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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 (May 2026). This Phase 2 trial studies Nivolumab for hodgkin lymphoma.

Phase 2RecruitingNational Research Center for Hematology, RussiaNCT07209059Data as of May 2026

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

Cancer type

Hodgkin Lymphoma

Disease stage

Required: Stage IIB (BULKY), III, IV

Performance status

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

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.

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