At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Dexamethasone, cyclophosphamide, rituximab (drug), Rituximab, ibrutinib (drug)
- How long the study runs
- Study runs about 121 months (dates as stated)
- About the drug or intervention
- Dexamethasone, cyclophosphamide, rituximab — drug: DRC Arm (chemotherapy) consists of dexamethasone, cyclophosphamide and rituximab treatment · Rituximab, ibrutinib — drug: RI Arm (chemotherapy free) consists of rituximab and ibrutinib treatment
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 148
- Started
- 2020-02-03
- Last checked
- 2024-05
Plain English Summary
What is this study?
- • Testing a new treatment for waldenstrom macroglobulinemia
- • Phase2/Phase3 - 148 participants
- • Waldenström's macroglobulinaemia (WM) is a rare type of slow growing lymphoma
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with waldenstrom macroglobulinemia
Where?
- • Bath - Royal United Hospital, Bath
- • Bournemouth - The Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust
- • Canterbury - East Kent Hospitals University NHS Foundation Trust
- • Cardiff - University Hospital of Wales
- • +21 more UK sites
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
Waldenström's macroglobulinaemia (WM) is a rare type of slow growing lymphoma. It develops when white blood cells grow abnormally. Typically a disease of the elderly, the median age of presentation is \>70 years and the current treatment for WM is unsatisfactory, with incomplete responses and inevitable recurrence. Therefore there is a need to find alternative treatments that are more effective, leading to lasting responses and improved quality of life. The RAINBOW study is a phase 2-3 trial assessing 'chemotherapy free' treatment as primary therapy for WM which can potentially improve response outcome, durability and importantly, reduce toxicity for WM patients. This approach will be done using the drug Ibrutinib, which in combination with rituximab (RI) will be the experimental arm. As there is no agreed standard on first-line therapy for WM, the control arm is the current treatment based on the most recently published clinical trial results. The control arm consists of rituximab, cyclophosphamide and dexamethasone (DCR), and is widely recommended by international consensus as appropriate treatment for first-line therapy for WM. In this study, 148 adults (aged ≥ 18 years) with treatment naïve WM will be randomised on a 1:1 ratio to either the treatment or control arm. Randomised treatment lasts for a maximum of 6 cycles and response will be assessed following 3 cycles of treatment and completion of randomised treatment at approximately 24 weeks after commencing treatment. RI patients may then have up to 5 years of Ibrutinib monotherapy. Patients will be seen regularly during treatment and then every 3 months for 5 years after treatment discontinuation. Patients will enter annual follow up for survival until the end of trial (including progressed patients). The study will be conducted at NHS hospitals and is expected to last 9 years and 6 months.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years and over
- Who can join: All genders
Biomarkers mentioned
What the study is looking for
- ✓Patients ≥ 18 years
- ✓Confirmed diagnosis of WM (according to consensus panel / WHO criteria) with measurable IgM paraprotein
- ✓Previously untreated disease at any stage requiring therapy at the discretion of the treating physician. Suggested...
- ✓haematological suppression to Hb \<10g/dl, or neutrophils \<1.5x109/l or platelets \<150x109/l
- ✓clinical evidence of hyperviscosity
Who cannot take part
- ✗Prior therapy for WM
- ✗Lymphoplasmacytic lymphoma with no detectable serum IgM paraprotein
- ✗CNS involvement with WM
- ✗Autoimmune cytopenias
- ✗Major surgery within 4 weeks prior to randomisation
See the full criteria
Where Is This Study? (25 UK sites)
Royal United Hospital, Bath
Bath, United Kingdom
The Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust
Bournemouth, United Kingdom
Research Development & Support
clinicalresearch@bournemouth.ac.uk01202 961200East Kent Hospitals University NHS Foundation Trust
Canterbury, United Kingdom
Caroline Cowley, Research & Innovation/Clinical Trials Unit Manager
ekhuft.researchandinnovation@nhs.net01227 783169University Hospital of Wales
Cardiff, United Kingdom
Colchester Hospital
Colchester, United Kingdom
Mid Yorkshire NHS Trust
Dewsbury, United Kingdom
Royal Devon University Hospital
Exeter, United Kingdom
Medway Maritime Hospital
Gillingham, United Kingdom
Castle Hill Hospital
Hull, United Kingdom
James Illingworth
hyp-tr.development.research@nhs.net01482 461883 or 461903NHS Lanarkshire
Lanark, United Kingdom
St James's University Hospital
Leeds, United Kingdom
Leicester Royal Infirmary
Leicester, United Kingdom
Carolyn Maloney
uhl-tr.researchandinnovationadminmailbox@nhs.net0116 258 8351Barking, Havering and Redbridge University Hospitals NHS Trust
London, United Kingdom
Barts Health NHS Trust
London, United Kingdom
King's College Hospital
London, United Kingdom
Northwick Park Hospital
London, United Kingdom
University College London Hospitals NHS Foundation Trust
London, United Kingdom
Rajinder Sidhu - Associate Director, Research Governance and Operations
uclh.jro-communications@nhs.net020 3447 9825Christie NHS Foundation Trust
Manchester, United Kingdom
Norfolk and Norwich Hospital
Norwich, United Kingdom
Oxford University Hospital
Oxford, United Kingdom
University Hospitals Plymouth NHS Trust
Plymouth, United Kingdom
Salisbury NHS Foundation Trust
Salisbury, United Kingdom
Torbay & Newton Abbot Hospital
Torquay, United Kingdom
Royal Cornwall Hospital
Truro, United Kingdom
Hampshire Hospitals NHS Foundation Trust
Winchester, United Kingdom
How to Get in Touch
RAINBOW Trial Coordinator
Sponsor contactCONTACT
UCL CTC haematology trials team
Sponsor contactCONTACT
