Study on Rituximab and Drug Combination for Treating Aggressive B-cell Lymphoma and Leukemia in Children and Adolescents

3 1 1 1

What is this study about?

This clinical trial is focused on studying treatments for mature aggressive B-cell lymphoma and leukemia in children and adolescents. These are types of cancers that affect the blood and lymphatic system. The study will explore the effectiveness of various medications, including rituximab, abiraterone acetate, anhydrous cyclophosphamide, cytarabine, vinblastine sulfate, dexamethasone acetate, ifosfamide, methotrexate, etoposide, and vindesine sulfate. These medications are used in different combinations to see how well they work in treating these diseases.

The purpose of the study is to analyze how well patients do without experiencing any events like disease progression or relapse, which is referred to as event-free survival. The study will also look at how the immune system recovers after treatment, particularly focusing on the recovery of a type of white blood cell called CD19+ B-cells. Patients will receive different treatment plans, some including rituximab, to determine if adding this medication improves outcomes.

Participants in the study will receive treatment over a period of time, with some receiving a placebo to compare the effects. The study will monitor patients’ progress and health, aiming to find the most effective treatment plan for these aggressive cancers. The trial will help understand if certain medications can improve survival rates and how they affect the immune system’s recovery.

1 initial assessment

Upon joining the study, an initial assessment is conducted to confirm eligibility. This includes a review of medical history and a series of tests to ensure adequate liver, kidney, and heart function, unless affected by the lymphoma.

2 treatment initiation

Treatment begins with the administration of medications. The specific drugs and their administration routes include: prednisolone (intravenous), cyclophosphamide (intravenous), cytarabine (intrathecal and intravenous), vincristine (intravenous), doxorubicin (intravenous), dexamethasone (intravenous), ifosfamide (intravenous), rituximab (intravenous), methotrexate (intrathecal and intravenous), etoposide (intravenous), and vindesine (intravenous).

3 treatment cycles

The treatment is structured in cycles, with each cycle involving a combination of the medications listed. The frequency and dosage are determined based on the specific stage of the disease and the treatment protocol.

4 monitoring and adjustments

Regular monitoring is conducted to assess the response to treatment. This includes blood tests and imaging studies. Adjustments to the treatment plan may be made based on these results.

5 completion of treatment

Upon completion of the treatment cycles, a final assessment is conducted to evaluate the overall response to the therapy. This includes a comprehensive review of the patient’s health status.

6 follow-up

Follow-up is expected for at least two years after the initial diagnosis. This involves regular check-ups to monitor for any recurrence of the disease and to assess long-term health outcomes.

Who Can Join the Study?

  • The patient must have a new diagnosis of an aggressive type of mature B-cell Non-Hodgkin lymphoma, which includes types like Burkitt lymphoma, Burkitt leukemia, diffuse large B-cell lymphoma, or other mature B-cell lymphomas as classified by the World Health Organization (WHO).
  • There must be available slides or tissue samples for review by a pathology expert, unless the diagnosis is confirmed by specific tests.
  • The patient must be under 18 years old at the time of diagnosis.
  • The patient must receive diagnosis and treatment at one of the centers participating in the trial.
  • The patient must not have received any previous chemotherapy or treatment specifically for lymphoma. Steroids should not have been used for more than two days in the last month.
  • The patient must have proper liver, kidney, and heart function, unless these issues are caused by the lymphoma itself.
  • There must be a signed consent form from the patient and/or their parents or guardians agreeing to the treatment plan, participation in the study, and sharing of data.
  • The patient is expected to be followed up for at least two years after the initial diagnosis.
  • The patient must have a certificate of vaccination against hepatitis B or a negative test result for hepatitis B, showing no infection.

Who Cannot Join the Study?

  • Patients who have a different type of cancer than the one being studied.
  • Patients who are not within the specified age range for the study.
  • Patients who have other serious health conditions that might interfere with the study.
  • Patients who are unable to follow the study procedures or attend required visits.
  • Patients who are pregnant or breastfeeding.
  • Patients who have received certain treatments recently that could affect the study results.
  • Patients who have allergies or reactions to the study medications.
  • Patients who are participating in another clinical trial at the same time.
  • Patients who have a history of non-compliance with medical treatments.
  • Patients who have certain infections that could affect the study.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Medical University Of Graz Graz Austria
Region Oestergoetland Linkoping Sweden
University Hospital Jena KöR Jena Germany
University Medicine Greifswald Greifswald Germany
Universitaetsmedizin Goettingen Goettingen Germany
Center For Pediatric And Adolescent Medicine Of The Johannes Gutenberg University Mainz Mainz Germany
Universitaetsklinikum Heidelberg AöR Heidelberg Germany
Rostock University Medical Center Rostock Germany
Universitaet Leipzig Leipzig Germany
Medizinische Universitaet Innsbruck Innsbruck Austria
Technische Universitaet Dresden Dresden Germany
Oslo Universitetssykehus HF Oslo Norway
Medizinische Hochschule Hannover Hanover Germany
Kuopio University Hospital Kuopio Finland

Other Sites

Site Name City Country Status
Universitaetsklinikum Regensburg AöR Regensburg Germany
Region Skane Skanes Universitetssjukhus Lund Sweden
Karolinska University Hospital Solna Sweden
Universitaetsklinikum Mannheim GmbH Mannheim Germany
Klinikum Kassel GmbH Kassel Germany
Staedtisches Klinikum Braunschweig gGmbH Brunswick Germany
Klinikum Oldenburg AöR Oldenburg In Holstein Germany
Universitetssykehuset Nord-Norge HF Tromsø Norway
Klinik Hallerwiese-Cnopfsche Kinderklinik Nürnberg Germany
Universitaetsklinikum Erlangen AöR Erlangen Germany
Universitaetsklinikum Tuebingen AöR Tuebingen Germany
Tampere University Hospital Tampere Finland
Klinikum Der Landeshauptstadt Stuttgart gKAöR Stuttgart Germany
Universitaetsklinikum Magdeburg AöR Magdeburg Germany
Saarland University Hospital Homburg Germany
Evangelisches Klinikum Bethel gGmbH Bielefeld Germany
Turku University Hospital Turku Finland
Universitaetsklinikum Ulm AöR Ulm Germany
Aalborg University Hospital Aalborg Denmark
Kepler Universitaetsklinikum GmbH Linz Austria
Rheinische Friedrich-Wilhelms-Universitaet Bonn Bonn Germany
Justus-Liebig-Universitaet Giessen Giessen Germany
Medical Center – University Of Freiburg Freiburg Im Breisgau Germany
Rigshospitalet Copenhagen Denmark
Klinikum der Technischen Universitaet Muenchen (TUM Klinikum) Munich Germany
Region Vaesterbotten Umea Sweden
Klinikum Dortmund gGmbH Dortmund Germany
HELIOS Klinikum Krefeld GmbH Krefeld Germany
Staedtisches Klinikum Karlsruhe gGmbH Karlsruhe Germany
Universitaetsklinikum Aachen AöR Aachen Germany
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
St. Anna Kinderspital GmbH Vienna Austria
HELIOS Klinikum Berlin-Buch GmbH Berlin Germany
HELIOS Klinikum Erfurt GmbH Erfurt Germany
Asklepios Klinik Sankt Augustin GmbH Sankt Augustin Germany
Deutsches Herzzentrum Berlin Berlin Germany
St. Olavs Hospital HF Trondheim Norway
Queen Silvia Childrens Hospital – Sahlgrenska University Hospital – Vaestra Goetalandsregionen Gothenburg Sweden
Gemeinschaftskrankenhaus Herdecke gGmbH Herdecke Germany
Muehlenkreiskliniken AöR Minden Germany
Oulu University Hospital Oulu Finland
Odense University Hospital Odense Denmark
Klinikum Bremen-Mitte gGmbH Bremen Germany
Westfaelische Wilhelms Universitaet Muenster Munster Germany
Uniklinikum Salzburg Salzburg Austria
Hxmqy Bivfyu Ht Bergen Norway
Ghieoslzupfyevzdhhuli Mcfepqhioxh gmesk Koblenz Germany
Hqoxnr Ktejoqrd Sopjhvzn Gbwv Schwerin Germany
Cvvw Twwdy Kgbdxdns gnovk Cottbus Germany
Uokjqlmaihv Wuxdivwnzizwmcc &yokxfu Vkdevxoyk Kogibhe unb Jakjmnbjswwk Dumowoo Datteln Germany
Ultzsprcxw Htgbjwyk Cbtuqpo Cologne Germany
Fqoddmkw ntwyvzlen Mtxno a Hgfyluy Prague Czechia
Ubxtwxs Uahosshzku Hhzzbuld Uppsala Sweden
Uettiptfzvykmsfrtbque Dsqcebacksx Azi Duesseldorf Germany
Hnghqokh Uxcgojqbhq Cmnmciv Hngynepc Helsinki Finland
Agqhrx Udydmikngm Hnffsdlm Aarhus Denmark
Legieq Mnzyfqykmn Uwzeyhxsnu Ow Mhynzn Munich Germany
Gwwjhs Ussgzmohkz Fqnayezln Frankfurt Germany
Uvllopgbpwfacsaalkzvu Wvqfnzjcd Ass Wuerzburg Germany
Uefzotzdjw Mntgcmc Chbzzg Hrxyhjsatlewxvsca Hamburg Germany
Uumbxafzbguhdxdqcgtbd Engej Apz Essen Germany
Mkgimwizrzpbygutfixecgorli Hyorkmfzfcqvzpza Halle (Saale) Germany
Ucontwnxuzubekrdbrees Agzfembi Augsburg Germany

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
21.08.2017
Czechia Czechia
Not recruiting
21.08.2017
Denmark Denmark
Not recruiting
21.08.2017
Finland Finland
Not recruiting
21.08.2017
Germany Germany
Not recruiting
21.08.2017
Norway Norway
Not recruiting
21.08.2017
Sweden Sweden
Not recruiting
21.08.2017

Trial locations

Rituximab is a medication used in this trial to treat children and adolescents with aggressive B-cell lymphoma and leukemia. It is being tested to see if it can improve survival rates when used in different treatment stages. The trial is examining whether using rituximab alone or in combination with standard chemotherapy can help patients live longer without the disease coming back. The study also looks at how the immune system recovers after treatment with rituximab.

Standard Chemotherapy (S-CTX) refers to the usual treatment given to patients with aggressive B-cell lymphoma and leukemia. This therapy involves using a combination of drugs to kill cancer cells and stop them from growing. In this trial, standard chemotherapy is used as a baseline treatment to compare the effects of adding rituximab. The goal is to determine if the addition of rituximab can improve the outcomes for patients.

Mature Aggressive B-cell Lymphoma and Leukemia in Children and Adolescents – This disease involves the rapid growth of B-cells, a type of white blood cell, which can form tumors in lymph nodes or other parts of the body. In children and adolescents, it can manifest as either lymphoma, which primarily affects the lymphatic system, or leukemia, which affects the blood and bone marrow. The disease progresses quickly, often requiring immediate medical attention. It can lead to symptoms such as swollen lymph nodes, fever, night sweats, and weight loss. The aggressive nature of the disease means it can spread rapidly to other organs if not managed promptly.

Trial ID:
2023-505509-18-00
Protocol code:
B-NHL 2013
NCT ID:
NCT03206671
Trial Phase:
Therapeutic confirmatory (Phase III)

Other Trials to Consider

  • Venetoclax plus drug combination versus drug combination alone in children with relapsed acute myeloid leukemia

    Recruiting

    3 1 1 1
    Austria Belgium Czechia Denmark Finland France +8
  • A study to evaluate the efficacy and safety of depemokimab and salbutamol sulfate in patients with chronic obstructive pulmonary disease and type 2 inflammation.

    Recruiting

    3 1 1
    Belgium Bulgaria Denmark France Germany Greece +6