Votrient (pazopanib)

Indications for Prior Authorization

Votrient (pazopanib)
  • For diagnosis of Renal Cell Carcinoma (RCC)
    Indicated for the treatment of patients with advanced renal cell carcinoma (RCC).

  • For diagnosis of Soft tissue sarcoma (STS)
    Indicated for the treatment of adults with advanced soft tissue sarcoma (STS) who have received prior chemotherapy.

    Limitation of Use: The efficacy of Votrient for the treatment of patients with adipocytic STS or gastrointestinal stromal tumors has not been demonstrated.

Criteria

Brand Votrient, Generic pazopanib*

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)
For diagnosis of Renal Cell Carcinoma (RCC)

  • Diagnosis of renal cell carcinoma
  • AND
  • One of the following: [2]
    • Disease has relapsed
    • Diagnosis of stage IV disease
    AND
  • Trial or intolerance to generic pazopanib (applies to brand Votrient only)
  • AND
  • One of the following: [2]
    • One of the following:
      • Both of the following:
        • Used in the treatment of non-clear cell renal cell carcinoma
        • Trial and failure, contraindication or intolerance to generic sunitinib
        OR
      • For continuation of prior therapy
      OR
    • Patient has clear cell renal cell carcinoma
Brand Votrient, Generic pazopanib*

Prior Authorization (Reauthorization)

Length of Approval: 12 Month(s)
For diagnosis of Renal Cell Carcinoma (RCC)

  • Patient does not show evidence of progressive disease while on therapy
  • AND
  • Trial or intolerance to generic pazopanib (applies to brand Votrient only)
  • AND
  • One of the following:
    • One of the following:
      • Both of the following:
        • Used in the treatment of non-clear cell renal cell carcinoma
        • Trial and failure, contraindication or intolerance to generic sunitinib
        OR
      • For continuation of prior therapy
      OR
    • Patient has clear cell renal cell carcinoma
Brand Votrient, Generic pazopanib*

Prior Authorization (Initial Authorization)

Length of Approval: 12 Month(s)
For diagnosis of Soft tissue sarcoma (STS)

  • Diagnosis of advanced soft tissue sarcoma (STS) [4, A]
  • AND
  • Trial or intolerance to generic pazopanib (Applies to Brand Votrient only)
Brand Votrient, Generic pazopanib*

Prior Authorization (Reauthorization)

Length of Approval: 12 Month(s)
For diagnosis of Soft tissue sarcoma (STS)

  • Patient does not show evidence of progressive disease while on therapy
  • AND
  • Trial or intolerance to generic pazopanib (Applies to Brand Votrient only)
P & T Revisions

2026-04-01, 2025-12-09, 2025-03-03, 2024-02-19, 2023-11-23, 2023-06-22, 2023-06-08, 2023-03-21, 2023-03-21, 2022-08-01, 2022-03-02, 2021-09-27, 2021-05-25, 2021-04-13, 2020-03-12

  1. Votrient Prescribing Information. Novartis Pharmaceuticals. East Hanover, NJ. January 2024.
  2. National comprehensive cancer network (NCCN). Clinical practice guidelines in oncology. Kidney cancer v.1.2026. Available at: https://www.nccn.org/professionals/physician_gls/pdf/kidney.pdf. Accessed April 1, 2026.
  3. PALETTE: a randomized, double-blind, phase III trial of pazopanib versus placebo in patients (pts) with soft-tissue sarcoma (STS) whose disease has progressed during or following prior chemotherapy-An EORTC STBSG Global Network Study (EORTC 62072). Available at: www.asco.org/ascov2/Meetings/Abstracts?&vmview=abst_detail_view&confID=102&abstractID=83283. Accessed April 30, 2012.
  4. National comprehensive cancer network (NCCN). Clinical practice guidelines in oncology. Soft tissue sarcoma v.3.2026. Available at: http://www.nccn.org/professionals/physician_gls/PDF/sarcoma.pdf. Accessed April 1, 2026.

  1. Votrient is an active drug in anthracycline pretreated STS patients with an increase in median PFS of 13 weeks. [3]

  • 2026-04-01: 2026 Annual Review. Updated trial and failure criteria where applicable to standard verbiage with removal of "and failure". Operational note added. References updated.
  • 2025-12-09: Addition of new strength of generic. Added IL statute operational note.
  • 2025-03-03: 2025 Annual Review. Background updates only.
  • 2024-02-19: 2024 Annual Review
  • 2023-11-23: Addition of generic Votrient, PA applied.
  • 2023-06-22: Removed Oncology specialist requirement
  • 2023-06-08: Update for Soft Tissue Sarcoma to remove criterion that requires "patient received at least one prior chemotherapy."
  • 2023-03-21: Annual Review: Updated Soft Tissue Sarcoma criteria to remove listed chemotherapy examples.
  • 2023-03-21: COT allowance to support formulary strategy for non-clear cell renal cell carcinoma.
  • 2022-08-01: Guideline Update
  • 2022-03-02: No criteria changes, updated references.
  • 2021-09-27: Addition of EHB formulary to guideline, no changes to criteria
  • 2021-05-25: Addition of EHB formulary to guideline, no changes to criteria
  • 2021-04-13: 2021 Annual Review: no changes. Updated GPIs
  • 2020-03-12: Annual Review: updated background & references