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Clinical Trials/KCT0004506
KCT0004506
Recruiting
未知

Perfusion CT to Predict Progression-free Survival and Response Rate in Bevacizumab and Paclitaxel Treantment of Platinum-Resistant Persistent or Recurrent Epithelial Ovarian, Fallopian Tube, or Peritoneal Carcinoma

Seoul National University Hospital0 sites184 target enrollmentTBD
ConditionsNeoplasms

Overview

Phase
未知
Intervention
Not specified
Conditions
Neoplasms
Sponsor
Seoul National University Hospital
Enrollment
184
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional Study
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1 Registration to Step 0
  • 1\.1 Patient must be female \= 18 years of age.
  • 1\.2 Pateint must have epithelial ovarian, fallopian tube, or primary peritoneal cancer. This includes high\-grade serous ovarian cancer, endometroid, clear cell, mixed epithelial, undifferentiated carcinoma, transitional cell carcinoma histologies.
  • 1\.3 Patient must have suspected platinum\-resistant disease (disease progression \= 6 months of platinum therapy).
  • 1\.4 Patient must be expected to undergo therapy with bevacizumab in combination with paclitaxel at recommended standard of care doses if suspected recurrence is confirmed with imaging. Patient must be able and willing to provide written informed consent.
  • 1\.5 Patient must have a life expectancy of \= 3 months.3
  • 1\.6 Patient must have adequate bone marrow, coagulation, renal, and hepatic function; eGFR(glomerular filtration rate) calculation \= 60 mL/min/1\.73 m2 (within 28 days of screening CT submission)
  • 1\.7 Patient must demonstrate an ECOG(Eastern Cooperative Onocology Group) performance status of 0\-2\.
  • 2 Registration to Step 1
  • Note: The ACR(American College of Radiology) Imaging Core Lab will evaluate the potential target lesion once all required images are received and inform the site within five business days if patient is eligible and may be registered to Step 1 and scheduled for perfusion CT imaging. The local site will receive notification of eligibility via RAVE.

Exclusion Criteria

  • 1\.1 Patients with carcinosarcoma, non\-epithelial, low grade tumors, or tumors with low malignant potential are excluded.
  • 1\.2 Patient must not have undergone therapy with any VEGF monoclonal antibodies in the last twelve weeks. Patient must not have received any small molecule anti\-VEGF drug within the previous 4 weeks.
  • 1\.3 Patient must not have undergone major surgery or radiotherapy to the pelvis or abdomen within previous 4 weeks.
  • 1\.4 Patients must not have known contraindications to bevacizumab, including but not limited to abdominal fistula, GI perforation, intra\-abdominal abscess, thrombotic or hemorrhagic disorders, uncontrolled hypertension or active clinically significant cardiovascular disease, non\-healing wound, ulcer, or bone fracture within previous 4 weeks.
  • 1\.5 Patient must not have untreated or symptomatic CNS(Central nervous system) metastasis.
  • 1\.6 Patient must not have another active (within past 3 years) or concurrent malignancy. Resected basal cell skin cancer is allowed within past 3 years.
  • 1\.7 Patient must not have contraindication to iodinated contrast.

Outcomes

Primary Outcomes

Not specified

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