Chronic Myeloid Leukemia Clinical Trial
Official title:
Long Term Follow-up of Ph+ CML Patients Achieving Complete Cytogenetic Remission With Interferon Based Therapy
Objectives
This is an observational study aimed at updating the overall survival (OS), the progression
free survival (PFS) to accelerated-blastic (AB) phase and the complete cytogenetic response
(CCgR) duration of the CML patients who between 1986 and 2001 were treated with an IFN based
therapy (either alone or in combination) and who obtained a CCgR. It also aims at analysing
the clinical and biological features of this selected cohort of patients with persisting CCgR
after treatment with IFN.
Study design This study is an observational retrospective multicenter study.
Assessment and Follow-up Patients' demographic data and retrospective collection of CML
cytogenetic and molecular data will be reported in the "Assessment and Follow-up FORM".
In this FORM the events related to therapy, disease and survival will also be reported.
Duration of the study:
The recruitment period is estimated in approximately 2 years.
Study rational
- IFN, either alone or in combination with AC, prolonged survival of Ph+ CML patients, in
early chronic phase, mainly in those patients achieving the CCgR
- CCgR became the surrogate marker for survival duration and the main target of IFN
therapy
- CCgR were rare events accounting for less than 10% of the cytogenetic responsive
patients
- These cases can be considered as a fascinating elite of patients who have the highest
sensitivity to IFN and are the most likely candidates for prolonged survival and
possibly cure
- From 1986 to 2001, more than 1200 CML patients either enrolled in different national
trials or referred in single Institutions have been treated frontline with IFN based
therapy
- In 2001, data on 317 CCgRs were reported by the EICML group
- They included 214 cases treated with IFN alone collected from the database of 9 national
study groups in Austria, Belgium, Netherlands, France, Germany, Italy, Spain, Sweden and
United Kingdom and 103 cases treated with IFN alone collected from single Institutions
in Italy, France, and United Kingdom.
- The study did not include the patients achieving CCgR with IFN + LDAC
- The contribution of Italy was of 119 cases: 59 from national studies and 60 from single
Institutions
- The follow-up of these patients is stopped at 2000 and from 2000 thereafter almost CML
patients were treated with IM
- We don't know if the patients who had achieved a CCgR with IFN based therapy continued
or discontinued IFN, or crossed to IM therapy
- We don't know if they maintained a CCgR with or without therapy
- We don't know if the patients who achieved a CCgR with IFN and crossed to IM had the
same cytogenetic and molecular response, PFS and OS as the majority of the patients
unresponsive to IFN who were treated with IM
- We don't know the clinical and biological features of these selected cohort of patients
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05400122 -
Natural Killer (NK) Cells in Combination With Interleukin-2 (IL-2) and Transforming Growth Factor Beta (TGFbeta) Receptor I Inhibitor Vactosertib in Cancer
|
Phase 1 | |
Completed |
NCT02057185 -
Occupational Status and Hematological Disease
|
||
Recruiting |
NCT03326310 -
Selumetinib and Azacitidine in High Risk Chronic Blood Cancers
|
Phase 1 | |
Recruiting |
NCT04621851 -
Retro-prospective Observational Study on Risk of Progression in CP-CML Patients Eligible for TKI Discontinuation
|
||
Completed |
NCT01207440 -
Ponatinib for Chronic Myeloid Leukemia (CML) Evaluation and Ph+ Acute Lymphoblastic Leukemia (ALL)
|
Phase 2 | |
Not yet recruiting |
NCT06409936 -
PEARL Study: PotEntial of Asciminib in the eaRly Treatment of CML
|
Phase 2 | |
Active, not recruiting |
NCT02917720 -
2nd or 3rd TKI-stop After 2 Years Nilotinib Pre-treatment in CML-patients
|
Phase 2 | |
Not yet recruiting |
NCT02883036 -
Vitro Study of Tigecycline to Treat Chronic Myeloid Leukemia
|
N/A | |
Withdrawn |
NCT01188889 -
RAD001 in Patients With Chronic Phase Chronic Myeloid Leukemia w/ Molecular Disease.
|
Phase 1/Phase 2 | |
Completed |
NCT01795716 -
Bioequivalence Study of Mesylate Imatinib Capsule in Chronic Myeloid Leukemia Body
|
Phase 1 | |
Completed |
NCT00988013 -
Intensity Modulated Total Marrow Irradiation (IM-TMI) for Advanced Hematologic Malignancies
|
N/A | |
Approved for marketing |
NCT00905593 -
Nilotinib in Adult Patients With Imatinib-resistant or Intolerant Chronic Myeloid Leukemia in Blast Crisis, Accelerated Phase or Chronic Phase
|
Phase 3 | |
Terminated |
NCT00573378 -
Imatinib or Nilotinib With Pegylated Interferon-α2b in Chronic Myeloid Leukemia
|
Phase 2 | |
Completed |
NCT00469014 -
Busulfan, Fludarabine, Clofarabine With Allogeneic Stem Cell Transplantation for Acute Myeloid Leukemia
|
Phase 2 | |
Terminated |
NCT00522990 -
Study to Assess the Safety of Escalating Doses of AT9283, in Patients With Leukemias
|
Phase 1/Phase 2 | |
Completed |
NCT00257647 -
Use of SV40 Vectors to Treat Chronic Myeloid Leukemia (CML)
|
N/A | |
Unknown status |
NCT00598624 -
Clinical Trial to Evaluate the Safety and Efficacy of Treosulfan Based Conditioning Prior to Allogeneic Haematopoietic Stem Cell Transplantation (HSCT)
|
Phase 2 | |
Completed |
NCT00219739 -
STI571 ProspectIve RandomIzed Trial: SPIRIT
|
Phase 3 | |
Completed |
NCT06148493 -
Real-World Usage of Asciminib Among Patients With Chronic Myeloid Leukemia in Chronic Phase in the United States Using a Large Claims Database
|
||
Completed |
NCT00375219 -
Homoharringtonine (Omacetaxine Mepesuccinate) in Treating Patients With Chronic Myeloid Leukemia (CML) With the T315I BCR-ABL Gene Mutation
|
Phase 2 |