What is the next treatment for a 14‑year‑old girl with Hodgkin lymphoma relapsed after ABVD?

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Last updated: February 15, 2026View editorial policy

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Next Treatment for Relapsed Hodgkin Lymphoma After ABVD

For this 14-year-old girl with Hodgkin lymphoma relapsed after ABVD, the next treatment should be 2-3 cycles of platinum-based salvage chemotherapy (DHAP, ICE, or IGEV) followed by high-dose chemotherapy with autologous stem cell transplantation (ASCT). 1, 2

Immediate Next Steps

Confirm True Relapse

  • Obtain histological confirmation via biopsy before proceeding with salvage therapy, particularly if progression occurs in new sites, to rule out misdiagnosis or transformation 3
  • This is mandatory before any salvage treatment begins 3

Salvage Chemotherapy Regimen Selection

Choose one of the following platinum-based regimens: 1, 2

  • DHAP (dexamethasone/high-dose ara-C/cisplatin) - particularly recommended since she was previously treated with ABVD and the cumulative doxorubicin dose makes cardiac toxicity a concern 2
  • ICE (ifosfamide/carboplatin/etoposide) - equally effective alternative 1, 2
  • IGEV (ifosfamide/gemcitabine/vinorelbine) - demonstrates good activity with low toxicity profile 1, 2

Administer 2-3 cycles of the chosen salvage regimen to reduce tumor burden and mobilize stem cells prior to transplantation 1, 2

Critical Treatment Goals

  • The primary goal is achieving FDG-PET negativity (Deauville score ≤3), which defines chemosensitivity and dramatically impacts post-ASCT outcomes 2, 3
  • Chemosensitive disease (at minimum partial response) is required to proceed to transplantation 3

Definitive Treatment: High-Dose Chemotherapy with ASCT

If salvage chemotherapy achieves chemosensitive disease, proceed immediately to high-dose chemotherapy followed by ASCT - this is the treatment of choice for relapsed Hodgkin lymphoma and offers the only potentially curative option 1, 3

Evidence Supporting This Approach

  • Randomized trials demonstrate 3-year event-free survival of 53-55% with ASCT versus only 10-34% with conventional chemotherapy alone 3, 4
  • Five-year failure-free survival reaches 40-45% with ASCT 5, 6
  • ASCT significantly improves freedom from treatment failure (55% at 3 years) compared to continued conventional chemotherapy (34%) 4

Post-ASCT Management

After ASCT, administer brentuximab vedotin consolidation - this is now standard for high-risk patients, which includes relapsed disease 3

If Residual Disease Persists

  • Consider radiotherapy to residual nodal disease after salvage therapy if chemosensitive but with residual masses 2

Regimens to AVOID in This Patient

Do NOT use the following: 2

  • BEACOPPescalated as salvage therapy - risk of exceeding critical cumulative anthracycline dose (she already received doxorubicin in ABVD), significant hematologic toxicity, and potential impairment of stem cell mobilization 2
  • Mini-BEAM or Dexa-BEAM - associated with significant toxic mortality 2
  • Dose-intensive sequential chemotherapy - does not improve prognosis compared to standard DHAP-based salvage 2

Special Considerations for Adolescent Patient

Age-Appropriate Factors

  • At 14 years old, she is well within the age range for aggressive salvage therapy and ASCT (guidelines specify patients up to 60 years) 1
  • Reproductive counseling is mandatory before salvage treatment because chemotherapy can cause permanent fertility damage 7
  • Pre-treatment cardiac and pulmonary function tests are required to identify patients at increased risk of complications 7

Prognosis

  • Despite relapse, the prognosis remains favorable with appropriate salvage therapy and ASCT 7
  • Achieving PET-negative status after salvage chemotherapy is the most important prognostic factor for post-transplant success 2, 3

If Refractory to Salvage Chemotherapy

If she fails to achieve chemosensitive disease after salvage chemotherapy, consider: 3

  • Single-agent brentuximab vedotin 3
  • Anti-PD-1 therapy (nivolumab or pembrolizumab) 3
  • Allogeneic stem cell transplantation in selected cases (though this remains experimental and should be conducted within clinical trials) 1, 3

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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