№ files_lp_4_process_3_112009
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Dataset detailing individual acute myeloid leukemia patients including sex, age at diagnosis, cytogenetic and molecular alterations, and induction chemotherapy regimens.
Year:
2026
Patient Count:
21
Sex Distribution:
11 Males, 10 Females
Age Range:
30–72 years
Cytogenetic Alterations:
normal, t(10;13), del(15), -Y, t(8;21), inv(16), der(5)t(5;?), t(7;21), t(11;19), +11, +13, add(10), add(12), -16, -18, +2mar
Molecular Alterations:
FLT3-ITD, NPM1mutA, TP53
Induction Chemotherapy Regimens:
3+7, ICE, 3+7 +FLT3 inhibitor
Ex-vivo Treatment Groups:
Senescence High, Senescence Low
In-vivo Treatment Group:
chemotherapy-treated patients
Data Type:
Patient clinical and molecular dataset
Source:
Clinical study cohort
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Protocol version:
6.0
Date:
18 September 2020
Study name:
rEECur
Study design:
International randomised controlled trial
Medical condition:
Recurrent and primary refractory Ewing sarcoma
Intervention:
Chemotherapy
Sponsor:
University of Birmingham
Sponsor protocol number:
RG_13-277
CRCTU number:
SA2015
EudraCT number:
2014-000259-99
ISRCTN reference number:
ISRCTN36453794
Chief Investigator:
Dr Martin McCabe
Coordinating institution:
Cancer Research UK Clinical Trials Unit, University of Birmingham
Geographic scope:
International
Participating regions:
United Kingdom, Germany, Italy, France, Spain, Scandinavia, Australia, New Zealand, Switzerland
Target population:
Patients with recurrent or primary refractory Ewing sarcoma
Regulatory status:
Ethics and regulatory approval required per participating country
Amendment history:
Substantial amendments between 2014 and 2016
Document type:
Clinical trial protocol
Randomisation method:
Centralised online randomisation
Trial phase:
Phase II (Germany-specific limitation noted)
Year:
2025
Region / City:
Canberra
Topic:
Medical Procedures, Oncology, Hematology
Document Type:
Procedure
Organization / Institution:
Canberra Health Services
Author:
Canberra Health Services
Target Audience:
Healthcare professionals involved in chemotherapy administration
Effective Period:
Ongoing
Approval Date:
2025-01-01
Date of Changes:
2025-01-01
Year:
2023
Region / City:
Canberra
Topic:
Chemotherapy Care
Document Type:
Guideline
Organization / Institution:
Canberra Health Services
Author:
Melissa O’Brien, A/g ED of CAS
Target Audience:
Clinical staff providing care to adult patients receiving chemotherapy
Effective Date:
24/04/2023
Amendment Date:
24/04/2023
Year:
2025
Region / City:
Australia
Topic:
Pharmaceutical benefits, chemotherapy, PBS
Document Type:
FAQ
Organization:
Pharmaceutical Benefits Scheme
Author:
Pharmaceutical Benefits Advisory Committee (PBAC)
Target Audience:
Healthcare providers, prescribers, patients
Effective Period:
From December 1, 2024
Approval Date:
Not specified
Modification Date:
Not specified
Contextual Description:
FAQ document providing detailed information on the changes in PBS listing for Opdualag and Vyxeos under the EFC Program, including prescription and claiming details.
Year:
2021
Region / city:
Australia
Topic:
Pharmaceutical Drug Submission
Document type:
Resubmission Request
Organization / institution:
PBAC
Author:
AbbVie Pty Ltd.
Target audience:
Healthcare professionals, PBAC
Validity period:
Not specified
Approval date:
2021
Date of amendments:
Not specified
Year:
2019
Region / City:
Wellington, New Zealand
Topic:
Colorectal cancer, chemotherapy regimens
Document type:
Draft definitions
Organization / Institution:
Ministry of Health, New Zealand
Author:
Ministry of Health
Target audience:
Medical oncologists, pharmacists, nurse specialists, other DHB staff
Period of validity:
Not specified
Approval date:
Not specified
Date of last modification:
Not specified
Note:
Year
Theme:
Healthcare, Oncology, Pharmaceutical Services
Document Type:
Agreement
Year:
2023
Region / City:
London, Norwich, Liverpool, UK
Topic:
Medical Research
Document Type:
Systematic Review with Meta-Analysis
Author:
Tristan D Boam, Melissa Gabriel, Rajeev Shukla, Paul D Losty
Target Audience:
Healthcare professionals, researchers in paediatric oncology
Period of Effect:
1990-2020
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
N/A
Region / City:
N/A
Topic:
Healthcare, Oncology, Nursing
Document Type:
Job Description
Organization:
Cherrybrook Cancer Services
Author:
N/A
Target Audience:
Healthcare professionals, Nurses
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
2014
Region / city:
Not specified
Subject:
Mortality following palliative chemotherapy
Document type:
Audit report
Institution:
Not specified
Author:
Rafael Silverman
Target audience:
Clinical departments and healthcare professionals involved in palliative care and chemotherapy
Period of validity:
Not specified
Approval date:
Not specified
Last reviewed:
2 May 2024
Contextual description:
A departmental audit assessing short-term mortality rates following palliative chemotherapy for solid tumours in a specific time period.
Year:
2012
Region / City:
Europe / Vienna
Theme:
Lung Cancer, Oncology
Document Type:
Survey
Organization / Institution:
European Society for Medical Oncology (ESMO)
Author:
Dr. Raffaele Califano
Target Audience:
Medical Oncologists, Radiation Oncologists
Period of Action:
Deadline end of February 2012
Approval Date:
N/A
Date of Changes:
N/A
Document Title:
Intrathecal Chemotherapy (ITC) Prescription and Checklist
Appendix:
Appendix 5
Field:
Oncology
Medical Procedure:
Intrathecal chemotherapy administration
Document Type:
Medical prescription form and procedural checklist
Purpose:
Recording prescription, dispensing, transfer, and administration details for intrathecal chemotherapy
Healthcare Setting:
Hospital oncology department
Responsible Roles:
Prescriber, Clinical Pharmacy, Checking Nurse
Drugs Mentioned:
Methotrexate, Cytarabine, Hydrocortisone, Rituximab
Administration Route:
Intrathecal
Form Sections:
Patient details, prescription record, dispensing and transfer, administration record, verification checklist
Verification Requirements:
Patient identity confirmation, consent verification, drug and dose validation, pharmacy release confirmation
Safety Controls:
Drug verification, route confirmation, preparation date check, volume restriction, ITC register verification
Associated Procedure:
Lumbar puncture
Usage Frequency:
Single occasion prescription
Record Handling:
Copy to lead oncology pharmacist and original filed in patient notes
Document Type:
Supplementary tables from a clinical research publication
Medical Topic:
Neuroblastoma treatment and response assessment
Treatment Agent:
Hu14.18K322A monoclonal antibody
Therapy Phase:
Induction chemotherapy
Assessment Method:
Curie score imaging evaluation
Number of Patients:
43 patients (42 at end of induction assessment)
Infusion Protocol:
Planned 4-hour antibody infusion with possible extension to 8 or 16 hours based on patient tolerance and physician discretion
Infusion Duration Categories:
4 hours daily for 4 days; extended to 8 hours; extended to 16 hours
Clinical Measurements:
Median Curie scores and proportions of patients with CS > 0 and CS > 2
Assessment Timepoints:
Pretherapy; after 2 cycles of therapy; end of induction
Patient Withdrawal:
One patient withdrew after course 4 of therapy
Year:
Not specified
Region / City:
Not specified
Theme:
Oncology, Hematology
Document Type:
Scientific Research
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Medical professionals, researchers
Action Period:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Region / City:
International / Multicenter
Subject:
Breast cancer, Vitamin D, Neoadjuvant chemotherapy
Document type:
Supplemental material for research article
Institution / Organization:
Academic research institutions
Authors:
Not specified
Study population:
Patients with breast cancer undergoing neoadjuvant chemotherapy
Data sources:
Medline, Embase, Cochrane Library, Web of Science
Methods:
Literature search, data extraction, quality assessment, subgroup and sensitivity analyses, meta-analysis
Outcome measures:
Overall pathological response, pathological complete response (pCR), event-free survival (EFS)
Period covered:
Not explicitly stated, studies pooled from multiple cohorts
Supplementary content:
Tables of search strategy, data extraction, baseline characteristics, quality assessment; figures for bias, funnel plots, subgroup and sensitivity analyses, forest plots
Year:
2022
Region / City:
United Kingdom
Topic:
Anti-Money Laundering
Document Type:
Policy & Procedures
Organization:
[Firm Name]
Author:
[Firm Name]
Target Audience:
Accountancy Firms, Money Laundering Reporting Officers (MLROs)
Effective Period:
Ongoing
Approval Date:
[MM/YY]
Date of Changes:
[MM/YY]
Year:
2019
Region / City:
United Kingdom
Subject:
Anti-money laundering compliance
Document Type:
Guidance
Author:
CIOT, ATT
Target Audience:
Small firms registered for AML Supervision with CIOT or ATT
Period of validity:
Ongoing
Approval Date:
8 April 2019
Modification Date:
N/A
Year:
2019
Region / City:
Hong Kong
Topic:
Anti-Money Laundering / Counter-Financing of Terrorism Compliance
Document Type:
Self-Assessment Checklist
Organization / Authority:
Securities and Futures Commission (SFC)
Target Audience:
Licensed Corporations (LCs) and Associated Entities (AEs)
Version:
April 2019
Responsible Officer:
Compliance Officer (CO) and Money Laundering Reporting Officer (MLRO)
Reference:
Guideline on Anti-Money Laundering and Counter-Financing of Terrorism for Licensed Corporations
Date of Completion:
as recorded by LC / AE
Note:
Year
Subject:
Anti-Money Laundering, Compliance, Financial Regulations
Document Type:
Template
Organization / Institution:
FINRA
Target Audience:
Small Firms, Financial Institutions, Compliance Officers
Year:
N/A
Region / city:
EMEA
Theme:
Anti-Money Laundering (AML) Requirements
Document type:
Regulatory information
Organ / institution:
CitiDirect
Author:
N/A
Target audience:
Banks and financial institutions across EMEA region
Effective period:
N/A
Approval date:
N/A
Modification date:
N/A
Context description:
Document provides an overview of AML regulatory documentation requirements for multiple countries across the EMEA region for banking institutions and payment authorization processes.