ActivePhase 2ACTRN12618001734257

ALL09 - SUbstitute BLinatumomab to Improve Minimal Residual Disease Eradication in Adolescents and Young Adults with Acute Lymphoblastic Leukaemia – The SUBLIME Study

ALL09 - Phase II Study of Blinatumomab as Induction Therapy in Adolescent and Young Adult Acute Lymphoblastic Leukaemia


Sponsor

Australasian Leukaemia and Lymphoma Group

Enrollment

55 participants

Start Date

Oct 1, 2019

Study Type

Interventional

Conditions

Summary

The purpose of this study is to determine if a new immune based therapy (called Blinatumomab) can help improve outcomes for patients with Acute Lymphoblastic Leukaemia. Who is it for? You may be eligible for this study if you are aged 15-40 and have been diagnosed with B-lineage Acute Lymphoblastic Leukaemia. Study details All participants in this study will be provided with Blinatumomab, that will be provided continuously through the vein over two cycles of 28 days using an infusion device. Participants will be provided with usual care outside of these two cycles. 79 days after commencing cycle 1, participants will need to take a blood test and a bone marrow sample will be collected. Blood and bone marrow samples will also be taken throughout the treatment period, however these are the same as you would have taken during standard treatment outside of the trial. It is hoped that this study will help to better understand how to successfully incorporate immune based therapy in adolescents and young adults with Acute Lymphoblastic Leukaemia.


Eligibility

Sex: Both males and femalesMin Age: 15 YearssMax Age: 40 Yearss

Inclusion Criteria7

  • A morphological diagnosis of B-lineage ALL by WHO criteria. All clinico-pathological sub-types will be eligible, except for mature B or Burkitt ALL;
  • Bone marrow blast count greater than or equal to 20%;
  • Adequate renal and hepatic function at Screening as defined by:
  • a. Total bilirubin less than 2.5 x ULN unless medically correctable
  • b. Serum creatinine less than or equal to 200 micromol/L unless medically correctable
  • Normal left ventricular ejection fraction, according to institutional criteria;
  • An ECOG performance status score of 0-3 at Screening.

Exclusion Criteria8

  • A diagnosis of T-lineage ALL by WHO criteria.
  • Patients known to have Philadelphia chromosome positive disease as defined by WHO criteria using standard karyotype and/or fluorescence in situ hybridization (FISH) analysis and/or BCR-ABL1 fusion transcript detection
  • Subjects aged less than 15 or more than 40 years at Screening;
  • Presence of serious cardiac, pulmonary, hepatic or renal disease;
  • Previous treatment for ALL or history of cancer (other than basal cell skin cancer or carcinoma of the cervix in situ, or other localised cancer treated by surgical excision only more than 5 years earlier without evidence of recurrence in the intervening period).
  • Positive for HIV, or evidence of uncontrolled Hepatitis B or C infection
  • Severe active infection
  • Women who are pregnant at the time of diagnosis will not be excluded from the trial per se. A management plan will be devised between patient, obstetrician and haematologist.

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Interventions

blinatumomab 28mcg/m^2 administered intravenously via an ambulatory infusion device. Dose is administered continuously, as the infusion device is taken home with the patient. The patient will require

blinatumomab 28mcg/m^2 administered intravenously via an ambulatory infusion device. Dose is administered continuously, as the infusion device is taken home with the patient. The patient will require minimal instruction on the use of the infusion device, as it is programmed and monitored by the nursing staff. Digital data is captured to track dose compliance in the ambulatory setting. Blinatumomab is administered continuously over 2 x 28 day cycles, first during induction and second during the consolidation treatment, representing a 2 month gap between blinatumomab cycles. Standard of care treatment is provided outside of these 2 28-day cycles. Standard of care in this trial is the approved BFM-2000 adapted pediatric protocol currently used in centres in Australia.


Locations(16)

The Royal Adelaide Hospital - Adelaide

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Royal North Shore Hospital - St Leonards

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

The Alfred - Melbourne

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Austin Health - Austin Hospital - Heidelberg

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

The Canberra Hospital - Garran

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Fiona Stanley Hospital - Murdoch

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Gosford Hospital - Gosford

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Monash Medical Centre - Clayton campus - Clayton

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Prince of Wales Hospital - Randwick

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Princess Alexandra Hospital - Woolloongabba

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Royal Prince Alfred Hospital - Camperdown

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

The Townsville Hospital - Douglas

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Westmead Hospital - Westmead

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Wollongong Hospital - Wollongong

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Royal Melbourne Hospital - City campus - Parkville

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

Peter MacCallum Cancer Centre - Melbourne

ACT,NSW,QLD,SA,TAS,WA,VIC, Australia

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