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OncoMatch/Clinical Trials/NCT05230680

Azacitidine-CHOP for Patients With Nodal T-cell Lymphoma With T-follicular Helper Phenotype (ACANTUS)

Is NCT05230680 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies ACHOP for t cell lymphoma.

Phase 1/2RecruitingWon Seog KimNCT05230680Data as of Jun 2026Location: South Korea

Treatment: ACHOPInduction treatment (every 3 weeks, total 6 cycles) * Azacitidine D-2, -1, 1 (level 1: 50mg/m2, level 2: 75mg/m2, level 3: 100mg/m2, level 4: 125mg/m2) * Cyclophosphamide 750mg/m2 d1 * Doxorubicin 50 mg/m2 d1 * Vincristine 1.4 mg/m2 (Max: 2 mg) d1 * Prednisolone 100mg PO d1-5 Maintenance treatment (every 4 weeks, total 12 cycles) * Azacitidine 75mg/m2 d1-5

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Extracted eligibility criteria

Treatments studied

Other

ACHOP

Cancer type

Non-Hodgkin Lymphoma

Performance status

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

Demographics

Ages 20–85

Prior therapy

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

Cannot have received: chemotherapy

Exception: short-term corticosteroids (for less than 8 days) prior to selection

Previously treated for T-cell lymphoma with immunotherapy or chemotherapy, except for short-term corticosteroids (for less than 8 days) prior to selection

Cannot have received: chemotherapy

History of chemotherapy for Hodgkin's or other non-Hodgkin's lymphoma in the last 5 years

Cannot have received: radiation therapy

Exception: localized to a single lymph node

Prior radiotherapy, except for those localized to a single lymph node

Cannot have received: doxorubicin (doxorubicin)

History of administration of doxorubicin at >200 mg/m²

Lab requirements

Blood counts

absolute neutrophil count (anc) ≥1,500/μl, platelets ≥100,000/μl (or anc ≥500/μl and platelets ≥50,000/ μl in the presence of bone marrow involvement)

Kidney function

serum cr ≤2.0mg/dl or egfr ≥ 30ml/min according to the cockroft-gault formula

Liver function

alt ≤2.5x upper limit of normal (uln) (or ≤5x uln in the presence of liver involvement), total bilirubin ≤2x uln (or ≤3x uln in the presence of liver involvement)

Cardiac function

lvef ≥45% on echocardiography or muga

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

Frequently asked questions

Is NCT05230680 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 85 years or younger and at least 20 years old.

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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