Orelabrutinib Combined With Obinutuzumab and Lenalidomide (OGL Regimen) as First-line Treatment for Marginal Zone Lymphoma.

Chinese Academy of Medical Sciences & Peking Union Medical College

Status and phase: Enrolling; Phase 2

Conditions: Marginal Zone Lymphoma

Treatments: Drug: Orelabrutinib, obinutuzumab, lenalidomide

Study type: Interventional

Funder types: Other

Identifiers

NCT06454968

PUMCH-NHL-017

Details and patient eligibility

About

This is a multicenter prospective single arm phase II study, and the purpose of this study is to evaluate the safety and efficacy of orelabrutinib combined with obinutuzumab and lenalidomide in untreated marginal zone lymphoma. The primary objective was the best complete response rate (CRR).

Full description

Marginal zone lymphomas (MZL) are a type of lymphoma that originates from the marginal zone tissue of the lymphoid follicles (Mucosa-associated lymphoid tissue, MALT), and include three subtypes: MALT lymphoma, nodal MZL, and splenic MZL. The incidence of MZL is second only to diffuse large B-cell lymphoma (DLBCL) and follicular lymphoma (FL), accounting for approximately 7.8% of all non-Hodgkin lymphomas (NHL). MZL is considered an indolent lymphoma, with patients generally having a better overall survival prognosis. Despite this, some patients still face the challenges of disease relapse or transformation into large cell lymphoma, leading to a poor prognosis.

We conduct this prospective, phase II, single-arm clinical study to initially explore the efficacy and safety of Orelabrutinib combined with obinutuzumab and lenalidomide in patients with previously untreated marginal zone lymphoma. The patients will be treated with 6 cycles of OGL regimen. Patients with CR/PR after 6 cycles of OGL treatment will be treated with 6 cycles of single-agent orelabrutinib regimen.

Enrollment: 45 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age ≥ 18 years, either sex.

• Histopathologically confirmed B-cell non-Hodgkin lymphoma MZL (splenic, nodal, or extra-nodal).

• At least 1 measurable lesion

• Eligible for treatment: meets the GELF criteria, or has clinical symptoms/organ dysfunction related to the disease

• Patients who are not suitable for local radiotherapy or whose condition progresses after local treatment, and those not suitable for local radiotherapy include the following situations:

  • Ann Arbor non-continuous Stage II or Stage III-IV non-gastric MALT and nodal MZL
  • SMZL (Splenic Marginal Zone Lymphoma)
  • Gastric MALT with Lugano Stage II2/IIE/IV

• ECOG performance status (PS) score of 0-2.

• Expected survival time is ≥3 months

• Sign the Informed consent

Exclusion criteria

• Currently has other malignant tumors;
• Lymphoma involving the central nervous system
• Allergic to any of the study drugs;
• Active infection or uncontrolled HBV infection (DNA>105/ml), HIV/AIDS, or other severe infectious diseases;
• Pregnant or lactating women and women of childbearing age who are unwilling to use contraception;
• Any other conditions deemed unsuitable for participation in this trial by the investigator.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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45 participants in 1 patient group

OGL

Experimental group

Description:

Orelabrutinib: 150mg qd d1-d21/C1-C6 obinutuzumab: 1000mg iv d1,d8,d15/c1, 1000mg iv d1/C2-C6 lenalidomide：25mg po qd d1-14/C1-C6 Orelabrutinib: 150mg qd d1-d28/C7-C12

Treatment:

Drug: Orelabrutinib, obinutuzumab, lenalidomide