RareWays is a research directory. It helps you understand the science. It is not medical advice. Always discuss your care options with your healthcare team.

Coverage: 2020-01-01 onwards, with up to 300 results per query from PubMed and Europe PMC and separate limits on other sources. This is a selected index, not a complete literature search.

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ICD ORPHA:391cHL

Classic Hodgkin Lymphoma

Classic Hodgkin lymphoma is a cancer of the lymphatic system, the network that helps the body fight infection. It is marked by abnormal Reed-Sternberg cells and usually appears as painless swollen lymph nodes, often in the neck, chest or armpits. Treatment usually involves chemotherapy, sometimes with radiotherapy or immunotherapy, and many people are cured.

This overview is general information, not an individual medical assessment. Research is selected automatically and may include mismatches. How we select and explain research.

458
Articles
155
Trials (13 AU)
Data refreshed
20 October 2026
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Common Questions

What is Classic Hodgkin Lymphoma?

Classic Hodgkin lymphoma is a cancer of the lymphatic system, the network that helps the body fight infection. It is marked by abnormal Reed-Sternberg cells and usually appears as painless swollen lymph nodes, often in the neck, chest or armpits. Treatment usually involves chemotherapy, sometimes with radiotherapy or immunotherapy, and many people are cured.

How many clinical trials are available for Classic Hodgkin Lymphoma?

RareWays currently indexes 155 clinical trials for Classic Hodgkin Lymphoma, of which 23 are actively recruiting. These counts cover indexed trials across countries, not just your country. An Australian site does not necessarily mean that site is recruiting. Check locations, eligibility and current availability with the study team.

Where does the research data for Classic Hodgkin Lymphoma come from?

RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is refreshed automatically every day. All articles and trials link directly to their original sources.

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