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Lenalidomide (Revlimid®) Plus Low-dose Dexamethasone (Ld x 4 Cycles) Then Stem Cell Collection Followed by Randomization to Continued Ld or Stem Cell Transplantation (SCT) Plus Maintenance L

14 marzo 2019 aggiornato da: Memorial Sloan Kettering Cancer Center

A Phase II Clinical Trial for Untreated Patients With Multiple Myeloma Eligible for Stem Cell Transplant: Lenalidomide (Revlimid®) Plus Low-dose Dexamethasone (Ld x 4 Cycles) Then Stem Cell Collection Followed by Randomization to Continued Ld or Stem Cell Transplantation (SCT) Plus Maintenance L

The purpose of this study is to compare the effects, good and bad, of two ways to treat patients with standard-risk symptomatic multiple myeloma. Patients with standard-risk myeloma have myeloma with specific features: levels of 2 blood tests have to be in a specific range and there can be no myeloma tumors found outside of the bones or bone marrow, the areas where myeloma is usually discovered. In past clinical studies, patients with standard-risk myeloma have done well with intensive therapy in the form of stem cell transplant. But multiple myeloma is not curable and, although it may respond to standard treatments including stem cell transplant, myeloma always recurs.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Effettivo)

67

Fase

  • Fase 2

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

    • New Jersey
      • Basking Ridge, New Jersey, Stati Uniti
        • Memoral Sloan Kettering Cancer Center
    • New York
      • Commack, New York, Stati Uniti, 11725
        • Memorial Sloan-Kettering Cancer Center @ Suffolk
      • Harrison, New York, Stati Uniti, 10604
        • Memorial Sloan Kettering West Harrison
      • New York, New York, Stati Uniti, 10065
        • Memorial Sloan Kettering Cancer Center
      • Rockville Centre, New York, Stati Uniti
        • Memorial Sloan Kettering at Mercy Medical Center
      • Sleepy Hollow, New York, Stati Uniti, 10591
        • Memoral Sloan Kettering Cancer Center at Phelps
      • Sleepy Hollow, New York, Stati Uniti, 10591
        • Memorial Sloan Kettering Cancer Center at Phelps Memorial Hospital Center

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

Da 18 anni a 75 anni (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • Age ≥ 18 and ≤ 75
  • Histologic and serologic findings from MSKCC confirming the diagnosis of multiple myeloma. Standard diagnostic criteria for multiple myeloma will be used, as per the revised International Myeloma Working Group diagnostic criteria.
  • Patients must have symptomatic multiple myeloma without advanced organ damage (such as multiple fractures or advanced bone disease causing immobilization, renal failure, spinal cord compression, or organ compromise due to soft tissue plasmacytoma). If immediate therapy with radiation and high-dose steroids (eg, for cord compression) or with bortezomib-based therapy (eg, for renal failure) is required, the patient is not eligible for this trial.
  • Patients may have received 1 cycle of prior therapy with dexamethasone for multiple myeloma.
  • Adequate organ function is required, defined as follows:
  • ANC ≥ 1,500/μl and platelets ≥ 100,000/μl (unless low ANC and platelets are due to multiple myeloma)
  • Serum bilirubin ≤ 2.0 mg/dl
  • AST, ALT and alkaline phosphatase < 3 times the upper limit of laboratory normal
  • Adequate renal function as assessed by calculated creatinine using Cockcroft-Gault estimation of CrCl (see Appendix I): Subjects must have calculated creatinine clearance ≥ 30ml/min by Cockcroft-Gault formula
  • Performance status (ECOG) ≤ 2 (Appendix E).
  • Eligible for SCT with LVEF ≥ 50% by MUGA or ECHO, and diffusing capacity > 50% predicted by pulmonary function testing
  • Ability to understand the investigational nature of this study and to give informed consent
  • All study participants must be registered into the mandatory Revlimid REMS® program, and be willing and able to comply with the requirements the of Revlimid REMS® program
  • Females of childbearing potential (FCBP)† must have a negative serum or urine pregnancy test with a sensitivity of at least 50 mIU/mL within 10 - 14 days prior to and again within 24 hours prior to prescribing lenalidomide for cycle 1 (prescriptions must be filled within 7 days) and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control, one highly effective method and one additional effective method AT THE SAME TIME, at least 28 days before she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree not to father a child and agree to use a latex condom during sexual contact with females of child bearing potential even if they have had a successful vasectomy. See Appendix C: Risks of Fetal Exposure, Pregnancy Testing Guidelines and Acceptable Birth Control Methods.
  • Able to take aspirin 325mg or 81mg daily as prophylactic anticoagulation (patients intolerant to ASA may use Coumadin or low molecular weight heparin).

Exclusion Criteria:

  • Prior treatment for myeloma except for one cycle of dexamethasone
  • History of thromboembolic disease within the past 6 months regardless of anticoagulation
  • Myocardial infarction within 6 months prior to enrollment, or New York Hospital Association (NYHA) Class III or IV heart failure (see APPENDIX F), uncontrolled angina, severe uncontrolled ventricular arrhythmias, electrocardiographic evidence of acute ischemia or active conduction system abnormalities.
  • Pregnant or breast-feeding women are excluded due to the potential teratogenicity of lenalidomide.
  • Concurrent active malignancy other than non-melanoma skin cancers or carcinoma-insitu of the cervix, or presence of myelodysplastic or myeloproliferative disease. Patients with prior malignancies with a disease-free interval of ≥ 5 years are eligible.
  • Patients who have had prior malignancies within the past 5 years but are considered to be "cured" with a low likelihood of recurrence may be eligible at the discretion of the Principal Investigator.
  • Active hepatitis B or C infection
  • HIV 1 or 2 positivity
  • Any other medical condition or laboratory evaluation that, in the treating physician's or principal investigator's opinion, makes the patient unsuitable to participate in this clinical trial

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: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Stem cell transplant x 1 or x 2

All patients on this study start with the same treatment, lenalidomide and dexamethasone by mouth. After patients have received 4 cycles of lenalidomide and dexamethasone and are within 2 weeks of completing stem cell collection, they are randomized (like the toss of a coin) to either :

  • stem cell transplant right after collection
  • continue lenalidomide and dexamethasone, saving stem cell transplant for a later time.

After 4 cycles of Ld, eligible patients will undergo stem cell mobilization and collection with standard-of-care cyclophosphamide and Neupogen (G-CSF) or with plerixafor G-CSF. Mobilization with cyclophosphamide is preferred, but plerixafor is also allowed. Ld will be held for at least 2 weeks prior to stem cell mobilization.

On the SCT arm, patients not achieving VGPR by 3 months after the 1st SCT will undergo a 2nd SCT. All patients, after one or two SCT, will receive maintenance L.

Altri nomi:
  • In the initial 4 cycles of therapy, pts will receive oral lenalidomide at the
  • starting dose of 25mg on days 1-21 every 28 days (1 cycle) with dose
  • adjustments for creatinine clearance (CRCL) & dose reductions for toxicity.
  • Pts will receive low-dose oral dexamethasone at 40mg weekly on days 1, 8, 15 &
  • 22 of each 28-day cycle with dose reductions as below for toxicity (the weekly
  • dose could be split over 2 days in the week i.e. 20mg on days 1, 4, 8, 11, 15,
  • 18, 22, & 25 for better tolerance). For SCT, pts are adm to hosp. High-dose
  • melphalan is admin in a single dose on day -2 or split dose on days -3 & -2,
  • through a cvc. Melphalan doseadjustments are made for age & CRCL,. Pts with
  • CRCL,> 51ml/min receive melphalan at 200mg/m2. Pts with CRCL < 51ml/min
  • (to be evaluated within 2 weeks of SCT) will receive 140mg/m2. Pts > 70 years
  • old receive 140mg/m2 also. Each SCT in a tandem SCT is a clinically discrete
  • event & these rules of dose adjustment apply to each SCT. It is possible,
  • that pts will get different doses of melphalan in tandem SCT
Sperimentale: Continue lenalidomide and dexamethasone

All patients on this study start with the same treatment, lenalidomide and dexamethasone by mouth. After patients have received 4 cycles of lenalidomide and dexamethasone and are within 2 weeks of completing stem cell collection, they are randomized (like the toss of a coin) to either :

stem cell transplant right after collection

  • continue lenalidomide and dexamethasone
  • saving stem cell transplant for a later time.
Patients will then be randomized to continued Ld or high-dose melphalan with SCT. On the SCT arm patients not achieving VGPR by 3 months after the 1st SCT will undergo a 2nd SCT. All patients after one or two SCT, will receive maintenance L.
Altri nomi:
  • In the initial 4 cycles of therapy, pts will receive oral lenalidomide at the
  • starting dose of 25mg on days 1-21 every 28 days (one cycle) with dose
  • adjustments for creatinine clearance and dose reductions. Pts will receive
  • low-dose oral dexamethasone at 40mg weekly on days 1, 8, 15 & 22 of each
  • 28-day cycle with dose reductions (the weekly dose could be split over 2 days
  • in the week i.e. 20mg on days 1, 4, 8, 11, 15, 18, 22, & 25 for better
  • tolerance). For continued Ld, pts will resume Ld at the last dose tolerated
  • during the initial 4 cycles, with prophylactics & dose reductions as indicated.
  • Lenalidomide will be continued until progression of disease, if as tolerated.
  • Low-dose dexamethasone will be continued for 1 year (from the start of initial
  • treatment), as tolerated. Dose adjustments will follow guidelines. Pts will
  • be seen every 3 months by their physician & their disease will be reassessed.
  • Pts will also have a CBC & pregnancy test performed monthly.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Progression Free Survival (PFS) Rate at 2 Years After Enrollment in Untreated Patients With Multiple Myeloma.
Lasso di tempo: 2 years
2 years

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Sopravvivenza globale
Lasso di tempo: fino a 4 anni
fino a 4 anni
Number of Participants With VGPR + CR Rate
Lasso di tempo: 2 years

VGPR/Very Good Partial Response + CR/Complete Response (>/= VGPR) for each study arm

Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR

2 years
Overall Response Rates
Lasso di tempo: 2 years
Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR
2 years

Collaboratori e investigatori

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

Investigatori

  • Investigatore principale: Hani Hassoun, MD, Memorial Sloan Kettering Cancer Center

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

10 dicembre 2008

Completamento primario (Effettivo)

1 luglio 2018

Completamento dello studio (Effettivo)

1 luglio 2018

Date di iscrizione allo studio

Primo inviato

11 dicembre 2008

Primo inviato che soddisfa i criteri di controllo qualità

11 dicembre 2008

Primo Inserito (Stima)

12 dicembre 2008

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

15 marzo 2019

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 marzo 2019

Ultimo verificato

1 agosto 2018

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 .

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