English Summary: Spanish-Language HCL Webinar with Dr. Jacqueline Barrientos
In May 2025, the Hairy Cell Leukemia Foundation proudly hosted our first fully Spanish-language educational webinar, led by renowned hematologist Dr. Jacqueline Barrientos from the Mount Sinai Medical Center in Miami. This event marked a significant milestone in our ongoing commitment to reach and support Spanish-speaking patients and families affected by hairy cell leukemia (HCL).
Dr. Barrientos delivered a clear, empathetic, and insightful presentation on HCL, covering key topics such as diagnosis, current treatment options, and the latest advances in targeted therapies. Below are the highlights from this valuable session:
Understanding the Basics of HCL
Hairy cell leukemia is a rare disease, accounting for only 1.4% of lymphomas and 2% of all leukemias.
Approximately 1,000 to 1,500 cases are diagnosed annually in the U.S. Many oncologists may see only one case in their entire career.
It primarily affects men between the ages of 55 and 60, though it can also occur in younger or older individuals. The male-to-female ratio is 4:1.
Diagnosis: Accuracy is Crucial
Diagnosis requires a bone marrow biopsy, as aspiration often yields insufficient information.
Flow cytometry is used to identify B-cell markers such as CD19, CD20, CD11c, CD25, CD103, among others.
The most important marker is the BRAF V600E mutation, present in about 90% of classic HCL cases.
Dr. Barrientos emphasized the importance of distinguishing between classic HCL and the variant form, which is more aggressive and requires a different therapeutic approach.
When to Start Treatment vs. Watch and Wait
Not all newly diagnosed patients require immediate treatment. Around 10% can begin with “active surveillance.”
Treatment is recommended when:
Hemoglobin falls below 11 g/dL
Neutrophils drop below 1,000
Platelets fall below 100,000
There are frequent infections, intense fatigue, fever, night sweats, weight loss, or an enlarged spleen
Recommended First-Line Treatments
First-line therapies include cladribine and pentostatin, both purine analogs.
Cladribine is given for five consecutive days, and rituximab is added weekly for eight weeks.
Dr. Barrientos emphasized that even with dose adjustments, patients can achieve complete remission.
Advances and Clinical Trials
The combination of Vemurafenib (a BRAF inhibitor) with Rituximab has shown remarkable efficacy in relapsed patients.
Clinical trials have shown response rates close to 100%.
The combination doubled complete remission rates compared to Vemurafenib alone.
Combinations with Obinutuzumab (a more potent monoclonal antibody than Rituximab) have also been studied.
While drugs like Ibrutinib have been evaluated, their efficacy is limited and side effects can be significant.
The immunotoxin Moxetumomab showed promise but was withdrawn from the market.
Evaluating Treatment Response
Bone marrow should not be evaluated earlier than 4 to 6 months after treatment.
Complete remission is defined as:
Normal blood counts.
No evidence of hairy cells in bone marrow or peripheral blood using standard stains.
Spleen size has diminished.
Achieving minimal residual disease (MRD) negativity has been associated with longer-lasting remission.
A Success Story: Personalization and Hope
Dr. Barrientos shared an inspiring case: a 72-year-old patient with advanced kidney disease was diagnosed with HCL during evaluation for a transplant. Unable to receive standard chemotherapy, he was treated with adjusted doses of Vemurafenib and Rituximab. He achieved complete remission, received his kidney transplant, and is now living cancer-free and without dialysis—a clear example of personalized and collaborative medicine.
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