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The Combination of Rad001 and Rituximab In Patients With Non-hodgkin's Lymphomas ((RAD001-R))

14 marzo 2016 aggiornato da: The Lymphoma Academic Research Organisation

A Phase I/II Study Investigating the Combination of RAD001 and Rituximab in Patients With Non-Hodgkin's Lymphomas

This study is an open label, multicenter study with two phases:

  • Phase I is a dose escalation study of RAD001 in combination with one injection of Rituximab 375 mg/m² per week during 4 weeks (28 days) in patients CD20 positive non-Hodgkin's lymphomas to determine the dose limiting toxicities (DLTs) and maximum tolerated dose (MTD). The purpose of the study is to assess the feasibility of the combination based on - rate of dose limiting toxicities (DLT) and PK drug-drug interaction (DDI).
  • Phase II will define the efficacy and safety profile of RAD001 and Rituximab combination at the RP2D in patients with lymphomas.

Patients with lymphomas will be treated at the RP2D established during phase I and evaluated for clinical benefit rate, comprising complete responses (CR + CRu), partial responses (PR) and stable disease (SD), and time to progression using the IWG criteria for treatment response.

Induction therapy will follow the same schedule than during the phase I study.

Maintenance therapy: Monthly cycles for up to 2 years with:

  • Daily RAD001 at the same dose than during induction therapy.
  • Rituximab infusion every other cycle at 375 mg/m2 that correspond to the usual maintenance schedule for Rituximab.

Response to therapy will be assessed between day 42 and day 49, then every two months.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Effettivo)

21

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Lille, Francia, 59037
        • Service des Maladies du Sang - CHRU de Lille
      • Nantes, Francia, 44035
        • Service Hématologie - Hôtel Dieu de NANTES
      • Pierre-Bénite, Francia, 69495
        • Service Hématologie - CHU Lyon Sud
      • Rouen, Francia, 76038
        • Service Hématologie - Centre Henri Becquerel
      • Villejuif, Francia, 94805
        • Service Hématologie - Institut Gustave Roussy

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • Patients with relapsed or refractory of one of the following CD 20 positive B-cell Lymphoma:

    • Mantle cell, Marginal zone, lymphocytic, follicular lymphoma
    • Histological transformation from low grade to high grade
  • Must have had at least one previous chemotherapy regimen and not more than 5 previous chemotherapy regimens.
  • Disease is measurable: existence of a bidimensional lesion greater than 2 cm in its longer diameter or malignant lymphocytosis greater than 5000 x 109/L
  • Recovery from any non-hematological toxicity derived from previous treatments. The presence of alopecia and NCI-CTC grade < 2 symptomatic peripheral neuropathy is allowed.
  • Age ≥18 years old;
  • Eastern Co-operative Oncology Group (ECOG) performance status 0-1;
  • Adequate liver and renal function, defined by total bilirubin ≤2.5 x institutional upper limit of normal (ULN) or ≤5 x ULN if liver is involved by malignancy as judged by the investigator (explanation must be provided) and creatinine ≤ 221 μmol/L ;
  • Fasting serum cholesterol ≤7.75 mmol/L AND fasting triglycerides ≤ 2.5 x ULN. NOTE: In case one or both of these thresholds are exceeded, the patient can only be included after initiation of appropriate lipid lowering medication.
  • Adequate bone marrow function, defined by absolute neutrophil count (ANC) ≥1000/mm3 and platelet count ≥100,000/mm3, unless due to disease;
  • At least 3 weeks since previous chemotherapy, biological therapy, radiation therapy, major surgery, or other investigational cancer therapy that is considered disease-directed and have recovered from prior toxicities to Grade 0-1;
  • All men of reproductive potential and women† of child-bearing potential (WOCBP) must agree to practice effective contraception during the entire study period and for one month after the last study treatment, unless documentation of infertility exists.

    † A woman patient is considered to have childbearing potential unless she meets at least one of the following criteria 1) Age > 50 years and naturally amenorrhoeic for > 1 year (amenorrhoea following cancer therapy does not rule out childbearing potential); or 2) Premature ovarian failure confirmed by a specialist gynaecologist or 3) Previous bilateral salpingo-oophorectomy, or hysterectomy, or 4) XY genotype, turner syndrome, uterine agenesis.

  • Able to understand and willingness to sign the informed consent form.

Exclusion Criteria:

  • Uncontrolled clinically significant inter-current illness including, but not limited to, ongoing to active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements. Patients receiving antibiotics for infections that are under control may be included in the study;
  • Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of RAD001 (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small bowel resection)
  • Patients receiving chronic, systemic treatment with corticosteroids (at a dose equivalent or greater than 20 mg prednisone per day) or another immunosuppressive agent. Topical or inhaled corticosteroids are allowed.
  • Patients should not receive immunization with attenuated live vaccines within one week of study entry or during study period. Close contact with those who have received attenuated live vaccines should be avoided during treatment with everolimus. Examples of live vaccines include intranasal influenza, measles, mumps, rubella, oral polio, BCG, yellow fever, varicella and TY21a typhoid vaccines.
  • Patients who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study such as:

    • symptomatic congestive heart failure of New York heart Association Class III or IV
    • unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction within 6 months of start of study drug, serious uncontrolled cardiac arrhythmia or any other clinically significant cardiac disease
    • severely impaired lung function as defined as spirometry and DLCO that is 50% of the normal predicted value and/or 02 saturation that is 88% or less at rest on room air
    • uncontrolled diabetes as defined by fasting serum glucose >1.5 x ULN (Note: Optimal glycemic control should be achieved before starting trial therapy.)
    • active (acute or chronic) or uncontrolled severe infections
    • liver disease such as cirrhosis or severe hepatic impairment (Child-Pugh class C).
  • Leptomeningeal or uncontrolled CNS localization
  • Concurrent malignancy, except patients with early stage squamous cell carcinoma of the skin, basal cell carcinoma of the skin, localized prostate cancer, or cervical intraepithelial neoplasia;
  • Treatment with any other investigational drugs within the preceding 4 weeks
  • Known HIV-positive (since such patients are at increased risk of lethal infections when treated with potentially marrow-suppressive therapy);
  • Known active hepatitis A, B, or C, or history of hepatitis A, B or C;
  • Women who are pregnant or lactating
  • Male patient whose sexual partner(s) are WOCBP who are not willing to use adequate contraception, during the study and for 8 weeks after the end of treatment
  • Patients who have received prior treatment with an mTOR inhibitor (e.g., sirolimus, temsirolimus, everolimus).
  • Patients with a known hypersensitivity to everolimus or other rapamycin (e.g., sirolimus, temsirolimus) or to its excipients
  • History of noncompliance to medical regimen
  • Patients unwilling to or unable to comply with the protocol

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Everolimus and rituximab
One injection of Rituximab 375 mg/m2 per week during 28 days followed by one Rituximab infusion every other cycle at 375 mg/m2 associated with everolimus at 5mg or 10 mg every day or 5 mg every other day.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Phase I part: Determination of the Recommended Dose of RAD001 in combination with rituximab.
Lasso di tempo: 28 days
Determination of recommended dose will be based on safety parameters and particularly on incidence of DLTs .
28 days
Phase II part: Complete Response Rate (CR+CRu)
Lasso di tempo: 2 years
Assessment of response will be based on the International Workshop to Standardize Response criteria for NHL (Criteria for evaluation of response in Non-Hodgkin's lymphoma Cheson,1999)
2 years

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
OVERALL RESPONSE RATE
Lasso di tempo: 2 years
The same disease response assessment used for complete response rate will be considered to determine the Overall Response Rate. Patient is defined as a responder if he/she has a complete response (CR/CRu) or partial response (PR) at the end of treatment. A descriptive analysis will also be performed considering as nonresponders all patients who relapsed or died during treatment phase even if they were prematurely withdrawn as responder.
2 years
PROGRESSION-FREE SURVIVAL
Lasso di tempo: Up to 4 years
Progression-Free Survival will be measured from the date of inclusion to the date of first documented disease progression, relapse or death from any cause. Responding patients and patients who are lost to follow up will be censored at their last tumor assessment date.
Up to 4 years
OVERALL SURVIVAL
Lasso di tempo: Up to 4 years
Overall survival will be measured from the date of inclusion to the date of death from any cause. Patients who are alive at the time of analysis will be censored at the date of the last contact.
Up to 4 years
DURATION OF RESPONSE
Lasso di tempo: Up to 4 years
Duration of response will be measured from the date of first documentation of a response (CR/CRu or PR after induction or at the end of treatment) to the date of first documented evidence of progression/relapse or death from any cause. Responding patients and patients who are lost to follow up will be censored at their last tumor assessment date.
Up to 4 years

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Vincent RIBRAG, Doctor, Service Hématologie, Institut Gustave Roussy

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 dicembre 2011

Completamento primario (Effettivo)

1 giugno 2013

Completamento dello studio (Effettivo)

1 dicembre 2015

Date di iscrizione allo studio

Primo inviato

26 ottobre 2011

Primo inviato che soddisfa i criteri di controllo qualità

29 marzo 2012

Primo Inserito (Stima)

30 marzo 2012

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

15 marzo 2016

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 marzo 2016

Ultimo verificato

1 marzo 2016

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Everolimus and rituximab

3
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