All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a Healthcare Professional. If you are a patient or carer, please visit the Lymphoma Coalition.

The Lymphoma Hub uses cookies on this website. They help us give you the best online experience. By continuing to use our website without changing your cookie settings, you agree to our use of cookies in accordance with our updated Cookie Policy

Introducing

Now you can personalise
your Lymphoma Hub experience!

Bookmark content to read later

Select your specific areas of interest

View content recommended for you

Find out more
  TRANSLATE

The Lymphoma Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the Lymphoma Hub cannot guarantee the accuracy of translated content. The Lymphoma Hub and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.

Steering CommitteeAbout UsNewsletterContact
LOADING
You're logged in! Click here any time to manage your account or log out.
LOADING
You're logged in! Click here any time to manage your account or log out.
2018-07-25T08:36:22.000Z

EHA 2018 | Durable responses seen with moxetumomab pasudotox in R/R HCL

Jul 25, 2018
Share:

Bookmark this article

On Saturday 16th June an oral abstract session took place at the 23rd Congress of the European Hematology Association (EHA). Abstract S856 was presented by Francis Giles, Developmental Therapeutics Consortium, Chicago, US, on the use of moxetumomab pasudotox in heavily pretreated patients with relapsed/refractory (R/R) hairy cell leukemia (HCL) (NCT01829711).

Study Overview

  • The study was single-arm, open-label at 34 centers across 14 countries
  • N = 80 patients received 40 μg/kg IV on Days 1,3 and 5 of 28-day treatment cycles until disease progression or unacceptable toxicity
  • The primary endpoint was the rate of durable complete response (CR) that was defined by CR with hematologic remission of ≥181 days
  • The secondary endpoints were overall response rate (ORR), CR rate, progression-free survival (PFS), duration of response (DOR), tolerability and safety

Key Findings

  • The durable CR as assessed by a blinded independent review was 30% (95% CI, 20%–41%)
  • 34% (n = 27) of patients demonstrated CR with MRD-negativity according to immunohistochemistry (95% CI, 24%–45%)
  • The ORR as assessed by a blinded independent review was 75% (95% CI, 64%–84%)
  • 80% achieved hematologic remission with a median onset of 1.1 months
  • The median duration of hematologic remission from CR was not reached
  • Most frequent treatment-related adverse events (AEs) Grade ≥3 was lymphocyte count decrease (7.5%) and hemolytic uremic syndrome (5%)

The findings of this study demonstrated that moxetumomab pasudotox had durable responses in patients with R/R HCL. Dr Giles concluded that moxetumomab pasudotox also eradicated MRD in a substantial proportion of patients.

  1. Giles F. Moxetumomab pasudotox in heavily pretreated patients with relapsed/refractory hairy cell leukemia: Results of a pivotal international study. Abstract S856. 23rd Congress of EHA, Stockholm, Sweden

Understanding your specialty helps us to deliver the most relevant and engaging content.

Please spare a moment to share yours.

Please select or type your specialty

  Thank you

Newsletter

Subscribe to get the best content related to lymphoma & CLL delivered to your inbox