Hodgkin Lymphoma (HL) – Summary for Oncology Pharmacist
Definition
A malignant lymphoma characterized by the presence of Reed–Sternberg cells (large, binucleated B cells, CD30+ and CD15+), typically arising from germinal center B-cells.
Epidemiology
- Bimodal age distribution: peaks at 15–35 and >55 years
- Slight male predominance
- High cure rate (>85%) with modern therapies
Subtypes (WHO Classification)
- Classical Hodgkin Lymphoma (cHL) (95%):
- Nodular sclerosis (most common)
- Mixed cellularity
- Lymphocyte-rich
- Lymphocyte-depleted
- Nodular lymphocyte-predominant HL (NLPHL) (CD20+, CD30–, CD15–)
Clinical Features
- Painless lymphadenopathy (often cervical, mediastinal)
- B symptoms: fever, night sweats, weight loss
- Alcohol-induced pain at lymph nodes (rare, but specific)
- Fatigue, pruritus, splenomegaly
Diagnosis
- Excisional lymph node biopsy (not FNA)
- Histology: Reed–Sternberg cells in an inflammatory background
- Immunohistochemistry: CD30+, CD15+, PAX5+, CD20 variable
- PET-CT for staging and response assessment
- Bone marrow biopsy if advanced stage or cytopenias
Staging (Ann Arbor System)
- Stage I–IV based on nodal/extranodal spread
- A = no B symptoms, B = presence of B symptoms
- Bulky disease = mass >10 cm or mediastinal mass >1/3 thoracic diameter
Treatment Regimens
First-line:
- ABVD: doxorubicin, bleomycin, vinblastine, dacarbazine
- Given every 28 days x 4–6 cycles
- A+AVD (brentuximab + doxorubicin, vinblastine, dacarbazine) – for advanced-stage, especially CD30+
- BEACOPP: escalated in high-risk patients (more toxic)
Relapsed/Refractory HL
- Salvage chemo (e.g., ICE, DHAP, GDP) followed by autologous stem cell transplant (ASCT)
- Brentuximab vedotin (anti-CD30 ADC)
- Checkpoint inhibitors: nivolumab, pembrolizumab (especially post-ASCT)
Key Toxicities to Monitor
- Doxorubicin → cardiotoxicity
- Bleomycin → pulmonary toxicity (monitor DLCO, avoid in older adults or lung disease)
- Vinblastine → neuropathy, constipation
- Brentuximab vedotin → neuropathy, neutropenia
- Myelosuppression, secondary malignancies
Monitoring
- CBC, renal/hepatic panels
- Pulmonary function (bleomycin)
- Ejection fraction (doxorubicin)
- Interim PET-CT after 2 cycles (Deauville score)
- Long-term: secondary malignancy, infertility, hypothyroidism (after neck radiation), cardiopulmonary toxicity
Prognosis
- Highly curable with frontline therapy
- Early-stage: >90% cure rate
- Advanced-stage: ~70–80%
- Poor prognostic markers: B symptoms, bulky disease, high ESR, extranodal involvement

