ID

41372

Beskrivning

Study ID: 111476 Clinical Study ID: 111476 Study Title: An open, single-arm trial to assess the clinical activity of recMAGE-A3 + AS15 in patients with unresectable MAGE-A3-positive metastatic cutaneous melanoma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00942162 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Antigen-Specific Cancer Immunotherapeutic Study Indication: Melanoma

Nyckelord

Versioner (2)
  1. 2020-09-14 2020-09-14 -
  2. 2020-10-30 2020-10-30 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

14 september 2020

DOI

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Creative Commons BY 4.0
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Clinical activity of recMAGE-A3 + AS15 in patients with metastatic cutaneous melanoma NCT00942162

Engelsk

Radiotherapy; Local Surgery

1 Formulär  
Administrative
Beskrivning

Administrative

Alias
UMLS CUI-1
C1320722
Patient Number
Beskrivning

Patient Number

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Radiotherapy
Beskrivning

Radiotherapy

Alias
UMLS CUI-1
C1522449
Has the patient received low-dose radiotherapy during the study treatment period?
Beskrivning

If yes → Please record radiotherapy details below.

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C1708745
UMLS CUI [2,1]
C0347984
UMLS CUI [2,2]
C0008976
Radiotherapy
Beskrivning

Radiotherapy

Alias
UMLS CUI-1
C1522449
Radiotherapy Site
Beskrivning

Radiotherapy Site

Datatyp

integer

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C1515974
Other site, specify
Beskrivning

Other site, specify

Datatyp

text

Alias
UMLS CUI [1,1]
C1515974
UMLS CUI [1,2]
C0205394
UMLS CUI [1,3]
C2348235
Cumulative dose
Beskrivning

Cumulative dose

Datatyp

float

Alias
UMLS CUI [1]
C2986497
Units
Beskrivning

Units

Datatyp

text

Alias
UMLS CUI [1]
C1519795
Date of first administration
Beskrivning

Date of first administration

Datatyp

date

Alias
UMLS CUI [1]
C3173309
Date of last administration
Beskrivning

Date of last administration

Datatyp

date

Alias
UMLS CUI [1,1]
C1762893
UMLS CUI [1,2]
C1533734
Status of the lesion before radiotherapy
Beskrivning

Status of the lesion before radiotherapy

Datatyp

text

Alias
UMLS CUI [1,1]
C0449438
UMLS CUI [1,2]
C0221198
UMLS CUI [2,1]
C1522449
UMLS CUI [2,2]
C0332152
Type of lesion (Radiotherapy)
Beskrivning

Type of lesion (Radiotherapy)

Datatyp

text

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0332307
UMLS CUI [2]
C1522449
If target lesion, specify number (Radiotherapy)
Beskrivning

If target lesion, specify number (Radiotherapy)

Datatyp

integer

Alias
UMLS CUI [1,1]
C1521840
UMLS CUI [1,2]
C0221198
UMLS CUI [2]
C2348235
UMLS CUI [3]
C0237753
UMLS CUI [4]
C1522449
Local Surgery
Beskrivning

Local Surgery

Alias
UMLS CUI-1
C0543467
UMLS CUI-2
C0205276
Have some lesions been resected during the study treatment period?
Beskrivning

If Yes, please record surgery details below

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0728940
UMLS CUI [2,1]
C0347984
UMLS CUI [2,2]
C0008976
Local Surgery
Beskrivning

Local Surgery

Alias
UMLS CUI-1
C0543467
UMLS CUI-2
C0205276
Surgery Site
Beskrivning

Surgery Site

Datatyp

integer

Alias
UMLS CUI [1,1]
C1515974
UMLS CUI [1,2]
C0543467
Date of surgery
Beskrivning

Date of surgery

Datatyp

date

Alias
UMLS CUI [1]
C3258210
Status of the lesion before surgery
Beskrivning

Status of the lesion before surgery

Datatyp

text

Alias
UMLS CUI [1,1]
C0449438
UMLS CUI [1,2]
C0221198
UMLS CUI [2,1]
C0543467
UMLS CUI [2,2]
C0332152
Type of lesion (Surgery)
Beskrivning

Type of lesion (Surgery)

Datatyp

text

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0332307
UMLS CUI [2]
C0543467
If target lesion, specify number (Surgery)
Beskrivning

If target lesion, specify number (Surgery)

Datatyp

integer

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C1521840
UMLS CUI [2,1]
C0237753
UMLS CUI [2,2]
C2348235
UMLS CUI [3]
C0543467
Tillbaka till toppen

Similar models

Radiotherapy; Local Surgery

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administrative
C1320722 (UMLS CUI-1)
Patient Number
Item
Patient Number
text
C2348585 (UMLS CUI [1])
Item Group
Radiotherapy
C1522449 (UMLS CUI-1)
Has the patient received low-dose radiotherapy during the study treatment period?
Item
Has the patient received low-dose radiotherapy during the study treatment period?
boolean
C1522449 (UMLS CUI [1,1])
C1708745 (UMLS CUI [1,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Item Group
Radiotherapy
C1522449 (UMLS CUI-1)
Item
Radiotherapy Site
integer
C1522449 (UMLS CUI [1,1])
C1515974 (UMLS CUI [1,2])
Site
Code List
Radiotherapy Site
CL Item
Primary tumor/recurrence  (1)
CL Item
Lymphnode regional  (2)
CL Item
Lymphnode distant  (3)
CL Item
Cutaneous/subcutaneous regional  (4)
CL Item
Cutaneous/subcutaneous distant  (5)
CL Item
Confluent skin lesions regional  (6)
CL Item
Confluent skin lesions distant  (7)
CL Item
Lung  (9)
CL Item
Brain  (10)
CL Item
Other site (99)
Other site, specify
Item
Other site, specify
text
C1515974 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
Cumulative dose
Item
Cumulative dose
float
C2986497 (UMLS CUI [1])
Item
Units
text
C1519795 (UMLS CUI [1])
Units
Code List
Units
CL Item
Grays  (Gy)
CL Item
Centigrays  (cGy)
CL Item
x100 Rads (rd)
Date of first administration
Item
Date of first administration
date
C3173309 (UMLS CUI [1])
Date of last administration
Item
Date of last administration
date
C1762893 (UMLS CUI [1,1])
C1533734 (UMLS CUI [1,2])
Item
Status of the lesion before radiotherapy
text
C0449438 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
Status of the lesion before radiotherapy
Code List
Status of the lesion before radiotherapy
CL Item
Progressive lesion  (PD)
CL Item
Stable lesion  (SD)
CL Item
Regressive lesion  (Reg)
CL Item
New lesion (New)
Item
Type of lesion (Radiotherapy)
text
C0221198 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2])
Type of lesion
Code List
Type of lesion (Radiotherapy)
CL Item
Target lesion  (TG)
CL Item
Non-Target lesion (NT)
If target lesion, specify number (Radiotherapy)
Item
If target lesion, specify number (Radiotherapy)
integer
C1521840 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C2348235 (UMLS CUI [2])
C0237753 (UMLS CUI [3])
C1522449 (UMLS CUI [4])
Item Group
Local Surgery
C0543467 (UMLS CUI-1)
C0205276 (UMLS CUI-2)
Have some lesions been resected during the study treatment period?
Item
Have some lesions been resected during the study treatment period?
boolean
C0221198 (UMLS CUI [1,1])
C0728940 (UMLS CUI [1,2])
C0347984 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Item Group
Local Surgery
C0543467 (UMLS CUI-1)
C0205276 (UMLS CUI-2)
Item
Surgery Site
integer
C1515974 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
Surgery Site
Code List
Surgery Site
CL Item
Primary tumor/recurrence  (1)
CL Item
Lymphnode regional  (2)
CL Item
Lymphnode distant  (3)
CL Item
Cutaneous/subcutaneous regional  (4)
CL Item
Cutaneous/subcutaneous distant  (5)
CL Item
Confluent skin lesions regional  (6)
CL Item
Confluent skin lesions distant  (7)
CL Item
Lung  (9)
CL Item
Brain  (10)
CL Item
Other site (99)
Date of surgery
Item
Date of surgery
date
C3258210 (UMLS CUI [1])
Item
Status of the lesion before surgery
text
C0449438 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C0543467 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
Status of the lesion before surgery
Code List
Status of the lesion before surgery
CL Item
Progressive lesion  (PD)
CL Item
Stable lesion  (SD)
CL Item
Regressive lesion  (Reg)
CL Item
New lesion (New)
Item
Type of lesion (Surgery)
text
C0221198 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C0543467 (UMLS CUI [2])
Type of lesion
Code List
Type of lesion (Surgery)
CL Item
Target lesion  (TG)
CL Item
Non-Target lesion (NT)
If target lesion, specify number (Surgery)
Item
If target lesion, specify number (Surgery)
integer
C0221198 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
C0237753 (UMLS CUI [2,1])
C2348235 (UMLS CUI [2,2])
C0543467 (UMLS CUI [3])
Tillbaka till toppen 

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