Chronic Myeloid LeukemiaPhase 2BESTNCT02810990
Bosutinib in Elderly Chronic Myeloid Leukemia
A Phase 2 study testing Bosutinib in people with Chronic Myeloid Leukemia, run by Gruppo Italiano Malattie EMatologiche dell'Adulto at 45 sites in Italy.
Trial summary
The objective of the present study is to evaluate a new drug called bosutinib as it is believed that this agent may be able to predict an excellent prognosis in patients that did not obtain any benefit with other drugs before. Still, this needs to be proved and we hope this study is able to do so. Read more about this study
- Who is it for?
- Ages 60 years and older
- Conditions the study is for
- Chronic Myeloid Leukemia
- What is being tested?
- Bosutinib
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 65 participants
- Where
- 45 sitesItaly
- Study dates
- 17 Nov 2016to 22 Jun 2022
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Molecular confirmed diagnosis of BCR-ABL1+ CML
- Chronic phase CML (ELN 2013 criteria)
- 60 years of age or older
- Prior first-line treatment with any other TKIs
- Intolerance to prior treatment, based on investigator and patient assessment or failure of prior treatment according to any one of the ELN 2013 criteria, as listed below
- Non complete hematologic response (CHR) at 3 months
Show all 17Show fewer
- No cytogenetic response (Ph+ > 95%) at 6 months
- Less than Partial Cytogenetic Response (PCyR) (Ph+ >35%) at 6 months
- BCR-ABL1 > 10% at 6 months
- Non complete CyR (CCyR) (Ph+ > 0) at 12 months
- BCR-ABL1 > 1% at 12 months
- Loss of CHR at any time
- Loss of CCyR at any time
- Confirmed loss of major molecular response (MMR) (BCR-ABL1 > 0.1%) in two consecutive tests, of which one > 1%, at any time
- An effective form of contraception from enrolment through 30 days after the end of treatment
- Signed written informed consent according to ICH/EU/GCP and national and local laws prior to any study procedures
- Willingness and ability to comply with scheduled visits and study procedures.
Who cannot join
- Accelerated or blastic phase CML (according to ELN 2013 criteria)
- Patients with the T315I or the V299L mutation
- Patients previously treated with 2 TKIs or more
- Compelled to take medications that are known to be associated with Torsades de Pointes and/or with significant QTc prolongation
- Any condition or illness that, in the opinion of the Investigator, would compromise patient safety or interfere with the evaluation of the drug
- HBV markers positivity
- Lack of informed consent
Trial locations and contacts
45 sites in 1 country.
45 sites in 1 country
Italy45 sites
S.O.C. di Ematologia - Azienda Ospedaliera - SS. Antonio e Biagio e Cesare Arrigo
Alessandria
Azienda Ospedaliero - Universitaria Ospedali Riuniti Umberto I - G.M. LANCISI - G. SALESI
Ancona
UO Ematologia con trapianto-Università degli Studi di Bari Aldo Moro
Bari
Fausto Castagnetti
Bologna
Istituto di Ematologia "Lorenzo e A. Seragnoli" - Policlinico S. Orsola - Malpighi
Bologna
ASL N.8 - Ospedale "A. Businco" - Struttura Complessa di Ematologia e CTMO
Cagliari
Università di Catania - Cattedra di Ematologia - Ospedale "Ferrarotto"
Catania
S.C. Ematologia ASO S. Croce e Carle
Cuneo
Arcispedale Sant'Anna Dipartimento di Scienze Mediche Sezione di Ematologia
Ferrara
Policlinico di Careggi
Florence
Struttura Complessa di Ematologia Ospedali Riuniti Foggia
Foggia
IRCCS_AOU San Martino-IST-Ematologia 1-Monoblocco 11°piano- lato ponente
Genova
ASL Le/1 P.O. Vito Fazzi - U.O. di Ematologia ed UTIE
Lecce
Istituto Scientifico Romagnoli per lo Studio e la Cura dei Tumori- IRST
Meldola
Policlinico G. Martino Dipartimento di Medicina Interna - U.O. Messina
Messina
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico UOC Oncoematologia
Milan
U.O. Ematologia e Trapianto di MIdollo - Ist.Scientifico Ospedale San Raffaele
Milan
Unità Trapianto di Midollo Ist. Nazionale Tumori
Milan
Azienda Ospedaliera "S.Gerardo"
Monza
Azienda Università degli Studi di Napoli "Federico II" - Facoltà di Medicina e Chirurgia
Naples
S.C.D.U. Ematologia - Università del Piemonte Orientale Amedeo Avogadro
Novara
Dip. di Scienze Cliniche e Biologiche - Ospedale S. Luigi Gonzaga-Medicina Interna 2
Orbassano
Università degli Studi di Padova - Ematologia ed Immunologia Clinica
Padova
U.O. di Ematologia con trapianto - A.U. Policlinico "Paolo Giaccone"
Palermo
Cattedra di Ematologia CTMO Università degli Studi di Parma
Parma
S.C. Ematologia - Fondazione IRCCS Policlinico S. Matteo
Pavia
Dipartimento di Oncologia ed Ematologia - AUSL Ospedale G. da Saliceto
Piacenza
Ematologia - Ospedale San Carlo
Potenza
Dipartimento Oncologico - Ospedale S.Maria delle Croci
Ravenna
Unità Operativa Complessa di Ematologia - Arcispedale S. Maria Nuova
Reggio Emilia
Ospedale "Infermi"
Rimini
U.O. di Ematologia - Centro Oncologico Basilicata
Rionero in Vulture
Complesso Ospedaliero S. Giovanni Addolorata
Roma
Divisione Ematologia - Università Campus Bio-Medico
Roma
Padiglione Cesalpino - I piano - Divisione di Ematologia - Ospedale S. Camillo
Roma
Università Cattolica del Sacro Cuore - Policlinico A. Gemelli
Roma
UOC Pronto Soccorso - Dipartimento Biotecnologie Cellulari Università di Roma "Sapienza"
Roma
Istituto di Ematologia - IRCCS Ospedale Casa Sollievo della Sofferenza
San Giovanni Rotondo
U.O.C. Ematologia e Trapianti - A.O. Senese - Policlinico " Le Scotte"
Siena
A.O. Santa Maria - Terni S.C Oncoematologia
Terni
Divisione di Ematologia - "Città della Salute e della Scienza di Torino"
Torino
S.C. Ematologia 2 A.O. Città della Salute e della Scienza di Torino San Giovanni Battista
Torino
Clinica Ematologica-Centro Trapianti e Terapie cellulari
Udine
Medicina Interna I - Ospedale di Circolo
Varese
A. O. - Istituti Ospitalieri di Verona- Div. di Ematologia - Policlinico G.B. Rossi
Verona
About this study
Official title: Bosutinib Efficacy, Safety, Tolerability (BEST) Study in Elderly Chronic Myeloid Leukemia Patients Failing Front-line Treatment With Other Tyrosine Kinase Inhibitors
The objective of the present study is to evaluate a new drug called bosutinib as it is believed that this agent may be able to predict an excellent prognosis in patients that did not obtain any benefit with other drugs before. Still, this needs to be proved and we hope this study is able to do so.
Read the detailed description
Bosutinib is a potent tyrosine kinase inhibitor (TKI) active at nM concentration on BCR-ABL1 and most BCR-ABL1 mutations. Bosutinib has been approved by the FDA and the EMA for the treatment of patients with Ph+/BCR-ABL1+ chronic myeloid leukemia who fail treatment with other TKIs, first or second line. The goal of second-line treatment of CML is to achieve a response that would predict for a survival equal to, or very close to, the survival of non leukemic people, that is to say to achieve a complete cytogenetic response (CCyR) or a major molecular response (MMR). To achieve that goal, it is necessary to find and keep the right balance between activity, safety, and tolerability. There are no studies comparing TKIs in second-line. From phase 2, single-arm, studies, the reported efficacy of Bosutinib is similar to the reported efficacy of dasatinib and nilotinib. The median age of newly diagnosed CML patients is about 56 years, and at least 40% of all newly diagnosed patients are more than 60 years old. Particularly for these patients, the choice of the TKI must take into account the safety and the tolerability profile of the TKIs. The use of dasatinib and nilotinib is burdened by pleural and pulmonary complications, by infections, and by cardiovascular, thrombotic and metabolic (diabetes mellitus, dyslipidemia) complications. These complications are more frequent and more clinically relevant in the elderly. The safety and tolerability of Bosutinib has been reported in first- as well as in second- and third-line. The standard dose (500 mg once daily) is tolerated and safe, but at that dose several adverse events (AEs) limit the tolerability, require dose reduction or interruption, and affect patient quality of life, including diarrhea, nausea, vomiting, skin rash. Also an increase of AST, ALT and lipase are of concern and a cause of treatment discontinuation. On the contrary, an increased frequency of infections and of pleuro-pulmonary, cardiovascular, thrombotic, and metabolic AEs has not been reported. The reported hematologic toxicity of Bosutinib is at least as low as, or even lower than, that reported for the other TKIs, in spite of the fact that Bosutinib is a dual, BCR-ABL1 and src inhibitor. Until today, all studies of TKIs in CML have tested a fixed initial dose, providing for dose adjustment in case of toxicity (dose decrease) or in case of unsatisfactory response (dose increase). No study so far was designed to test the adaptation of the dose to the response, taking advantage of the fact that the efficacy of TKI treatment can be assessed rapidly and precisely by measuring the BCR-ABL1 transcripts level with real-time PCR (RT-PCR) in peripheral blood cells. An RT-PCR monthly for the first few months provides the best assessment of the response to treatment. We predict that a more flexible strategy of treatment (adapting the dose to the response) will result into a more convenient balance between activity and toxicity, hence into a better outcome. Based on these premises, it is proposed to test the activity, the safety, and the tolerability of Bosutinib, second-line, beginning with a low dose and adjusting subsequent doses based on molecular response, and on AEs, in a population of elderly patients. In almost all prior studies of TKIs in second- or third-line, the primary efficacy was assessed using cytogenetic response, both major and complete, at different time points. To make the results of this study comparable to the results of prior studies, the cytogenetic response will be evaluated as specified in section 5, but since the response to therapy and the evaluation of the efficacy of therapy are more and more based on molecular response, dose adaptation and efficacy evaluation will be based primarily on molecular response.
- Conditions
- Chronic Myeloid Leukemia
- Being tested
- Bosutinib
- Keywords
- bosutinib, chronic myeloid leukemia
- Medical subject headings
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BosutinibDrug
Bosutinib is given orally accordingly with this scheme:
- 200 mg OD: starting dose ("wash-in" period) at week 1 and week 2 B. 300 mg OD: from week 3 to the end of week 16
At the end of week 12 evaluation of molecular response (BCR-ABL1 level by RT-Q-PCR).
Bosutinib dose is then managed as follows :
C1. if BCR-ABL1 ≤1% at week 12: 300 mg OD from week 17 to week 52 C2. if BCR-ABL1 > 1% at week 12: 400 mg OD from week 17 to week 52
All the responsive patients who are still on Bosutinib at the end of week 52, will continue Bosutinib at the same dose (300 mg OD or 400 mg OD) for the next two years ( if tolerated and in absence of safety concerns).
| Study group | Role | What they receive |
|---|---|---|
| Bosutinib treatment | Experimental | Not described Receives: Drug: Bosutinib |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of patients who are in major molecular response (MMR)
Measured: One year treatment
Secondary outcomes (7)
Number of patients who obtain molecular response
Measured: At 6 and 12 months from treatment start
Number of patients discontinuing treatment for failure, adverse events or other reasons
Measured: At 12 and 36 months
Number of Adverse Events (AEs)
Measured: At 36 months
Number of patients alive
Measured: At 36 months
Number of patients on treatment at 200, 300 and 400 mg or more daily
Measured: At 6, 12 and 36 months
Number and type of BCR-ABL1 mutations
Measured: At 36 months
Patient reported quality of life
Measured: At 3, 6, and 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Jun 2016 (estimated)
- Study start17 Nov 2016
- Primary completion30 Apr 2020
- Study completion22 Jun 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Myeloid LeukemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 65 participants (actual)
Sponsor and investigators
- Lead sponsor
- Gruppo Italiano Malattie EMatologiche dell'Adulto
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Fausto Castagnetti, Study chair, Department of Hematology, S. Orsola-Malpighi University of Bologna
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02810990
- Sponsor's protocol ID
- CML1516
- Other IDs
- 2016-002216-40, 2016
- Acronym
- BEST
- Status last verified
- Feb 2023
- First submitted
- 15 Jun 2016
- Last updated
- 3 Feb 2023
- Results posted
- No
- Data monitoring committee
- Yes
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Feb 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Bosutinib Efficacy, Safety, Tolerability (BEST) Study in Elderly Chronic Myeloid Leukemia Patients Failing Front-line Treatment With Other Tyrosine Kinase Inhibitors
- ClinicalTrials.gov ID
- NCT02810990
- Acronym / sponsor ID
- BEST / CML1516
- Conditions
- Chronic Myeloid Leukemia
- Keywords
- bosutinib, chronic myeloid leukemia
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 65 participants (actual)
- Lead sponsor
- Gruppo Italiano Malattie EMatologiche dell'AdultoUniversity, hospital or other
- Study start
- 17 Nov 2016 (actual)
- Primary completion
- 30 Apr 2020 (actual)
- Study completion
- 22 Jun 2022 (actual)
- First posted
- 23 Jun 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The objective of the present study is to evaluate a new drug called bosutinib as it is believed that this agent may be able to predict an excellent prognosis in patients that did not obtain any benefit with other drugs before. Still, this needs to be proved and we hope this study is able to do so.
Detailed description
Bosutinib is a potent tyrosine kinase inhibitor (TKI) active at nM concentration on BCR-ABL1 and most BCR-ABL1 mutations. Bosutinib has been approved by the FDA and the EMA for the treatment of patients with Ph+/BCR-ABL1+ chronic myeloid leukemia who fail treatment with other TKIs, first or second line. The goal of second-line treatment of CML is to achieve a response that would predict for a survival equal to, or very close to, the survival of non leukemic people, that is to say to achieve a complete cytogenetic response (CCyR) or a major molecular response (MMR). To achieve that goal, it is necessary to find and keep the right balance between activity, safety, and tolerability. There are no studies comparing TKIs in second-line. From phase 2, single-arm, studies, the reported efficacy of Bosutinib is similar to the reported efficacy of dasatinib and nilotinib. The median age of newly diagnosed CML patients is about 56 years, and at least 40% of all newly diagnosed patients are more than 60 years old. Particularly for these patients, the choice of the TKI must take into account the safety and the tolerability profile of the TKIs. The use of dasatinib and nilotinib is burdened by pleural and pulmonary complications, by infections, and by cardiovascular, thrombotic and metabolic (diabetes mellitus, dyslipidemia) complications. These complications are more frequent and more clinically relevant in the elderly. The safety and tolerability of Bosutinib has been reported in first- as well as in second- and third-line. The standard dose (500 mg once daily) is tolerated and safe, but at that dose several adverse events (AEs) limit the tolerability, require dose reduction or interruption, and affect patient quality of life, including diarrhea, nausea, vomiting, skin rash. Also an increase of AST, ALT and lipase are of concern and a cause of treatment discontinuation. On the contrary, an increased frequency of infections and of pleuro-pulmonary, cardiovascular, thrombotic, and metabolic AEs has not been reported. The reported hematologic toxicity of Bosutinib is at least as low as, or even lower than, that reported for the other TKIs, in spite of the fact that Bosutinib is a dual, BCR-ABL1 and src inhibitor. Until today, all studies of TKIs in CML have tested a fixed initial dose, providing for dose adjustment in case of toxicity (dose decrease) or in case of unsatisfactory response (dose increase). No study so far was designed to test the adaptation of the dose to the response, taking advantage of the fact that the efficacy of TKI treatment can be assessed rapidly and precisely by measuring the BCR-ABL1 transcripts level with real-time PCR (RT-PCR) in peripheral blood cells. An RT-PCR monthly for the first few months provides the best assessment of the response to treatment. We predict that a more flexible strategy of treatment (adapting the dose to the response) will result into a more convenient balance between activity and toxicity, hence into a better outcome. Based on these premises, it is proposed to test the activity, the safety, and the tolerability of Bosutinib, second-line, beginning with a low dose and adjusting subsequent doses based on molecular response, and on AEs, in a population of elderly patients. In almost all prior studies of TKIs in second- or third-line, the primary efficacy was assessed using cytogenetic response, both major and complete, at different time points. To make the results of this study comparable to the results of prior studies, the cytogenetic response will be evaluated as specified in section 5, but since the response to therapy and the evaluation of the efficacy of therapy are more and more based on molecular response, dose adaptation and efficacy evaluation will be based primarily on molecular response.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Bosutinib treatment | Experimental | Drug: Bosutinib |
Who may qualify
- Ages
- 60 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (17 listed)
- Molecular confirmed diagnosis of BCR-ABL1+ CML
- Chronic phase CML (ELN 2013 criteria)
- 60 years of age or older
- Prior first-line treatment with any other TKIs
- Intolerance to prior treatment, based on investigator and patient assessment or failure of prior treatment according to any one of the ELN 2013 criteria, as listed below
Key exclusion criteria (7 listed)
- Accelerated or blastic phase CML (according to ELN 2013 criteria)
- Patients with the T315I or the V299L mutation
- Patients previously treated with 2 TKIs or more
- Compelled to take medications that are known to be associated with Torsades de Pointes and/or with significant QTc prolongation
- Any condition or illness that, in the opinion of the Investigator, would compromise patient safety or interfere with the evaluation of the drug
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BosutinibBosutinib is given orally accordingly with this scheme: A. 200 mg OD: starting dose ("wash-in" period) at week 1 and week 2 B. 300 mg OD: from week 3 to the end of week 16 At the end of week 12 evaluation of molecular response (BCR-ABL1 level by RT-Q-PCR). Bosutinib dose is then managed as follows : C1. if BCR-ABL1 ≤1% at week 12: 300 mg OD from week 17 to week 52 C2. if BCR-ABL1 > 1% at week 12: 400 mg OD from week 17 to week 52 All the responsive patients who are still on Bosutinib at the end of week 52, will continue Bosutinib at the same dose (300 mg OD or 400 mg OD) for the next two years ( if tolerated and in absence of safety concerns). | Drug | Bosutinib treatment |
Primary outcome
Number of patients who are in major molecular response (MMR)
Time frame: One year treatment
7 secondary outcomes
Number of patients who obtain molecular response
Time frame: At 6 and 12 months from treatment start
Number of patients discontinuing treatment for failure, adverse events or other reasons
Time frame: At 12 and 36 months
Number of Adverse Events (AEs)
Time frame: At 36 months
Number of patients alive
Time frame: At 36 months
Number of patients on treatment at 200, 300 and 400 mg or more daily
Time frame: At 6, 12 and 36 months
Number and type of BCR-ABL1 mutations
Time frame: At 36 months
Patient reported quality of life
Time frame: At 3, 6, and 12 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Feb 2023.
- GIMEMA Foundation websiteLink provided by the sponsor.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Fausto Castagnetti study chair
Department of Hematology, S. Orsola-Malpighi University of Bologna
45 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Bosutinib in people with Chronic Myeloid Leukemia, run by Gruppo Italiano Malattie EMatologiche dell'Adulto at 45 sites in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 17 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 3 Feb 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 45 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of patients who are in major molecular response (MMR) (time frame: One year treatment). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Feb 2023.