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)

  1. Classical Hodgkin Lymphoma (cHL) (95%):
    • Nodular sclerosis (most common)
    • Mixed cellularity
    • Lymphocyte-rich
    • Lymphocyte-depleted
  2. 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

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:

Radiation therapy:

  • Often used in early-stage or bulky disease
  • Involved-site radiation (ISRT)

Relapsed/Refractory HL

Key Toxicities to Monitor

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
Synonyms
Hodgkin lymphoma's, HL
Links