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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Hodgkin lymphoma

Haematology and transfusion · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

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Airway, vena caval or spinal compression

Stridor, orthopnoea, facial swelling, venous congestion, tamponade, focal neurology or sphincter dysfunction from bulky nodal disease requires immediate anatomical stabilisation before routine staging.

Action: Use ABCDE assessment, keep a patient with mediastinal compression in the tolerated position, involve anaesthesia, respiratory, oncology and surgery urgently, obtain tissue before corticosteroids when safely possible, and use emergency radiotherapy, systemic treatment, stenting or decompression according to anatomy and pathology certainty.

Synopsis

Recognise Hodgkin lymphoma, obtain adequate tissue before steroids, stage with PET-CT and deliver response-adapted curative treatment while reducing pulmonary, cardiac, fertility and second-cancer harm.

  • Painless cervical or supraclavicular lymphadenopathy, mediastinal mass, pruritus and B symptoms are typical; alcohol-induced node pain is memorable but uncommon and non-diagnostic.
  • Reference-standard diagnosis is an excision or adequate core biopsy showing architecture, Reed–Sternberg morphology and the appropriate immunophenotype; fine-needle aspiration is inadequate.
  • Avoid corticosteroids before biopsy unless life-saving because lymphoma can melt rapidly and leave non-diagnostic tissue.
  • Baseline staging uses FDG PET-CT; it usually removes the need for routine bone-marrow biopsy in classical Hodgkin lymphoma.
  • Record Ann Arbor stage, bulky disease, B symptoms and early-stage favourable or unfavourable factors; treatment is curative and risk adapted rather than stage number alone.
  • Early favourable classical disease often receives two ABVD cycles followed by 20 Gy involved-site radiotherapy; other early groups use more chemotherapy or 30 Gy according to BSH protocol and PET response.
  • Advanced disease uses PET-adapted chemotherapy; after a negative interim PET, bleomycin is commonly omitted from later ABVD-derived cycles to reduce pulmonary toxicity.
  • NICE supports brentuximab vedotin with doxorubicin, vinblastine and dacarbazine for untreated stage III or IV CD30-positive adult Hodgkin lymphoma.
  • Interim PET is interpreted with the Deauville five-point scale and must be timed and acted on through the same protocol; inflammation can produce false positivity.
  • Discuss sperm, oocyte or embryo preservation before gonadotoxic treatment whenever delay is safe, and provide long-term cardiac, thyroid, breast, lung and second-cancer follow-up based on exposure.

Key red flags

Stridor, severe orthopnoea, superior vena cava obstruction, pericardial compromise or inability to lie flat makes sedation and supine biopsy hazardous and needs senior airway planning.

New weakness, sensory level, radicular pain or bladder or bowel dysfunction suggests malignant spinal cord compression and requires urgent MRI and dexamethasone through the MSCC pathway.

Rapid clinical decline, high LDH, lysis chemistry or an atypical extranodal pattern should prompt review for non-Hodgkin lymphoma, infection or transformation rather than assumption of ordinary classical Hodgkin lymphoma.

Fever during treatment is neutropenic sepsis until assessed; bleomycin-associated cough or hypoxaemia requires immediate drug review and pulmonary investigation.

Mediastinal compression

Cough, chest pressure, facial swelling, orthopnoea, stridor or inability to lie flat requires urgent anatomical and anaesthetic assessment.

Investigation priorities

01
Reference standard: excision biopsyFirst stepReference standard

Preserve nodal architecture and enough tissue for confident subtype and differential diagnosis.

02
First-line staging: FDG PET-CTFirst line

Map nodal, splenic, marrow and extranodal disease and establish a metabolic baseline.

Management branches

Persistent nodeObtain architecture before steroids

Unexplained lymphadenopathy or mediastinal mass persists or progresses.

  1. Assess compression, infection, HIV and alternative cancer and obtain FBC, ESR, organ and viral baseline.
  2. Arrange excision biopsy or multiple large cores with specialist tissue handling before corticosteroids when safe.
  3. Review integrated pathology, then stage confirmed disease with PET-CT and classify early risk or advanced disease.

Key medicines

ABVDGive doxorubicin 25 mg/m², bleomycin 10,000 IU/m², vinblastine 6 mg/m² and dacarbazine 375 mg/m² intravenously on days 1 and 15 of each 28-day cycle for the protocol-defined number of cycles.Use independent chemotherapy verification, vesicant precautions and cumulative anthracycline assessment. Monitor bleomycin lung injury, neutropenic sepsis, neuropathy, liver toxicity and fertility; stop and investigate bleomycin for new cough or hypoxaemia and avoid pregnancy.
Brentuximab vedotin with AVDGive brentuximab vedotin 1.2 mg/kg IV, maximum 120 mg, on days 1 and 15 of a 28-day cycle with protocol doxorubicin 25 mg/m², vinblastine 6 mg/m² and dacarbazine 375 mg/m² for six cycles.Give primary G-CSF prophylaxis according to the regimen. Monitor peripheral neuropathy, neutropenia, infection, infusion reaction, pancreatitis and liver toxicity; use dose modifications for neuropathy and severe organ impairment and prevent pregnancy during and after treatment.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • British Society for Haematology first-line classical Hodgkin guidelineUK tissue, staging, early and advanced response-adapted treatment guidance.
  • NICE TA1059 brentuximab combination recommendationsCurrent NHS first-line option for stage III or IV CD30-positive adult disease.
  • NICE TA524 brentuximab for relapsed Hodgkin lymphomaCommissioned relapsed and refractory CD30-positive populations.
  • NICE NG47 haematological cancers recommendationsUK specialist diagnostic, treatment and survivorship service standards.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom