Clinical Trials Directory

Trials / Completed

CompletedNCT01616238

A Study for Older Adults With Acute Lymphoblastic Leukaemia

A Phase 2 Study for Older Adults With Acute Lymphoblastic Leukaemia

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
126 (actual)
Sponsor
University College, London · Academic / Other
Sex
All
Age
55 Years
Healthy volunteers
Not accepted

Summary

The NCRI Adult ALL sub-group propose to collaborate with the Dutch/Belgian group HOVON to carry out a prospective, non randomised multi-arm study (including a choice of regimen intensity) to investigate the safety, tolerability and feasibility of a standardised therapy protocol for patients ≥ 60 years old with de novo ALL. The overall aim is define a basic standard of care upon which trials of novel therapies will be based in future. The design of the study will enable collection of a comprehensive dataset regarding the clinical outcome, Complete Response Rate (CR) and Minimal Residual Disease (MRD) response rates in a previously completely uncharacterised population, thus providing the essential platform for designing future randomised advanced phase studies in which new therapeutic approaches and novel therapies can be prospectively investigated.

Detailed description

The study will 1. establish baseline expectations for Event Free Survival (EFS), Overall Survival (OS), MRD responses and quality of life measures for older patients of all ages and pre-morbid states; 2. disclose how best to use knowledge of pre-morbid characteristics to apply the appropriate intensity of therapy in order to balance the best disease related outcomes against quality of life; 3. establish national standards of care for this patient group; 4. provide the essential platform for careful design of future randomised advanced phase studies of new therapeutic approaches and agents.

Conditions

Interventions

TypeNameDescription
DRUGChemotherapyTreatment for all pathways consists of Induction, Intensification (where applicable), Consolidation and Maintenance therapy during which combination chemotherapy is given for up to 2.5 years.

Timeline

Start date
2012-12-01
Primary completion
2018-12-21
Completion
2023-02-01
First posted
2012-06-11
Last updated
2023-08-16

Locations

34 sites across 2 countries: Netherlands, United Kingdom

Source: ClinicalTrials.gov record NCT01616238. Inclusion in this directory is not an endorsement.