ID
27984
Descrição
ADVANCED PROSTATE CANCER DATA COLLECTION Version 2.3.1 Revised: April 10th, 2017, International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ Conditions:All patients with advanced prostate cancer, either having metastatic disease or biochemical recurrence progressing after salvage treatment or ineligible for salvage treatment. Patients with biochemical recurrence treated with salvage therapy are referred to the localized prostate cancer set Treatment Approaches: Hormonal Therapy | Chemotherapy | Immunotherapy | Radiopharmaceuticals | Radiation | Interventions for Complications of Local Progression Questionnaires used in this form: Expanded Prostate Cancer Index Composite (EPIC-26) The EPIC-26 is free for all health care organizations, and a license is not needed. The scoring guide may be found at http://www.med.umich.edu/urology/research/EPIC/EPIC-26-Scoring-1.2007.pdf Utilization of Sexual Medications/Devices: The Utilization of Sexual Medications/Devices is free for all health care organizations, and a license is not needed. Refer to http:// dx.doi.org/10.1016/j.urology.2006.01.077 for more information
Link
Palavras-chave
Versões (4)
- 07/12/2017 07/12/2017 -
- 29/11/2018 29/11/2018 - Sarah Riepenhausen
- 29/11/2018 29/11/2018 - Sarah Riepenhausen
- 30/04/2020 30/04/2020 - Sarah Riepenhausen
Titular dos direitos
ICHOM
Transferido a
7 de dezembro de 2017
DOI
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Licença
Creative Commons BY-NC 3.0
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ICHOM Advanced Prostate Cancer
ICHOM Advanced Prostate Cancer
- StudyEvent: ODM
Descrição
Demographic factors
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical or patient-reported
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0421451
Descrição
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical reported RESPONSE OPTIONS: Numerical value of height in cm or in
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0005890
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Descrição
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical reported RESPONSE OPTIONS: Numerical value of weight in kg or lbs
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0005910
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Descrição
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported RESPONSE OPTIONS: Numerical value of height in cm or in
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0005890
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Descrição
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported RESPONSE OPTIONS: Numerical value of weight in kg or lbs
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0005910
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
text
Alias
- UMLS CUI [1]
- C0015031
Descrição
The level of schooling is defined in each country as per ISCED [International Standard Classification] INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0013658
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0024819
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0024819
Descrição
Baseline Clinical Factors
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical RESPONSE OPTIONS: Numerical value of hemoglobin level in g/L
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C0011900
Descrição
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0009488
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported RESPONSE OPTIONS: Ordinal values from 0 to 10, with 'No pain' marked at '0' and 'Worst pain imaginable' marked at '10'
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0582148
Descrição
A first degree relative is a father, brother, or son INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C1532320
Descrição
Baseline Tumor Factors
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical RESPONSE OPTIONS: Numerical value of PSA ng/mL
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0201544
Descrição
Pathologic staging preferred, if available cT0: No evidence of primary tumor cT1: if not able to select T1a, T1b or T1c: Clinically inapparent tumor neither palpable nor visible by imaging cT1a: Tumor incidental histologic finding in 5 percent or less of tissue resected cT1b: Tumor incidental histologic finding in more than 5 percent of tissue resected cT1c: Tumor identified by needle biopsy (eg, because of elevated PSA) cT2: if not able to select T2a, T2b or T2c: Tumor confined within prostate* cT2a: Tumor involves one-half of one lobe or less cT2b: Tumor involves more than one-half of one lobe but not both lobes cT2c: Tumor involves both lobes cT3: if not able to select T3a, T3b or T3c: Tumor extends through the prostate capsule cT3a: Extracapsular extension (unilateral or bilateral) cT3b: Tumor invades seminal vesicle(s) cT4: Tumor is fixed or invades adjacent structures other than seminal vesicles such as external sphincter, rectum, bladder, levator muscles, and/or pelvic wall cTX: Primary tumor cannot be assessed INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0600139
- UMLS CUI [1,2]
- C1300072
- UMLS CUI [1,3]
- C0205210
Descrição
Pathologic staging preferred, if available cNo: regional lymph node metastasis cN1: Metastasis in regional lymph node(s) cNX: Regional lymph nodes were not assessed INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0600139
- UMLS CUI [1,2]
- C0456532
- UMLS CUI [1,3]
- C0205210
Descrição
Pathologic staging preferred, if available pT2: if not able to select T2a, T2b or T2c: Organ confined pT2a: Unilateral, one-half of one side or less pT2b: Unilateral, involving more than one-half of side but not both sides pT2c: Bilateral disease pT3: if not able to select T3a, T3b: Extraprostatic extension pT3a: Extraprostatic extension or microscopic invasion of bladder neck pT3b: Seminal vesicle invasion pT4: Invasion of rectum, levator muscles, and/or pelvic wall pTX: Primary tumor cannot be assessed INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0600139
- UMLS CUI [1,2]
- C1300072
- UMLS CUI [1,3]
- C1521733
Descrição
Pathologic staging preferred, if available pN0: No positive regional nodes pN1: Metastases in regional node(s) pNX: Regional nodes not sampled INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0600139
- UMLS CUI [1,2]
- C0456532
- UMLS CUI [1,3]
- C1521733
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0332326
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on Gleason score (GLEASON) TIMING: Baseline REPORTING SOUCE: Clinical RESPONSE OPTIONS: 2-10
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0332326
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on Gleason score (GLEASON) TIMING: Baseline REPORTING SOUCE: Clinical RESPONSE OPTIONS: 2-10
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0332326
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0807944
Descrição
High burden is indicated as any of the following criteria (from: CHAARTED (randomized clinical trial in the US): - Visceral metastases (extranodal) - Bone metastases with at least 4 bone lesions OR at least 1 bone lesion outside of the vertebral column or pelvis. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0449279
Descrição
Treatment Factors
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0332152
- UMLS CUI [1,2]
- C0033573
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on prior prostatectomy (prostatectx) TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0332152
- UMLS CUI [1,2]
- C0033573
- UMLS CUI [1,3]
- C0011008
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0279134
- UMLS CUI [1,2]
- C1708063
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0279134
- UMLS CUI [1,2]
- C1706721
- UMLS CUI [2,1]
- C0279134
- UMLS CUI [2,2]
- C0085405
Descrição
Use of any of the following treatments to induce castrate levels of serum testosterone: 1. LHRH or GnRH agonist or antagonist 2. Bilateral orchiectomies INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0279492
Descrição
Any medication that treats the prostate cancer taken by mouth, through a vein, or injected, other than ADT INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C1515119
- UMLS CUI [1,2]
- C1514463
Descrição
Both anti-resorptive medications or denosumab are relevant INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0012544
- UMLS CUI [2]
- C3839270
Descrição
Treatment Variables
Descrição
INCLUSION CRITERIA: All patients TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0279492
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on Androgen Deprivation Therapy (ADTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0279492
- UMLS CUI [1,2]
- C0808070
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on Androgen Deprivation Therapy (ADTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0279492
- UMLS CUI [1,2]
- C0806020
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on Androgen Deprivation Therapy (ADTX), and no end date is entered (ADTXSTOPDATE) TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0279492
- UMLS CUI [1,2]
- C0549178
Descrição
INCLUSION CRITERIA: All patients TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0279025
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on hormonal therapy (HORMONTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0279025
- UMLS CUI [1,2]
- C0808070
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on hormonal therapy (HORMONTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0279025
- UMLS CUI [1,2]
- C0806020
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on hormonal therapy (HORMONTX), and no end date is entered (HORMONTXSTOPDATE) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0279025
- UMLS CUI [1,2]
- C0549178
Descrição
INCLUSION CRITERIA: All patients TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0392920
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on chemotherapy (CHEMOTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1302181
- UMLS CUI [1,2]
- C3173309
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on chemotherapy (CHEMOTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1302181
- UMLS CUI [1,2]
- C0806020
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on chemotherapy (CHEMOTX), and no end date is entered (CHEMOTXSTOPDATE) TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0549178
- UMLS CUI [1,2]
- C0392920
Descrição
INCLUSION CRITERIA: All patients TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0021083
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on immunotherapy (IMMUNOTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0021083
- UMLS CUI [1,2]
- C0808070
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on immunotherapy (IMMUNOTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0021083
- UMLS CUI [1,2]
- C0806020
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on immunotherapy (IMMUNOTX), and no end date is entered (IMMUNOTXSTOPDATE) TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0021083
- UMLS CUI [1,2]
- C0549178
Descrição
INCLUSION CRITERIA: All patients TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0182638
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on radiopharmaceuticals (RADIOPHARM) TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0182638
- UMLS CUI [1,2]
- C3173309
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on radiopharmaceuticals (RADIOPHARM) TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0182638
- UMLS CUI [1,2]
- C1531784
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on radiotherapy (RADIOTX), and no end date is entered (RADIOTXSTOPDATE) TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0182638
- UMLS CUI [1,2]
- C0549178
Descrição
Could be one of the following procedures: - TURP (transurethral resection of the prostate) - Ureteral stent - Percutaneous nephrostomy tube - Suprapubic catheter placement - Chronic foley catheter / self intermittent catheterization INCLUSION CRITERIA: All patients TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Multiple answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0184661
- UMLS CUI [1,2]
- C0027643
Descrição
INCLUSION CRITERIA: All patients If answered 'TURP' on interventions for complications due to local progression (LOCPROGTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0040771
- UMLS CUI [1,2]
- C0011008
Descrição
INCLUSION CRITERIA: All patients If answered 'ureteral stent' on interventions for complications due to local progression (LOCPROGTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0183518
- UMLS CUI [1,2]
- C0011008
Descrição
INCLUSION CRITERIA: All patients If answered 'percutaneous nephrostomy tube' on interventions for complications due to local progression (LOCPROGTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0564457
- UMLS CUI [1,2]
- C0011008
Descrição
INCLUSION CRITERIA: All patients If answered 'suprapubic catheter placement' on interventions for complications due to local progression (LOCPROGTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0150798
- UMLS CUI [1,2]
- C0011008
Descrição
INCLUSION CRITERIA: All patients If answered 'chronic foley catheter / self intermittent catheterization' on interventions for complications due to local progression (LOCPROGTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0179804
- UMLS CUI [1,2]
- C0011008
Descrição
INCLUSION CRITERIA: All patients TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0012544
- UMLS CUI [2]
- C1690432
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on bisphosphonates or denosumab (BISPHOSTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0012544
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [2,1]
- C1690432
- UMLS CUI [2,2]
- C0808070
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on bisphosphonates or denosumab (BISPHOSTX) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0012544
- UMLS CUI [1,2]
- C1690432
- UMLS CUI [1,3]
- C0806020
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on bisphosphonates or denosumab (BISPHOSTX), and no end date is entered (BISPHOSTXSTOPDATE) TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0012544
- UMLS CUI [1,2]
- C0549178
- UMLS CUI [2,1]
- C1690432
- UMLS CUI [2,2]
- C0549178
Descrição
Acute Complications of Treatment
Descrição
A CTCAE v 4 grace III complication or higher means that the patient had to be admitted to the hospital. See http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf for a list of domains and grades of complications INCLUSION CRITERIA: Patients with systemic therapy If answered 'yes' on chemotherapy, immunotherapy or hormonaltherapy (CHEMOTX or IMMUNOTX or HORMONTX) TIMING: Update at least annually REPORTING SOUCE: Clinical TYPE: Multiple answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C1516728
- UMLS CUI [1,3]
- C1515119
Descrição
INCLUSION CRITERIA: Patients with systemic therapy If answered 'Other' on CTCAE grade III-IV complications due to systemic therapy (excluding ADT) (COMPLSYS) TIMING: Update at least annually REPORTING SOUCE: Clinical RESPONSE OPTIONS: CTCAE grade III-IV complication due to systemic therapy (excluding ADT)
Tipo de dados
text
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C1516728
- UMLS CUI [1,3]
- C1515119
Descrição
INCLUSION CRITERIA: Patients with systemic therapy If answered Cytopenias on CTCAE grade III-IV complications due to systemic therapy (excluding ADT) (COMPLSYS) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0010828
- UMLS CUI [1,2]
- C0011008
Descrição
INCLUSION CRITERIA: Patients with systemic therapy If answered Infection on CTCAE grade III-IV complications due to systemic therapy (excluding ADT) (COMPLSYS) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009450
- UMLS CUI [1,2]
- C2316983
Descrição
INCLUSION CRITERIA: Patients with systemic therapy If answered Vomiting, diarrhea, constipation, other GI toxicity on CTCAE grade III-IV complications due to systemic therapy (excluding ADT) (COMPLSYS) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C0521362
- UMLS CUI [1,3]
- C0011008
Descrição
INCLUSION CRITERIA: Patients with systemic therapy If answered Neuropathy on CTCAE grade III-IV complications due to systemic therapy (excluding ADT) (COMPLSYS) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0442874
- UMLS CUI [1,2]
- C0011008
Descrição
INCLUSION CRITERIA: Patients with systemic therapy If answered Cardiovascular toxicity on CTCAE grade III-IV complications due to systemic therapy (excluding ADT) (COMPLSYS) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0007222
- UMLS CUI [1,2]
- C2316983
Descrição
INCLUSION CRITERIA: Patients with systemic therapy If answered Other on CTCAE grade III-IV complications due to systemic therapy (excluding ADT) (COMPLSYS) TIMING: Update at least annually REPORTING SOUCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C0011008
Descrição
Degree of health
Descrição
ECOG / WHO scale: - PS = 0 normal activity level; - PS = 1 restricted with strenuous activity, but can do light activity; - PS = 2 active >/= 50% of day; - PS = 3 spends >50% of day in chair or bed; - PS = 4 totally confined to bed INCLUSION CRITERIA: All patients TIMING: Baseline 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C1520224
- UMLS CUI [1,2]
- C1298650
Descrição
ECOG / WHO scale: - PS = 0 normal activity level; - PS = 1 restricted with strenuous activity, but can do light activity; - PS = 2 active >/= 50% of day; - PS = 3 spends >50% of day in chair or bed; - PS = 4 totally confined to bed INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Multiple answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0002771
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289637
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289645
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289630
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289641
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289629
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289644
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289625
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289626
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289631
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289627
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289636
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289634
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4287870
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289649
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289633
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289647
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289646
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289628
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289639
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289648
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289632
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289638
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289643
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289640
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289635
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C4289642
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C3899191
Descrição
INCLUSION CRITERIA: All patients TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C3827672
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02)TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0663448
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02) TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C2366566
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02)TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C3828613
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02) TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C3827672
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' to using medications or devices to aid or improve erections (LIBID_Q02) TIMING: Baseline 3 months post initiation of treatment 6 months post initiation of treatment 1 year post initiation of treatment Tracked ongoing annually for life REPORTING SOUCE: Patient-reported TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C1115771
Descrição
EORTCQLQC
Descrição
Survival and disease control
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on procedures needed for local progression (LOCPROGTX) TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Clinical TYPE: Multiple Answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0184661
- UMLS CUI [1,2]
- C0449258
Descrição
INCLUSION CRITERIA: All patients TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0242656
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on symptomatic skeletal related event (SSRE) TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0441471
- UMLS CUI [1,2]
- C0037253
- UMLS CUI [1,3]
- C0011008
Descrição
INCLUSION CRITERIA: Patients without known metastasis TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Clinical TYPE: Single Answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C2939420
Descrição
INCLUSION CRITERIA: Patients without known metastasis If answered 'yes' on development of metastasis (METADEV) TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C2316983
- UMLS CUI [1,2]
- C0027627
Descrição
Castration-resistant disease is defined as two successive PSA rises at least one week apart, or the development or progression of radiographically proven metastatic lesions, in the setting of castrate levels of testosterone (<50 ng/mL) INCLUSION CRITERIA: Patients that are not yet castration resistant TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Clinical TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C3658267
Descrição
INCLUSION CRITERIA: Patients that are not yet castration resistant If answered 'yes' on development of castration-resistant disease (CRPCDATE) TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Clinical
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C3658267
- UMLS CUI [1,2]
- C2316983
Descrição
INCLUSION CRITERIA: All patients TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Administrative data (Death registry) TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1]
- C0011065
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on overall survival (OVERALLSURV) TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Administrative data (Death registry)
Tipo de dados
date
Unidades de medida
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1148348
Descrição
INCLUSION CRITERIA: All patients If answered 'yes' on overall survival (OVERALLSURV) TIMING: 1 year post initiation of treatment Tracked ongoing annually for life (when hospital is able to track this ongoing) REPORTING SOURCE: Administrative data (Death registry) TYPE: Single answer
Tipo de dados
integer
Alias
- UMLS CUI [1,1]
- C0007465
- UMLS CUI [1,2]
- C0596130
- UMLS CUI [1,3]
- C0600139
Similar models
ICHOM Advanced Prostate Cancer
- StudyEvent: ODM
C1519795 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,2])
C1300072 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,3])
C0456532 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,3])
C1300072 (UMLS CUI [1,2])
C1521733 (UMLS CUI [1,3])
C0456532 (UMLS CUI [1,2])
C1521733 (UMLS CUI [1,3])
C0033573 (UMLS CUI [1,2])
C0033573 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C1708063 (UMLS CUI [1,2])
C1706721 (UMLS CUI [1,2])
C0279134 (UMLS CUI [2,1])
C0085405 (UMLS CUI [2,2])
C1514463 (UMLS CUI [1,2])
C3839270 (UMLS CUI [2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C3173309 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C3173309 (UMLS CUI [1,2])
C1531784 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,2])
C0027643 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1690432 (UMLS CUI [2])
C0808070 (UMLS CUI [1,2])
C1690432 (UMLS CUI [2,1])
C0808070 (UMLS CUI [2,2])
C1690432 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,3])
C0549178 (UMLS CUI [1,2])
C1690432 (UMLS CUI [2,1])
C0549178 (UMLS CUI [2,2])
C1516728 (UMLS CUI [1,2])
C1515119 (UMLS CUI [1,3])
C1516728 (UMLS CUI [1,2])
C1515119 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C2316983 (UMLS CUI [1,2])
C0521362 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C2316983 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1298650 (UMLS CUI [1,2])
C0449258 (UMLS CUI [1,2])
C0037253 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0027627 (UMLS CUI [1,2])
C2316983 (UMLS CUI [1,2])
C0596130 (UMLS CUI [1,2])
C0600139 (UMLS CUI [1,3])