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Velcade (Bortezomib - PS341) in the Treatment of Patients Over 18 Years With Ph+ Leukemia

21. november 2008 opdateret af: University of Bologna

A Phase II Study of Velcade (Bortezomib - PS341) in the Treatment of Patients Over 18 Years With Ph+ Leukemia

Ph+ leukemias (i.e.Chronic Myelogenous Leukemia (CML) and (Ph+) Acute Lymphoblastic Leukemia are malignant clonal disorder of the hemopoietic stem cell due to reciprocal translocation of genetic material between chromosome 9 and 22 giving rise to the translocation t(9;22) (q2.2; q2.1). The translocation causes the formation of a new hybrid gene (bcr-abl) that codes for a 185 kb or 210 kb cytoplasmic protein (P185 and P210 respectively) that by autophosphorylation activates a number of signaling pathways involved in cell proliferation, maturation, apoptosis and adhesion, leading to the malignant cell transformation1-3. The course of the disease goes on through a chronic phase (CP), usually lasting some years, that is characterized by a massive myeloid hyperplasia with hyperleukocytosis and splenomegaly. The CP is almost always followed by an accelerated or blastic phase (ABP) where the leukemic process acquires the characteristics of acute leukemia. The ABP usually lasts some months and terminates with the death of the patient3.

The frequency of CML in western countries ranges between 10 and 15 per million persons (age - standardized). It is rare in children. The median age is 55 years.

Current treatment of CML includes conventional chemotherapy, allogeneic bone marrow transplantation (allo BMT), alpha-interferon (alpha-IFN)and imatinib.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

3

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Bologna, Italien, 40138
        • Policlinico "S.Orsola-Malpighi"-Istituto di Ematologia "L e A Seragnoli"

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria for chronic phase patients :

  1. Age >/=18 years
  2. Ph positive
  3. Absence of a CHR after 3 months on imatinib
  4. Loss of a previously obtained CHR on imatinib alone
  5. Absence of a CCgR within 12 months on imatinib alone
  6. Loss of a previously obtained CCgR on imatinib alone
  7. Written informed consent

Exclusion Criteria for chronic phase patients :

  1. Age <18
  2. Performance status (ECOG/WHO) > 2 (see Appendix 2)
  3. Inability to provide written informed consent
  4. Pregnancy
  5. Accelerated or blastic phase
  6. Formal refusal of any recommendation of a safe contraception
  7. Alcohol or drug addiction
  8. Altered hepatic or renal function as defined by AST/ALT or bilirubin > 3 times upper normal limits (UNL)
  9. Serum creatinine > 265 umol/l or >3.0 mg/dl
  10. Any other disease or condition that by the advise of the responsible physician would make the treatment dangerous for the patient or would make the patient ineligible for the study, including physical, psychiatric, social and behavioural problems.

Inclusion criteria for accelerated and blastic phase or acute lymphoblastic leukemia Ph+ patients:

  1. Age >/=18 years
  2. Ph positive
  3. Loss of a previous hematological response to imatinib alone, with further progression to ABP (see section 14 for definitions)
  4. Performance status (ECOG/WHO)
  5. Written informed consent

Exclusion criteria for accelerated and blastic phase or acute lymphoblastic leukemia Ph+ patients:

  1. Age <18
  2. Performance status (ECOG/WHO) > 2 (see Appendix 2)
  3. Inability to provide written informed consent
  4. Pregnancy
  5. Chronic Phase disease
  6. Formal refusal of any recommendation of a safe contraception
  7. Alcohol or drug addiction
  8. Altered hepatic or renal function as defined by AST/ALT or bilirubin > 3 times upper normal limits (UNL)
  9. Serum creatinine > 265 umol/l or >3.0 mg/dl
  10. Any other disease or condition that by the advise of the responsible physician would make the treatment dangerous for the patient or would make the patient ineligible for the study, including physical, psychiatric, social and behavioural problems.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Giovanni Martinelli, MD, Istituto di Ematologia "L e A Seragnoli" Policlinico S.Orsola-Malpighi di Bologna

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. juli 2006

Primær færdiggørelse (Faktiske)

1. februar 2008

Studieafslutning (Faktiske)

1. februar 2008

Datoer for studieregistrering

Først indsendt

2. august 2007

Først indsendt, der opfyldte QC-kriterier

2. august 2007

Først opslået (Skøn)

3. august 2007

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

24. november 2008

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

21. november 2008

Sidst verificeret

1. november 2008

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Andre undersøgelses-id-numre

  • CML/033-26866138-CAN
  • EUDRACT 2004-002977-22

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Bortezomib

3
Abonner