Informations:
Erreur:
ID
22082
Description
Randomized, Open Label Multi-Center Study Comparing Cabazitaxel at 20 mg/m² and at 25 mg/m² Every 3 Weeks in Combination With Prednisone for the Treatment of Metastatic Castration Resistant Prostate Cancer Previously Treated With a Docetaxel-Containing Regimen Other drug name: Jevtana® Study Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT01308580 Sponsor: Sanofi
Lien
https://clinicaltrials.gov/ct2/show/NCT01308580
Mots-clés
Versions (1)
- 18/05/2017 18/05/2017 -
Téléchargé le
18 mai 2017
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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CRFs Cabazitaxel Prostate Cancer DRKS00006520 NCT01308580 Cycle 2
CRFs Cabazitaxel Prostate Cancer NCT01308580 Cycle 2
- StudyEvent: ODM
Similar models
CRFs Cabazitaxel Prostate Cancer NCT01308580 Cycle 2
- StudyEvent: ODM
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Date of visit
Item
Date of visit:
date
C1320303 (UMLS CUI [1])
Item Group
Vital Signs - Day 01 - Not applicable if already done within 8 days prior to infusion.
C0518766 (UMLS CUI-1)
Assessment Date
Item
Date performed:
date
C2985720 (UMLS CUI [1])
Body Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
Systolic Blood Pressure
Item
Systolic Blood Pressure
float
C0871470 (UMLS CUI [1])
Diastolic Blood Pressure
Item
Diastolic Blood Pressure
float
C0428883 (UMLS CUI [1])
Heart Rate
Item
Heart Rate
float
C0018810 (UMLS CUI [1])
CL Item
0 (1)
CL Item
1 (2)
CL Item
2 (3)
CL Item
3 (4)
CL Item
4 (5)
Item Group
Laboratory Tests Hematology - Repeat on Day 01, 08 and Day 15.
C0022885 (UMLS CUI-1)
C0474523 (UMLS CUI-2)
C0474523 (UMLS CUI-2)
Laboratory Test Date
Item
Date
text
C2826641 (UMLS CUI [1])
Hemoglobin
Item
Hemoglobin
text
C0019046 (UMLS CUI [1])
Platelets
Item
Platelet Count (Thrombocyte Count)
float
C0005821 (UMLS CUI [1])
White Blood Cell Count
Item
White Blood Cell Count (Leukocyte Count)
float
C0023508 (UMLS CUI [1])
Neutrophils
Item
Neutrophils
float
C0948762 (UMLS CUI [1])
Lymphocytes
Item
Lymphocytes
float
C0024264 (UMLS CUI [1])
Monocytes
Item
Monocytes
float
C0026473 (UMLS CUI [1])
Eosinophils
Item
Eosinophils
float
C0200638 (UMLS CUI [1])
Basophils
Item
Basophils
float
C0200641 (UMLS CUI [1])
Item Group
Laboratory Tests Biochemistry - Repeat on Day 08, 15 (Sodium, Potassium, Calcium, Phosphorus, Blood Urea Nitrogen, Magnesium, Creatinine)
C0022885 (UMLS CUI-1)
C0005477 (UMLS CUI-2)
C0005477 (UMLS CUI-2)
Laboratory Test Biochemistry Date
Item
Date
date
C2826641 (UMLS CUI [1,1])
C0005477 (UMLS CUI [1,2])
C0005477 (UMLS CUI [1,2])
Sodium
Item
Sodium
float
C0337443 (UMLS CUI [1])
Potassium
Item
Potassium
float
C0202194 (UMLS CUI [1])
Calcium
Item
Calcium
float
C0201925 (UMLS CUI [1])
Phosphorus
Item
Phosphorus
float
C0031705 (UMLS CUI [1])
Blood Urea Nitrogen
Item
Blood urea nitrogen
float
C0005845 (UMLS CUI [1])
Magnesium
Item
Magnesium
float
C0373675 (UMLS CUI [1])
Total Proteins
Item
Total Proteins
float
C0555903 (UMLS CUI [1])
Albumin
Item
Albumin
float
C0201838 (UMLS CUI [1])
Blood Glucose
Item
Glucose
float
C0202042 (UMLS CUI [1])
AST
Item
AST (SGOT - ASAT)
float
C0201899 (UMLS CUI [1])
AST: Upper Limit
Item
AST (SGOT - ASAT): Normal Range - Upper Limit
float
C0201899 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
C1519815 (UMLS CUI [1,2])
ALT
Item
ALT (SGPT - ALAT)
float
C0201836 (UMLS CUI [1])
ALT: Upper Limit
Item
ALT (SGPT - ALAT): Normal Range - Upper Limit
float
C0201836 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
C1519815 (UMLS CUI [1,2])
Alkaline Phosphatase
Item
Alkaline Phosphatase
float
C0201850 (UMLS CUI [1])
Alkaline Phosphatase: Upper Limit
Item
Alkaline Phosphatase: Normal Range - Upper Limit
float
C0201850 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
C1519815 (UMLS CUI [1,2])
Total Bilirubin
Item
Total Bilirubin
float
C0201913 (UMLS CUI [1])
Total Bilirubin: Upper Limit
Item
Total Bilirubin: Normal Range - Upper Limit
float
C0201913 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
C1519815 (UMLS CUI [1,2])
Creatinine
Item
Creatinine
float
C0201976 (UMLS CUI [1])
Creatinine
Item
Creatinine: Normal Range - Upper Limit
float
C0201976 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
C1519815 (UMLS CUI [1,2])
Lactate Dehydrogenase
Item
Lactate Dehydrogenase
float
C0202113 (UMLS CUI [1])
Lactate Dehydrogenase: Upper Limit
Item
Lactate Dehydrogenase: Normal Range - Upper Limit
float
C0202113 (UMLS CUI [1,1])
C1519815 (UMLS CUI [1,2])
C1519815 (UMLS CUI [1,2])
Date of ECG
Item
Date performed:
date
C2826640 (UMLS CUI [1])
CL Item
Normal (Normal)
CL Item
Abnormal (Abnormal)
ECG finding abnormal
Item
Interpretation - If abnormal, clinically significant?
boolean
C0438154 (UMLS CUI [1,1])
C2826279 (UMLS CUI [1,2])
C2826279 (UMLS CUI [1,2])
Item Group
Medication - Pre Medication: Record all medications that the subject has taken prior to the Day 01 study treatment as premedication.
C0033045 (UMLS CUI-1)
Medication
Item
Drug/Medication (Brand or generic name)
text
C0013227 (UMLS CUI [1])
CL Item
Prophylaxis (Prophylaxis)
Total daily dose
Item
Dosage (Total daily dose)
float
C2348070 (UMLS CUI [1])
Dose Unit
Item
Dose Unit
text
C2826646 (UMLS CUI [1])
Administration Route
Item
Route
text
C0013153 (UMLS CUI [1])
Premedication: Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1,1])
C0033045 (UMLS CUI [1,2])
C0033045 (UMLS CUI [1,2])
Premedication: End Date
Item
End Date
date
C0806020 (UMLS CUI [1,1])
C0033045 (UMLS CUI [1,2])
C0033045 (UMLS CUI [1,2])
Item Group
Investigational Product Administration - Prednisone/ Prednisolone
C0304229 (UMLS CUI-1)
C1533734 (UMLS CUI-2)
C0032952 (UMLS CUI-3)
C1533734 (UMLS CUI-2)
C0032952 (UMLS CUI-3)
Prednisone: Intended Daily Dose
Item
Intended Daily Dose
float
C0032952 (UMLS CUI [1,1])
C1283828 (UMLS CUI [1,2])
C2348070 (UMLS CUI [1,3])
C1283828 (UMLS CUI [1,2])
C2348070 (UMLS CUI [1,3])
Prednisone: Actual Total Dose
Item
Actual Total Dose
float
C0032952 (UMLS CUI [1,1])
C3174092 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,2])
Prednisone: Number of day with no intake
Item
Number of day with no intake
float
C0032952 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,3])
C0332453 (UMLS CUI [1,4])
C0449788 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,3])
C0332453 (UMLS CUI [1,4])
Item Group
Investigational Product Administration - Cabazitaxel
C0304229 (UMLS CUI-1)
C1533734 (UMLS CUI-2)
C2830183 (UMLS CUI-3)
C1533734 (UMLS CUI-2)
C2830183 (UMLS CUI-3)
Item
Scheduled Period
text
C2830183 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,2])
CL Item
Day 01 (Day 01)
Cabazitaxel: Batch Number
Item
Batch Number
text
C2830183 (UMLS CUI [1,1])
C3641829 (UMLS CUI [1,2])
C3641829 (UMLS CUI [1,2])
Cabazitaxel: Start Date
Item
Start Date
date
C2830183 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
Cabazitaxel: Intended Dose
Item
Intended Dose
float
C2830183 (UMLS CUI [1,1])
C1283828 (UMLS CUI [1,2])
C2348070 (UMLS CUI [1,3])
C1283828 (UMLS CUI [1,2])
C2348070 (UMLS CUI [1,3])
Item
Administration Route
text
C2830183 (UMLS CUI [1,1])
C0013153 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,2])
CL Item
IV (IV)
Cabazitaxel: Actual Dose
Item
Actual Dose
float
C2830183 (UMLS CUI [1,1])
C3174092 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,2])
Item Group
If dose interrupted and readministered, please report the information below: Cabazitaxel
C1512900 (UMLS CUI-1)
C2830183 (UMLS CUI-2)
C2830183 (UMLS CUI-2)
Interruption Cabazitaxel: Scheduled Period
Item
Scheduled Period
text
C1512900 (UMLS CUI [1,1])
C2830183 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C2830183 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
Interruption Cabazitaxel: Batch Number
Item
Batch Number
text
C1512900 (UMLS CUI [1,1])
C2830183 (UMLS CUI [1,2])
C3641829 (UMLS CUI [1,3])
C2830183 (UMLS CUI [1,2])
C3641829 (UMLS CUI [1,3])
Interruption Cabazitaxel: Start Date
Item
Start Date
date
C1512900 (UMLS CUI [1,1])
C2830183 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C2830183 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
Item
Administration Route
text
C1512900 (UMLS CUI [1,1])
C2830183 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
C2830183 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
CL Item
IV (IV)
Interruption Cabazitaxel: Actual Dose
Item
Actual Dose
float
C1512900 (UMLS CUI [1,1])
C2830183 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,3])
C2830183 (UMLS CUI [1,2])
C3174092 (UMLS CUI [1,3])
Item Group
Circulating free plasma DNA - Blood Sampling
C4289789 (UMLS CUI-1)
C0005834 (UMLS CUI-2)
C0005834 (UMLS CUI-2)
(Circulating free plasma DNA: Date of Sample
Item
Date of Sample
date
C4289789 (UMLS CUI [1,1])
C1317250 (UMLS CUI [1,2])
C1317250 (UMLS CUI [1,2])
Macroscopic Hematuria
Item
Does the patient experience Macroscopic Hematuria during this cycle?
boolean
C0473237 (UMLS CUI [1])
Item
If YES, specify the cause:
text
C0473237 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,2])
CL Item
Local infection* (Local infection*)
CL Item
Bladder mucositis (non infectious)* (Bladder mucositis (non infectious)*)
CL Item
Local progression/ obstruction** (Local progression/ obstruction**)
CL Item
Anticoagulation/ Aspirin therapy** (Anticoagulation/ Aspirin therapy**)
CL Item
Thrombocytopenia** (Thrombocytopenia**)
CL Item
No cause identified** (No cause identified**)
CL Item
Stones* (Stones*)
CL Item
Non steroid anti-inflammatory drug** (Non steroid anti-inflammatory drug**)
CL Item
Other (Other)
Macroscopic Hematuria: Cause Specification
Item
If YES and OTHER, specify:
text
C0473237 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C0015127 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
Macroscopic Hematuria: Examination
Item
Did you perform specific exams to document the cause?
boolean
C0473237 (UMLS CUI [1,1])
C0582103 (UMLS CUI [1,2])
C0582103 (UMLS CUI [1,2])
Item Group
Tumor Assessment - Recist 1.1 (to follow until radiological progression) - Target Lesion (Previously identified). Note: If new lesion appears, please report it on the specific page "Tumor assessment (new lesion)".
C3889740 (UMLS CUI-1)
C2986546 (UMLS CUI-2)
C2986546 (UMLS CUI-2)
Target Lesion Number
Item
Lesion Number - The Lesion number should be entered and saved to display "Lesion location" and "Lesion Description (Subsite). The lesion number entered should be similar to the lesion number from "Target Lesion (at Baseline)".
float
C0449791 (UMLS CUI [1,1])
C2986546 (UMLS CUI [1,2])
C2986546 (UMLS CUI [1,2])
Target Lesion Location
Item
Lesion Location
text
C0450429 (UMLS CUI [1,1])
C2986546 (UMLS CUI [1,2])
C2986546 (UMLS CUI [1,2])
Target Lesion Description
Item
Lesion Description (Subsite)
text
C0678257 (UMLS CUI [1,1])
C2986546 (UMLS CUI [1,2])
C2986546 (UMLS CUI [1,2])
Target Lesion Assessment Date
Item
Date of Assessment
date
C2986546 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
C2985720 (UMLS CUI [1,2])
Target Lesion Method of Measurement
Item
Method of Tumor Measurement
text
C1299991 (UMLS CUI [1,1])
C2986546 (UMLS CUI [1,2])
C2986546 (UMLS CUI [1,2])
Target Lesion Diameter
Item
Measurement of Target Lesion: Diameter
float
C2986546 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,2])
Item Group
Tumor Assessment - Recist 1.1 (to follow until radiological progression) - Non-Target Lesion (Previously identified). Note: If new lesion appears, please report it on the specific page "Tumor assessment (new lesion)".
C3889740 (UMLS CUI-1)
C2986547 (UMLS CUI-2)
C2986547 (UMLS CUI-2)
Non-Target Lesion Assessment Date
Item
Date of Assessment
date
C2985720 (UMLS CUI [1,1])
C2986547 (UMLS CUI [1,2])
C2986547 (UMLS CUI [1,2])
Item
Overall Response of Non-Target Lesions:
text
C3272903 (UMLS CUI [1,1])
C2986547 (UMLS CUI [1,2])
C2986547 (UMLS CUI [1,2])
CL Item
CR (CR)
CL Item
Non CR/Non PD (Non CR/Non PD)
CL Item
PD (PD)
CL Item
NE (NE)
Overall Response of Non-Target Lesion Specification
Item
If Response is NE, Please Specify the Reason:
text
C3272903 (UMLS CUI [1,1])
C2986547 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C2986547 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
Non-Target Lesion Progressive Disease Location
Item
If Response is PD, Please Specify the Concerned Non-Target Lesion(s) Below:
text
C2986547 (UMLS CUI [1,1])
C1335499 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,3])
C1335499 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,3])
Item Group
Tumor Assessment - New Lesion
C3889740 (UMLS CUI-1)
C2986548 (UMLS CUI-2)
C2986548 (UMLS CUI-2)
New Lesion Location
Item
Lesion Location
text
C2986548 (UMLS CUI [1,1])
C0450429 (UMLS CUI [1,2])
C0450429 (UMLS CUI [1,2])
New Lesion Description
Item
New Lesion Description (Specify Exact Location)
text
C2986548 (UMLS CUI [1,1])
C0678257 (UMLS CUI [1,2])
C0678257 (UMLS CUI [1,2])
New Lesion Assessment Date
Item
Date of Assessment
date
C2986548 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
C2985720 (UMLS CUI [1,2])
New Lesion Method of Measurement
Item
Method of Tumor Measurement
text
C2986548 (UMLS CUI [1,1])
C1299991 (UMLS CUI [1,2])
C1299991 (UMLS CUI [1,2])
Bone Scan Hot Spot
Item
In case of Bone scan done, indicate the total number of Hot spots:
float
C0203668 (UMLS CUI [1,1])
C0203637 (UMLS CUI [1,2])
C0203637 (UMLS CUI [1,2])
Item Group
Tumor Markers - to follow until PSA progression - to be performed prior to the next study drug infusion.
C0041365 (UMLS CUI-1)
Tumor Markers: Assessment Date
Item
Date of evaluation
date
C0041365 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
C2985720 (UMLS CUI [1,2])
CL Item
PSA (PSA)
Tumor Markers: PSA Test Value
Item
PSA Test Value
float
C0041365 (UMLS CUI [1,1])
C0201544 (UMLS CUI [1,2])
C1275372 (UMLS CUI [1,3])
C0201544 (UMLS CUI [1,2])
C1275372 (UMLS CUI [1,3])
Tumor Markers: PSA Test Unit
Item
PSA Test: Unit
text
C0041365 (UMLS CUI [1,1])
C0201544 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
C0201544 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
Tumor Markers: PSA Test Lower Limit
Item
PSA Test: Normal Range - Lower Limit
text
C0041365 (UMLS CUI [1,1])
C0201544 (UMLS CUI [1,2])
C1518030 (UMLS CUI [1,3])
C0201544 (UMLS CUI [1,2])
C1518030 (UMLS CUI [1,3])
Tumor Markers: PSA Test Upper Limit
Item
PSA Test: Normal Range - Upper Limit
text
C0041365 (UMLS CUI [1,1])
C0201544 (UMLS CUI [1,2])
C1519815 (UMLS CUI [1,3])
C0201544 (UMLS CUI [1,2])
C1519815 (UMLS CUI [1,3])
Item Group
Present Pain Intensity and Analgesic Questionnaire for Cancer Pain (to follow until the first documented progression).
C0596240 (UMLS CUI-1)
C0034394 (UMLS CUI-2)
C0034394 (UMLS CUI-2)
Cancer Pain Questionnaire: Complete
Item
Was the Patient questionnaire completed for this visit?
boolean
C0596240 (UMLS CUI [1,1])
C0034394 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
C0034394 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
Item
If NO, please specify the primary reason:
text
C0596240 (UMLS CUI [1,1])
C0034394 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,3])
C0034394 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,3])
CL Item
Subject is unable due to toxicity disease (Subject is unable due to toxicity disease)
CL Item
Failure to distribute the questionnaire (Failure to distribute the questionnaire)
CL Item
Patient refusal (Patient refusal)
CL Item
Death (Death)
CL Item
Patient did not wish to show up (Patient did not wish to show up)
CL Item
Translation not available (Translation not available)
CL Item
Other (Other)
Cancer Pain Questionnaire: Primary Reason Specification
Item
If NO and OTHER, Specify:
text
C0596240 (UMLS CUI [1,1])
C0034394 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C0034394 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
Pain Assessment: Date
Item
If YES, Please complete the PAIN ASSESSMENT below: Date Corresponds to current cycle (7 days prior to dosing Day 1) Date
date
C1161170 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
C2985720 (UMLS CUI [1,2])
Present Pain Intensity
Item
If YES, Please complete the PAIN ASSESSMENT below: Date Corresponds to current cycle (7 days prior to dosing Day 1) Present Pain Intensity
float
C1320357 (UMLS CUI [1])
Analgesic Score
Item
If YES, Please complete the PAIN ASSESSMENT below: Date Corresponds to current cycle (7 days prior to dosing Day 1) Analgesic Score
text
C3202977 (UMLS CUI [1,1])
C0449820 (UMLS CUI [1,2])
C0449820 (UMLS CUI [1,2])
CL Item
Not evaluable (Not evaluable)
CL Item
Previously reported progression (Previously reported progression)
CL Item
No progression (No progression)
CL Item
Progression (please specify the assessment) (Progression (please specify the assessment))
Item
Disease Status: Progression - please specify the assessment:
text
C1335499 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,2])
Code List
Disease Status: Progression - please specify the assessment:
CL Item
Tumor assessment (Tumor assessment)
CL Item
PSA (PSA)
CL Item
Pain (Pain)
Item Group
FACT P Questionnaire (to follow until the first documented progression).
C3641634 (UMLS CUI-1)
FACT P Questionnaire
Item
Was the assessment performed at this visit?
boolean
C3641634 (UMLS CUI [1])
Item
If NO, please specify the primary reason:
text
C1549995 (UMLS CUI [1,1])
C3641634 (UMLS CUI [1,2])
C3641634 (UMLS CUI [1,2])
CL Item
Subject is unable due to toxicity disease (Subject is unable due to toxicity disease)
CL Item
Failure to distribute the questionnaire (Failure to distribute the questionnaire)
CL Item
Patient refusal (Patient refusal)
CL Item
Death (Death)
CL Item
Patient did not wish to show up (Patient did not wish to show up)
CL Item
Translation not available (Translation not available)
CL Item
Other (Other)
FACT P Questionnaire: Primary Reason Specification
Item
If OTHER, Specify:
text
C1549995 (UMLS CUI [1,1])
C3641634 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
C3641634 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
FACT P Questionnaire: Date
Item
If YES, Please indicate how true each statement has been for the patient during the past 7 days: Date performed
date
C0011008 (UMLS CUI [1,1])
C1549995 (UMLS CUI [1,2])
C1549995 (UMLS CUI [1,2])
Item Group
FACT P Questionnaire - Physical Well-Being: If YES, Please indicate how true each statement has been for the patient during the past 7 days.
C0517226 (UMLS CUI-1)
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item
Because of my physical condition, I have trouble meeting the needs of my family
text
C4287855 (UMLS CUI [1])
Code List
Because of my physical condition, I have trouble meeting the needs of my family
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Somewhat (Somewhat)
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Very Much (Very Much)
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I am bothered by side effects of treatment.
text
C4289375 (UMLS CUI [1])
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Somewhat (Somewhat)
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Somewhat (Somewhat)
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A little bit (A little bit)
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Not answered (Not answered)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item Group
FACT P Questionnaire - Social/ Family Well-Being: If YES, Please indicate how true each statement has been for the patient during the past 7 days.
C3476515 (UMLS CUI-1)
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item
I get emotional support from my friends.
text
C0600015 (UMLS CUI [1,1])
C0079382 (UMLS CUI [1,2])
C0079382 (UMLS CUI [1,2])
CL Item
A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Somewhat (Somewhat)
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Item
My family has accepted my illness.
text
C0278069 (UMLS CUI [1,1])
C0015576 (UMLS CUI [1,2])
C0015576 (UMLS CUI [1,2])
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A little bit (A little bit)
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Not answered (Not answered)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item
I am satisfied with my family communication about my illness.
text
C2984054 (UMLS CUI [1])
Code List
I am satisfied with my family communication about my illness.
CL Item
A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item
I feel close to my partner (or the person who is my main support).
text
C2984059 (UMLS CUI [1])
Code List
I feel close to my partner (or the person who is my main support).
CL Item
A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item
(If the patient prefers not to answer to the following question, please tick for this question NOT ANSWERED.) I am satisfied with my sex life.
text
C2984060 (UMLS CUI [1])
Code List
(If the patient prefers not to answer to the following question, please tick for this question NOT ANSWERED.) I am satisfied with my sex life.
CL Item
A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item Group
FACT P Questionnaire - Emotional Well-Being: If YES, Please indicate how true each statement has been for the patient during the past 7 days.
C2984554 (UMLS CUI-1)
CL Item
A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item
I am losing hope in the fight against my illness.
text
C2984056 (UMLS CUI [1])
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Somewhat (Somewhat)
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A little bit (A little bit)
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Not answered (Not answered)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Item
I worry that my condition will get worse.
text
C2984075 (UMLS CUI [1])
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item Group
FACT P Quesionnaire - Functional Well-Being: If YES, Please indicate how true each statement has been for the patient during the past 7 days.
C3483376 (UMLS CUI-1)
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item
I am content with the quality of my life right now.
text
C0034380 (UMLS CUI [1])
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item Group
FACT P Questionnaire - Additional Concerns: If YES, Please indicate how true each statement has been for the patient during the past 7 days.
C3482667 (UMLS CUI-1)
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A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
Item
I have aches and pains that bother me.
text
C3830278 (UMLS CUI [1,1])
C0030193 (UMLS CUI [1,2])
C0030193 (UMLS CUI [1,2])
CL Item
A little bit (A little bit)
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Not answered (Not answered)
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Item
I have certain parts of my body where I experience pain.
text
C3641636 (UMLS CUI [1])
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A little bit (A little bit)
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Not answered (Not answered)
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Somewhat (Somewhat)
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Item
My pain keeps me from doing things I want to do.
text
C3641680 (UMLS CUI [1])
Code List
My pain keeps me from doing things I want to do.
CL Item
A little bit (A little bit)
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Not answered (Not answered)
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Not at all (Not at all)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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A little bit (A little bit)
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A little bit (A little bit)
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Not answered (Not answered)
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Item
My problems with urinating limit my activities.
text
C3641641 (UMLS CUI [1])
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A little bit (A little bit)
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Not answered (Not answered)
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Somewhat (Somewhat)
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Very Much (Very Much)
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A little bit (A little bit)
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Not answered (Not answered)
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Quite a bit (Quite a bit)
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Somewhat (Somewhat)
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Very Much (Very Much)
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