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NCT00565851 · OUTCOME

Progression Free Survival (Surgery Analysis)

Carboplatin, Paclitaxel and Gemcitabine Hydrochloride With or Without Bevacizumab After Surgery in Treating Patients With Recurrent Ovarian, Epithelial, Primary Peritoneal, or Fallopian Tube Cancer · Source last updated 2025-12-30

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

Measure
MEDIAN
Unit
Months
Interval / dispersion
95% Confidence Interval
Time frame
Radiographic assessment of disease (in patients with measurable and non-measurable disease) was conducted Every three months for two years and then every 6 months after completion of chemotherapy during the maintenance/surveillance phase.

What was measured

Progression-free survival was defined as the time from randomization to cancer progression as shown on radiography, according to the RECIST version 1.0 criteria, an increase in the CA125 level according to Gynecologic Cancer InterGroup (GCIG) criteria, global deterioration of health, or death from any cause.

Analysis population: All randomized patients who were eligible for the surgery analysis (data were combined and analyzed according to randomized surgical assignment, regardless of chemotherapy regimen, as pre-specified in the study protocol).

Groups in this outcome

No Cytoreductive Surgery

All patients enrolled in the study who did not receive cytoreductive surgery and included in the surgery analysis

Cytoreductive Surgery

All patients enrolled in the study who received secondary cytoreductive surgery and were included in the surgery analysis

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
No Cytoreductive Surgery245
Cytoreductive Surgery240

Reported measurements

Source class 1
Values in Months · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
No Cytoreductive Surgery16.2Not reported14.219.6Not reported
Cytoreductive Surgery18.9Not reported16.821.0Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        14.2
        upper Limit
        19.6
        value
        16.2
      2. group Id
        OG001
        lower Limit
        16.8
        upper Limit
        21.0
        value
        18.9
denoms
  1. counts
    1. group Id
      OG000
      value
      245
    2. group Id
      OG001
      value
      240
    units
    Participants
description
Progression-free survival was defined as the time from randomization to cancer progression as shown on radiography, according to the RECIST version 1.0 criteria, an increase in the CA125 level according to Gynecologic Cancer InterGroup (GCIG) criteria, global deterioration of health, or death from any cause.
dispersion Type
95% Confidence Interval
groups
  1. description
    All patients enrolled in the study who did not receive cytoreductive surgery and included in the surgery analysis
    id
    OG000
    title
    No Cytoreductive Surgery
  2. description
    All patients enrolled in the study who received secondary cytoreductive surgery and were included in the surgery analysis
    id
    OG001
    title
    Cytoreductive Surgery
param Type
MEDIAN
population Description
All randomized patients who were eligible for the surgery analysis (data were combined and analyzed according to randomized surgical assignment, regardless of chemotherapy regimen, as pre-specified in the study protocol).
reporting Status
POSTED
time Frame
Radiographic assessment of disease (in patients with measurable and non-measurable disease) was conducted Every three months for two years and then every 6 months after completion of chemotherapy during the maintenance/surveillance phase.
title
Progression Free Survival (Surgery Analysis)
type
SECONDARY
unit Of Measure
Months

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice