R-CDOP Combined With Intrathecal Methotrexate for DLBCL Patients With High-risk of CNS Relapse

Official title

A Phase II Study of R-CDOP Combined With Intrathecal Methotrexate for Diffuse Large B-cell Lymphoma Patients With High-risk of Central Nervous System Relapse

Overview

This is a double-center, single-arm, phase 2 study to evaluate the efficacy and safety of R-CDOP regimen combined with intrathecal methotrexate in chemo-naive diffuse large B-cell lymphoma patients with high-risk of CNS relapse.

Detailed description

Diffuse large B-cell lymphoma is the most common subtype of non-Hodgkin's lymphoma, accounting for 31% of all non-Hodgkin's lymphomas. At present, the standard treatment is R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) Regimen. In DLBCL, central nervous system recurrence is rare, but once it occurs, it is often fatal. The prognosis of patients with central recurrence of DLBCL is very poor, and the median survival time is only 3.5-7 months.The CNS relapse rate of the R-CHOP regimen combined with MTX (methotrexate) intrathecal in high CNS-IPI DLBCL patients is approximately 12%.

This study was a phase II, prospective, single arm，double-center study, which requires a total of 83 DLBCL patients with high-risk of CNS relapse.

Patients will receive a total of 6-8 cycles of R-CDOP regimen, repeated every 3 weeks. Intrathecal MTX will be administered after the 1st-5th cycle of chemotherapy. All the patients will receive a mid-treatment PET scan after 4 cycles of chemotherapy. Patient achieves CR (complete response) after 4 cycles will continue to receive another 2 cycles of treatment. For those who achieve PR, another 4 cycles of chemotherapy will given.

Interventions

• Drug R-CDOP+intrathecal MTX
  R-CDOP+intrathecal MTX： * Rituximab 375 mg / m\^2，D1 * Cyclophosphamide 750 mg / m\^2，D2 * Doxorubicin Hydrochloride Liposome Injection 35mg / m\^2，D2 * Vincristine 1.4mg/m\^2 (dose capped at 2 mg)，D2 * Prednisone 50 mg， bid D2-6 * Cycle1-5：Intrathecal MTX 12 mg + DXM 5 mg after chemotherapy （PK patients will be given 24 h after chemotherapy）

Primary outcome measures

• 2-year central nervous system relapse rate [Time frame: up to 6 years after the start of the study]
• Concentration of doxorubicin in cerebrospinal fluid after using doxorubicin hydrochloride liposome injection [Time frame: up to 4 years after the start of the study]

Secondary outcome measures (10)

• Objective response rate (ORR) [Time frame: 2 years after enrollment of final patient]
• 2-year progression-free survival (PFS) rate [Time frame: 2 years after enrollment of final patient]
• 2-year event-free survival (EFS) rate [Time frame: 2 years after enrollment of final patient]
• Overall Survival (OS) [Time frame: 2 years after enrollment of final patient]
• Adverse events [Time frame: Since the signing of informed consent forms to 30 days after the last cycle]
• Cmax（maximum concentration） [Time frame: Time from zero to Tmax]
• Tmax（maximum time） [Time frame: Time from zero to Cmax]
• T1/2（drug half time） [Time frame: The time it takes for blood concentration levels to drop by half]
• AUC（0-∞）（area under the curve） [Time frame: Time from zero to ∞]
• AUC （0-t）（area under the curve from time zero to the last observation time [Time frame: Time from zero to the last observation time]

Eligibility criteria

Inclusion criteria

• Age range from 18 to 75 years;
• ECOG performance status: 0-2;
• Histopathologically confirmed untreated diffuse large B-cell lymphoma (cell origin can be distinguished according to Hans algorithm) , And fulfilled the following criteria for high-risk CNS recurrence:

• CNS-IPI 4-6;
• The lymphoma involved testis, breast (excluding unilateral breast and less than 5 cm mass), adrenal gland, kidney, paranasal sinus, paravertebral, and bone marrow and other sites;
• PCLBCL-leg;
• Subjects have at least one measurable lesion: the long axis of the lymph node shall be>1.5 cm, the long axis of the extranodal lesions shall be>1.0 cm;
• Bone marrow hematopoiesis was essentially normal: WBC≥3.5 ×10\^9/L, ANC≥1.5×10\^9/L, PLT≥80×10\^9/L, Hb≥90 g/L. Abnormal peripheral blood indices, as a result of lymphoma invading the bone marrow or spleen, permitted enrollment at the discretion of the investigator;
• Liver function: total bilirubin, ALT, AST < 1.5×UNL (upper limit of normal);
• Renal function: Cr < 1.5×UNL and creatinine clearance≥30 ml/min;
• Echocardiography or nuclide cardiac function testing with LVEF≥50%;
• Patients in the reproductive period agreed to appropriate contraception. Women in the reproductive period had a negative serum pregnancy test within 2 weeks before enrollment;
• Consent to provide pathological tissue specimens (wax blocks within half a year or 20 slides for paraffin tissue sections);
• Life expectancy≥3 months;
• Signed informed consent;

Exclusion criteria

• Patients with a known history of severe allergy to humanized or murine mAbs, or any contraindication to R-CDOP, intrathecal MTX;
• Patients with evidence of CNS involvement (baseline cerebrospinal fluid, imaging, symptoms);
• Special types of diffuse large B-cell lymphoma patients who are not suitable for induction therapy with R-CDOP, such as PMBCL, double-hit large B-cell lymphoma, etc;
• Clinically significant cardiac conditions, including severe cardiac insufficiency: New York Heart Association (NYHA) cardiac insufficiency class IV, unstable angina, acute myocardial infarction within 6 months prior to screening, congestive heart failure, and Q-Tc interval greater than 500 ms;
• Those who had a second degree or greater operation within three weeks before treatment;
• Diagnosed with a malignancy other than lymphoma or under treatment, with the following exceptions:

• Had received treatment with curative intent and had not developed malignancy with known active disease ≥ 5 years prior to enrollment;
• Basal cell carcinoma of the skin (other than melanoma) that has been adequately treated with no evidence of disease;
• Carcinoma in situ of the cervix that has been adequately treated with no evidence of disease;
• Had significant coagulation abnormalities;
• Any previous antilymphoma therapy other than short-term corticosteroids (up to 10 days);
• Those with severe active infection;
• Other serious, uncontrolled concomitant conditions that may affect protocol adherence or interfere with interpretation of results include uncontrolled diabetes mellitus, or pulmonary disease (interstitial pneumonia, obstructive pulmonary disease, and a history of symptomatic bronchospasm), hypertension, and others;
• HBV (HBsAg positive and HBV-DNA ≥ 104 IU / ml), HCV (HCV antibody positive and HCV-RNA measurable); And subjects with other acquired, congenital immunodeficiency diseases, including but not limited to those with HIV infection;
• Pregnant or lactating women;

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

China · 2 centers

• Dongmei Ji — Shanghai
• Cancer Hospital affilicaited to Xinjiang Medical University — Ürümqi

Identifiers

NCT: NCT05257018 · CSPC-DMS-LM-K001

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗