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HLHRUXO: Ruxolitinib Therapy for HLH

HLHRUXO: Use of a Response-Adapted Ruxolitinib-containing Regimen for the Treatment of Hemophagocytic Lymphohistiocytosis

Categories:

Histiocytosis Treatment

Immunodeficiency Diseases Treatment

Diseases Treated:

Hemophagocytic Lymphohistiocytosis

Eligibility Overview:

  • 6 weeks to 22 years old
  • Newly diagnosed hemophagocytic lymphohistiocytosis (HLH)
  • Relapsed or refractory HLH
  1. Brief Summary

    This is a multi-institution Phase Ib/II study to determine the efficacy and tolerability of a response-adapted regimen incorporating ruxolitinib (Jakafi®), dexamethasone and etoposide as frontline therapy for patients with newly diagnosed hemophagocytic lymphohistiocytosis or as salvage therapy for patients with relapsed/refractory HLH. The trial will be coordinated by the North American Consortium of Histiocytosis  (NACHO) with enrollment at St. Jude and nine9 additional sites throughout the United States.

    HLH is a rare and often fatal disorder of the immune system characterized by the overwhelming activation of T cells and macrophages, which secrete high levels of cytokines and mediate significant tissue damage. Current treatment primarily focuses on decreasing inflammation and treating any underlying triggers by using agents such as high-dose steroids, etoposide, ATG and alemtuzumab. Although these treatments have helped reduce mortality, they are associated with short- and long-term toxicities and five-year survival remains around 60%.

    A novel immunomodulatory agent such as ruxolitinib offers a rational therapy that can be used instead of, or in some cases, in addition to, other HLH-directed therapies, such as etoposide. In preclinical studies, ruxolitinib decreased the manifestations of HLH, reduced CNS inflammation and significantly increased survival.

    Primary Objective

    • To determine the efficacy and tolerability of a response-adapted ruxolitinib-containing regimen for patients with newly diagnosed HLH.

    Secondary Objectives

    • To describe the efficacy and tolerability of a response-adapted ruxolitinib-containing regimen for patients with relapsed/refractory HLH
    • To describe the overall response and outcome for patients with newly diagnosed or relapsed/refractory HLH who are treated with this regimen

    Eligibility Criteria

    Inclusion criteria include:

    •  ≥6 weeks and ≤22 years old
    • Newly diagnosed HLH
    • History of HLH unresponsive to prior therapy
    • Exclusion Criteria include but are not limited to:
    • Weighs less than 3 kg
    • Isolated CNS disease
    • Life expectancy less than 2 weeks
    • Likely to require less than 4 weeks of therapy
    • Severe organ dysfunction
    • Taking rifampin, St. John’s Wort or any JAK inhibitor
    • Taking another investigational agent or enrolled on another treatment protocol

    Study Design

    Multi-site Phase Ib/II, two-arm (Frontline and Salvage), non-randomized clinical trial.

    Study Sites

    St. Jude Children’s Research Hospital
    Memphis, Tennessee

    Collaborating sites in the U.S.

  2. About this study

    This study will test a new drug therapy for hemophagocytic lymphohistiocytosis . This condition is also known as HLH or HLH disease.

    The drug in this study is called ruxolitinib  (Jakafi). The U.S. Food and Drug Administration (FDA) has approved ruxolitinib to treat adults with certain blood disorders. The FDA has also approved the drug to treat a condition called steroid refractory graft-versus-host disease in adults and children at least 12 years old.

    Research suggests ruxolitinib may reduce the immune system inflammation that happens with HLH. Studies also suggest ruxolitinib may work better than other HLH therapies.

    Although studies have found that ruxolitinib is safe in children with cancer, we do not know the safest and best dose of this drug in children with HLH. This study will only use doses of ruxolitinib that have been shown to be safe when given to children with cancer.

    Purpose of this clinical trial

    This main goal of this study is to find out if ruxolitinib will improve the survival rate for children with HLH.

    Eligibility overview

    • 6 weeks to 22 years old
    • Newly diagnosed HLH
    • History of HLH unresponsive to prior therapy
  3. HLHRUXO
    Sponsors: St. Jude Children’s Research Hospital
    ClinicalTrials.gov identifier NCT04551131
    Trial Start Date: January 2021
    Estimated Enrollment: 62 (all sites combined)
    Study Type: Interventional
    Study Phase: Phase I/II
    Conditions: HLH
    Ages: 6 weeks to 22 years old
    Principal investigator: Melissa Hines, MD
    Co-principal investigator Kim Nichols, MD
    Study Sites: St. Jude Children’s Research Hospital and collaborating sites outside the U.S.
    For a consultation or to discuss HLHRUXO: St. Jude Physician/Patient Referral Office
    1-888-226-4343
    referralinfo@stjude.org

St. Jude Children’s Research Hospital
262 Danny Thomas Place
Memphis, TN 38105  USA
Voice: 1-888-226-4343 or 901-595-4055
24-Hour Emergency Access Pager: 1-800-349-4334
Email: referralinfo@stjude.org

The above information is intended to provide only a basic description about a research protocol that may be currently active at St. Jude. The details made available here may not be the most up-to-date information on protocols used by St. Jude. To receive full details about a protocol and its status and or use at St. Jude, a physician must contact St. Jude directly.