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Record W2106168795 · doi:10.1016/j.bbmt.2009.12.142

The Impact Of Prior Exposure To Rituximab On Autologous Stem Cell Transplantation In Patients With Follicular And Transformed Lymphoma

2010· article· en· W2106168795 on OpenAlexaffabout
Alexandra Muccilli, Steve Doucette, Sheryl McDiarmid, Lothar Huebsch, Mitchell Sabloff

Bibliographic record

VenueBiology of Blood and Marrow Transplantation · 2010
Typearticle
Languageen
FieldMedicine
TopicLymphoma Diagnosis and Treatment
Canadian institutionsOttawa Hospital
Fundersnot available
KeywordsRituximabMedicineAutologous stem-cell transplantationFollicular lymphomaLymphomaInternal medicineCD20OncologyTransplantationChemotherapyRetrospective cohort studyGastroenterologySurgery

Abstract

fetched live from OpenAlex

Introduction: Addition of rituximab to chemotherapy (CT) for follicular lymphoma (FL) has been shown to improve many outcome parameters. Often, high-dose therapy is followed by autologous stem-cell transplantation (ASCT) after 1, 2 or more relapses. Kang et al. (BMT (2007) 40, 973) investigated whether prior exposure to rituximab had any influence on a subsequent ASCT and found no differences in the outcomes analyzed. However, there has been evidence suggesting that that such prior exposure may alter the phenotype of these tumour cells so that they no longer express CD20, and thus potentially altering their behaviour. Methods: We performed a retrospective review on all patients having received an ASCT at the Ottawa Hospital with an initial diagnosis of FL. They were grouped into four categories according to their prior exposure to or lack of prior exposure to rituximab and according to their pre-ASCT diagnosis, non-transformed FL (FL-NT) vs. transformed (FL-T). Results: 259 patients who underwent an autoHSCT for FL were divided into 4 groups: 184 FL non-transformed (FL-NT) (31 patients received rituximab and 153 did not), and 75 FL-transformed (FL-T) (24 patients received rituximab and 51 did not). The 5-year progression-free survivals (PFS) were 61.2% and 27.6%, respectively (p<0.0001) and the overall survivals (OS) were 72.5% and 39.3%, respectively, (p<0.0001). In the FL-NT group, no differences existed in PFS or OS between FL-NT rituximab-naïve and rituximab-treated patients (5-year PFS 61% vs. 64%, p=0.69; 5-year OS 73% vs. 68%, p=0.80). Within the FL-T group, the subsequent 5-year PFS of the rituximab-naive vs. pre-treated groups were 22% and 55% (p =0.20), respectively, and the 5-year OS were 36% and 51% (p=0.39), respectively. Prior exposure to R had a positive effect (Hazard Ratio (HR): 0.44, 95% CI 0.20-0.97, p=0.04) on PFS and OS (HR: 0.5, 95% CI 0.21-1.18, p=0.11). Pre-treatment with rituximab in FL-NT prior to ASCT does not adversely impact ASCT outcomes. There is a suggestion of an increase in the number of patients with FL-T being transplanted in the post-rituximab era and as expected, the FL-T had a poorer outcome than the FL-NT patients. However, prior exposure to rituximab appeared to demonstrate a trend toward an improved OS within the FL-T group. In summary, previous rituximab exposure may be associated with an increased rate of transformation, leading to the poorer outcome of patients originally diagnosed with FL-NT.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation 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 score0.003
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.003
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)0.0010.000

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 head0.004
GPT teacher head0.221
Teacher spread0.217 · 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 source (direct Gemma or distilled Codex), 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
Published2010
Admission routes2
Has abstractyes

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