Phase II Front-line Ponatinib in Adult Philadelphia+/BCR-ABL+ Acute Lymphoblastic Leukemia.

Acute Lymphoblastic Leukemia Clinical Trial

— LAL1811  

Official title:

Front-line Treatment of Philadelphia Positive/BCR-ABL Positive Acute Lymphoblastic Leukemia With Ponatinib, a New Potent Tyrosine Kinase Inhibitor.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01641107
• Other study ID #: LAL1811
• Secondary ID: 2012-002761-35
• Status: Completed
• Phase: Phase 2
• Start date: December 4, 2014
• Est. completion date: September 30, 2021

Study information

• Verified date: November 2021
• Source: Incyte Corporation
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Drug resistance resulting from emergence of Imatinib-resistant BCR-ABL clones is a significant problem in Ph positive ALL patients because after a very good initial response to one TKI inhibitor, many patients relapse within one year, relapse being almost always associated with a BCR-ABL kinase domain point mutation. The patients who relapse after treatment with one TKI can be rescued to remission with another TKI, but the second remission is usually shorter than the previous one. A more potent TKI inhibitor, and pan-active not only on all the BCR-ABL variants (including the second generation TKI resistant T315I mutant), but also on others molecular targets can do better. In this context, Ponatinib is a novel synthetic orally active tyrosine kinase inhibitor (TKI), specifically developed to inhibit BCR-ABL, the fusion protein that is the product of the Philadelphia chromosome (Ph) in chronic myeloid leukemia (CML) and in a subset of acute lymphoblastic leukemia (Ph+ ALL). It potently inhibits the BCR-ABL protein as well as mutated forms of the protein that arise in patients resistant to prior therapies with TKIs. Ponatinib has been demonstrated to inhibit all the mutations that have been detected so far, in vitro and in vivo and to uniformly suppress the emerge of single-mutant clones in a mutagenesis assay. In the Phase II study, 41% of Philadelphia chromosome positive acute lymphoblastic leukemia patients treated with Ponatinib achieved major hematologic response, 47% had a major cytogenetic response, 38% obtained a complete cytogenetic response, showing that Ponatinib provides significant benefit despite previous intolerance or refractoriness to other TKIs. The Phase I trial showed that patients with a more recent diagnosis had increased rates of major molecular response: 79% for 14 patients with 0 to 5 years since diagnosis vs. 29% for 14 patients with more than 5 to 9 years since diagnosis (P=0.02) and 27% for 15 patients with more than 9 to 24 years since diagnosis (P=0.009). These characteristics support the hypothesis for a role of Ponatinib not only in patients resistant to prior TKI therapy but also in untreated ALL Ph+ patients, in order to prevent the emergence of resistant caused by the selection of mutated Ph+ clones and in order to avoid rapid progression of the disease.

Description:

This is a multi-center, phase 2, single arm unblinded trial of oral Ponatinib in patients with Ph+ Acute Lymphoblastic Leukemia. Patients will receive daily oral administration of Ponatinib at a dose of 45 mg/day for 6 weeks (defined as one course) for 8 courses, same dose and schedule, for a total of 48 weeks. Each patient will be followed for the subsequent 24 months, every 3 month, providing survival information and monitoring serious adverse event.

Each patient should be treated for a minimum of 6 weeks. Then a patient can be discontinued in the following situation:

• at the end of first course (6 weeks), in case of lack of CHR;

• at the end of third course (18 weeks), in case of lack of CCgR;

• any time in case of loss of CHR or CCgR.

If they remain on therapy after 48 weeks, they will be able to continue treatment during the extension phase of the study, if it is of interest of the patient, or they will be allowed to receive any treatment that is in their interest. For all the patients remaining on trial, response, outcome and toxicity will be followed for the subsequent 24 months.The 6-weeks periodicity must be rigidly respected, irrespective of the temporary discontinuation of study drug (eg, if a patient will take Ponatinib only for 4 weeks and will remain off-treatment for the subsequent two weeks because of AE, when the 7th week begins this patient will restart Ponatinib as a second course, as per protocol). Prednisone (P) will be administered to all patients for 7-14 days, before Ponatinib, so as to make it possible to wait for the results of cytogenetic and molecular tests, and to evaluate the response to P alone, hence for another 21 days. Intrathecal therapy (IT) with MTX/AraC/DEX is mandatory, every 28 days, in patients without clinical-cytologic evidence of meningeal involvement. In patients with CNS disease, IT is performed twice weekly until a complete clearance of cerebrospinal fluid blast cells is achieved, hence once weekly for 4 weeks, hence once monthly.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: September 30, 2021
• Est. primary completion date: April 24, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. To be classified as having Ph+ ALL, patients must have >20% blasts in bone marrow at the time of diagnosis and no prior history of CML.

2. Patients with previously untreated Ph+ and/or BCR/ABL + ALL:

• age = 60 years old or

• age = 18 years old, but unfit for program of intensive therapy and allogeneic SCT

3. Adequate hepatic function as defined by the following criteria:

• total serum bilirubin =1.5 x upper limit of normal (ULN), unless due to Gilbert's syndrome

• alanine aminotransferase (ALT) =2.5 × ULN

• aspartate aminotransferase (AST) =2.5 × ULN.

4. Adequate pancreatic function as defined by the following criterion:

• serum lipase and amylase =1.5 × ULN.

5. For females of childbearing potential, a negative pregnancy test must be documented prior to randomization.

6. Female and male patients who are fertile must agree to use an effective form of contraception with their sexual partners from randomization through 4 months after the end of treatment.

7. Signed written informed consent according to ICH/EU/GCP and national local laws.

Exclusion Criteria:

1. WHO performance status = 50% (Karnofsky) or = 3 (ECOG).

2. Active HBV or HCV hepatitis, or AST/ALT = 2.5 x ULN and bilirubin = 1.5 x ULN.

3. History of acute pancreatitis within 1 year of study or history of chronic pancreatitis.

4. History of alcohol abuse.

5. Ongoing or active infections.

6. Uncontrolled hypertriglyceridemia (triglycerides >450 mg/dL).

7. Clinically significant, uncontrolled, or active cardiovascular disease, specifically including, but not restricted to:

• any history of myocardial infarction, stroke, or revascularization

• unstable angina or transient ischemic attack within 6 months prior to enrollment

• congestive heart failure within 6 months prior to enrollment, or left ventricular ejection fraction (LVEF) less than lower limit of normal per local institutional standards within 6 months prior to enrollment

• history of clinically significant (as determined by the treating physician) atrial arrhythmia

• any history of ventricular arrhythmia

• any history of venous thromboembolism including deep venous thrombosis or pulmonary embolism .

8. Uncontrolled hypertension (diastolic blood pressure >90 mm Hg; systolic >140 mm Hg). Patients with hypertension should be under treatment on study entry to effect blood pressure control.

9. Taking medications that are known to be associated with Torsades de Pointes.

10. Taking any medications or herbal supplements that are known to be strong inhibitors of CYP3A4 within at least 14 days before the first dose of ponatinib.

11. Creatinine level > 2.5mg/dl or Glomerular Filtration Rate (GFR) < 20 ml/min or proteinuria > 3.5 g/day.

12. Impairment of gastrointestinal (GI) function, or a GI disease that may significantly alter the absorption of study drugs (e.g. rare hereditary problems of galactose intolerance , the Lapp lactase deficiency or glucose-galactose malabsorption, severe malabsorption syndrome, or extended small bowel resection).

13. Patients who are currently receiving treatment with any of the medications listed in Appendix E if the medications cannot be either discontinued or switched to a different medication prior to starting study drug. The medications listed in Appendix E have the potential to prolong QT.

14. Patients who have received any investigational drug = 4 weeks.

15. Patients who have undergone major surgery = 2 weeks prior to starting study drug or who have not recovered from side effects of such therapy.

16. Patients who are pregnant or breast feeding and adults of reproductive potential not employing an effective method of birth control (women of childbearing potential must have a negative serum pregnancy test within 48 hrs prior to administration of Ponatinib). Post menopausal women must be amenorrhoeic for at least 12 months to be considered of non-childbearing potential. Male and female patients must agree to employ an effective barrier method of birth control throughout the study and for up to 4 months following discontinuation of study drugs.

17. Patients with a history of another primary malignancy that is currently clinically significant or currently requires active intervention.

18. Patients unwilling or unable to comply with the protocol.

Related Conditions & MeSH terms

• Acute Lymphoblastic Leukemia
• BCR-ABL Positive
• Leukemia
• Leukemia, Lymphoid
• Philadelphia Positive
• Precursor Cell Lymphoblastic Leukemia-Lymphoma

Intervention

Drug:
• Ponatinib
Treatment: Patients will receive daily oral administration of Ponatinib at a dose of 45 mg/day for 6 weeks (defined as one course) for 8 courses, same dose and schedule, for a total of 48 weeks. Each patient will be followed for the subsequent 24 months, every 3 month, providing survival information and monitoring serious adverse event. Each patient should be treated for a minimum of 6 weeks. Patients must be discontinued from the trial in the event of myocardial infarction or stroke, or for development or progression of arterial disease necessitating revascularization. Once a complete hematologic response has been achieved, with a platelet count = 50x109/L, patients can be treated with aspirin and/or a statin as clinically indicated, at investigator discretion.

Locations

Country	Name	City	State
Italy	S.O.C. di Ematologia - Azienda Ospedaliera - SS. Antonio e Biagio e Cesare Arrigo	Alessandria
Italy	Azienda Ospedaliero - Universitaria Ospedali Riuniti Umberto I - G.M. LANCISI - G. SALESI	Ancona
Italy	Dipartimento Area Medica - Presidio Ospedaliero "C. e G.Mazzoni"	Ascoli
Italy	Az.Ospedaliera S.G.Moscati	Avellino
Italy	Azienda Ospedaliera - Papa Giovanni XXIII	Bergamo
Italy	Istituto di Ematologia "Lorenzo e A. Seragnoli" - Università degli Studi di Bologna - Policlinico S. Orsola - Malpighi	Bologna
Italy	ASL N.8 - Ospedale "A. Businco" - Struttura Complessa di Ematologia e CTMO	Cagliari
Italy	Università di Catania - Cattedra di Ematologia - Ospedale "Ferrarotto"	Catania
Italy	Azienda Ospedaliero Universitaria Arcispedale Sant'Anna Dipartimento di Scienze Mediche Sezione di Ematologia e Fisiopatologia dell'Emostasi	Ferrara
Italy	Policlinico di Careggi	Firenze
Italy	Divisione Ematologia 1 - Azienda Ospedaliera Universitaria "San Martino"	Genova
Italy	ASL Le/1 P.O. Vito Fazzi - U.O. di Ematologia ed UTIE	Lecce
Italy	Unità Operativa Complessa - Medicina Generale - Sezione di Ematologia - Ospedale Versilia USL 12 Toscana	Lido di Camaiore
Italy	Istituto Scientifico Romagnoli per lo Studio e la Cura dei Tumori- IRST	Meldola
Italy	U.O. di Ematologia- Ospedale dell'Angelo - Mestre	Mestre
Italy	Ospedale Niguarda " Ca Granda"	Milano
Italy	UO Ematologia - AOU Policlinico di Modena	Modena
Italy	S.C.D.U. Ematologia - DIMECS e Dipartimento Oncologico - Università del Piemonte Orientale Amedeo Avogadro	Novara
Italy	Dip. di Scienze Cliniche e Biologiche - Ospedale S. Luigi Gonzaga-Medicina Interna 2	Orbassano
Italy	Università degli Studi di Padova - Ematologia ed Immunologia Clinica	Padova
Italy	Ospedali Riuniti "Villa Sofia-Cervello"	Palermo
Italy	S.C. Ematologia - Fondazione IRCCS Policlinico S. Matteo	Pavia
Italy	Sezione di Ematologia ed Immunologia Clinica - Ospedale S.Maria della Misericordia	Perugia
Italy	Div. di Ematologia di Muraglia - CTMO Ospedale San Salvator	Pesaro
Italy	U.O. Ematologia Clinica - Azienda USL di Pescara	Pescara
Italy	Unità Operativa Ematologia e Centro Trapianti - Dipartimento di Oncologia ed Ematologia - AUSL Ospedale di Piacenza	Piacenza
Italy	Università di Pisa - Azienda Ospedaliera Pisana - Dipartimento di Oncologia, dei Trapianti e delle nuove Tecnologie in Medicina - Divisione di Ematologia	Pisa
Italy	Dipartimento Oncologico - Ospedale S.Maria delle Croci	Ravenna
Italy	Dipartimento Emato-Oncologia A.O."Bianchi-Melacrino-Morelli"	Reggio Calabria
Italy	Ospedale "Infermi"	Rimini
Italy	Complesso Ospedaliero S. Giovanni Addolorata	Roma
Italy	S.C. di Ematologia e Trapianti - I.F.O. Istituto Nazionale Tumori Regina Elena	Roma
Italy	U.O.C. Ematologia - Ospedale S.Eugenio	Roma
Italy	Università degli Studi "Sapienza" - Dip Biotecnologie Cellulari ed Ematologia - Divisione di Ematologia	Roma
Italy	Università degli Studi - Policlinico di Tor Vergata	Roma
Italy	UOC di Ematologia e Trapianti di Cellule Staminali Emopoietiche - AOU San Giovanni di Dio e Ruggi D'Aragona	Salerno
Italy	U.O.C. Ematologia e Trapianti - A.O. Senese - Policlinico " Le Scotte"	Siena
Italy	Dipartimento di Oncologia ed Ematologia S.C. Ematologia 2 A.O. Città della Salute e della Scienza di Torino San Giovanni Battista	Torino
Italy	Azienda U.L.S.S.9 - U.O. di Ematologia	Treviso
Italy	Clinica Ematologica - Policlinico Universitario	Udine
Italy	Università degli Studi di Verona - A. O. - Istituti Ospitalieri di Verona- Div. di Ematologia - Policlinico G.B. Rossi	Verona
Italy	ULSS N.6 Osp. S. Bortolo	Vicenza

Sponsors (1)

Lead Sponsor	Collaborator
Incyte Corporation

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of patients who are in Complete Hematological Response (CHR).	The primary endpoint is the proportion of patients who are in CHR at 6 months, calculated on the total number of patients who have been enroled and have received at least one dose of the first drug (prednisone).	At 6 months from study entry.
Secondary	The rate of Complete Hematological Response (CHR).	CHR requires that all of the following are present: Bone marrow with less than 5% blast cells; Peripheral blood differential without blasts; PMN = 1.5 x 109/L; PLT = 100 x 109/L; No evidence of extramedullary involvement from leukemia	At 6, 12, 24, 36 and 48 weeks from study entry.
Secondary	The rate of complete Cytogenetic Response (CgR).	CgR is defined based on the percentage of Ph pos metaphases, as evaluated by chromosome banding analysis (CBA) of at least 20 marrow cell metaphases: Complete (CCgR) if Ph pos 0; Partial (PCgR) if Ph pos 1-34%; Minor (mCgR) if Ph pos 35-65%; Minimal or none (min/none CgR) if Ph pos > 65% If only interphase FISH data are available, the response can be defined only as non-complete or complete - to be complete by FISH, it is required that less than 1% of nuclei (minimum number 200) have a positive signal.	At 6, 12, 24, 36 and 48 weeks from study entry.
Secondary	Duration of Complete Cytogenetic Response (CCgR).	Duration of CCgR is measured by the date of the achievement of CCgR to the date of CCgR loss.	After four years from study entry.
Secondary	The rate of Complete Molecular Response (CMoIR).	Molecular response is classified as: • Complete if by RT-Q-PCR the BCR-ABL: ABL ratio is below 0.01, with a sensitivity of at least 30,000 molecules of ABL.	At 12, 24, 36 and 48 weeks from study entry.
Secondary	The rate of major molecular response.	Molecular response (MR) is classified as: • Major (MMolR) if by RT-Q-PCR the BCR-ABL: ABL ratio is lower than 0.10, with a sensitivity of at least 30,000 molecules of ABL.	At 12, 24, 36 and 48 weeks from study entry.
Secondary	Duration of Complete molecular response (CMR).	Duration of CMR is measured by the date of the achievement of CMR to the date of CMR loss.	After four years from study entry.
Secondary	Type and number of BCR-ABL kinase domain mutations.		At the end of the study. At four years after enrollment of first patient.
Secondary	Percentage of relationships between the response and the biomarkers.		At six months from study entry.
Secondary	Event Free Survival.	Events are induction failure, relapse and death whichever comes first.	After four years from study entry.
Secondary	Overall survival	Overall survival is measured in all patients from the data of enrolment to the date of death, by any causes.	At the end of study. After four years from enrolment.
Secondary	Failure Free Survival		After four years from study entry.
Secondary	Rate of Rate of side effects, adverse events and serious adverse events.		After four years from study entry.

External Links

•   Gimema Foundation Website