Status:

NOT_YET_RECRUITING

Cabo-POLARIS : A Trial to Evaluate Cabozantinib Among Haemodialysied Patients

Lead Sponsor:

Centre Hospitalier Universitaire de Besancon

Conditions:

Cancer of Kidney

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

Among patients with renal cell carcinoma (RCC), 2.7 to 4.7 % of patients are at risk of progressing to dialysis or transplantation after partial and radical nephrectomy respectively. Of note, similar ...

Eligibility Criteria

Inclusion

  • Main Inclusion Criteria:
  • Documented histological diagnosis of advanced or metastatic renal cell cancer with a clear-cell or papillary component.
  • Must have received at least one prior line of systemic therapy.
  • Undergoing haemodialysis for more than 3 months without major complications that might confound the results of the trial, or is not in the best interest of the participant to participate, in the opinion of the treating investigator
  • Recovery to baseline or ≤ Grade 1 CTCAE v.4.0 from toxicities related to any prior treatments, unless AE(s) are considered clinically nonsignificant by the investigator and/or stable on supportive therapy.
  • Age eighteen years or older on the day of consent.
  • Karnofsky Performance Status (KPS) score of ≥ 70%.
  • Adequate organ and marrow function.
  • Main exclusion Criteria:
  • Prior treatment with cabozantinib.
  • Kidney cancer without clear-cell or papillary component.
  • Receipt of any type of small molecule kinase inhibitor (including investigational kinase inhibitor) within 2 weeks before cabozantinib initiation.
  • Receipt of any type of anticancer antibody within 2 weeks before randomization. For investigational antibody the delay is 4 weeks.
  • 5 Major surgery within 4 weeks or major radiotherapy within 2 weeks prior to starting cabozantinib. Previous palliative radiotherapy (≤ 10 fractions) for metastatic lesions is permitted, provided that this has been completed at least 48 hours prior to starting cabozantinib. Subjects with clinically relevant ongoing complications from prior radiation therapy are not eligible. Subjects with clinically relevant ongoing complications from prior surgery are not eligible.
  • 6\. Known brain metastases or spinal compression unless adequately treated with radiotherapy and/or surgery (including radiosurgery) and stable for at least 6 weeks before randomization. Eligible subjects must be neurologically asymptomatic and without corticosteroid treatment at the time of randomization. Patients with a past history of meningeal carcinomatosis are not eligible.
  • 7\. The subject has uncontrolled, significant intercurrent or recent illness including, but not limited to, the following conditions:
  • 7a. Cardiovascular disorders
  • 7b Active infection requiring systemic treatment.
  • 7c. Gastrointestinal (GI) disorders including those associated with a high risk of perforation or fistula formation
  • 7d. Clinically significant haematuria, hematemesis, or haemoptysis of \> 0.5 teaspoon (2.5 ml) of red blood, or other history of significant bleeding (eg, pulmonary haemorrhage) within 3 months before randomization.
  • 7e. Cavitating pulmonary lesion(s) or known endobronchial disease manifestation.
  • 7f. Lesions invading major pulmonary blood vessels. 7g. Other clinically significant disorders.
  • 8\. Corrected QT interval \> 480 msec within 1 month before randomization. Three ECGs must be performed. If the average of these three consecutive results for QTcF is ≤ 480 msec, the subject meets eligibility in this regard.
  • 9\. - Existence of a past history of cancer within 3 years prior to inclusion into the study (excluding cured localized cancer such as non-melanomatous skin cancers, superficial bladder cancers, or in situ for breast or uterine cervical cancer, and localized prostate cancer without biochemical PSA relapse).

Exclusion

    Key Trial Info

    Start Date :

    June 1 2022

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    March 1 2027

    Estimated Enrollment :

    24 Patients enrolled

    Trial Details

    Trial ID

    NCT05241561

    Start Date

    June 1 2022

    End Date

    March 1 2027

    Last Update

    June 1 2022

    Active Locations (1)

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    Centre Hospitalier Universitaire de Besançon

    Besançon, France