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NCT00721513 · OUTCOME

Best Overall Response Rate

Docetaxel, Cisplatin, and Fluorouracil Followed By Cetuximab and Radiation Therapy in Treating Patients With Locally Advanced Head and Neck Cancer · Source last updated 2020-04-07

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

Measure
COUNT_OF_PARTICIPANTS
Unit
Participants
Interval / dispersion
Not reported
Time frame
up to 2 years

What was measured

Defined as rate of complete and partial responses (at least 30% decrease in the sum of the longest diameter of target lesions), measured by CT scan or MRI of the head and neck after completion of multimodality treatment with induction TPF (Docetaxel, cisplatin and fluorouracil) chemotherapy followed by combined ERT. We will use RECIST (Response Evaluation Criteria In Solid Tumors) (Therasse et al, 2000) for evaluation of response.

Groups in this outcome

TPFChemotherapy + Concomitant Cetuximab & RT

Taxotere/Cisplatinum/5-Fluorouracil (TPF) Chemotherapy Followed by Concomitant Cetuximab \& Radiation Therapy cetuximab cisplatin docetaxel fluorouracil computed tomography positron emission tomography quality-of-life assessment 3-dimensional conformal radiation therapy intensity-modulated radiation therapy

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

Analysis denominator · Participants

GroupSource count
TPFChemotherapy + Concomitant Cetuximab & RT20

Reported measurements

Source class 1

Complete response

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
TPFChemotherapy + Concomitant Cetuximab & RT5Not reportedNot reportedNot reportedNot reported

Partial response

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
TPFChemotherapy + Concomitant Cetuximab & RT10Not reportedNot reportedNot reportedNot reported

Progression of disease

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
TPFChemotherapy + Concomitant Cetuximab & RT4Not reportedNot reportedNot reportedNot reported

Stable disease

Values in Participants · Interval/dispersion: Not reported
GroupValueSpreadLowerUpperComment
TPFChemotherapy + Concomitant Cetuximab & RT1Not reportedNot reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        value
        5
      title
      Complete response
    2. measurements
      1. group Id
        OG000
        value
        10
      title
      Partial response
    3. measurements
      1. group Id
        OG000
        value
        4
      title
      Progression of disease
    4. measurements
      1. group Id
        OG000
        value
        1
      title
      Stable disease
denoms
  1. counts
    1. group Id
      OG000
      value
      20
    units
    Participants
description
Defined as rate of complete and partial responses (at least 30% decrease in the sum of the longest diameter of target lesions), measured by CT scan or MRI of the head and neck after completion of multimodality treatment with induction TPF (Docetaxel, cisplatin and fluorouracil) chemotherapy followed by combined ERT. We will use RECIST (Response Evaluation Criteria In Solid Tumors) (Therasse et al, 2000) for evaluation of response.
groups
  1. description
    Taxotere/Cisplatinum/5-Fluorouracil (TPF) Chemotherapy Followed by Concomitant Cetuximab \& Radiation Therapy cetuximab cisplatin docetaxel fluorouracil computed tomography positron emission tomography quality-of-life assessment 3-dimensional conformal radiation therapy intensity-modulated radiation therapy
    id
    OG000
    title
    TPFChemotherapy + Concomitant Cetuximab & RT
param Type
COUNT_OF_PARTICIPANTS
reporting Status
POSTED
time Frame
up to 2 years
title
Best Overall Response Rate
type
SECONDARY
unit Of Measure
Participants

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice