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NCT05245656RecruitingPhase 2

A Study Comparing Rituximab/Bendamustin(RB) Alternating With Rituximab/Bendamustin/Cytarabin(RBAC) With RB Therapy in Elderly Patients With Mentle Cell Lymphoma

A Randomized Phase II Trial Comparing Rituximab/Bendamustine(RB) Alternating With Rituximab/Bendamustine/Cytarabine(RBAC) With RB as Induction Therapy in Elderly Patients With Newly Diagnosed and Transplant-ineligible Mantle Cell Lymphoma

Source: ClinicalTrials.gov · Last updated 23 Apr 2026

Brief summary (registry, in English)

This is a phase 2, multicenter, open-label, active-controlled randomized trial to determine efficacy and safety of rituximab/bendamustine (RB) alternating with rituximab/bendamustine/cytarabine (RBAC) compared with standard RB alone in the first-line treatment of elderly patients with mantle cell lymphoma, who are not eligible for high-dose therapy followed by autologous stem cell transplantation.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
90 (estimated)
First submitted
8 Feb 2022
Start date
18 Oct 2022
Primary completion date
31 Dec 2029
Lead sponsor
Kim, Seok Jin
NCT number
NCT05245656

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 90
  • From 18 Oct 2022 to the primary completion date, 31 Dec 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior treatment for Hodgkin lymphoma or non-Hodgkin lymphoma within the last 5 years.
  • HBsAg (+) or anti-HBc Ab (+) (patients will be eligible if they receive appropriate prophylactic antiviral therapy using entecavir, tenofovir, and so on)
  • History of prior hepatitis C infection (patients positive for HCV IgG will be eligible if they are negative for HCV-RNA)
  • concomitant administration of any other experimental drugs under investigation
  • major surgical procedure or significant trauma within 28 days before start of study treatment, open biopsy within 7 days before start of study treatment

Other illness

  • Ann Arbor stage 1 disease
  • Active malignancy within the past 3 years except for localized non-melanoma skin cancer, papillary thyroid cancer, cervical carcinoma in situ, breast cancer in situ, or localized prostate cancer that has been definitely treated,
  • Known history of human immunodeficiency virus (HIV) infection
  • any serious illness or medical conditions that are unstable or could jeopardize the safety of the patient and his/her compliance in the study
    • Congestive heart failure ≥ NYHA class 3
    • Acute coronary syndrome within 6 months (unstable angina or new-onset angina, myocardial infarct, or ventricular arrhythmia)
    • History of significant neurological or psychological disorder including dementia and seizure disorder
    • Severe chronic obstructive pulmonary disease with hypoxemia
    • Cerebrovascular disease including transient ischemic attack within the past 6 months
    • Non-healing wound, ulcer, or bone fracture
    • Active uncontrolled bacterial, viral, or fungal infection requiring systemic therapy
  • Known hypersensitivity to bendamustine, rituximab, cytarabine, or mannitol

Other

  • In-situ mantle cell lymphoma
  • Central nervous system involvement
  • If the patient's partner is a woman who could possibly get pregnant, men who didn't have a vasectomy must agree to use medically recommended methods for adequate contraception (tubal ligation, intrauterine devices, or barriers \[diaphragm, cervical cap\] in the patient's partner and the use of condoms in men) when sexually active.

Who the study is looking for

  • newly diagnosed, previously untreated, histologically confirmed CD20+ mantle cell lymphoma, confirmed by WHO classification criteria
  • age ≥70 years or 60-69 years if the patients are ineligible for high-dose therapy with autologous stem cell transplantation.
  • ECOG performance status 2 or less
  • Adequate organ functions
    • adequate heart function: LVEF ≥50% by echocardiography or MUGA
    • adequate renal function: serum creatinine ≤ 2.0mg/dL or CrCl ≥40 mL/min based on the Cockcroft-Gault method
    • adequate hepatic function: ≤2.5 times the upper limit of ALT (≤5 times the upper limit of ALT if the elevation is attributed by underlying lymphoma) and ≤2 times the upper limit of ALT (≤3 times the upper limit of total bilirubin if the elevation is attributed by underlying lymphoma)
    • adequate hematologic function: absolute neutrophil counts (ANC) ≥ 1,500/mL, platelet counts ≥ 100,000/mL (any ANC and platelet counts are allowed, if they were related to bone marrow involvement)
  • Written informed consent

Age in the registry: 60 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Samsung Medical Center
Coordinator of this site? Confirm its status
SeoulSouth KoreaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.