- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07573436
Loncastuximab Tesirine and Rituximab as First-line Therapy in Patients With Post-transplant Lymphoproliferative Disorder (PLUTO) (PLUTO)
A Phase 1/2 Study of Loncastuximab Tesirine and Rituximab as First-line Therapy in Patients With Post-transplant Lymphoproliferative Disorder (PLUTO)
The purpose of phase I of this clinical trial is to learn the recommended dose of the drugs loncastuximab tesirine and rituximab in participants with post-transplant lymphoproliferative disorders (PTLD).
The purpose of phase II of this clinical trial is to learn if the drugs loncastuximab tesirine and rituximab are effective in participants with post-transplant lymphoproliferative disorders (PTLD).
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Rachel Kingsford
- Numéro de téléphone: 801-585-0115
- E-mail: rachel.kingsford@hci.utah.edu
Sauvegarde des contacts de l'étude
- Nom: Narendranath Epperla, MD
- Numéro de téléphone: 801-585-0255
- E-mail: naren.epperla@hci.utah.edu
Lieux d'étude
-
-
Utah
-
Salt Lake City, Utah, États-Unis, 84112
- Huntsman Cancer Institute at University of Utah
-
Contact:
- Rachel Kingsford
- Numéro de téléphone: 801-585-0115
- E-mail: rachel.kingsford@hci.utah.edu
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Subject aged ≥ 18 years.
Histologically confirmed B-cell PTLD (monomorphic and polymorphic) following solid organ transplantation; with or without EBV association.
--Note: Subjects with classic Hodgkin-like PTLD are excluded.
- Measurable disease as defined by the 2014 Lugano Classification as assessed by positron-emission tomography (PET)- computed tomography (CT) or by CT or magnetic resonance imaging (MRI) if the tumor is not fluorodeoxyglucose (FDG)-avid on screening
- ECOG Performance Status ≤ 2.
Adequate organ function as defined as:
Hematologic:
- Absolute neutrophil count (ANC) ≥ 1000/mm3
- Platelet count ≥ 75,000/mm3
- Hemoglobin ≥ 8 g/dL
Hepatic:
- Bilirubin ≤1.5 x upper limit of normal (ULN) or ≤3 x ULN with document liver involvement and/ or Gilbert's disease
- Transaminases (AST or ALT) ≤ 3 x ULN or ≤ 5 x ULN with documented liver involvement
Renal:
- Estimated creatinine clearance ≥ 60 mL/min by Cockcroft-Gault formula.
For female subjects: Negative pregnancy test or evidence of post-menopausal status. The post-menopausal status will be defined as having been amenorrheic for 12 months without an alternative medical cause. The following age-specific requirements apply:
Women < 50 years of age:
- Amenorrheic for ≥ 12 months following cessation of exogenous hormonal treatments; and
- Luteinizing hormone and follicle-stimulating hormone levels in the post-menopausal range for the institution; or
- Underwent surgical sterilization (bilateral oophorectomy or hysterectomy).
Women ≥ 50 years of age:
- Amenorrheic for 12 months or more following cessation of all exogenous hormonal treatments; or
- Had radiation-induced menopause with last menses >1 year ago; or
- Had chemotherapy-induced menopause with last menses >1 year ago; or
- Underwent surgical sterilization (bilateral oophorectomy, bilateral salpingectomy, or hysterectomy).
- Female subjects of childbearing potential and male subjects with a sexual partner of childbearing potential must agree to use a highly effective method of contraception and the lactation requirements as described in Sections 5.4.1 and 5.4.2.
- Subjects or their legal representatives must be able to read, understand, and provide informed consent to participate in the trial.
- Willing and capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in the protocol
Exclusion Criteria:
- PTLD following liquid transplantation
- CNS involvement
- Prior treatment for PTLD with the exception of radiation, antivirals, steroids and reduced immunosuppression
- Human immunodeficiency virus (HIV) infection
- Major surgery within 4 weeks prior to enrolment
- History of bleeding diathesis (e.g., von Willebrand's disease), hemophilia, or active bleeding.
- Subjects with chronic liver disease with hepatic impairment Child-Pugh class C
- Pregnant or lactating or intending to become pregnant during the study
- Active autoimmune disease which, in the opinion of the investigator, may negatively impact subject safety or interfere with study participation.
- The diagnosis of another malignancy which, in the opinion of the investigator, is likely to negatively impact subject safety or interfere with study participation.
Significant medical diseases or conditions including those requiring substantial changes in concomitant medications, as assessed by the investigator, that would substantially increase the risk-to-benefit ratio of participating in the study. This includes, but is not limited to the following conditions:
Cardiovascular disorders:
- Congestive heart failure New York Heart Association Class III or IV, unstable angina pectoris, serious cardiac arrhythmias.
- Myocardial infarction (MI) within 6 months before the first dose.
- QTc prolongation defined as a QTcF > 480 ms.
- Congenital long QT syndrome or a corrected QT measure (QTc) interval of >480 ms at screening (unless secondary to pacemaker or bundle branch block).
- Grade 2 or higher edema (peripheral, pleural or ascites)
- Grade 1 or higher pericardial effusion
- Severe pulmonary disease
- Uncontrolled diabetes mellitus
- Severely immunocompromised state
- Any other condition that would, in the Investigator's judgment, contraindicate the subject's participation in the clinical study due to safety concerns or compliance with clinical study procedures.
- Active systemic bacterial, viral, fungal, or other infection requiring systemic treatment at time of screening
- Subjects with evidence of active hepatitis B infection, based on positive surface antigen or Hepatitis B DNA PCR are excluded. Subjects who are Hepatitis B core antibody positive must take prophylaxis with entecavir or equivalent and be willing to undergo monthly Hepatitis B DNA PCR testing
- Active hepatitis C infection
- Grade 2 or higher rash
- Clinically significant fluid accumulation in the third space
- Subjects taking prohibited medications as described in Section 6.8.1. A washout period of prohibited medications for a period of at least five half-lives or as clinically indicated should occur before the start of treatment.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation séquentielle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Dose Level 1 (starting dose): SD or PD
Dose Level 1:
This arm included participants who had SD (Stable Disease) or PD (Progressive Disease) after the first 6 weeks of treatment. Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they do not achieve a response, they will come off the study but will be monitored for survival. |
Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle.
Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Autres noms:
|
|
Expérimental: Dose Level 1 (starting dose): PR
Dose Level 1:
This arm included participants who had a Partial Response (PR) after the first 6 weeks of treatment. Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they achieve PR, they will have the option to receive either rituximab consolidation or R-CHOP (at the physician's discretion). |
Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle.
Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Autres noms:
|
|
Expérimental: Dose Level 1 (starting dose): CR
Dose Level 1:
This arm included participants who had a Complete Response (CR) after the first 6 weeks of treatment. Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they achieve a CR after 4 cycles of Lonca-R, they will receive rituximab consolidation (SOC). |
Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle.
Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Autres noms:
|
|
Expérimental: Dose Level 2: SD or PD
Dose Level 2:
This arm included participants who had SD (Stable Disease) or PD (Progressive Disease) after the first 6 weeks of treatment. Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they do not achieve a response, they will come off the study but will be monitored for survival. |
Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle.
Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Autres noms:
|
|
Expérimental: Dose Level 2: PR
Dose Level 2:
This arm included participants who had a Partial Response (PR) after the first 6 weeks of treatment. Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they achieve PR, they will have the option to receive either rituximab consolidation or R-CHOP (at the physician's discretion). |
Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle.
Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Autres noms:
|
|
Expérimental: Dose Level 2: CR
Dose Level 2:
This arm included participants who had a Complete Response (CR) after the first 6 weeks of treatment. Lonca-R will be administered for 4 cycles with response assessment at 6 weeks (+/- 1 week) following the last Lonca-R treatment. If they achieve a CR after 4 cycles of Lonca-R, they will receive rituximab consolidation (SOC). |
Lonca will be administered by IV at 75µg/kg every 3 weeks (DL1).
Rituximab or rituximab biosimilar will be administered by IV at 375 mg/m2 on Day 1 of every cycle.
Lonca will be administered first, followed by rituximab (with a 30 min wait time between the two agents)
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Phase I: Define Maximum Tolerated Dose (MTD) based on the rate of dose-limiting toxicities (DLTs) during the DLT evaluation period.
Délai: 4 years
|
To assess the Recommended Phase 2 Dose (RP2D) of loncastuximab tesirine and rituximab in participants with post-transplant lymphoproliferative disorders (PTLD).
|
4 years
|
|
Phase II: The complete response (CR) rate after 4 cycles of lonca-R per Lugano 2014 criteria1.
Délai: 4 years
|
To assess the efficacy of the combination of lonca-R based on CR rate after 4 cycles.
|
4 years
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
The frequency of adverse events (AEs) and serious adverse events (SAEs) characterized by type, severity (as defined by the NIH CTCAE, version 6.0), seriousness, duration, and relationship to study treatment.
Délai: 4 years
|
To assess the safety and tolerability of lonca-R in subjects with B-cell PTLD.
|
4 years
|
|
The overall response rate (ORR) after 4 cycles of lonca-R.
Délai: 4 years
|
To determine ORR after 4 cycles of lonca-R in subjects with B-cell PTLD.
|
4 years
|
|
The best complete response (CR) rate is defined as CR at the completion of 4 cycles of lonca-R or 4 cycles of lonca-R and 4 cycles of consolidation of rituximab monotherapy (every 3 weeks) in subjects with B-cell PTLD.
Délai: 4 years
|
To determine the best CR rate in subjects with B-cell PTLD.
|
4 years
|
|
Median and two year progression-free survival (PFS). PFS will be as defined as the time from study drug initiation to the time of documented disease progression (as assessed by Lugano Criteria), or death from any cause.
Délai: 4 years
|
To assess PFS.
|
4 years
|
|
Median and two year overall survival (OS). OS is defined as the time from initiation of treatment until death from any cause.
Délai: 4 years
|
To assess OS.
|
4 years
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Narendranath Epperla, MD, Huntsman Cancer Institute
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- HCI198713
Informations sur les médicaments et les dispositifs, documents d'étude
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