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Hodgkin lymphoma survival exceeds 90% in early-stage patients with modern therapy

Hodgkin lymphoma survival exceeds 90% in early-stage patients with modern therapy
Photo by Thomas Kinto / Unsplash
Key Takeaway
Consider that modern therapy yields >90% 5-year survival in early-stage Hodgkin lymphoma but long-term toxicities remain a concern.

This systematic review summarizes current outcomes and treatment paradigms in Hodgkin lymphoma. The authors report that 5-year survival rates in early-stage patients exceed 90%, and long-term remission rates in advanced-stage disease are above 75%. However, primary refractory disease occurs in 5%-10% of patients, and relapse rates range from 10% to 30%. These data reflect improvements with modern therapies including brentuximab vedotin and PD-1 inhibitors.

The review also highlights significant long-term toxicities, including secondary malignancies, cardiovascular disease, pulmonary fibrosis, and infertility. These adverse effects underscore the need for treatment de-escalation strategies and careful survivorship care.

The authors discuss paradigm shifts in treatment de-escalation, precision salvage approaches, the evolving role of transplantation, and the use of precision medicine tools. No specific limitations were noted in the review, but as a systematic review, the findings depend on the quality of included studies.

For clinicians, these results reinforce the high curability of Hodgkin lymphoma while emphasizing the importance of balancing efficacy with long-term toxicity. The review provides a comprehensive overview but does not offer new pooled effect estimates or comparative analyses.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
Hodgkin lymphoma (HL) is a B-cell–derived hematologic malignancy originating from germinal centre B cells. Owing to its remarkable sensitivity to chemotherapy and radiotherapy, HL has become one of the most curable adult malignancies. Over the past decades, treatment regimens such as ABVD and escalated BEACOPP, combined with radiotherapy, have achieved 5-year survival rates exceeding 90% in early-stage patients and long-term remission rates above 75% in advanced-stage disease. However, long-term toxicities associated with conventional therapies—including secondary malignancies, cardiovascular disease, pulmonary fibrosis, and infertility—have increasingly compromised survivors’ quality of life. Meanwhile, approximately 5%–10% of patients exhibit primary refractory disease, and 10%–30% eventually relapse.In recent years, the emergence of targeted and immunotherapeutic agents, particularly the anti-CD30 antibody–drug conjugate (brentuximab vedotin) and immune checkpoint inhibitors (e.g., PD-1 inhibitors), has profoundly reshaped the therapeutic landscape of HL. This review systematically summarises the epidemiological characteristics and biological foundations of HL, as well as the achievements and limitations of conventional therapies. We place particular emphasis on key clinical trial evidence in recent years and discuss paradigm shifts in four major areas: treatment de-escalation and toxicity reduction in frontline therapy, precision salvage strategies for relapsed/refractory HL, the evolving role of transplantation, and the application of precision medicine tools such as circulating tumour DNA (ctDNA) and molecular subtyping. We further explore how HL treatment is transitioning from a “cure-oriented” model focused solely on survival to a novel paradigm of “functional cure” that balances efficacy with long-term quality of life. We define “functional cure” as durable remission with minimal long−term toxicity, preserving organ function and quality of life—a unifying principle of modern HL management. Special attention is given to clinical decision-making in PD-1–exposed patients, emerging therapeutic targets, cellular therapies, and the growing role of real-world evidence. These insights aim to inform future individualised treatment strategies in HL.
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