic database search identified 3,168 records (excluding duplicates) that were screened at the title and abstract stage and 390 records were obtained and assessed for eligibility in full-text review of which 10 were included. In addition, conference abstracts, key regulatory and HTA agencies, and bibliographies of relevant SLRs captured in the database search were hand searched for additional relevant studies. Out of 870 additional records retrieved, 863 were excluded and 7 were included. Thus, this review identified 17 records pertaining to 12 unique studies investigating therapies in patients with wAIHA. All study populations consisted of participants with wAIHA or reported a wAIHA subgroup, except two studies that reported a mixed population (without reporting on the wAIHA subgroup) where 95.5% and 88% of participants had wAIHA. Most trials were at least 24 weeks long, with three extending for longer than two years. Five clinical trials were randomized whereas the remaining seven were single-arm trials. Four trials had control arms, three of which included placebo, and one control arm was prednisolone. Among the clinical trials included, five studied rituximab, in combination with prednisone, prednisolone, ibrutinib, or bortezomib. Three trials studied fostamatinib, while other studied treatments included pegcetacoplan, sovleplenib, parsaclisib, and rilzabrutinib. There were large differences in study design, eligibility criteria, country, average age, timing of study, and sample sizes between rituximab and studies investigating novel treatments. There are also large differences in endpoint definitions and timepoint of endpoint evaluation between rituximab and other studies. Bucher ITCs and NMAs were not feasible due to the absence of common treatment arms and could not account for important cross-trial differences due to their reliance on summary-level data. Comparisons between rituximab and registrational trials using unanchored population-adjusted methods such as MAIC and STC are also limited due to lack of overlap in patient populations in terms of treatment line, and differences in background corticosteroid use, which are both critical prognostic variables. Conclusions: An ITC using published rituximab interventional studies was found to not be feasible as it is unlikely to yield credible results due to lack of a common comparator and differences in key prognostic variables including patient characteristics and background corticosteroid use. Future work should consider de novo sources of real-world evidence for rituximab that more closely align with registrational trial characteristics and endpoint definitions. However, aligning timing of endpoint measurements between registration trials and real-world data to match definitions remains challenging.

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 score0.086
Threshold uncertainty score0.701

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)0.0000.000

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 head0.023
GPT teacher head0.307
Teacher spread0.284 · 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".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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