ID

40554

Descripción

COLORECTAL CANCER DATA COLLECTION Version 1.1.2 Revised: November 6th, 2017 http://www.ichom.org/ Notice: This work was conducted using resources from ICHOM, the International Consortium for Health Outcomes Measurement (www.ICHOM.org). The content is solely the responsibility of the authors and does not necessarily represent the official views of ICHOM. Conditions: All patients with newly pathologically diagnosed invasive colorectal cancer (stage I-IV) Excluded Conditions: Non-adenocarcinoma, non-primary colorectal tumors and patients with recurrent disease at baseline will be excluded. Treatment Approaches: Surgery | Radiotherapy | Chemotherapy | Targeted Therapy In this standard set (parts of) the following questionnaires/scores are used: European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30): Due to the need for a license, the EORTC QLQ-C30 questions are not included in this version of the standard set. European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C29): Due to the need for a license, the EORTC QLQ-C29 questions are not included in this version of the standard set. Memorial Sloan-Kettering Cancer Center (MSKCC) Bowel Function Instrument: Only 4 of the items used. According to ICHOM it is free to use for all health care organizations and no license is needed. Temple, L., Bacik, J., Savatta, S. et al. The Development of a Validated Instrument to Evaluate Bowel Function After Sphincter-Preserving Surgery for Rectal Cancer. Dis Colon Rectum (2005) 48: 1353. European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-LMC21): A license is needed for use of this questionnaire as well, however only one question is used. ICHOM was supported by Alliance of Dedicated Cancer Centers (CZ, DICA, Bowel Cancer Australia) for this standard set. Publication: Zerillo JA, Schouwenburg MG, van Bommel ACM, et al. An International Collaborative Standardizing a Comprehensive Patient-Centered Outcomes Measurement Set for Colorectal Cancer. JAMA Oncol. 2017;3(5):686–694. doi:10.1001/jamaoncol.2017.0417 For this version of the standard set, semantic annotation with UMLS CUIs has been added.

Link

http://www.ichom.org/

Palabras clave

Versiones (2)
  1. 11/9/18 11/9/18 - Sarah Riepenhausen
  2. 30/4/20 30/4/20 - Sarah Riepenhausen
Titular de derechos de autor

ICHOM

Subido en

30 de abril de 2020

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 4.0
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ICHOM Colorectal Cancer

Inglés

6 months post treatment Clinical Form

1 formularios  
Administrative Data
Descripción

Administrative Data

Alias
UMLS CUI-1
C1320722
Indicate the patient's medical record number
Descripción

This number will not be shared with ICHOM. In the case patient-level data is submitted to ICHOM for benchmarking or research purposes, a separate ICHOM Patient Identifier will be created and cross-linking between the ICHOM Patient Identifier and the medical record number will only be known at the treating institution INCLUSION CRITERIA: All patients TIMING: On all forms REPORTING SOURCE: Administrative or clinical RESPONSE OPTIONS: According to institution

Tipo de datos

integer

Alias
UMLS CUI [1]
C1269815
Patient's last name:
Descripción

The patients' name will not be shared with ICHOM.  INCLUSION CRITERIA: All patients TIMING: On all forms REPORTING SOURCE: Administrative or clinical

Tipo de datos

text

Alias
UMLS CUI [1]
C1299487
Treatment variables
Descripción

Treatment variables

Alias
UMLS CUI-1
C0087111
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 0 = No treatment
Descripción

INCLUSION CRITERIA: All patients TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Multiple answer

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C4086728
UMLS CUI [1,2]
C0746919
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 1 = Surgery
Descripción

INCLUSION CRITERIA: All patients TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Multiple answer

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C4086728
UMLS CUI [1,3]
C0543467
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 2 = Radiotherapy
Descripción

INCLUSION CRITERIA: All patients TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Multiple answer

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C4086728
UMLS CUI [1,3]
C1522449
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 3 = Chemotherapy
Descripción

INCLUSION CRITERIA: All patients TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Multiple answer

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C4086728
UMLS CUI [1,3]
C0392920
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 4 = Targeted therapy
Descripción

INCLUSION CRITERIA: All patients TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Multiple answer

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C4086728
UMLS CUI [1,3]
C2985566
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 5 = Best supportive care
Descripción

INCLUSION CRITERIA: All patients TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Multiple answer

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C4086728
UMLS CUI [1,3]
C0344211
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 999 = Unknown
Descripción

INCLUSION CRITERIA: All patients TIMING: 6 months, update at least annually up to 10 years REPORTING SOURCE: Clinical TYPE: Multiple answer

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C4086728
UMLS CUI [1,3]
C0439673
Indicate whether the patient received surgery during the last year:
Descripción

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 de datos

integer

Alias
UMLS CUI [1]
C0543467
Indicate the method of the surgical procedure:
Descripción

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 de datos

integer

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0332307
Provide the date of surgery:
Descripción

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 de datos

date

Unidades de medida
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C1628561
DD/MM/YYYY
Indicate whether the patient received radiotherapy during the last year
Descripción

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 de datos

integer

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C4086728
Indicate what type of radiotherapy:
Descripción

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 de datos

integer

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0332307
Provide the start date of radiotherapy:
Descripción

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 de datos

date

Unidades de medida
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C1522449
DD/MM/YYYY
Provide the stop date of radiotherapy:
Descripción

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 de datos

date

Unidades de medida
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0806020
DD/MM/YYYY
Indicate whether the patient received chemotherapy during the last year:
Descripción

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 de datos

integer

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C4086728
Provide the start date of chemotherapy:
Descripción

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 de datos

date

Unidades de medida
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0808070
DD/MM/YYYY
Provide the stop date of chemotherapy, if applicable:
Descripción

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 de datos

date

Unidades de medida
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0806020
DD/MM/YYYY
Indicate whether the patient received targeted therapy during the last year:
Descripción

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 de datos

integer

Alias
UMLS CUI [1,1]
C2985566
UMLS CUI [1,2]
C4086728
Provide the start date of targeted therapy:
Descripción

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 de datos

date

Unidades de medida
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C2985566
UMLS CUI [1,2]
C0808070
DD/MM/YYYY
Provide the stop date of targeted therapy, if applicable:
Descripción

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 de datos

date

Unidades de medida
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C2985566
UMLS CUI [1,2]
C0806020
DD/MM/YYYY
Survival and disease control
Descripción

Survival and disease control

Alias
UMLS CUI-1
C1148433
UMLS CUI-2
C4304384
Indicate whether there is a complete response
Descripción

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 de datos

integer

Alias
UMLS CUI [1]
C0242594
UMLS CUI [2]
C1275810
Indicate whether there is evidence of circumferential margin involvement:
Descripción

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 de datos

integer

Alias
UMLS CUI [1,1]
C0728940
UMLS CUI [1,2]
C0229985
UMLS CUI [1,3]
C0449438
Disutility of care
Descripción

Disutility of care

Alias
UMLS CUI-1
C4062984
Indicate whether the patient received a stoma (ileostomy/colostomy):
Descripción

INCLUSION CRITERIA: Only if the patient received surgery. TIMING: Updated at least 6 months after treatment REPORTING SOURCE: Clinical TYPE: Single answer

Tipo de datos

integer

Alias
UMLS CUI [1]
C1955856
Provide the date of stoma surgery:
Descripción

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 de datos

date

Unidades de medida
  • DD/MM/YYYY
Alias
UMLS CUI [1,1]
C1955856
UMLS CUI [1,2]
C0011008
DD/MM/YYYY
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  0 = No complication
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0549184
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  1 = Complication requiring intervention (surgical, radiological, endoscopic)
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0184661
UMLS CUI [1,3]
C1514873
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  2 = Complication leading to prolonged hospitalization ( >14days)
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0745041
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  3 = Complication leading to unplanned readmission
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0600290
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  4 = Complication leading to ICU admission
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0583239
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  5 = Complication leading to discontinuing of treatment
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0457454
UMLS CUI [1,3]
C0087111
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  6 = Complication leading to reduced dosing
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C1707814
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  7 = Complication leading to death
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0011065
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  8 = Complication, but did not result in any of the above mentioned
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0205394
UMLS CUI [1,3]
C1274040
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  999 = Unknown
Descripción

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 de datos

boolean

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0439673
Provide the date of death:
Descripción

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 de datos

date

Unidades de medida
  • DD/MM/YYYY
Alias
UMLS CUI [1]
C1148348
DD/MM/YYYY
Indicate whether the complication is attributable to colorectal cancer treatment:
Descripción

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 de datos

integer

Alias
UMLS CUI [1,1]
C0009566
UMLS CUI [1,2]
C0596130
UMLS CUI [1,3]
C0920425
Please indicate the type of complication:
Descripción

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 de datos

integer

Alias
UMLS CUI [1]
C3258281
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Similar models

6 months post treatment Clinical Form

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Patient ID
Item
Indicate the patient's medical record number
integer
C1269815 (UMLS CUI [1])
Patient's last name
Item
Patient's last name:
text
C1299487 (UMLS CUI [1])
Item Group
Treatment variables
C0087111 (UMLS CUI-1)
Treatment: None
Item
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 0 = No treatment
boolean
C4086728 (UMLS CUI [1,1])
C0746919 (UMLS CUI [1,2])
Treatment: Surgery
Item
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 1 = Surgery
boolean
C0087111 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
C0543467 (UMLS CUI [1,3])
Treatment: Radiotherapy
Item
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 2 = Radiotherapy
boolean
C0087111 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,3])
Treatment: Chemotherapy
Item
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 3 = Chemotherapy
boolean
C0087111 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
Treatment: Targeted Therapy
Item
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 4 = Targeted therapy
boolean
C0087111 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
C2985566 (UMLS CUI [1,3])
Treatment: Best supportive care
Item
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 5 = Best supportive care
boolean
C0087111 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
C0344211 (UMLS CUI [1,3])
Treatment: Unknown
Item
Indicate whether the patient received one of the following treatment during the last year: (select all that apply) 999 = Unknown
boolean
C0087111 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
C0439673 (UMLS CUI [1,3])
Item
Indicate whether the patient received surgery during the last year:
integer
C0543467 (UMLS CUI [1])
Treatment
Code List
Indicate whether the patient received surgery during the last year:
CL Item
Hemicolectomy right (1)
C0192861 (UMLS CUI-1)
(Comment:en)
CL Item
Extended colectomy right (2)
C0400043 (UMLS CUI-1)
(Comment:en)
CL Item
Transverse resection (3)
C0192863 (UMLS CUI-1)
(Comment:en)
CL Item
Hemicolectomy left (4)
C0192865 (UMLS CUI-1)
C0546535 (UMLS CUI-2)
(Comment:en)
CL Item
Subtotal colectomy (5)
C0149750 (UMLS CUI-1)
C0728939 (UMLS CUI-2)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
CL Item
Total colectomy (6)
C0192871 (UMLS CUI-1)
(Comment:en)
CL Item
Sigmoid resection (7)
C0192866 (UMLS CUI-1)
(Comment:en)
CL Item
Anterior resection (8)
C0193083 (UMLS CUI-1)
(Comment:en)
CL Item
Low anterior resection (LAR) (9)
C1282272 (UMLS CUI-1)
(Comment:en)
CL Item
Abdomino-perineal resection (APR) (10)
C2004459 (UMLS CUI-1)
(Comment:en)
CL Item
Proctectomy with coloanal (11)
C0193062 (UMLS CUI-1)
C2985529 (UMLS CUI-2)
(Comment:en)
CL Item
Other (12)
C0205394 (UMLS CUI-1)
(Comment:en)
Item
Indicate the method of the surgical procedure:
integer
C0543467 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Treatment
Code List
Indicate the method of the surgical procedure:
CL Item
Endoscopic (for colon tumors) (1)
C0282493 (UMLS CUI-1)
(Comment:en)
CL Item
Transabdominal open (2)
C0348025 (UMLS CUI-1)
C0198482 (UMLS CUI-2)
(Comment:en)
CL Item
Transabdominal minimally invasive (laparoscopic/robotic) (3)
C0198482 (UMLS CUI-1)
C0282624 (UMLS CUI-2)
(Comment:en)
CL Item
Transanal open (4)
C0543467 (UMLS CUI-1)
C0589371 (UMLS CUI-2)
C0348025 (UMLS CUI-3)
(Comment:en)
CL Item
Transanal endoscopic (TEMS/SPTS)/minimally invasive (TAMIS) (5)
C0543467 (UMLS CUI-1)
C0589371 (UMLS CUI-2)
C0282624 (UMLS CUI-3)
C0282493 (UMLS CUI-4)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
CL Item
Other (6)
C0205394 (UMLS CUI-1)
(Comment:en)
Surgery date
Item
Provide the date of surgery:
date
C1628561 (UMLS CUI [1])
Item
Indicate whether the patient received radiotherapy during the last year
integer
C1522449 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
Radiotherapy
Code List
Indicate whether the patient received radiotherapy during the last year
CL Item
Neoadjuvant  (1)
C1298676 (UMLS CUI-1)
(Comment:en)
CL Item
Adjuvant  (2)
C1298675 (UMLS CUI-1)
(Comment:en)
CL Item
Definitive (3)
C2986592 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate what type of radiotherapy:
integer
C1522449 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Radiotherapy
Code List
Indicate what type of radiotherapy:
CL Item
Long course without chemotherapy  (1)
C1522449 (UMLS CUI-1)
C0443252 (UMLS CUI-2)
(Comment:en)
CL Item
Long course chemoradiation  (2)
C0443252 (UMLS CUI-1)
C0436307 (UMLS CUI-2)
(Comment:en)
CL Item
Brachytherapy  (3)
C0006098 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
C1522449 (UMLS CUI-2)
(Comment:en)
CL Item
Short course  (0)
C0443303 (UMLS CUI-1)
C1522449 (UMLS CUI-2)
(Comment:en)
CL Item
Intraoperative radiation therapy (ORT)  (4)
C0338240 (UMLS CUI-1)
(Comment:en)
CL Item
Other  (5)
C1522449 (UMLS CUI-1)
C0205394 (UMLS CUI-2)
(Comment:en)
Start of radiotherapy
Item
Provide the start date of radiotherapy:
date
C0808070 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
End of radiotherapy
Item
Provide the stop date of radiotherapy:
date
C1522449 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Item
Indicate whether the patient received chemotherapy during the last year:
integer
C0392920 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
Chemotherapy
Code List
Indicate whether the patient received chemotherapy during the last year:
CL Item
Neoadjuvant (1)
C1298676 (UMLS CUI-1)
(Comment:en)
CL Item
Adjuvant (2)
C1298675 (UMLS CUI-1)
(Comment:en)
CL Item
Definitive (3)
C2986592 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Start of chemotherapy
Item
Provide the start date of chemotherapy:
date
C0392920 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
End of chemotherapy
Item
Provide the stop date of chemotherapy, if applicable:
date
C0392920 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Item
Indicate whether the patient received targeted therapy during the last year:
integer
C2985566 (UMLS CUI [1,1])
C4086728 (UMLS CUI [1,2])
Targeted therapy
Code List
Indicate whether the patient received targeted therapy during the last year:
CL Item
Cetuximab (1)
C0995188 (UMLS CUI-1)
(Comment:en)
CL Item
Bevacizumab (2)
C0796392 (UMLS CUI-1)
(Comment:en)
CL Item
Panitumumab (3)
C0879427 (UMLS CUI-1)
(Comment:en)
CL Item
Ramucirumab (4)
C2742502 (UMLS CUI-1)
(Comment:en)
CL Item
Aflibercept (5)
C1134659 (UMLS CUI-1)
(Comment:en)
CL Item
Regorafenib (6)
C2980094 (UMLS CUI-1)
(Comment:en)
CL Item
Other (7)
C0205394 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Start of targeted therapy
Item
Provide the start date of targeted therapy:
date
C2985566 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
End of targeted therapy
Item
Provide the stop date of targeted therapy, if applicable:
date
C2985566 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Item Group
Survival and disease control
C1148433 (UMLS CUI-1)
C4304384 (UMLS CUI-2)
Item
Indicate whether there is a complete response
integer
C0242594 (UMLS CUI [1])
C1275810 (UMLS CUI [2])
Residual invasive cancer
Code List
Indicate whether there is a complete response
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Indicate whether there is evidence of circumferential margin involvement:
integer
C0728940 (UMLS CUI [1,1])
C0229985 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
Residual invasive cancer
Code List
Indicate whether there is evidence of circumferential margin involvement:
CL Item
Positive (<= 1mm) (0)
C1709603 (UMLS CUI-1)
(Comment:en)
CL Item
Negative (>1mm) (1)
C1709157 (UMLS CUI-1)
(Comment:en)
CL Item
Not reported (999)
C1549114 (UMLS CUI-1)
(Comment:en)
Item Group
Disutility of care
C4062984 (UMLS CUI-1)
Item
Indicate whether the patient received a stoma (ileostomy/colostomy):
integer
C1955856 (UMLS CUI [1])
Stoma
Code List
Indicate whether the patient received a stoma (ileostomy/colostomy):
CL Item
No (0)
C1298908 (UMLS CUI-1)
C1955856 (UMLS CUI-2)
(Comment:en)
CL Item
Temporary (1)
C0205374 (UMLS CUI-1)
C1955856 (UMLS CUI-2)
(Comment:en)
CL Item
Permanent (2)
C0205355 (UMLS CUI-1)
C1955856 (UMLS CUI-2)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Stoma date
Item
Provide the date of stoma surgery:
date
C1955856 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Complications: None
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  0 = No complication
boolean
C0009566 (UMLS CUI [1,1])
C0549184 (UMLS CUI [1,2])
Complications: Requiring intervention
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  1 = Complication requiring intervention (surgical, radiological, endoscopic)
boolean
C0009566 (UMLS CUI [1,1])
C0184661 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
Complications: prolonged hospitalisation
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  2 = Complication leading to prolonged hospitalization ( >14days)
boolean
C0009566 (UMLS CUI [1,1])
C0745041 (UMLS CUI [1,2])
Complications: unplanned readmission
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  3 = Complication leading to unplanned readmission
boolean
C0009566 (UMLS CUI [1,1])
C0600290 (UMLS CUI [1,2])
Complications: ICU admission
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  4 = Complication leading to ICU admission
boolean
C0009566 (UMLS CUI [1,1])
C0583239 (UMLS CUI [1,2])
Complications: discontinuation of treatment
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  5 = Complication leading to discontinuing of treatment
boolean
C0009566 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
Complications: Reduction of dosing
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  6 = Complication leading to reduced dosing
boolean
C0009566 (UMLS CUI [1,1])
C1707814 (UMLS CUI [1,2])
Complications: Death
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  7 = Complication leading to death
boolean
C0009566 (UMLS CUI [1,1])
C0011065 (UMLS CUI [1,2])
Complications: other result
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  8 = Complication, but did not result in any of the above mentioned
boolean
C0009566 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
Complications: Unknown
Item
Indicate whether the patient experienced a complication while on treatment or up to 90 days after initiation of treatment (multiple answers possible):  999 = Unknown
boolean
C0009566 (UMLS CUI [1,1])
C0439673 (UMLS CUI [1,2])
Date of death
Item
Provide the date of death:
date
C1148348 (UMLS CUI [1])
Item
Indicate whether the complication is attributable to colorectal cancer treatment:
integer
C0009566 (UMLS CUI [1,1])
C0596130 (UMLS CUI [1,2])
C0920425 (UMLS CUI [1,3])
Residual invasive cancer
Code List
Indicate whether the complication is attributable to colorectal cancer treatment:
CL Item
No (0)
C1298908 (UMLS CUI-1)
(Comment:en)
CL Item
Yes (1)
C1705108 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
Item
Please indicate the type of complication:
integer
C3258281 (UMLS CUI [1])
Complication type
Code List
Please indicate the type of complication:
CL Item
Leakage (0)
C0919691 (UMLS CUI-1)
(Comment:en)
CL Item
Breakdown of anastomosis (1)
C0332853 (UMLS CUI-1)
C3203359 (UMLS CUI-2)
(Comment:en)
CL Item
Wound Infection (2)
C0043241 (UMLS CUI-1)
(Comment:en)
CL Item
Thromboembolic (3)
C0040038 (UMLS CUI-1)
(Comment:en)
CL Item
Hematoma (4)
C0018944 (UMLS CUI-1)
(Comment:en)
CL Item
Stoma related complications (5)
C0009566 (UMLS CUI-1)
C1955856 (UMLS CUI-2)
(Comment:en)
CL Item
Skin desquamation (6)
C0237849 (UMLS CUI-1)
(Comment:en)
CL Item
Dysuria (7)
C0013428 (UMLS CUI-1)
(Comment:en)
CL Item
Dehydration (8)
C0011175 (UMLS CUI-1)
(Comment:en)
CL Item
Weight loss (9)
C1262477 (UMLS CUI-1)
(Comment:en)
CL Item
Febrile neuropathy (10)
C0442874 (UMLS CUI-1)
C0015967 (UMLS CUI-2)
(Comment:en)
CL Item
Neutropenic sepsis (11)
C0853697 (UMLS CUI-1)
C0243026 (UMLS CUI-2)
(Comment:en)
CL Item
Mucositis (12)
C0333355 (UMLS CUI-1)
(Comment:en)
CL Item
skin toxicity (13)
C1167791 (UMLS CUI-1)
(Comment:en)
CL Item
Neurotoxicity (14)
C0235032 (UMLS CUI-1)
(Comment:en)
CL Item
Unknown (999)
C0439673 (UMLS CUI-1)
(Comment:en)
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