ID
27979
Descrizione
BREAST CANCER DATA COLLECTION Version 1.1.0 Revised: September 13th, 2017, International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ Conditions: All patients with newly pathologically diagnosed invasive colorectal cancer (stage I-IV) Treatment Approaches: Surgery | Radiotherapy | Chemotherapy | Targeted Therapy
collegamento
Keywords
versioni (3)
- 07/12/17 07/12/17 -
- 11/09/18 11/09/18 - Sarah Riepenhausen
- 30/04/20 30/04/20 - Sarah Riepenhausen
Titolare del copyright
ICHOM
Caricato su
7 dicembre 2017
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 3.0
Commenti del modello :
Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.
Commenti del gruppo di articoli per :
Commenti dell'articolo per :
Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.
ICHOM Colorectal Cancer
ICHOM Colorectal Cancer
- StudyEvent: ODM
Descrizione
Demographic Factors
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0079399
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0421451
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0015031
Descrizione
This is based upon the International Standard Classification of Education for the United States, and reflects standards in the U.S. Please adapt questions according to your country’s guidelines. Primary refers to the first 8 years of formal education in elementary school in the US. Secondary school refers to the last four years of statutory formal education (grade 9-12) at high school in the US. Tertiary refers to colleges or universities, including undergraduate and postgraduate education in the US. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0013658
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0439849
Descrizione
Baseline Clinical Factors
Descrizione
Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Patient-reported TYPE: Multiple answer Separate multiple entries with "";""
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0009488
Descrizione
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical RESPONSE OPTIONS: Numerical value of height in cm or in
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0005890
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0005890
- UMLS CUI [1,2]
- C1519795
Descrizione
Height and weight are used to calculate BMI INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical RESPONSE OPTION: Numerical value of weight in kg or lbs
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0005910
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0005910
- UMLS CUI [1,2]
- C1519795
Descrizione
ECOG/WHO Scale: WHO 0 = normal activity level WHO 1 = restricted with physically strenuous activity WHO 2 = active >/= 50% of day WHO 3 = spends > 50% of day in chair or bed WHO 4 = totally confined to bed or chair INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1520224
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0945985
Descrizione
Familial Adenomatosis Polyposis is caused by a germline mutation of the APC gene. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0032580
Descrizione
Lynch syndrome is caused by a mutation of one of the DNA mismatch repair (MMR) genes or the EPCAM gene. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4289650
- UMLS CUI [2]
- C1155661
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0021390
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0679557
Descrizione
Defined as two or more distinct primary tumors, separated by normal bowel and not due to direct extension or metastasis. Of note: If yes, please collect information on highest TNM stage. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0677930
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0872338
Descrizione
INCLUSION CRITERIA: All patients with rectal cancer receiving surgery/radiotherapy TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Numerical value; Please enter "999" if distance is unknown.
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0872338
- UMLS CUI [1,2]
- C0007113
Descrizione
Only select cT4 if not able to select cT4a or cT4b. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C1300072
- UMLS CUI [1,2]
- C0205210
Descrizione
Only select cN1 or cN2 if not able to select cN1a-c or cN2a-b. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0456532
- UMLS CUI [1,2]
- C0205210
Descrizione
Only select cM1 if not able to select cM1a or cM1b. INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C1302548
- UMLS CUI [1,2]
- C0205210
Descrizione
INCLUSION CRITERIA: If the patient received surgery or biopsy TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0919553
Descrizione
INCLUSION CRITERIA: If the patient received surgery or biopsy TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0812241
Descrizione
INCLUSION CRITERIA: If the patient received surgery or biopsy TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C2747837
Descrizione
INCLUSION CRITERIA: If the patient received surgery or biopsy TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0920269
Descrizione
Only select pT4 if not able to select pT4a or pT4b. INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C1300072
- UMLS CUI [1,2]
- C1521733
Descrizione
Only select pN1 or pN2 if not able to select pN1a-c or pN2a-b. INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0456532
- UMLS CUI [1,2]
- C1521733
Descrizione
Only select pM1 if not able to select pM1a or pM1b. INCLUSION CRITERIA: If the patient received surgery or biopsy TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C1302548
- UMLS CUI [1,2]
- C1521733
Descrizione
INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Numerical value; Please enter "999" if number of resected lymph nodes is unknown.
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0024204
- UMLS CUI [1,2]
- C0728940
Descrizione
INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Numerical value; Please enter "999" if number of involved lymph nodes is unknown.
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0806692
Descrizione
INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Multiple answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1708790
Descrizione
INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1300724
Descrizione
INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0229985
Descrizione
Baseline Treatment Factors
Descrizione
INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4049774
Descrizione
INCLUSION CRITERIA: If the patient received surgery TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0151664
Descrizione
INCLUSION CRITERIA: All patients TIMING: Baseline REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C1283828
Descrizione
Treatment variables
Descrizione
INCLUSION CRITERIA: All patients TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Multiple answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0087111
Descrizione
INCLUSION CRITERIA: If answered "surgery" on treatment [TREATMENT] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0543467
Descrizione
INCLUSION CRITERIA: If yes answered "yes" on surgery [SURGERY] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0683312
- UMLS CUI [1,2]
- C0543467
Descrizione
INCLUSION CRITERIA: If yes answered "yes" on surgery [SURGERY] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Date, Please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1628561
Descrizione
INCLUSION CRITERIA: If answered "radiotherapy" on treatment [TREATMENT] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1522449
Descrizione
INCLUSION CRITERIA: If answered "yes" on radiotherapy [RADIOTX] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Multiple answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C1522449
- UMLS CUI [1,2]
- C1521902
Descrizione
INCLUSION CRITERIA: If answered "yes" on radiotherapy [RADIOTX] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Date, Please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0436382
Descrizione
INCLUSION CRITERIA: If answered "yes" on radiotherapy [RADIOTX] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Date, Please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0436385
Descrizione
INCLUSION CRITERIA: If answered "chemotherapy" on treatment [TREATMENT] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0392920
Descrizione
INCLUSION CRITERIA: If answered "chemotherapy" on treatment TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0392920
- UMLS CUI [1,2]
- C0332307
Descrizione
INCLUSION CRITERIA: If answered "chemotherapy" on treatment TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Date, please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1302181
- UMLS CUI [1,2]
- C3173309
Descrizione
INCLUSION CRITERIA: If answered "chemotherapy" on treatment TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Date, please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1302181
- UMLS CUI [1,2]
- C0806020
Descrizione
INCLUSION CRITERIA: If answered "targeted therapy" on treatment [TREATMENT] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single Answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C2985566
Descrizione
INCLUSION CRITERIA: If answered "yes on targeted therapy [TARGETTX] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Date, please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C2985566
- UMLS CUI [1,2]
- C3173309
Descrizione
INCLUSION CRITERIA: If answered "yes on targeted therapy [TARGETTX] TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Date, please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C2985566
- UMLS CUI [1,2]
- C1531784
Descrizione
Survival and disease control
Descrizione
In case of pathologic evaluation: a pathologic complete response is defined as no evidence of residual invasive cancer of the complete resected specimen and all sampled regional lymph nodes. In case of diagnostic evaluation only: a clinical complete response is defined when there is no sign of tumor after all diagnostic tests (e.g. MRI/endoscopy) INCLUSION CRITERIA: Only if patient received neo-adjuvant therapy for rectal cancer. TIMING: Update at least 6 months after treatment REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0242594
Descrizione
INCLUSION CRITERIA: Only if the patient received surgery for rectal cancer. TIMING: Update at least 6 months after treatment REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0728940
- UMLS CUI [1,2]
- C0229985
- UMLS CUI [1,3]
- C0449438
Descrizione
INCLUSION CRITERIA: Only if the patient is treated with curative intent. TIMING: 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0034897
Descrizione
INCLUSION CRITERIA: Only if answered "yes" on recurrence [RECUR] TIMING: 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0034897
- UMLS CUI [1,2]
- C0332307
Descrizione
INCLUSION CRITERIA: Only if answered "yes" on recurrence [RECUR] TIMING: 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Clinical TYPE: Date, Please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0807712
Descrizione
INCLUSION CRITERIA: Only if the patient has advanced disease. TIMING: 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0242656
Descrizione
INCLUSION CRITERIA: Only if answered "yes" on progression [PROGRESS] TIMING: 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0242656
- UMLS CUI [1,2]
- C0430022
Descrizione
INCLUSION CRITERIA: Only if answered "yes" on progression [PROGRESS] TIMING: 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Clinical TYPE: Date, Please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0242656
- UMLS CUI [1,2]
- C0011008
Descrizione
INCLUSION CRITERIA: All patients TIMING: 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Administrative TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0011065
Descrizione
INCLUSION CRITERIA: If answered "yes" on patient died [DEATH] TIMING: 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Administrative TYPE: Date, Please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1148348
Descrizione
INCLUSION CRITERIA: If answered "yes" on patient died [DEATH] TIMING: 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Administrative TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0007465
Descrizione
Disutility of care
Descrizione
INCLUSION CRITERIA: Only if the patient received surgery. TIMING: Updated at least 6 months after treatment REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C1955856
Descrizione
INCLUSION CRITERIA: If answered "yes" on stoma [STOMA] TIMING: Updated at least 6 months after treatment REPORTING SOURCE: Clinical TYPE: Date, Please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C1955856
- UMLS CUI [1,2]
- C0011008
Descrizione
These response options are based on the Clavien-Dindo classification for surgical complications and the Common Terminology Criteria version 4 (CTCAE v4). To collect the most severe complications, grade 3 -5 of both classification systems are included in the Standard Set. INCLUSION CRITERIA: Only if the patient received treatment. TIMING: Updated at least 6 months after treatment REPORTING SOURCE: Clinical TYPE: Multiple answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0009566
Descrizione
INCLUSION CRITERIA: If answered "Complication leading to death" on experience of complication [COMPLIMPACT] TIMING: Updated at least 6 months after treatment REPORTING SOURCE: Clinical TYPE: Date, Please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C1148348
Descrizione
INCLUSION CRITERIA: If answered "yes" on experience of complication [COMPLIMPACT] TIMING: Updated at least 6 months after treatment REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0009566
- UMLS CUI [1,2]
- C0596130
- UMLS CUI [1,3]
- C0920425
Descrizione
INCLUSION CRITERIA: If answered "yes" on complication attributable to colorectal cancer treatment [COMPLTX] TIMING: Updated at least 6 months after treatment REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3258281
Descrizione
Quality of death
Descrizione
INCLUSION CRITERIA: If answered "yes" on patient died [DEATH] TIMING: 1 year post treatment, tracked annually REPORTING SOURCE: Administrative TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0421611
Descrizione
INCLUSION CRITERIA: If answered "yes" on patient died [DEATH] TIMING: 1 year post treatment, tracked annually REPORTING SOURCE: Administrative or clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0085555
Descrizione
INCLUSION CRITERIA: If answered "yes" on patient died [DEATH] TIMING: 1 year post treatment, tracked annually REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0421611
- UMLS CUI [1,2]
- C0558295
Descrizione
INCLUSION CRITERIA: If answered "yes" on patient died [DEATH] TIMING: 1 year post treatment, tracked annually REPORTING SOURCE: Clinical TYPE: Date, Please enter "999" if date is unknown
Tipo di dati
date
Unità di misura
- DD/MM/YYYY
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0920316
Descrizione
Emergency visits should not be included. INCLUSION CRITERIA: If answered "yes" on patient died [DEATH] TIMING: 1 year post treatment, tracked annually REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0184666
Descrizione
Emergency visits should not be included. INCLUSION CRITERIA: If answered "yes" on patient died [DEATH] TIMING: 1 year post treatment, tracked annually REPORTING SOURCE: Clinical TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0184666
Descrizione
Degree of health
Descrizione
INCLUSION CRITERIA: Patients with surgery/radiotherapy TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0453855
- UMLS CUI [1,2]
- C2128962
Descrizione
INCLUSION CRITERIA: Patients with surgery/radiotherapy TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0452428
- UMLS CUI [1,2]
- C2128962
Descrizione
INCLUSION CRITERIA: Patients with surgery/radiotherapy TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0439801
- UMLS CUI [1,2]
- C0453855
- UMLS CUI [1,3]
- C1290944
Descrizione
INCLUSION CRITERIA: Patients with surgery/radiotherapy TIMING: Baseline, 6 months, 1 year post treatment, tracked annually up to 10 years REPORTING SOURCE: Patient-reported TYPE: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0439801
- UMLS CUI [1,2]
- C0452428
- UMLS CUI [1,3]
- C1290944
Descrizione
EORTCQLQC
Similar models
ICHOM Colorectal Cancer
- StudyEvent: ODM
C1519795 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C1155661 (UMLS CUI [2])
C0007113 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,2])
C1521733 (UMLS CUI [1,2])
C1521733 (UMLS CUI [1,2])
C1521733 (UMLS CUI [1,2])
C0728940 (UMLS CUI [1,2])
C1283828 (UMLS CUI [1,2])
C0543467 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,2])
C3173309 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C3173309 (UMLS CUI [1,2])
C1531784 (UMLS CUI [1,2])
C0229985 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
C0332307 (UMLS CUI [1,2])
C0430022 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0596130 (UMLS CUI [1,2])
C0920425 (UMLS CUI [1,3])
C0558295 (UMLS CUI [1,2])
C0920316 (UMLS CUI [1,2])
C2128962 (UMLS CUI [1,2])
C2128962 (UMLS CUI [1,2])
C0453855 (UMLS CUI [1,2])
C1290944 (UMLS CUI [1,3])
C0452428 (UMLS CUI [1,2])
C1290944 (UMLS CUI [1,3])