Status:

ACTIVE_NOT_RECRUITING

Impact of Antihypertensive Therapy on Recurrence Risk of Ovarian Cancer for Bevacizumab-associated Hypertension

Lead Sponsor:

Groupe Hospitalier Pitie-Salpetriere

Collaborating Sponsors:

Dr Floriane Jochum, Principal Investigator

Institut Curie

Conditions:

Ovarian Cancer

Antiangiogenic-Associated Hypertension

Eligibility:

FEMALE

18+ years

Brief Summary

Antiangiogenic therapies like bevacizumab, have notably improved cancer treatment, including for gynecological cancers, by inhibiting the vascular endothelial growth factor and thus limiting tumor gro...

Detailed Description

Antiangiogenic therapies, such as bevacizumab, have significantly improved the treatment landscape of various cancers, including gynecological types. Bevacizumab is a humanized monoclonal IgG1 antibod...

Eligibility Criteria

Inclusion

  • women with newly ovarian cancer diagnosis (FIGO III to IV)
  • age over 18 years old at time of ovarian cancer diagnosis
  • diagnosed between January 1, 2011 and December 31, 2020
  • with debulking ovarian cancer surgery and adjuvant chemotherapy

Exclusion

  • not in the "Regime general" "Sécurité Sociale" reimbursement system
  • without standard chemotherapy protocol (carbotaxol every 3 weeks or weekly)
  • history of heart failure or heart surgery, cardiovascular infarction or any coronaropathy disease, cerebro-vascular disease, arteriopathy of the lower limb, within the year before ovarian cancer surgery. Patients with history of hypertension without any complications were not excluded.
  • bevacizumab initiation prior to debulking surgery
  • combination of antihypertensive classes prior bevaizumab or as the first-line hypertensive therapy of bevacizumab-associated hypertension
  • antihypertensive monotherapy from other classes than CCBs and ACEi (ARBs, beta-blockers, diuretics etc...) as the anti-hypertensive therapy. Therapy could be initiated before ovarian surgery.
  • Complementary analysis :
  • \- patients treated by ARBs

Key Trial Info

Start Date :

May 20 2024

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

August 31 2024

Estimated Enrollment :

9464 Patients enrolled

Trial Details

Trial ID

NCT06515678

Start Date

May 20 2024

End Date

August 31 2024

Last Update

July 26 2024

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Institut Curie

Paris, France, 75005

2

Pitié-Salpêtrière

Paris, France, 75013