Sandbox: HCL therapy: Difference between revisions

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:* [[Interferon alpha]]
:* [[Interferon alpha]]
:* [[Vemurafenib]]
:* [[Vemurafenib]]
* The preferred drug for the initial treatment of hairy cell leukemia is either [[cladribine]] or [[pentostatin]].
* The preferred drug for the initial treatment of hairy cell leukemia could be either [[cladribine]] or [[pentostatin]].
* Hairy cell leukemia patients who demonstrate a complete response after initial medical therapy should be managed by follow-up and close observation for any signs of relapse.
* A complete response for therapy is defined by the following criteria:
:* Absence of disease symptoms
:* Absence of [[splenomegaly]] on physical exam
:* Recovery of the patients blood counts to the normal limits
:* Absence of malignant leukemic cells on blood smear or bone marrow aspiration

Revision as of 23:33, 29 October 2015

Overview

Medical Therapy

  • The mainstay of therapy for hairy cell leukemia patients is chemotherapy.
  • Asymptomatic hairy cell leukemia patients, with no indications for therapy, may be managed by observation and close follow-up.
  • Indications to initiate medical therapy among patients with hairy cell leukemia include:
  • The presence of systemic symptoms such as fever, night sweats, and significant weight loss
  • The presence of subcostal abdominal discomfort due splenic distension
  • Positive history of recurrent infections.
  • Hemoglobin concentration lower than 12 g/dl
  • Platelets count lower than 100,000/mcl
  • Absolute neutrophil count lower than 1000/mcl
  • Pharmacological agents used for the treatment of hairy cell leukemia patients include:
  • The preferred drug for the initial treatment of hairy cell leukemia could be either cladribine or pentostatin.
  • Hairy cell leukemia patients who demonstrate a complete response after initial medical therapy should be managed by follow-up and close observation for any signs of relapse.
  • A complete response for therapy is defined by the following criteria:
  • Absence of disease symptoms
  • Absence of splenomegaly on physical exam
  • Recovery of the patients blood counts to the normal limits
  • Absence of malignant leukemic cells on blood smear or bone marrow aspiration