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OncoMatch/Clinical Trials/NCT04922567

Efficacy and Safety of Lenalidomide Plus CHOP vs CHOP in Patients With Untreated Peripheral T-Cell Lymphoma

Is NCT04922567 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments for peripheral t-cell lymphoma.

Phase 2RecruitingSecond Affiliated Hospital, School of Medicine, Zhejiang UniversityNCT04922567Data as of Jun 2026Location: China

Treatment: Lenalidomide · Cyclophosphamide · Doxorubicin · Vincristine · PrednisoneThis study aims to compare the efficacy and safety of lenalidomide plus CHOP (L-CHOP) versus CHOP alone in patients with previously untreated peripheral T-cell lymphoma (PTCL)

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Extracted eligibility criteria

Treatments studied

Chemotherapy

CyclophosphamideDoxorubicinVincristine

Endocrine / hormonal

Lenalidomide

Other

Prednisone

Cancer type

Non-Hodgkin Lymphoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: any anti-tumor therapy

Exception: prephase treatment specified for this study

Lab requirements

Blood counts

absolute neutrophil count(ANC)≥1.5×10^9/L, hemoglobin(Hb)≥90g/L, platelet(PLT)≥100×10^12/L

Kidney function

creatine ≤2.0×ULN

Liver function

total bilirubin ≤2.0mg/dl, transaminases≤3×ULN

Cardiac function

no obvious abnormal function of heart; decompensated heart failure, dilated cardiomyopathy, coronary heart disease of non-corresponding ST-segment in ECG diagnosis, or myocardial infarction within 6 months excluded

Fit chemotherapy indications and basic requirements, including no obvious abnormal function of heart, liver, lung and kidney: creatine ≤2.0×ULN, total bilirubin ≤2.0mg/dl, transaminases≤3×ULN. Normal peripheral hemogram: absolute neutrophil count(ANC)≥1.5×10^9/L, hemoglobin(Hb)≥90g/L, platelet(PLT)≥100×10^12/L. Hemogram abnormality: ANC<1.5×10^9/L; or hemoglobin<90 g/L; or PLT<100×10^9/L. Known hepatic and renal insufficiency (creatine>2.0×ULN, total bilirubin>2.0 mg/dl,transaminases>3.0×ULN). Patients with decompensated heart failure; or with dilated cardiomyopathy; or with coronary heart disease of non-corresponding ST-segment in ECG diagnosis; or with myocardial infarction within 6 months.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT04922567 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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