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Related Concept Videos

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Treatment Resistent Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
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Related Experiment Video

Updated: May 27, 2026

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
12:40

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors

Published on: December 7, 2014

Decrease in JAK2 V617F allele burden is not a prerequisite to clinical response in patients with polycythemia vera.

Emil Kuriakose1, Katherine Vandris, Y Lynn Wang

  • 1Weill Cornell Medical College, Department of Medicine, Division of Hematology and Medical Oncology, New York, NY 10021, USA.

Haematologica
|November 22, 2011
PubMed
Summary
This summary is machine-generated.

A reduction in the JAK2(V617F) allele burden is not required for patients with polycythemia vera to achieve hematologic remission. Molecular response is not consistently accompanied by clinical response in polycythemia vera.

Related Experiment Videos

Last Updated: May 27, 2026

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
12:40

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors

Published on: December 7, 2014

Area of Science:

  • Hematology
  • Molecular Biology
  • Oncology

Background:

  • The JAK2(V617F) allele burden is a potential marker for monitoring polycythemia vera treatment response.
  • Its role as a prerequisite for hematologic remission remains unclear.

Purpose of the Study:

  • To determine if a reduction in the JAK2(V617F) allele burden is necessary for achieving hematologic remission in polycythemia vera patients undergoing cytoreductive therapy.

Main Methods:

  • A cohort of 73 polycythemia vera patients treated with interferon or non-interferon therapies were analyzed.
  • Hematologic response was assessed using Polycythemia Vera Study Group criteria.
  • Molecular response was evaluated using European Leukemia Net criteria for JAK2(V617F) allele burden reduction.

Main Results:

  • High rates of hematologic response were observed with both interferon (89.1%) and non-interferon (59.3%) treatments.
  • Molecular response rates were low across all treatment groups (15.2% for interferon, 7.4% for non-interferon).
  • There was poor statistical agreement between hematologic and molecular responses.

Conclusions:

  • Hematologic response in polycythemia vera is often not associated with a reduction in the JAK2(V617F) allele burden.
  • Quantitative changes in the JAK2(V617F) allele burden are not a mandatory requirement for clinical response in polycythemia vera.