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European Stop Tyrosine Kinase Inhibitor Study (EURO-SKI)

Primary Purpose

Chronic Myeloid Leukemia

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Stopping treatment with TKI
Sponsored by
European LeukemiaNet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Myeloid Leukemia focused on measuring TKI, CML, Stopping, chronic phase, in remission

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • CML in CP under treatment with TKI in first line or in second line because of toxicity to first line TKI or with TKI in combination
  • Duration of TKI treatment before enrolment at least 3 years
  • At least complete molecular remission MR4
  • Before inclusion confirmation of CMR4 through a EUTOS-CMR laboratory
  • Baseline data and documentation on treatment before study entry available
  • Both sexes but fertile women only if using effective contraceptive
  • Health insurance coverage
  • 18 years or older

Exclusion Criteria:

  • Under 18 years old
  • Hospitalized patients without ability to give informed consent
  • Adults under law protection or without ability to consent
  • Previous or planned allogeneic stem cell transplantation

Sites / Locations

  • Fakultní nemocnice
  • Fakultní nemocnice Hradec Králové
  • University Hospital Olomouc
  • University Hospital Plzen
  • Fakultni nemocnice Kralovske Vinohrady
  • Ústav hematologie a krevní transfuze
  • Odense University Hospital
  • Helsinki University Central Hospital
  • CHU d'Angers
  • Institut Bergonié
  • Université Victor Segalen
  • Hôpital André Mignot
  • Chu Estaing
  • Hôpital Claude Huriez
  • Hôpital Édouard Herriot
  • Institut Paoli-Calmettes (IPC)
  • Centre Hospitalier Universitaire (CHU) de Nantes
  • Hôpital de l'Archet
  • Hôpital Saint-Louis
  • Hôpital Necker-Enfants Malades
  • Hopital de la Milétrie, Centre Hospitalier Universitaire (CHU) de Poitiers
  • Hôpital Pontchaillou
  • Hôpital Purpan
  • CHU de Tours
  • Hôpital de Brabois
  • Uniklinik RWTH
  • Universitätsklinikum
  • Klinikum
  • Universitätsklinikum
  • Klinikum Kempten-Oberallgäu
  • Universitätsmedizin Mannheim, Universität Heidelberg
  • Universitätsklinikum Giessen und Marburg GmbH
  • MVZ Klinikum Straubing GmbH
  • University of Athens, Society of Hematology
  • VU Academic Medical Center
  • Albert Schweitzer Hospital
  • Oslo universitetssykehus HF Rikshospitalet
  • Stavanger University Hospital
  • University Hospital of Northern Norway
  • Norwegian University of Science and Technology
  • Instituto Português de Oncologia Francisco Gentil
  • Karoliniska Univ hospital Huddinge
  • Univ hospital Linköping
  • Sunderby hospital
  • Lunds Universitet
  • Karoliniska Univ sjh Solna
  • Länssj Sundsvall
  • Norrlands Univ hospital
  • Uppsala University hospital
  • Univ hospital Örebro

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Stop treatment

Arm Description

TKI treatment will be stopped in CML patients with very deep molecular responses for at least one year and at least 3 years TKI treatment

Outcomes

Primary Outcome Measures

molecular relapse-free survival
Evaluation of molecular relapse-free survival after stopping TKI (survival without molecular relapse defined by BCR-ABL1 > 0.1% on the IS at one time point (loss of major molecular response, MMR))

Secondary Outcome Measures

Overall and progression-free survival
Overall and progression-free survival and the probabilities of a restart of TKI without prior molecular relapse
Treatment costs
Saved treatment costs / country from the time off TKI therapy considering also the more frequent PCR monitoring
QoL
Patient reported QoL and symptom burden over time
Time to recovery
Analysing the time to recovery of CMR4 after loss of MMR

Full Information

First Posted
May 8, 2012
Last Updated
October 29, 2021
Sponsor
European LeukemiaNet
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1. Study Identification

Unique Protocol Identification Number
NCT01596114
Brief Title
European Stop Tyrosine Kinase Inhibitor Study
Acronym
EURO-SKI
Official Title
Multicenter Trial Estimating the Persistence of Molecular Remission in Chronic Myeloid Leukemia After Stopping TKI
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
May 30, 2012 (Actual)
Primary Completion Date
December 3, 2014 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
European LeukemiaNet

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The EURO-SKI is a multicenter open label, uncontrolled trial estimating the persistence of molecular remission in Chronic Myeloid Leukemia (CML) patients after stopping Tyrosine Kinase Inhibitor (TKI). Main goal is the assessment of the duration of major molecular response (MMR) or better after stopping TKI therapy. Secondary goals include: Identification of clinical and biological factors affecting the persistence of complete molecular remission after stopping TKI (e.g. level of Complete molecular remission (CMR), risk score, duration of TKI treatment, type of TKI pretreatment) Evaluation of quality of life (QoL) in patients stopping TKI Evaluation of medico-economic impact of stopping TKI Estimating the number of patients in CMR who are eligible for stopping TKI therapy by setting up a screening log Time to recovery of CMR There will be no randomised comparison. Based on the experience of the STIM trial (Mahon et al., Lancet Onc 2010) we expect an overall six-month molecular-relapse-free survival probability of at least 40%. An interim analysis will be performed after a pilot phase where 200 patients have been observed for at least six months. Formally, it is planned to test the null hypothesis H0: Six-month molecular relapse-free survival probability P ≤ 40% against the alternative hypothesis H1: Six-month molecular-relapse-free survival probability P > 40%. Eligible are adult CML patients in chronic phase on TKI treatment in CMR for at least one year (> 4 log reduction of BCR-ABL transcripts on IS, TKI treatment for at least 3 years, confirmed by a PCR within a standardized CMR laboratory). Clinical and biological monitoring will be performed during 3 years: Associated scientific projects are performed. Recruitment period: 2 years; follow up: 3 years. Planned patient recruitment in main phase: n=500

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Myeloid Leukemia
Keywords
TKI, CML, Stopping, chronic phase, in remission

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
868 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Stop treatment
Arm Type
Experimental
Arm Description
TKI treatment will be stopped in CML patients with very deep molecular responses for at least one year and at least 3 years TKI treatment
Intervention Type
Other
Intervention Name(s)
Stopping treatment with TKI
Intervention Description
stopping until loss of MMR
Primary Outcome Measure Information:
Title
molecular relapse-free survival
Description
Evaluation of molecular relapse-free survival after stopping TKI (survival without molecular relapse defined by BCR-ABL1 > 0.1% on the IS at one time point (loss of major molecular response, MMR))
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Overall and progression-free survival
Description
Overall and progression-free survival and the probabilities of a restart of TKI without prior molecular relapse
Time Frame
3 years
Title
Treatment costs
Description
Saved treatment costs / country from the time off TKI therapy considering also the more frequent PCR monitoring
Time Frame
3 years
Title
QoL
Description
Patient reported QoL and symptom burden over time
Time Frame
3 years
Title
Time to recovery
Description
Analysing the time to recovery of CMR4 after loss of MMR
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: CML in CP under treatment with TKI in first line or in second line because of toxicity to first line TKI or with TKI in combination Duration of TKI treatment before enrolment at least 3 years At least complete molecular remission MR4 Before inclusion confirmation of CMR4 through a EUTOS-CMR laboratory Baseline data and documentation on treatment before study entry available Both sexes but fertile women only if using effective contraceptive Health insurance coverage 18 years or older Exclusion Criteria: Under 18 years old Hospitalized patients without ability to give informed consent Adults under law protection or without ability to consent Previous or planned allogeneic stem cell transplantation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susanne Saussele, Prof. Dr.
Organizational Affiliation
Universitätsmedizin Mannheim, Universität Heidelberg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fakultní nemocnice
City
Brno
ZIP/Postal Code
625 00
Country
Czechia
Facility Name
Fakultní nemocnice Hradec Králové
City
Hradec Kralove
ZIP/Postal Code
50005
Country
Czechia
Facility Name
University Hospital Olomouc
City
Olomouc
ZIP/Postal Code
775 20
Country
Czechia
Facility Name
University Hospital Plzen
City
Plzen
ZIP/Postal Code
30460
Country
Czechia
Facility Name
Fakultni nemocnice Kralovske Vinohrady
City
Prague
ZIP/Postal Code
100 34
Country
Czechia
Facility Name
Ústav hematologie a krevní transfuze
City
Prague
ZIP/Postal Code
12820
Country
Czechia
Facility Name
Odense University Hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark
Facility Name
Helsinki University Central Hospital
City
Helsinki
ZIP/Postal Code
00029 HUCH
Country
Finland
Facility Name
CHU d'Angers
City
Angers
ZIP/Postal Code
49933
Country
France
Facility Name
Institut Bergonié
City
Bordeaux
ZIP/Postal Code
33000
Country
France
Facility Name
Université Victor Segalen
City
Bordeaux
ZIP/Postal Code
33076
Country
France
Facility Name
Hôpital André Mignot
City
Chesnay cedex
ZIP/Postal Code
78157
Country
France
Facility Name
Chu Estaing
City
Clermont Ferrand
ZIP/Postal Code
63003
Country
France
Facility Name
Hôpital Claude Huriez
City
Lille
ZIP/Postal Code
59037
Country
France
Facility Name
Hôpital Édouard Herriot
City
Lyon
ZIP/Postal Code
69437
Country
France
Facility Name
Institut Paoli-Calmettes (IPC)
City
Marseille
ZIP/Postal Code
13273
Country
France
Facility Name
Centre Hospitalier Universitaire (CHU) de Nantes
City
Nantes
ZIP/Postal Code
44093
Country
France
Facility Name
Hôpital de l'Archet
City
Nice
ZIP/Postal Code
06200
Country
France
Facility Name
Hôpital Saint-Louis
City
Paris cedex 10
ZIP/Postal Code
75475
Country
France
Facility Name
Hôpital Necker-Enfants Malades
City
Paris Cedex 15
ZIP/Postal Code
75743
Country
France
Facility Name
Hopital de la Milétrie, Centre Hospitalier Universitaire (CHU) de Poitiers
City
Poitiers
ZIP/Postal Code
86021
Country
France
Facility Name
Hôpital Pontchaillou
City
Rennes
ZIP/Postal Code
35033
Country
France
Facility Name
Hôpital Purpan
City
Toulouse
ZIP/Postal Code
31059
Country
France
Facility Name
CHU de Tours
City
Tours
ZIP/Postal Code
37044
Country
France
Facility Name
Hôpital de Brabois
City
Vandoeuvre-lès-Nancy
ZIP/Postal Code
54511
Country
France
Facility Name
Uniklinik RWTH
City
Aachen
ZIP/Postal Code
52074
Country
Germany
Facility Name
Universitätsklinikum
City
Bonn
ZIP/Postal Code
53105
Country
Germany
Facility Name
Klinikum
City
Chemnitz
ZIP/Postal Code
09113
Country
Germany
Facility Name
Universitätsklinikum
City
Jena
ZIP/Postal Code
07747
Country
Germany
Facility Name
Klinikum Kempten-Oberallgäu
City
Kempten
ZIP/Postal Code
87439
Country
Germany
Facility Name
Universitätsmedizin Mannheim, Universität Heidelberg
City
Mannheim
ZIP/Postal Code
68163
Country
Germany
Facility Name
Universitätsklinikum Giessen und Marburg GmbH
City
Marburg
ZIP/Postal Code
35033
Country
Germany
Facility Name
MVZ Klinikum Straubing GmbH
City
Straubing
ZIP/Postal Code
94315
Country
Germany
Facility Name
University of Athens, Society of Hematology
City
Athens
ZIP/Postal Code
11526
Country
Greece
Facility Name
VU Academic Medical Center
City
Amsterdam
ZIP/Postal Code
1007 MB
Country
Netherlands
Facility Name
Albert Schweitzer Hospital
City
Dordrecht
ZIP/Postal Code
3300
Country
Netherlands
Facility Name
Oslo universitetssykehus HF Rikshospitalet
City
Oslo
ZIP/Postal Code
0372
Country
Norway
Facility Name
Stavanger University Hospital
City
Stavanger
ZIP/Postal Code
4068
Country
Norway
Facility Name
University Hospital of Northern Norway
City
Tromsø
ZIP/Postal Code
9038
Country
Norway
Facility Name
Norwegian University of Science and Technology
City
Trondheim
ZIP/Postal Code
7489
Country
Norway
Facility Name
Instituto Português de Oncologia Francisco Gentil
City
Lisboa
ZIP/Postal Code
1099-023
Country
Portugal
Facility Name
Karoliniska Univ hospital Huddinge
City
Huddinge
ZIP/Postal Code
141 86
Country
Sweden
Facility Name
Univ hospital Linköping
City
Linköping
ZIP/Postal Code
581 85
Country
Sweden
Facility Name
Sunderby hospital
City
Luleå
ZIP/Postal Code
971 80
Country
Sweden
Facility Name
Lunds Universitet
City
Lund
ZIP/Postal Code
221 85
Country
Sweden
Facility Name
Karoliniska Univ sjh Solna
City
Stockholm
ZIP/Postal Code
171 76
Country
Sweden
Facility Name
Länssj Sundsvall
City
Sundsvall
ZIP/Postal Code
851 86
Country
Sweden
Facility Name
Norrlands Univ hospital
City
Umeå
ZIP/Postal Code
901 85
Country
Sweden
Facility Name
Uppsala University hospital
City
Uppsala
ZIP/Postal Code
751 85
Country
Sweden
Facility Name
Univ hospital Örebro
City
Örebro
ZIP/Postal Code
701 85
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
33589755
Citation
Richter J, Lubking A, Soderlund S, Lotfi K, Markevarn B, Sjalander A, Stenke L, Deneberg S, Ahlstrand E, Myhr-Eriksson K, Panayiotidis P, Gedde-Dahl T, Zackova D, Mayer J, Olsson-Stromberg U, Mahon FX, Saussele S, Hjorth-Hansen H, Koskenvesa P. Molecular status 36 months after TKI discontinuation in CML is highly predictive for subsequent loss of MMR-final report from AFTER-SKI. Leukemia. 2021 Aug;35(8):2416-2418. doi: 10.1038/s41375-021-01173-w. Epub 2021 Feb 15. No abstract available.
Results Reference
background
PubMed Identifier
32058176
Citation
Soderlund S, Persson I, Ilander M, Guilhot J, Hjorth-Hansen H, Koskenvesa P, Richter J, Saussele S, Mustjoki S, Olsson-Stromberg U. Plasma proteomics of biomarkers for inflammation or cancer cannot predict relapse in chronic myeloid leukaemia patients stopping tyrosine kinase inhibitor therapy. Leuk Res. 2020 Mar;90:106310. doi: 10.1016/j.leukres.2020.106310. Epub 2020 Jan 23.
Results Reference
background
PubMed Identifier
29980572
Citation
Bouillon AS, Ventura Ferreira MS, Awad SA, Richter J, Hochhaus A, Kunzmann V, Dengler J, Janssen J, Ossenkoppele G, Westerweel PE, Te Boekhorst PAW, Mahon FX, Hjorth-Hansen H, Isfort S, Fioretos T, Hummel S, Schemionek M, Wilop S, Koschmieder S, Saussele S, Mustjoki S, Beier F, Brummendorf TH. Telomere shortening correlates with leukemic stem cell burden at diagnosis of chronic myeloid leukemia. Blood Adv. 2018 Jul 10;2(13):1572-1579. doi: 10.1182/bloodadvances.2018017772.
Results Reference
background
PubMed Identifier
28074067
Citation
Schutz C, Inselmann S, Saussele S, Dietz CT, Mu Ller MC, Eigendorff E, Brendel CA, Metzelder SK, Bru Mmendorf TH, Waller C, Dengler J, Goebeler ME, Herbst R, Freunek G, Hanzel S, Illmer T, Wang Y, Lange T, Finkernagel F, Hehlmann R, Huber M, Neubauer A, Hochhaus A, Guilhot J, Xavier Mahon F, Pfirrmann M, Burchert A. Expression of the CTLA-4 ligand CD86 on plasmacytoid dendritic cells (pDC) predicts risk of disease recurrence after treatment discontinuation in CML. Leukemia. 2017 Apr;31(4):829-836. doi: 10.1038/leu.2017.9. Epub 2017 Jan 11. Erratum In: Leukemia. 2018 Jan 30;:
Results Reference
background
PubMed Identifier
29735299
Citation
Saussele S, Richter J, Guilhot J, Gruber FX, Hjorth-Hansen H, Almeida A, Janssen JJWM, Mayer J, Koskenvesa P, Panayiotidis P, Olsson-Stromberg U, Martinez-Lopez J, Rousselot P, Vestergaard H, Ehrencrona H, Kairisto V, Machova Polakova K, Muller MC, Mustjoki S, Berger MG, Fabarius A, Hofmann WK, Hochhaus A, Pfirrmann M, Mahon FX; EURO-SKI investigators. Discontinuation of tyrosine kinase inhibitor therapy in chronic myeloid leukaemia (EURO-SKI): a prespecified interim analysis of a prospective, multicentre, non-randomised, trial. Lancet Oncol. 2018 Jun;19(6):747-757. doi: 10.1016/S1470-2045(18)30192-X. Epub 2018 May 4.
Results Reference
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PubMed Identifier
27890936
Citation
Ilander M, Olsson-Stromberg U, Schlums H, Guilhot J, Bruck O, Lahteenmaki H, Kasanen T, Koskenvesa P, Soderlund S, Hoglund M, Markevarn B, Sjalander A, Lotfi K, Dreimane A, Lubking A, Holm E, Bjoreman M, Lehmann S, Stenke L, Ohm L, Gedde-Dahl T, Majeed W, Ehrencrona H, Koskela S, Saussele S, Mahon FX, Porkka K, Hjorth-Hansen H, Bryceson YT, Richter J, Mustjoki S. Increased proportion of mature NK cells is associated with successful imatinib discontinuation in chronic myeloid leukemia. Leukemia. 2017 May;31(5):1108-1116. doi: 10.1038/leu.2016.360. Epub 2016 Nov 28.
Results Reference
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PubMed Identifier
29510895
Citation
Rinaldetti S, Pfirrmann M, Manz K, Guilhot J, Dietz C, Panagiotidis P, Spiess B, Seifarth W, Fabarius A, Muller M, Pagoni M, Dimou M, Dengler J, Waller CF, Brummendorf TH, Herbst R, Burchert A, Janbetaen C, Goebeler ME, Jost PJ, Hanzel S, Schafhausen P, Prange-Krex G, Illmer T, Janzen V, Klausmann M, Eckert R, Buschel G, Kiani A, Hofmann WK, Mahon FX, Saussele S. Effect of ABCG2, OCT1, and ABCB1 (MDR1) Gene Expression on Treatment-Free Remission in a EURO-SKI Subtrial. Clin Lymphoma Myeloma Leuk. 2018 Apr;18(4):266-271. doi: 10.1016/j.clml.2018.02.004. Epub 2018 Feb 8.
Results Reference
result

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European Stop Tyrosine Kinase Inhibitor Study

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