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Lenalidomide & Adriamycin & Dexamethasone (RAD) in Newly Diagnosed, Multiple Myeloma Patients (RAD)

14 października 2016 zaktualizowane przez: Meletios A. Dimopoulos

Phase II Open Label Study for the Assessment of the Efficacy and Safety of Lenalidomide & Adriamycin & Low Dose Dexamethasone (RAD) in Newly Diagnosed, Symptomatic Multiple Myeloma Patients

This study is to assess the efficacy and safety of lenalidomide in combination with adriamycin and low dose dexamethasone in newly diagnosed patients with symptomatic multiple myeloma as well as to collect information regarding the effect of this regimen on angiogenesis and bone remodeling of the study population.

Przegląd badań

Status

Zakończony

Warunki

Szczegółowy opis

This is a Phase II, non randomized, non- comparative, open label trial which assess the efficacy and safety of lenalidomide, adriamycin and low dose dexamethasone combination (RAD) in 45 newly diagnosed patients with symptomatic multiple myeloma as well as to collect information regarding the effect of this regimen on angiogenesis and bone remodeling of the study population. The recruitment period is estimated for 5 months while the treatment period and the follow up period 4 months and 1 month respectively. During the treatment initiation visit the response to the combination RAD according the International Myeloma Working Group (IMWG) criteria will be evaluated, biochemical markers of bone metabolism and angiogenic cytokines will be measured as well. IMWG Response evaluation will be repeated the day 1 of each treatment cycle as well as at the response evaluation visit. Finally biochemical markers of bone metabolism and angiogenic cytokines will be measured once more at the end of treatment visit.

Typ studiów

Interwencyjne

Zapisy (Rzeczywisty)

45

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Lokalizacje studiów

      • Patra, Grecja, 26504
        • University General Hospital of Patras
      • Thessaloniki, Grecja, 54007
        • Theageneio Anticancer Hospital of Thessaloniki
    • Attica
      • Athens, Attica, Grecja, 11528
        • General Hospital of Athens "Alexandra"
      • Athens, Attica, Grecja, 11527
        • General Hospital of Athens "G. Gennimatas"

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

18 lat do 70 lat (Dorosły, Starszy dorosły)

Akceptuje zdrowych ochotników

Nie

Płeć kwalifikująca się do nauki

Wszystko

Opis

Inclusion Criteria:

  1. Subjects able to read and understand the Informed Consent Form (ICF).
  2. Subjects willing to participate in the study and comply with its procedures.
  3. Subjects who have signed the ICF
  4. Newly diagnosed patients with symptomatic MM according to the criteria of IMWG
  5. Subjects eligible for autologous stem cell transplantation
  6. Age 18-70 years, of either sex
  7. karnofsky ≥ 60
  8. Platelets ≥ 100x109/L
  9. Neutrophils ≥ 1.5x109/L
  10. Alanine transaminase (ALT) & Aspartate transaminase (AST) ≤ 3-fold of upper normal limit
  11. Bilirubin ≤ 2-fold of upper normal limit
  12. Creatinine clearance ≥60 ml/min
  13. Expected survival ≥ 6 months as per PI's clinical judgment
  14. Subjects able to tolerate aspirin, low molecular weight heparin or coumarinic agents as prophylactic anticoagulation
  15. Female subject of childbearing potential must have 2 negative serum pregnancy tests (hCG) at Screening (once within 10-14 days and once 24 h before the study drug administration) and if sexually active must be using two medically acceptable, highly effective, adequate forms of birth control (ie, failure rate <1% per year when used consistently and correctly) prior to Screening and and for time period at least 28 days before the study drug administration and agree to continue using it while being in the study (Screening and Treatment Periods including dose interruptions). A female subject should continue using a highly effective method of birth control for 30 days following the end of treatment.
  16. A male subject must agree to use an adequate form of contraception for the duration of the study, while taking the study drug, during dose interruptions at for at least 28 days after the last dose of study drug even if he has had a successful vasectomy and agree to have sexual relations only with women who use a highly effective birth control method.
  17. Subjects must be free of any clinically significant disease (other than MM) that would interfere with study evaluations

Exclusion Criteria:

  1. Pregnancy, breastfeeding οr intention of pregnancy during the trial
  2. Suspected or known hypersensitivity to any of the study drugs
  3. Ongoing severe infection requiring intravenous antibiotic treatment
  4. Prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, in-situ cervical cancer, or other cancer from which the subject has been disease-free for at least 5 years. Concurrent prostate cancer for which the patient is receiving therapy will not be considered an exclusion if the Prostatic specific antigen (PSA) has been stable for 3 years
  5. Solitary bone or solitary extramedullary plasmacytoma as the only evidence of plasma cell dyscrasia
  6. Myocardial infraction within 6 months before enrollment, New York Heart Association (NYHA) Class II or greater heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmia, clinically significant pericardial disease, or electrocardiographic evidence of acute ischemic or active conduction system abnormalities
  7. Uncontrolled medical problems such as diabetes, coronary artery disease, hypertension, unstable angina, arrhythmia, pulmonary, hepatic and renal diseases unless renal insufficiency is considered to be secondary to MM
  8. Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the subject from signing the ICF
  9. Any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she will participate in the study or confounds the ability to interpret data from the study
  10. Subjects with any clinical condition that would affect study's outcome
  11. Participation in another interventional clinical trial in the 4 weeks preceding enrollment or planning to participate in another interventional clinical trial during the planned period of this study, except of the clinical trials that implicate drugs of supportive treatment

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Lenalidomide, adriamycin & dexamethasone
Lenalidomide 25 mg administered orally for the first 21 days of each 28-day-cycle, plus Adriamycin i.v. on days 1,2,3 & 4 of every cycle, plus Dexamethasone 40 mg orally on days 1, 8, 15 & 22 of every cycle for 4 cycles
Lenalidomide 25 mg by mouth for the first 21 days of a 28-day-cycle for 4 cycles
Inne nazwy:
  • Combination of Lenalidomide, adriamycin & dexamethasone
Adriamycin as intravenous bolus infusion at a dose of 9 mg/m2, on days 1-4 of a 28-day cycle for 4 cycles
Inne nazwy:
  • Combination of Lenalidomide, adriamycin & dexamethasone
Dexamethasone by mouth at a dose of 40 mg, on days 1, 8, 15, and 22 of a 28-day cycle for 4 cycles
Inne nazwy:
  • Combination of Lenalidomide, adriamycin & dexamethasone

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Overall response rate
Ramy czasowe: 142 days
Assessment of the overall response rate of study population to RAD regimen (including stringent complete response, complete response, very good partial response, partial response and stable disease) according to the uniform criteria of IMWG (International Myeloma Working Group) regarding the response to multiple myeloma therapy
142 days

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Progression-free survival (PFS)
Ramy czasowe: 142 days
142 days
Time to progression (TTP)
Ramy czasowe: 142 days
142 days
Time to Next Therapy (TtNT)
Ramy czasowe: 142 days
142 days
Number and severity of Adverse events as a measure of safety and toxicity profile
Ramy czasowe: 142 days
Adverse events will be assessed at each visit and graded according to the National Cancer Institute Common Toxicity Criteria (version 2.0)
142 days

Inne miary wyników

Miara wyniku
Opis środka
Ramy czasowe
Number of stem cell collected before Autologous Stem Cell Transplantation (ASCT)
Ramy czasowe: 142 days
142 days
Dickkopf-1 (DKK-1)
Ramy czasowe: 1 day
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Dickkopf-1 (DKK-1)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
C-telopeptide of type-I collagen (CTX)
Ramy czasowe: 1 day
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
C-telopeptide of type-I collagen (CTX)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
Tartrate-resistant acid phosphatase isoform-5b (TRACP-5b)
Ramy czasowe: 1 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 days
Tartrate-resistant acid phosphatase isoform-5b (TRACP-5b)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
Bone-alkaline phosphatase (bALP)
Ramy czasowe: 1 day
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Bone-alkaline phosphatase (bALP)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
Osteocalcin (OC)
Ramy czasowe: 1 day
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Osteocalcin (OC)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
C-terminal propeptide of procollagen type-I (CICP)
Ramy czasowe: 1 day
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
C-terminal propeptide of procollagen type-I (CICP)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
Soluble and total RANKL (sRANKL, tRANKL)
Ramy czasowe: 1 day
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Soluble and total RANKL (sRANKL, tRANKL)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
Osteoprotegerin (OPG)
Ramy czasowe: 1 day
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Osteoprotegerin (OPG)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
Osteopontin (OPN)
Ramy czasowe: 1 day
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Osteopontin (OPN)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
Macrophage inflammatory protein 1-alpha (MIP-1α)
Ramy czasowe: 1 day
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Macrophage inflammatory protein 1-alpha (MIP-1α)
Ramy czasowe: 112 days
Biochemical markers of bone remodeling will be measured in the serum of patients at therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
Angiopoietin-1 & -2
Ramy czasowe: 1 day
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Angiopoietin-1 & -2
Ramy czasowe: 112 days
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
Angiogenin
Ramy czasowe: 1 day
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Angiogenin
Ramy czasowe: 112 days
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
VEGF
Ramy czasowe: 1 day
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
Vascular endothelial growth factor (VEGF)
Ramy czasowe: 112 days
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
VEGF-A
Ramy czasowe: 1 day
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
VEGF-A
Ramy czasowe: 112 days
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days
basic fibroblast growth factor (bFGF)
Ramy czasowe: 1 day
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
1 day
basic fibroblast growth factor (bFGF)
Ramy czasowe: 112 days
Angiogenic cytokines, which will be evaluated in the serum of patients during therapy commencement on Day 1 of cycle 1 and at therapy completion on day 28 of cycle 4. 28-days-cycle
112 days

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Śledczy

  • Główny śledczy: Meletios Dimopoulos, Doctor, General Hospital of Athens "Alexandra"
  • Główny śledczy: Eirini Katodritou, Doctor, Theageneio Anticancer Hospital of Thessaloniki
  • Główny śledczy: Nikolaos Anagnostopoulos, Doctor, General Hospital of Athens "G. Gennimatas''
  • Główny śledczy: Argirios Symeonidis, Doctor, University General Hospital of Patras

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów

1 listopada 2014

Zakończenie podstawowe (Rzeczywisty)

1 lipca 2016

Ukończenie studiów (Rzeczywisty)

1 lipca 2016

Daty rejestracji na studia

Pierwszy przesłany

5 czerwca 2015

Pierwszy przesłany, który spełnia kryteria kontroli jakości

10 czerwca 2015

Pierwszy wysłany (Oszacować)

15 czerwca 2015

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Oszacować)

17 października 2016

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

14 października 2016

Ostatnia weryfikacja

1 października 2016

Więcej informacji

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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