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Comparison · NCT04033991-b46c07cc

Participants With mRCC and/or aRCC: First Line Sunitinib Treatment vs Participants With mRCC and/or aRCC: Second Line Axitinib Treatment: Number of Participants With Karnofsky Performance Status (KPS) Less Than 80 Percent (%)

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Participants With mRCC and/or aRCC: First Line Sunitinib Treatment vs Participants With mRCC and/or aRCC: Second Line Axitinib Treatment: Number of Participants With Karnofsky Performance Status (KPS) Less Than 80 Percent (%). Trial comparisons, record NCT04033991-b46c07cc. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04033991-b46c07cc

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1430.1180.173wilson
Risk in group 20.2310.1650.314wilson
Risk difference, group 1 minus group 2-0.0883-0.175-0.0158newcombe hybrid score
Risk ratio, group 1 over group 20.6180.4240.902log
Odds ratio, group 1 over group 20.5550.3440.895log
Number needed to treat, for one fewer participant with the outcome on Participants With mRCC and/or aRCC: First Line Sunitinib Treatment than on Participants With mRCC and/or aRCC: Second Line Axitinib Treatment
11.35.7263.4from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Participants With mRCC and/or aRCC: First Line Sunitinib Treatment
Participants who met the selection criteria, diagnosed with mRCC and/or aRCC, received sunitinib as first-line treatment from 2002 till 30 June 2018, according to normal routine healthcare practice in real-world setting, were included in this reporting arm. Data of these participants were derived from Christie NHS database.
89622OG000
Group 2Participants With mRCC and/or aRCC: Second Line Axitinib Treatment
Participants who met the selection criteria, diagnosed with mRCC and/or aRCC, received axitinib as second-line treatment from 2002 till 30 June 2018, according to normal routine healthcare practice in real-world setting, were included in this reporting arm. Data of these participants were derived from Christie NHS database.
28121OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Number of Participants With Karnofsky Performance Status (KPS) Less Than 80 Percent (%)
Description
KPS: used for rating participant activities of daily living on scale from 0-100, higher score = participant is better able to carry out daily activities. Score range: 100 = normal no complaints; no disease evidence, 90 = able to carry normal activity; minor signs/symptoms of disease, 80 = normal activity with effort; some signs/symptoms, 70 = cares for self; unable to carry on normal activity, 60 = requires occasional assistance, but able to care for most personal needs, 50 = requires considerable assistance and frequent medical care, 40 = disabled; requires special care, assistance, 30 = severely disabled; hospital admission is indicated although death not imminent, 20 = very sick; hospital admission necessary, 10 = moribund; fatal processes progressing rapidly and 0 = dead. The lower the score the worse is survival for most serious illnesses. Here, number of participants with KPS \<80% were reported.
Time frame
Baseline (data retrieved and observed retrospectively for approximately 1.2 years)
Population
Analysis population included all eligible participants with mRCC and/or aRCC, received sunitinib as first-line treatment and/or axitinib as second-line treatment from 2002 till 30 June 2018.

Source ClinicalTrials.gov

Trial

Title
Study of Patients With Metastatic and/or Advanced Renal Cell Carcinoma, Treated With Sunitinib/Axitinib.
NCT number
NCT04033991
Phases
Conditions
Carcinoma, Renal Cell
Interventions
Sunitinib, Axitinib
Lead sponsor
Pfizer
Results first posted
2022-02-18

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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