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Assessment of sensitivity and therapeutic response to next-line therapy in Chronic Myeloid Leukaemia (CML)

Response Post Tyrosine Kinase Inhibitor: Assesment of sensitivity and therapeutic response to next-line therapy in Chronic Myeloid Leukaemia (CML).

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12610000055000
Acronym
CML10 RESIST
Enrollment
679
Registered
2010-01-19
Start date
2010-06-08
Completion date
2015-11-30
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The target population for this study includes CML patients of any age residing in Australia or New Zealand with CML who have stopped TKI for any reason. Patients will be observed by there regular clinician and data submitted to the central trial coordinating centre.

Interventions

This an observational study, collecting data at regular intervals (6monthly) on subjects for five years. Observing current treatment, change in treatment and rationale for change

Sponsors

Australasian Leukaemia and Lymphoma Group (ALLG)
Lead SponsorOther Collaborative groups

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No

Inclusion criteria

Patients of any age Currently recieving Tyrosine Kinase Inhibitor(TKI) Patients with Philadelphia Positive or Breakpoint Cluster Region (BCR) V-abl Abelson murine leukaemia viral oncogene homolog1 (ABL) confirmed CML. Patients in any phase of CML including those with relapsed CML following allogeneic stem cell transplantation Patients who can provide written informed consent. Minors must have parental/legal guardian consent and assent where required

Exclusion criteria

If in the investigator's opinion the patient is unlikely candidate for follow-up information due to unavailability. Previous enrolment to the same registry.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026