Recurrent or Refractory B Cell Acute Lymphoblastic Leukaemia Clinical Trial
— MARALLOfficial title:
Phase I/II Study Combining Humanised Anti-CD20 (Veltuzumab), Anti-CD22 (Epratuzumab) and Both Monoclonal Antibodies With Intensive Chemotherapy in Adults With Recurrent or Refractory B-precursor Acute Lymphoblastic Leukaemia (ALL)
| Verified date | July 2014 |
| Source | Queen Mary University of London |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The treatment of adult B-cell acute lymphoblastic leukaemia (ALL) has progressed considerably
in the past 3 decades, particularly due to intensification of chemotherapies, improved
supportive care and the incorporation of stem cell transplantation. However, the maximum
tolerability of standard chemotherapeutics has been reached in ALL. Using conventional
chemotherapy, 80-85% of adults with ALL will achieve a complete remission (CR). Unfortunately
treatment at relapse is generally unsuccessful and rarely results, in long-term survival (7%
survival at 5 years). Therefore, the investigators are exploring novel treatment strategies
through the use of monoclonal antibodies (MoAbs) directed at surface antigens on leukaemic
blasts. Using MoAbs directed against surface proteins on B cells has had excellent results in
other B-cell diseases such as low and high grade non-Hodgkin lymphomas, without additional
toxicity. There has also been limited evidence from small studies and case reports of the
efficacy of MoAbs in ALL.
This is a Phase I/II study to determine the safety and tolerability of the combination of
veltuzumab and epratuzumab with intensive chemotherapy in patients with relapsed B-cell ALL.
A maximum of 51 patients will be treated with a combination of UKALL XII induction
chemotherapy and the monoclonal antibodies veltuzumab and epratuzumab. Veltuzumab and
epratuzumab are humanised monoclonal antibodies that target CD20 and CD22 surface proteins,
respectively. Both of these proteins are expressed on ALL tumour B cells.
One group of patients will receive modified UKALL XII chemotherapy + veltuzumab; a second,
modified UKALL XII chemotherapy + epratuzumab and if limited toxicity is found in these first
2 groups, a third group will receive, modified UKALL XII chemotherapy + both veltuzumab and
epratuzumab. Patients will be assessed for safety, tolerability and disease response. Safety
and tolerability will be measured by the number of Dose Limiting Toxicities (DLTs) in each
group. Disease response will be measured by the microscopic appearance of patient bone marrow
samples at day 29, and by molecular tests for tumour cells in bone marrow.
| Status | Unknown status |
| Enrollment | 55 |
| Est. completion date | August 2014 |
| Est. primary completion date | August 2014 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 16 Years and older |
| Eligibility |
Inclusion Criteria: 1. Aged 16 years or over 2. Confirmed diagnosis of recurrent or refractory B-precursor ALL [according to the WHO classification]. 3. Greater than 5% blasts in the bone marrow 4. WHO/ECOG performance status of 0-2 and well enough to receive intensive combination chemotherapy. 5. Negative pregnancy test in women of childbearing potential. Women will not be considered of child bearing potential if they have undergone surgical removal of the uterus or are post menopausal and have been amenorrhoeic for at least 24 months. 6. Patients must have adequate organ function: - Renal function - serum creatinine <2.5 x ULN or eGFR>50ml/min (measured EDTA or estimated creatinine clearance e.g Cockcroft & Gault) - Liver function (bilirubin/ALT <2.5 x ULN) 7. Patients must be able to comply with the study schedule. Exclusion Criteria: 1. Patients should not have received chemotherapy for current episode of relapsed ALL (except corticosteroids for a maximum of 10 days, before joining the study). 2. Patients with co-morbidities: e.g. uncontrolled hypertension and or poorly controlled diabetes which in the PI's opinion makes them unsuitable for the study. 3. Patients with severe psychiatric disorders which in the PI's opinion makes them unsuitable for trial participation. 4. Females of childbearing potential and all males must be willing to use an effective method of contraception (hormonal or barrier method of birth control; abstinence) for the duration of the study and for up to 3 months after the last dose of study medication. Note: Subjects are not considered of child bearing potential if they are surgically sterile (they have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or they are postmenopausal. 5. Females of childbearing potential must have a negative pregnancy test within 7 days prior to starting the study. 6. Females must not be breastfeeding. 7. Patients may not receive any other investigational agent during the study. 8. Patients should not have received any antibody therapy within 3 months of joining this study. |
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | University Hospitals Birmingham NHS Foundation | Birmingham | |
| United Kingdom | University of Bristol Foundation Trust | Bristol | |
| United Kingdom | University Hospital of Wales | Cardiff | |
| United Kingdom | Beatson West of Scotland Cancer Centre | Glasgow | |
| United Kingdom | Leeds Teaching Hospitals NHS Trust | Leeds | |
| United Kingdom | Barts and the London NHS Trust | London | |
| United Kingdom | Royal Free Hampstead NHS Trust | London | |
| United Kingdom | Newcastle University | Newcastle | |
| United Kingdom | Nottingham City Hospital | Nottingham | |
| United Kingdom | Plymouth Hospitals NHS Trust | Plymouth |
| Lead Sponsor | Collaborator |
|---|---|
| Queen Mary University of London | Immunomedics, Inc. |
United Kingdom,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | The total number of dose limiting toxicity events (DLTs) to measure safety and tolerability | The primary objective is to assess the safety and tolerability of the combination of veltuzumab and/or epratuzumab with intensive chemotherapy for recurrent or refractory adult B-precursor ALL. | Day 29 | |
| Secondary | Morphological and molecular remission in bone marrow | Achievement of morphological complete remission on Day 29 bone marrow Efficacy of treatment to achieve MRD negativity, and investigate a possible association between the intensity of CD20 and CD22 antigen expression and treatment activity. |
Day 29 |