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Enregistrement W4417022354 · doi:10.1182/blood-2025-5488

Subgroup analysis in pediatric patients from the Phase 3 study of tabelecleucel for allogeneic or solid organ transplant recipients with Epstein–Barr virus-driven post-transplant lymphoproliferative disease after failure of rituximab or rituximab and chemotherapy (ALLELE)

2025· article· en· W4417022354 sur OpenAlexaff
Sonali Chaudhury, Ran Reshef, Sarah Nikiforow, Diane M. George, Neena Kapoor, Michael Kent, Joerg Krueger, Theresa Cole, Pere Barba, Eduardo Olavarría, Roberta Valenti, Anke Friedetzky, Sandrine Roye, Susan E. Prockop

Notice bibliographique

RevueBlood · 2025
Typearticle
Langueen
DomaineMedicine
ThématiqueViral-associated cancers and disorders
Établissements canadiensHospital for Sick Children
Organismes subventionnairesnon disponible
Mots-clésRituximabPopulationSubgroup analysisLymphoproliferative disordersHazard ratioPhases of clinical researchTransplantationSalvage therapyClinical trial

Résumé

récupéré en direct d'OpenAlex

Abstract Background: Epstein–Barr virus-associated post-transplant lymphoproliferative disease (EBV+ PTLD) is an ultra-rare complication with low survival if initial treatment fails. Tabelecleucel is an off-the-shelf allogenic EBV-specific cytotoxic T cell therapy. Results from the overall population have been presented previously (Ghobadi et al. ASH 2024). Here we report for the first time, results from 12 pediatric patients who have participated in the ALLELE trial. Methods: ALLELE is a multicenter, open-label phase 3 trial. Eligibility criteria allow patients of any age to be included. During the trial, patients received intravenous tabelecleucel at 2 x 106 cells/kg on days 1, 8, and 15 in 35-day cycles. Response to treatment was evaluated by independent oncologic response adjudication (IORA) based on clinical and radiographic evidence collected during each treatment cycle. After treatment, disease status was evaluated for up to 2 years and survival status up to 5 years. The primary objective of the trial was objective response rate (ORR). Secondary objectives included rates of complete response (CR) and partial response (PR), time to response (TTR), duration of response (DOR), and overall survival (OS). Safety analyses were conducted in all patients who received at least one dose of tabelecleucel. Results: At data cutoff on 10 September 2024, a total of 86 patients (29 HCT and 57 SOT) ranging in age from 2.7–81.5 years were enrolled and treated with tabelecleucel. Of these patients, 12 were <17 years of age at the time of informed consent (3 HCT and 9 SOT). The median (range) age of pediatric patients was 8.8 (2.7–16.8) years. By age group, 2 patients were aged 2–<6 years, 5 were 6–<12 years and 5 were 12–<17 years. At the time of initial PTLD diagnosis, there were 9 pediatric patients with stage III (n=4) or stage IV (n=5) disease (Lugano classification with LYRIC modification), and 3 patients with the stage unknown. All 12 patients had extranodal disease and 8 had lymph node disease at screening. The median (range) time from PTLD diagnosis to receiving the first tabelecleucel dose was 2.99 (0.6–43.8) months. The ORR in patients <17 years of age was 50.0% (6/12 patients): CR was reported in 4/12 patients (1 HCT and 3 SOT), and PR was observed in 2/12 patients (1 HCT and 1 SOT). These results are consistent with the ORR for the overall population of 47.7% (41/86 patients). For the 6 patients who responded to treatment, the median (range) TTR was 1.6 (0.9–4.7) months. Two of the responders had a durable response of more than 6 months. Three of the responders, at the time of data cutoff, were censored with no disease progression or death. After a median (range) follow-up time of 5.2 (1.1–52.7) months, at time of data cutoff 50% (6/12 patients) were still alive, including 5 treatment responders and 1 non-responder. Serious adverse events (SAEs) were reported in 6 patients; in 2 cases they were deemed related to study treatment. Fatal SAEs were reported in 2 patients, neither of which was related to treatment. There were no reports of tumor flare reactions, infusion reactions, cytokine release syndrome, immune effector cell associated neurotoxicity, transmission of infectious diseases, graft vs host disease, or transplant rejection. Tabelecleucel showed a favorable safety profile consistent with that reported in the overall population. Conclusion: This analysis of 12 pediatric patients from the ALLELE trial suggests that the risk/benefit profile in the pediatric subgroup is consistent with that reported in the overall population, with an ORR of 50% (6/12 patients) and 5/6 treatment responders still alive at data cutoff. These findings support the use of tabelecleucel in pediatric patients with R/R EBV+ PTLD who have historically poor survival and very limited treatment options. The safety profile of tabelecleucel was favorable and no new concerns were identified for the pediatric population.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,002
score de la tête « metaresearch » (Gemma)0,003
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Observationnel · Signal consensuel: aucune
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,002
Score d'incertitude au seuil0,012

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0020,003
Méta-épidémiologie (sens strict)0,0010,000
Méta-épidémiologie (sens large)0,0020,003
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,000
Communication savante0,0010,000
Science ouverte0,0000,000
Intégrité de la recherche0,0010,001
Charge utile insuffisante (le modèle a refusé de juger)0,0020,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,006
Tête enseignante GPT0,252
Écart entre enseignants0,246 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeObservationnel
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations0
Publié2025
Routes d'admission1
Résumé présentoui

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