RecruitingPhase 2NCT03899337

A Trial of CHOP-R Therapy, With or Without Acalabrutinib, in Patients With Newly Diagnosed Richter's Syndrome

A Phase II, Randomised Study of CHOP-R in Combination With Acalabrutinib Compared to CHOP-R in Patients With Newly Diagnosed Richter's Syndrome and a Platform for Initial Investigations Into Activity of Novel Treatments in Relapsed/Refractory and Newly Diagnosed Richter's Syndrome.


Sponsor

University of Birmingham

Enrollment

105 participants

Start Date

Jul 23, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

The STELLAR trial will assess the effect of acalabrutinib taken in combination with CHOP-R compared to taking CHOP-R alone in patients with newly diagnosed Richter's Syndrome (RS). It will also be a platform to test other new drugs that show potential for treating RS. Chronic lymphocytic Leukaemia (CLL) is the most common blood cancer in adults, usually in their 70s or older. In a few patients, CLL can transform from a slow-growing cancer into an aggressive lymphoma called Richter's Syndrome. RS is very difficult to treat and patients have a short life-expectancy - usually a few months after diagnosis. Treatment for Richter's Syndrome in the UK is CHOP (four chemotherapy drugs) plus rituximab ('R' - an antibody treatment). The CHOP-R treatment is given as a standard of care for RS but has limited benefit - it is often temporary to extend life. Richter's Syndrome returns in most patients who then die from this disease. The STELLAR trial will investigate if a new drug called acalabrutinib, which is effective used by itself in patients with relapsed CLL and also some with Richter's Syndrome, will improve outcomes for newly diagnosed patients with RS. Acalabrutinib blocks a protein in CLL which can stop the cancer growing. Participants who have Richter's Syndrome and are suitable for CHOP-R will be recruited by specialised hospitals across the UK. People with another cancer, heart problems, or recent stroke cannot take part. Participants will have a lymph node biopsy, 3-4 bone marrow biopsies, blood samples, and PET-CT and CT scans. CHOP-R is given in a hospital every three weeks up to 6 times. All participants will receive CHOP-R; half will also receive acalabrutinib. When treatment with CHOP-R ends the patients who had acalabrutinib can continue to take it; patients who had CHOP-R alone may have acalabrutinib if their Richter's Syndrome returns after CHOP-R.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing whether adding a targeted drug called acalabrutinib to standard chemotherapy (CHOP-R) helps people newly diagnosed with Richter's Syndrome — a rare and aggressive cancer that can develop in some people with chronic lymphocytic leukemia (CLL). **You may be eligible if...** - You have CLL and have been newly diagnosed with a specific type of Richter's Syndrome (DLBCL type), confirmed by biopsy - You are 16 years of age or older - You are well enough to receive intensive chemotherapy (performance status 0-3) - You have not previously had CHOP or anthracycline-based chemotherapy **You may NOT be eligible if...** - You have previously received acalabrutinib or CHOP/anthracycline-containing chemotherapy - You were on ibrutinib and developed Richter's Syndrome within 4 weeks of stopping it - Cancer has spread to your brain or spinal fluid - You have active HIV, hepatitis B, or hepatitis C Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAcalabrutinib

100mg capsule, PO, BD

DRUGCyclophosphamide

750mg/m\^2, IV bolus

DRUGDoxorubicin

50mg/m\^2, IV bolus

DRUGVincristine

1.4mg/m\^2, IV infusion

DRUGPrednisolone

40mg/m\^2, PO, OD

DRUGRituximab

375mg/m\^2, IV infusion


Locations(16)

Belfast City Hospital

Belfast, United Kingdom

Royal Bournemouth Hospital

Bournemouth, United Kingdom

University Hospital of Wales

Cardiff, United Kingdom

Beatson West of Scotland Cancer Centre

Glasgow, United Kingdom

St James's University Hospital

Leeds, United Kingdom

Leicester Royal Infirmary

Leicester, United Kingdom

King's College Hospital

London, United Kingdom

St Bartholomew's Hospital

London, United Kingdom

University College London Hospital

London, United Kingdom

Christie Hospital

Manchester, United Kingdom

Norfolk and Norwich University Hospital

Norwich, United Kingdom

Nottingham City Hospital

Nottingham, United Kingdom

Churchill Hospital

Oxford, United Kingdom

Derriford Hospital

Plymouth, United Kingdom

Royal Hallamshire Hospital

Sheffield, United Kingdom

Southampton General Hospital

Southampton, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT03899337


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