A Randomized Phase III Study to Assess the Effect of a Longer Duration of Consolidation Treatment With Nilotinib on TFR in CP CML. (ENESTPath)

A Prospective, Randomized, Open Label, Two Arm Phase III Study to Evaluate Treatment Free Remission (TFR) Rate in Patients With Philadelphia-positive CML After Two Different Durations of Consolidation Treatment With Nilotinib 300mg BID.

This study aimed to assess the optimal duration of nilotinib 300 mg twice daily (BID) consolidation treatment in patients with Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML), in order that patients remained in treatment-free remission (≥MR4.0) without molecular relapse 12 months after starting the Treatment-Free Remission (TFR) phase.

Study Overview

• Status: Completed
• Conditions: Philadelphia Chromosome Positive (PH+) Chronic Myelogenous Leukemia in Chronic Phase (CML-CP)
• Intervention / Treatment: Drug: Nilotinib

Detailed Description

This was a prospective, randomized, open-label, multicenter Phase III study. The study design was made up of 3 phases:

• Nilotinib induction phase: 12 months
• Nilotinib consolidation phase: 12 or 24 months, depending on randomization
• Nilotinib treatment-free remission (TFR) phase: 24 or 36 months, depending on randomization.

Subjects were enrolled into the study and were treated with nilotinib 300mg twice daily (BID) for 24 months, during the induction (12 months) and consolidation (12 months) phases. At the end of the first 24 months of treatment, participants achieving a sustained molecular response (defined as ≥ MR4.0, in 4 out of 5 real-time quantitative polymerase chain reaction (RQ-PCR) assessments, including the last assessment, in the last 12 months) were randomized on a 1:1 basis to either:

1. suspend nilotinib treatment immediately and enter the TFR phase for 36 months (Nilotinib 24-month treatment arm), or
2. continue nilotinib treatment for a further 12 months (post-randomization consolidation phase), then suspend treatment and enter the TFR phase for 24 months (Nilotinib 36-month treatment arm).

Participants not achieving a sustained molecular response at 24 months from treatment start were not eligible for randomization and were treated at the discretion of the investigator according to standard practice. Information on survival, stem cell transplantation, and status of the patient's disease was collected until death or until 5 years from study entry, whichever came first. Additionally, for Nilotinib 36-month treatment arm, participants who did not achieve a sustained molecular response at 36 months from treatment start, discontinued from the study and were treated according to standard practice and followed up until death or until 5 years from study entry, whichever came first.

Participants relapsing during the TFR phase entered the nilotinib re-treatment phase of the study, and were re-treated with the same dose of nilotinib as they were on before the TFR phase. These patients remained on study until the completion of the 5-year study period unless prematurely withdrawn and discontinued from the study for any reason specified in the Protocol.

• Study Type: Interventional
• Enrollment (Actual): 620
• Phase: Phase 3

Contacts and Locations

Study Locations

• Austria
  • Graz, Austria, 8036
    • Novartis Investigative Site
  • Linz, Austria, A-4010
    • Novartis Investigative Site
  • Linz, Austria, 4010
    • Novartis Investigative Site
  • Rankweil, Austria, A-6830
    • Novartis Investigative Site
  • Salzburg, Austria, 5020
    • Novartis Investigative Site
  • Oberoesterreich
    • Linz, Oberoesterreich, Austria, A 4020
      • Novartis Investigative Site
• Belgium
  • Bruxelles, Belgium, 1070
    • Novartis Investigative Site
  • Liege, Belgium, 4000
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• Bulgaria
  • Pleven, Bulgaria, 5800
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  • Plovdiv, Bulgaria, 4002
    • Novartis Investigative Site
  • Sofia, Bulgaria, 1756
    • Novartis Investigative Site
  • Sofia, Bulgaria, 1431
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  • Varna, Bulgaria, 9000
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• Czechia
  • CZE
    • Hradec Kralove, CZE, Czechia, 500 05
      • Novartis Investigative Site
  • Czech Republic
    • Brno Bohunice, Czech Republic, Czechia, 625 00
      • Novartis Investigative Site
• Denmark
  • Holstebro, Denmark, DK-7500
    • Novartis Investigative Site
  • Roskilde, Denmark, 4000
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• Finland
  • HUS Helsinki, Finland, FIN-00029
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• France
  • Angers Cedex 1, France, 49033
    • Novartis Investigative Site
  • Bordeaux, France, 33076
    • Novartis Investigative Site
  • Bordeaux Cedex, France, 33000
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  • Chalon sur Saône, France, 71321
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  • Chambéry cedex, France, 73011
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  • Clermont Ferrand cedex 1, France, 63003
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  • Corbeil Essonnes, France, 91100
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  • Dunkerque, France, 59240
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  • Grenoble, France, 38043
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  • La Roche sur Yon cedex 9, France, 85925
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  • Lille, France, 59037
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  • Lille cedex, France, 59020
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  • Lyon Cedex, France, 69373
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  • Marseille, France, 13273
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  • Metz, France, 57085
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  • Metz, France, 57000
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  • Mulhouse cedex, France, 68070
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  • Nice Cedex, France, 06202
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  • Paris, France, 75012
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  • Perpignan, France, 66046
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  • Pontoise, France, F-95300
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  • Rouen Cedex 1, France, 76038
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  • Saint Priest en Jarez, France, 42271
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  • Toulouse, France, 31059
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  • Bayonne Cedex
    • Bayonne, Bayonne Cedex, France, 64109
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  • Cedex
    • Caen, Cedex, France, 14033
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  • Cedex 09
    • Le Mans, Cedex 09, France, 72037
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  • Cedex 10
    • Paris Cedex 10, Cedex 10, France, 75475
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• Germany
  • Augsburg, Germany, 86150
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  • Bayreuth, Germany, 95445
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  • Berlin, Germany, 13353
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  • Braunschweig, Germany, 38114
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  • Bremen, Germany, 28177
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  • Chemnitz, Germany, 09113
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  • Dresden, Germany, 01307
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  • Eisenach, Germany, 99817
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  • Frankfurt, Germany, 60596
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  • Georgsmarienhuette, Germany, 49124
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  • Halle, Germany, 06110
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  • Hamm, Germany, 59063
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  • Kiel, Germany, 24105
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  • Koeln, Germany, 50671
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  • Leipzig, Germany, 04103
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  • Lütten-Klein, Germany, 18107
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  • Magdeburg, Germany, 39104
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  • Marburg, Germany, 35039
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  • Muenchen, Germany, 81241
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  • Muenster, Germany, 48149
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  • Nuernberg, Germany, 90449
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  • Offenburg, Germany, 77654
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  • Potsdam, Germany, 14467
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  • Rostock, Germany, 18057
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  • Rostock, Germany, 18059
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  • Schorndorf, Germany, 73614
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  • Schwäbisch-Hall, Germany, 74523
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  • Stuttgart, Germany, 70174
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  • Velbert, Germany, 42551
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  • Westerstede, Germany, 26655
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  • Wiesbaden, Germany, 65191
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  • Wuerzburg, Germany, 97080
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  • Baden-Wuerttemberg
    • Mannheim, Baden-Wuerttemberg, Germany, 68305
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• Greece
  • Athens, Greece, 115 27
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  • Athens, Greece, 106 76
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  • Patras, Greece, 265 00
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  • GR
    • Athens, GR, Greece, 115 27
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    • Thessaloniki, GR, Greece, 570 10
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• Hungary
  • Budapest, Hungary, 1097
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  • Debrecen, Hungary, 4032
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  • Szeged, Hungary, H 6725
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• Italy
  • Napoli, Italy, 80131
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  • Novara, Italy, 28100
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  • Perugia, Italy, 06129
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  • AL
    • Alessandria, AL, Italy, 15100
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  • AN
    • Ancona, AN, Italy, 60126
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  • AV
    • Avellino, AV, Italy, 83100
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  • BA
    • Bari, BA, Italy, 70124
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  • BO
    • Bologna, BO, Italy, 40138
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  • BS
    • Brescia, BS, Italy, 25123
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  • CA
    • Cagliari, CA, Italy, 09126
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  • CR
    • Cremona, CR, Italy, 26100
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  • CT
    • Catania, CT, Italy, 95100
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  • FE
    • Cona, FE, Italy, 44100
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  • FG
    • San Giovanni Rotondo, FG, Italy, 71013
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  • FI
    • Firenze, FI, Italy, 50134
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  • GE
    • Genova, GE, Italy, 16132
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  • LE
    • Lecce, LE, Italy, 73100
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  • LI
    • Livorno, LI, Italy, 57124
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  • Lazio
    • Roma, Lazio, Italy, 00168
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  • ME
    • Messina, ME, Italy, 98125
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  • MI
    • Milano, MI, Italy, 20162
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    • Milano, MI, Italy, 20132
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    • Milano, MI, Italy, 20122
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  • MO
    • Modena, MO, Italy, 41124
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  • PA
    • Palermo, PA, Italy, 90127
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    • Palermo, PA, Italy, 90146
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  • PD
    • Padova, PD, Italy, 35128
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  • PE
    • Pescara, PE, Italy, 65124
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  • PI
    • Pisa, PI, Italy, 56126
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  • PR
    • Parma, PR, Italy, 43100
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  • PV
    • Pavia, PV, Italy, 27100
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  • PZ
    • Potenza, PZ, Italy, 85100
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  • RC
    • Reggio Calabria, RC, Italy, 89124
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  • RE
    • Reggio Emilia, RE, Italy, 42123
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  • RM
    • Roma, RM, Italy, 00144
      • Novartis Investigative Site
    • Roma, RM, Italy, 00161
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    • Roma, RM, Italy, 00133
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  • SA
    • Pagani, SA, Italy, 84016
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  • SI
    • Siena, SI, Italy, 53100
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  • TA
    • Taranto, TA, Italy, 74100
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  • TO
    • Orbassano, TO, Italy, 10043
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    • Torino, TO, Italy, 10126
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  • TV
    • Treviso, TV, Italy, 31100
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  • UD
    • Udine, UD, Italy, 33100
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  • VE
    • Mirano, VE, Italy, 30035
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    • Venezia, VE, Italy, 30174
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  • VI
    • Vicenza, VI, Italy, 36100
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  • VR
    • Verona, VR, Italy, 37126
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• Norway
  • Bergen, Norway, NO-5021
    • Novartis Investigative Site
  • Oslo, Norway, NO-0310
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• Poland
  • Chorzow, Poland, 41-500
    • Novartis Investigative Site
  • Gdansk, Poland, 80 952
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  • Katowice, Poland, 40-027
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  • Krakow, Poland, 30-510
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  • Olsztyn, Poland, 10 561
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  • Opole, Poland, 45-372
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  • Torun, Poland, 87 100
    • Novartis Investigative Site
  • Warszawa, Poland, 02 776
    • Novartis Investigative Site
  • Warszawa, Poland, 02 106
    • Novartis Investigative Site
• Portugal
  • Lisboa, Portugal, 1749-035
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  • Lisboa, Portugal, 1099 023
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  • Porto, Portugal, 4099-001
    • Novartis Investigative Site
  • Porto, Portugal, 4200-072
    • Novartis Investigative Site
  • Porto, Portugal, 4200 319
    • Novartis Investigative Site
• Romania
  • Bucharest, Romania, 030 171
    • Novartis Investigative Site
  • Bucharest, Romania, 500098
    • Novartis Investigative Site
  • Cluj-Napoca, Romania, 400124
    • Novartis Investigative Site
  • Iasi, Romania, 700483
    • Novartis Investigative Site
  • Sibiu, Romania, 550245
    • Novartis Investigative Site
  • Timisoara, Romania, 300 079
    • Novartis Investigative Site
  • District 2
    • Bucharest, District 2, Romania, 022328
      • Novartis Investigative Site
• Serbia
  • Belgrade, Serbia, 11000
    • Novartis Investigative Site
  • Belgrade, Serbia, 11070
    • Novartis Investigative Site
  • Nis, Serbia, 18000
    • Novartis Investigative Site
  • Novi Sad, Serbia
    • Novartis Investigative Site
• Slovakia
  • Bratislava, Slovakia, 85107
    • Novartis Investigative Site
  • Martin, Slovakia, 03601
    • Novartis Investigative Site
• Slovenia
  • Ljubljana, Slovenia, 1000
    • Novartis Investigative Site
• Spain
  • Granollers, Spain, 08402
    • Novartis Investigative Site
  • Madrid, Spain, 28041
    • Novartis Investigative Site
  • Madrid, Spain, 28034
    • Novartis Investigative Site
  • Madrid, Spain, 28046
    • Novartis Investigative Site
  • Madrid, Spain, 28006
    • Novartis Investigative Site
  • Madrid, Spain, 28040
    • Novartis Investigative Site
  • Madrid, Spain, 28009
    • Novartis Investigative Site
  • Madrid, Spain, 28222
    • Novartis Investigative Site
  • Madrid, Spain, 28031
    • Novartis Investigative Site
  • Murcia, Spain, 30008
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  • Santa Cruz de Tenerife, Spain, 38009
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  • Zaragoza, Spain, 50009
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  • Andalucia
    • Granada, Andalucia, Spain, 18014
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    • Jaen, Andalucia, Spain, 23007
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    • Malaga, Andalucia, Spain, 29010
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    • Sevilla, Andalucia, Spain, 41013
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    • Sevilla, Andalucia, Spain, 41009
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  • Barcelona
    • Sabadell, Barcelona, Spain, 08208
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  • Castilla Y Leon
    • León, Castilla Y Leon, Spain, 24071
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    • Salamanca, Castilla Y Leon, Spain, 37007
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    • Valladolid, Castilla Y Leon, Spain, 47011
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  • Catalunya
    • Badalona, Catalunya, Spain, 08916
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    • Barcelona, Catalunya, Spain, 08035
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    • Barcelona, Catalunya, Spain, 08036
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    • Barcelona, Catalunya, Spain, 08003
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    • Girona, Catalunya, Spain, 17007
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    • Hospitalet de LLobregat, Catalunya, Spain, 08907
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    • Tarragona, Catalunya, Spain, 43005
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  • Comunidad Valenciana
    • Alicante, Comunidad Valenciana, Spain, 03010
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    • Alzira, Comunidad Valenciana, Spain, 46600
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    • Valencia, Comunidad Valenciana, Spain, 46026
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  • Extremadura
    • Caceres, Extremadura, Spain, 10003
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  • Galicia
    • La Coruna, Galicia, Spain, 15006
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    • Pontevedra, Galicia, Spain, 36071
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    • Santiago de Compostela, Galicia, Spain, 15706
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  • Islas Baleares
    • Palma De Mallorca, Islas Baleares, Spain, 07120
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  • Navarra
    • Pamplona, Navarra, Spain, 31008
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  • Pais Vasco
    • San Sebastian, Pais Vasco, Spain, 20080
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• Sweden
  • Stockholm, Sweden, SE-171 76
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• United Kingdom
  • East Yorkshire, United Kingdom, HU16 5JQ
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  • Edinburgh, United Kingdom, EH4 2XU
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  • London, United Kingdom, EC1A 7BE
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  • London, United Kingdom, W12 0HS
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Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Key Inclusion Criteria:

• Confirmed diagnosis of chronic phase Ph+ CML
• Previous first-line treatment with imatinib for a minimum of 2 years;
• Patient in complete cytogenetic response;

Key Exclusion Criteria:

• Previous achievement of MR4.0 at study entry;
• Previous treatment with other target cells inhibitors other than imatinib;
• Patients with any history of detectable atypical Leukemia transcripts or patients with detectable atypical leukemia transcripts at screening;
• Previous anticancer agents for Chronic myeloid leukemia other than imatinib except for cytoreduction;
• Severe and/or uncontrolled concurrent medical disease that in the opinion of the investigator could cause unacceptable safety risks or compromise compliance with the protocol;
• History of other active malignancies within the 5 years prior to study entry with the exception of previous or concomitant basal cell skin cancer and previous carcinoma in situ treated curatively;
• Patients who have not recovered from prior surgery;
• Treatment with other investigational agents within 4 weeks of Day 1;
• Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of study drug

Other inclusion/exclusion criteria might apply.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Nilotinib 24-month treatment; Participants were treated with nilotinib 300mg BID for 24 months and, thereafter, entered the 36-month TFR phase	Drug: Nilotinib; Participants received a daily oral nilotinib dose of 300 mg BID, given as two 150 mg capsules BID.; Other Names: AMN107
Experimental: Nilotinib 36-month treatment; Participants were treated with nilotinib 300mg BID for 36 months and, thereafter, entered the 24-month TFR phase	Drug: Nilotinib; Participants received a daily oral nilotinib dose of 300 mg BID, given as two 150 mg capsules BID.; Other Names: AMN107
Experimental: Not randomized; Participants were treated with nolotinib 300mg BID for 24 months, but did not achieve a sustained molecular response after 24 months of treatment.	Drug: Nilotinib; Participants received a daily oral nilotinib dose of 300 mg BID, given as two 150 mg capsules BID.; Other Names: AMN107

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Percentage of Participants Who Remained in Treatment Free Remission (TFR) Without Molecular Relapse 12 Months After Entering the TFR Phase	Number of participants who remained in TFR (≥molecular response (MR) 4.0) without molecular relapse 12 months after entering the TFR phase (without re-starting nilotinib therapy) divided by the number of participants who entered the TFR phase and multiplied by 100. Molecular relapse during TFR is defined as the loss of major molecular response (MMR), or the confirmed loss of MR4.0 (defined by 3 consecutive tests less than MR4.0 assessed at 3 consecutive visits during TFR phase). Participants dropping out early from the study during the TFR phase were considered as unsuccessful TFR. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MMR is defined as≥3.0 log reduction in BCR-ABL transcripts compared to the standardized baseline or ≤0.1% BCR-ABL. MR4.0 is defined as either detectable disease≤0.01% BCR-ABL or undetectable disease in cDNA with≥10,000 ABL transcripts	12 months after entering the TFR phase, which is after 36 months from study treatment start for Nilotinib 24-month treatment arm and after 48 months from study treatment start for Nilotinib 36-month treatment arm

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Cumulative Incidence of MMR During the Pre-randomization Induction/Consolidation Phase Among Participants Without That Response at Study Entry	Number of participants who were in MMR during pre-randomization induction/consolidation phase divided by the number of participants without that response at baseline and multiplied by 100. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MMR is defined as ≥3.0 log reduction in BCR-ABL transcripts compared to the standardized baseline or ≤0.1% BCR-ABL.	From baseline up to 24 months after study treatment start
Cumulative Incidence of MMR During the Post-randomization Consolidation Phase Among Participants Without That Response at Study Entry	Number of participants who were in MMR during post-randomization consolidation phase divided by the number of participants without that response at baseline and multiplied by 100. Post-randomization consolidation phase corresponded to the 12-month additional treatment (after randomization) for Nilotinib 36-month treatment arm. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MMR is defined as ≥3.0 log reduction in BCR-ABL transcripts compared to the standardized baseline or ≤0.1% BCR-ABL.	From randomization (month 24 after study treatment start) up to 36 months after study treatment start
Cumulative Incidence of MR4.0 During the Pre-randomization Induction/Consolidation Phase Among Participants Without That Response at Study Entry	Number of participants who were in MR4.0 during the pre-randomization induction/consolidation phase divided by the number of participants without that response at baseline and multiplied by 100. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.0 is defined as either detectable disease ≤0.01% BCR-ABL IS or undetectable disease in cDNA with ≥10,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From baseline up to 24 months after study treatment start
Cumulative Incidence of MR4.0 During the Post-randomization Consolidation Phase Among Participants Without That Response at Study Entry	Number of participants who were in MR4.0 during the post-randomization consolidation phase divided by the number of participants without that response at baseline and multiplied by 100. Post-randomization consolidation phase corresponded to the 12-month additional treatment (after randomization) for Nilotinib 36-month treatment arm. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.0 is defined as either detectable disease ≤0.01% BCR-ABL IS or undetectable disease in cDNA with ≥10,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From randomization (month 24 after study treatment start) up to 36 months after study treatment start
Cumulative Incidence of MR4.5 During the Pre-randomization Induction/Consolidation Phase Among Participants Without That Response at Study Entry	Number of participants who were in MR4.5 during the pre-randomization induction/consolidation phase divided by the number of participants without that response at baseline and multiplied by 100. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.5 is defined as either detectable disease ≤ 0.0032% BCR-ABL IS; or undetectable disease within cDNA with ≥ 32,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From baseline up to 24 months after study treatment start
Cumulative Incidence of MR4.5 During the Post-randomization Consolidation Phase Among Participants Without That Response at Study Entry	Number of participants who were in MR4.5 during the post-randomization consolidation phase divided by the number of participants without that response at baseline and multiplied by 100. Post-randomization consolidation phase corresponded to the 12-month additional treatment (after randomization) for Nilotinib 36-month treatment arm. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.5 is defined as either detectable disease ≤ 0.0032% BCR-ABL IS; or undetectable disease within cDNA with ≥ 32,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From randomization (month 24 after study treatment start) up to 36 months after study treatment start
Cumulative Incidence of MMR During the Pre-randomization Induction/Consolidation Phase	Number of participants who were in MMR during the pre-randomization induction/consolidation phase divided by the number of enrolled participants and multiplied by 100. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MMR is defined as ≥3.0 log reduction in BCR-ABL transcripts compared to the standardized baseline or ≤0.1% BCR-ABL.	From baseline up to 24 months after study treatment start
Cumulative Incidence of MMR During the Post-randomization Consolidation Phase	Number of participants who were in MMR during the post-randomization consolidation phase divided by the number of enrolled participants and multiplied by 100. Post-randomization consolidation phase corresponded to the 12-month additional treatment (after randomization) for Nilotinib 36-month treatment arm. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MMR is defined as ≥3.0 log reduction in BCR-ABL transcripts compared to the standardized baseline or ≤0.1% BCR-ABL.	From randomization (month 24 after study treatment start) up to 36 months after study treatment start
Cumulative Incidence of MR4.0 During the Pre-randomization Induction/Consolidation Phase	Number of participants who were in MR4.0 during the pre-randomization induction/consolidation phase divided by the number of enrolled participants and multiplied by 100. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.0 is defined as either detectable disease ≤0.01% BCR-ABL IS or undetectable disease in cDNA with ≥10,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From baseline up to 24 months after study treatment start
Cumulative Incidence of MR4.0 During the Post-randomization Consolidation Phase	Number of participants who were in MR4.0 during the post-randomization consolidation phase divided by the number of enrolled participants and multiplied by 100. Post-randomization consolidation phase corresponded to the 12-month additional treatment (after randomization) for Nilotinib 36-month treatment arm. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.0 is defined as either detectable disease ≤0.01% BCR-ABL IS or undetectable disease in cDNA with ≥10,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From randomization (month 24 after study treatment start) up to 36 months after study treatment start
Cumulative Incidence of MR4.5 During the Pre-randomization Induction/Consolidation Phase	Number of participants who were in MR4.5 during the pre-randomization induction/consolidation phase divided by the number of enrolled participants and multiplied by 100. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.5 is defined as either detectable disease ≤ 0.0032% BCR-ABL IS; or undetectable disease within cDNA with ≥ 32,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From baseline up to 24 months after study treatment start
Cumulative Incidence of MR4.5 During the Post-randomization Consolidation Phase	Number of participants who were in MR4.5 during the post-randomization consolidation phase divided by the number of enrolled participants and multiplied by 100. Post-randomization consolidation phase corresponded to the 12-month additional treatment (after randomization) for Nilotinib 36-month treatment arm. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.5 is defined as either detectable disease ≤ 0.0032% BCR-ABL IS; or undetectable disease within cDNA with ≥ 32,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From randomization (month 24 after study treatment start) up to 36 months after study treatment start
Percentage of Participants Who Were in MMR During TFR Phase	Number of participants who were in MMR at selected timepoints divided by the number of participants in the TFR phase and multiplied by 100. Participants randomized in Nilotinib 36-month treatment arm had a maximum of 24 months of TFR phase, whereas participants randomized in Nilotinib 24-month treatment arm had a maximum of 36 months of TFR phase. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MMR is defined as ≥3.0 log reduction in BCR-ABL transcripts compared to the standardized baseline or ≤0.1% BCR-ABL.	From Month 1 after entering TFR phase up to 24 months after entering TFR phase for Nilotinib 36-month treatment arm and up to 36 months after entering TFR phase for Nilotinib 24-month treatment arm
Percentage of Participants Who Were in MR4.0 During the TFR Phase	Number of participants who were in MR4.0 at selected timepoints divided by the number of participants in the TFR phase and multiplied by 100. Participants randomized in Nilotinib 36-month treatment arm had a maximum of 24 months of TFR phase, whereas participants randomized in Nilotinib 24-month treatment arm had a maximum of 36 months of TFR phase. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.0 is defined as either detectable disease ≤0.01% BCR-ABL IS or undetectable disease in cDNA with ≥10,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From Month 1 after entering TFR phase up to 24 months after entering TFR phase for Nilotininb 36-months treatment arm and up to 36 months after entering TFR phase for Nilotinib 24-months treatment arm
Percentage of Participants Who Were in MR4.5 During the TFR Phase	Number of participants who were in MR4.5 at selected timepoints divided by the number of participants in the TFR phase and multiplied by 100. Participants randomized in Nilotinib 36-month treatment arm had a maximum of 24 months of TFR phase, whereas participants randomized in Nilotinib 24-month treatment arm had a maximum of 36 months of TFR phase. Confidence intervals were calculated based on the Exact Clopper-Pearson method. MR4.5 is defined as either detectable disease ≤ 0.0032% BCR-ABL IS; or undetectable disease within cDNA with ≥ 32,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From Month 1 after entering TFR phase up to 24 months after entering TFR phase for Nilotininb 36-month treatment arm and up to 36 months after entering TFR phase for Nilotinib 24-month treatment arm
BCR-ABL Ratio (Expressed as a Percentage) During the Induction/Consolidation Phase	BCR-ABL transcript ratio by international scale (IS) (expressed as a percentage) during the induction/consolidation phase. Participants randomized to Nilotinib 36-month treatment arm had 12-month additional consolidation phase (post-randomization).	From baseline up to 24 months after study treatment start for Nilotinib 24-month treatment arm and Not randomized participants; and up to 36 months after study treatment start for Nilotinib 36-month treatment arm.
BCR-ABL Ratio (Expressed as a Percentage) During the TFR Phase	BCR-ABL/control gene (ABL) transcript ratio by international scale (IS) (expressed as a percentage) during the TFR phase. BCR-ABL is the fusion gene from breakpoint cluster region and Abelson genes. Participants randomized in Nilotinib 36-month treatment arm had a maximum of 24 months of TFR phase, whereas participants randomized in Nilotinib 24-month treatment arm had a maximum of 36 months of TFR phase.	From Month 1 after entering TFR phase up to 24 months after entering TFR phase for Nilotinib 36-month treatment arm and up to 36 months after entering TFR phase for Nilotinib 24-month treatment arm
BCR-ABL Ratio (Expressed as a Percentage) During the Nilotinib Re-treatment Phase	BCR-ABL/control gene (ABL) transcript ratio by international scale (IS) (expressed as a percentage) during the nilotinib re-treatment phase. BCR-ABL is the fusion gene from breakpoint cluster region and Abelson genes.	From Day 1 after entering the re-treatment phase up to 24 months after entering re-treatment phase for Nilotinib 36-month treatment arm and 36 months after entering the re-treatment phase for Nilotinib 24-month treatment arm
Progression-free Survival (PFS) During the TFR Phase of the Study.	PFS is defined as the time from the date of start of the nilotinib TFR phase to the date of acelerated phase/blast crisis (AP/BC) or death, whichever came first. Participants randomized in Nilotinib 36-month treatment arm had a maximum of 24 months of TFR phase, whereas participants randomized in Nilotini 24-month treatment arm had a maximum of 36 months of TFR phase. Patients not known to have recurred or died on or before the cut-off date for PFS analysis were censored at the date of their last assessment (cytogenetic, hematology or extramedullary) for patients who were on study, and at the date of last contact for patients who were in follow-up.	From the start of the TFR phase to progression to AP/BC or death up to 24 months after entering TFR phase for Nilotininb 36-month treatment arm and up to 36 months after entering TFR phase for Nilotinib 24-month treatment arm
Treatment -Free Survival (TFS) During the TFR Phase of the Study	TFS is defined as the time from the start of the TFR phase to the date of the earliest of the following: loss of MMR, confirmed loss of MR4.0,re-start of nilotinib treatment, progression to AP/BC, or death from any cause. Patients not known to have had any of the events on or before the cut-off date were censored at the earlier of the date of their last assessment for patients who were still on study and the date of last contact for patients who were in follow-up. Participants randomized in Nilotinib 36-month treatment arm had a maximum of 24 months of TFR phase, whereas participants randomized in Nilotinib 24-month treatment arm had a maximum of 36 months of TFR phase. MMR is defined as ≥3.0 log reduction in BCR-ABL transcripts compared to the standardized baseline or ≤0.1%BCR-ABL. MR4.0 is defined as either detectable disease ≤0.01%BCR-ABL IS or undetectable disease in cDNA with ≥10,000 ABL transcripts (numbers of ABL transcripts in the same volume of cDNA used to test for BCR-ABL)	From the start of the TFR phase to the date of occurrence of treatment-free survival event, up to 24 months after entering TFR phase for Nilotinib 36-month treatment arm and up to 36 months after entering TFR phase for Nilotinib 24-month treatment arm
Overall Survival (OS) Rate During the TFR Phase of the Study.	OS is defined as the time from start of the TFR phase to the time of death due to any cause. Participants randomized in Nilotinib 36-month treatment arm had a maximum of 24 months of TFR phase, whereas participants randomized in Nilotini 24-month treatment arm had a maximum of 36 months of TFR phase. For participants without any event on or before the cut-off date, survival time will be censored at the date of their last assessment for patients who are still on study, and at the date of last contact for patients who are in follow-up.	From the start of the TFR phase to death due to any cause, assessed up to 24 months after entering TFR phase for Nilotinib 36-month treatment arm and up to 36 months after entering TFR phase for Nilotinib 24-month treatment arm

Collaborators and Investigators

• Sponsor: Novartis Pharmaceuticals

Publications and helpful links

General Publications

• Borghi L, Rosti G, Maggi A, Breccia M, Di Bona E, Iurlo A, La Barba G, Sportoletti P, Albano F, Galimberti S, Rivellini F, Cambrin GR, Capodanno I, Cuneo A, Bonifacio M, Sica S, Arcaini L, Capochiani E, Minotto C, Ciceri F, Crugnola M, Di Caprio L, Supekar S, Elena C, Baccarani M, Vegni E. Perspectives and Emotional Experiences of Patients With Chronic Myeloid Leukemia During ENESTPath Clinical Trial and Treatment-Free Remission: Rationale and Protocol of the Italian Substudy. Front Oncol. 2021 May 26;11:638689. doi: 10.3389/fonc.2021.638689. eCollection 2021.

Study record dates

Study Major Dates

• Study Start (Actual): April 15, 2013
• Primary Completion (Actual): July 8, 2020
• Study Completion (Actual): July 8, 2020

Study Registration Dates

• First Submitted: December 4, 2012
• First Submitted That Met QC Criteria: December 5, 2012
• First Posted (Estimate): December 6, 2012

Study Record Updates

• Last Update Posted (Actual): July 15, 2021
• Last Update Submitted That Met QC Criteria: June 23, 2021
• Last Verified: June 1, 2021

More Information

Terms related to this study

• Keywords: Adult; Chronic myelogenous leukemia (CML); Acute Lymphoid Leukemia; Chronic myeloid leukemia (CML); Acute Lymphoblastic Leukemia (ALL) Philadelphia chromosome positive; Suboptimal molecular response; Chronic myelocytic leukemia (CML)
• Additional Relevant MeSH Terms: Pathologic Processes; Neoplasms by Histologic Type; Neoplasms; Bone Marrow Diseases; Hematologic Diseases; Myeloproliferative Disorders; Chromosome Aberrations; Translocation, Genetic; Leukemia; Leukemia, Myeloid; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Philadelphia Chromosome
• Other Study ID Numbers: CAMN107AIC05; 2012-005124-15 (EudraCT Number)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES

IPD Plan Description

Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.

This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No