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OncoMatch/Clinical Trials/NCT07209059

PET-Adapted First-Line Therapy With Nivolumab for Advanced Hodgkin Lymphoma

Is NCT07209059 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Nivolumab for hodgkin lymphoma.

Phase 2RecruitingNational Research Center for Hematology, RussiaNCT07209059Data as of Jun 2026Location: Russia

Treatment: NivolumabThis is a single-center, open-label, phase 2 pilot study evaluating the efficacy and safety of a response-adapted first-line treatment strategy for patients with classical Hodgkin lymphoma (cHL) and unfavorable prognostic factors. The FINISH protocol (First-line Immuno-chemotherapy Navigated by Interim PET for Stratification and Hazard minimization In Hodgkin lymphoma) integrates nivolumab into induction therapy and tailors subsequent treatment based on interim PET-CT response. The study also includes exploratory monitoring of circulating tumor DNA (ctDNA) to investigate its role in early response assessment and residual disease detection.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Nivolumab

Cancer type

Hodgkin Lymphoma

Disease stage

Required: Stage IIB (BULKY), III, IV

Performance status

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

Demographics

Ages ≤ 60

Prior therapy

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

Cannot have received: chemotherapy

No prior chemotherapy, radiotherapy, or immunotherapy for lymphoma

Cannot have received: radiation therapy

No prior chemotherapy, radiotherapy, or immunotherapy for lymphoma

Cannot have received: immunotherapy

No prior chemotherapy, radiotherapy, or immunotherapy for lymphoma

Lab requirements

Kidney function

Serum creatinine ≤ 0.2 mmol/L; severe renal impairment (serum creatinine > 0.2 mmol/L) excluded unless lymphoma-related

Liver function

Absence of severe hepatic dysfunction; severe hepatic dysfunction excluded unless directly related to lymphoma

Cardiac function

Absence of severe cardiac dysfunction; congestive heart failure, unstable angina, recent myocardial infarction, or severe cardiac arrhythmias excluded

Adequate organ function, including: Serum creatinine ≤ 0.2 mmol/L; Absence of severe cardiac, pulmonary, hepatic, or renal dysfunction

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

Frequently asked questions

Is NCT07209059 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.

What disease stage is eligible?

Stage IIB (BULKY) or III or IV is required.

Is there an age limit?

Yes. Patients must be 60 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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