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    v1.0.31
    OpenPayerPolicy UpdatesPharmacy & Specialty DrugsClover Health Jevtana Prior Auth Policy | OpenPaye…
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    CurrentClover HealthPolicy C22983-A

    Jevtana (cabazitaxel) Coverage Criteria

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    This policy governs Clover Health prior authorization criteria for Jevtana (cabazitaxel) in patients with metastatic castration-resistant prostate cancer. It applies to providers requesting initiation or continuation of therapy.

    Policy Summary
    PayerClover Health
    PolicyJevtana (cabazitaxel) Coverage Criteria
    Policy CodePolicy C22983-A
    Change TypeNo material clinical or coverage changes
    Effective DateN/A
    Next Review DateN/A
    Key ActionSubmit prior authorization establishing the diagnosis, continuation status, treatment benefit and tolerability when applicable, and required prior-treatment history or intolerance/non-candidacy for initiation.
    SourceLink
    POLICY UPDATE CHANGES

    No material clinical or coverage changes in this revision.

    1Covered diagnosis
    3Specified prior therapies for initiation
    2Continuation benefit and safety requirements

    Coverage Criteria

    Continuation Therapy

    Covered when all of the following continuation requirements are met:

    Continuation therapy

    • Diagnosis: Metastatic castration-resistant prostate cancer
    • Current treatment: The patient is currently receiving therapy with the requested medication.
    • Treatment benefit: The patient is receiving benefit from therapy.

      No evidence of unacceptable toxicity and no evidence of disease progression while on the current regimen.

    Initiation Therapy

    Policy Summary
    PayerClover Health
    PolicyJevtana (cabazitaxel) Coverage Criteria
    Policy CodePolicy C22983-A
    Change TypeNo material clinical or coverage changes
    Effective DateN/A
    Next Review DateN/A
    Key ActionSubmit prior authorization establishing the diagnosis, continuation status, treatment benefit and tolerability when applicable, and required prior-treatment history or intolerance/non-candidacy for initiation.
    SourceLink
    On This Page
    Coverage CriteriaPrior Authorization and Provider RequirementsPolicy BackgroundJevtana InitiationJevtana ContinuationRequired Prior Treatment

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    For initiation, the diagnosis and both prior-treatment evaluation requirements must be met:

    Initiation therapy

    • Diagnosis: Metastatic castration-resistant prostate cancer
    • Previously treated with at least one

      • Docetaxel-containing regimen: Previously treated with a docetaxel-containing regimen.
      • Enzalutamide: Previously treated with enzalutamide (Xtandi).
      • Abiraterone: Previously treated with abiraterone (Zytiga).
    • Not a candidate for or intolerant to at least one

      • Docetaxel-containing regimen: Not a candidate for or intolerant to a docetaxel-containing regimen.
      • Enzalutamide: Not a candidate for or intolerant to enzalutamide (Xtandi).
      • Abiraterone: Not a candidate for or intolerant to abiraterone (Zytiga).

    Prior Authorization and Provider Requirements

    Prior Authorization

    Prior Authorization Required

    Jevtana requires prior authorization. For initiation or continuation requests, submit the patient's diagnosis, whether the patient is currently receiving Jevtana, evidence of treatment benefit, and applicable prior-treatment history and tolerability documentation.

    Documentation Required

    Prior Treatment and Intolerance or Non-Candidacy

    Document whether the patient was previously treated with any of the specified therapies and, when applicable, whether the patient was not a candidate for or was intolerant to any of them.

    • Docetaxel-containing regimen
    • Enzalutamide (Xtandi)
    • Abiraterone (Zytiga)
    Denial Risk

    Diagnosis, Continuation, and Treatment Benefit

    Approval requires documentation of metastatic castration-resistant prostate cancer. For continuation requests, confirm the patient is currently receiving Jevtana and is benefiting from therapy, with no unacceptable toxicity and no evidence of disease progression on the current regimen.

    • Diagnosis: metastatic castration-resistant prostate cancer
    • Continuation: patient is currently receiving the requested medication
    • Treatment benefit: no unacceptable toxicity and no disease progression
    Step Therapy

    Required Prior Therapy Evaluation

    Denial risk increases when the required prior-therapy evaluation has not been completed. Document whether the patient has previously received any of the following treatments: a docetaxel-containing regimen, enzalutamide, or abiraterone.

    • Docetaxel-containing regimen
    • Enzalutamide (Xtandi)
    • Abiraterone (Zytiga)

    Policy Background

    Jevtana (cabazitaxel) is evaluated for patients with metastatic castration-resistant prostate cancer. The policy distinguishes between initiation and continuation: initiation requires specified prior-treatment history and evaluation of candidacy or intolerance, while continuation requires that the patient is currently receiving Jevtana and continues to benefit without unacceptable toxicity or disease progression.

    Jevtana Initiation

    Jevtana Initiation

    Jevtana initiation requires both of the following:

    Initiation requirements

    • Previous treatment

      • Docetaxel-containing regimen: Previously treated with a docetaxel-containing regimen.
      • Enzalutamide: Previously treated with enzalutamide (Xtandi).
      • Abiraterone: Previously treated with abiraterone (Zytiga).
    • Non-candidacy or intolerance

      • Docetaxel-containing regimen: Not a candidate for or intolerant to a docetaxel-containing regimen.
      • Enzalutamide: Not a candidate for or intolerant to enzalutamide (Xtandi).
      • Abiraterone: Not a candidate for or intolerant to abiraterone (Zytiga).

    Jevtana Continuation

    Jevtana Continuation

    Jevtana continuation requires all of the following:

    Continuation requirements

    • Current therapy: The patient is currently receiving therapy with the requested medication.
    • Ongoing clinical benefit: The patient is receiving benefit from therapy.

      Benefit means no evidence of unacceptable toxicity and no evidence of disease progression while on the current regimen.