Expanded Treatment Protocol With LDK378 in ALK(+) NSCLC

Status: Recruiting
Phase: N/A
Diagnosis: Lung Cancer
NCT ID: NCT01947608 (View complete trial on ClinicalTrials.gov)
DFCI Protocol ID: 13-374

 

Novartis-sponsored, open-label, multi-center, interventional ETP to provide LDK378 to patients with ALK (+)NSCLC, who have been pre-treated with an ALK inhibitor; except in countries where ALK inhibitors are not approved or available. The protocol will further evaluate the safety of LDK378 in patients with ALK(+) NSCLC.

 

Conducting Institutions:
Massachusetts General Hospital, Dana-Farber Cancer Institute, Beth-Israel Deaconess Medical Center, Brigham and Women's Hospital

Overall PI:
Alice Shaw, MD, PhD, Massachusetts General Hospital

Site-responsible Investigators:
Daniel Costa, MD, Beth Israel Deaconess Medical Center
Leena Gandhi, MD, PhD, Dana-Farber Cancer Institute

Contacts:
Massachusetts General Hospital: Cancer Trials Call Center, 877-789-6100
Beth-Israel Deaconess Medical Center: Cancer Trials Call Center, 617-667-3060
Dana-Farber Cancer Institute: Kelly Masone, 617-632-3383, kmasone@partners.org

Eligibility Criteria

Inclusion Criteria (patients eligible for inclusion in this early treatment protocol have to meet all of the following criteria): 1. Histologically or cytologically confirmed diagnosis of NSCLC that carries an ALK rearrangement as assessed by approved FISH test (Abbott Molecular Inc), using Vysis breakapart probes (defined as 15% or more positive tumor cells); or the Ventana IHC test. If documentation of ALK rearrangement is not available, the test to confirm ALK rearrangement must be performed according to the above criterion, using a new tumor biopsy obtained prior to the first dose of ETP treatment (LDK378). Stage IIIB or IV NSCLC patient who does not qualify or have access to LDK378 through a clinical trial. 2. Age 18 years or older at the time of informed consent. 3. WHO performance status 0-2. 4. Patients must have received previous treatment with ALK inhibitor therapy for the treatment of locally advanced or metastatic NSCLC. Exposure to prior chemotherapy is not required. 5. Patients must have documented disease progression at enrollment. 6. Patients must have recovered from all toxicities related to prior anticancer therapies to grade ≤ 1 (CTCAE v 4.03). Exception to this criterion: patients with any grade of alopecia are allowed to enter the treatment. 7. The following laboratory criteria have been met: - Absolute neutrophil count (ANC) ≥ 1.5 x 109/L - Hemoglobin (Hgb) ≥ 8 g/dL - Platelets ≥ 75 x 109/L - Serum total bilirubin ≤ 1.5 x upper limit of normal (ULN), except for patients with Gilbert's syndrome who may be included if total bilirubin ≤ 3.0 x ULN and direct bilirubin ≤ 1.5 x ULN - Aspartate transaminase (AST) < 3.0 x ULN, except for patients with liver metastasis, who are only included if AST < 5 x ULN; alanine transaminase (ALT) < 3.0 x ULN, except for patients with liver metastasis, who are only included if ALT < 5 x ULN. - Calculated or measured creatinine clearance (CrCL) ≥ 30 mL/min 8. Patient must have the following laboratory values or have the following laboratory values corrected with supplements to be within normal limits at screening: - Potassium ≥ LLN - Magnesium ≥ LLN - Phosphorus ≥ LLN - Total calcium (corrected for serum albumin) ≥ LLN 9. Written informed consent for the ETP protocol must be obtained prior to any screening procedures. If consent cannot be expressed in writing, it must be formally documented and witnessed, ideally via an independent trusted witness. 10. Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests and other ETP procedures. Exclusion Criteria (patients eligible for this ETP must not meet any of the following criteria): 1. Patients with known hypersensitivity to any of the excipients of LDK378 (microcrystalline cellulose, mannitol, crospovidone, colloidal silicon dioxide and magnesium stearate). 2. Patients with symptomatic CNS metastases who are neurologically unstable or have required increasing doses of steroids within the 2 weeks prior to ETP entry to manage CNS symptoms. 3. Prior therapy with LDK378. 4. The patient is less than 5 half-lives from prior ALK inhibitor or targeted therapy (for adequate wash-out) without recovery from treatment toxicities to < grade 1 or to their pretreatment levels. 5. Chemotherapy or an investigational therapy ≤ 3 weeks prior to starting the LDK378 treatment who have not recovered from side effects of such treatment toxicities to < grade 1 or to their pre- treatment toxicities levels. 6. Radiotherapy to the chest ≤ 4 weeks prior to starting the LDK378 treatment or patients who have not recovered from radiotherapy-related toxicities. Non-chest radiotherapy or palliative radiotherapy for bone lesions ≤ 2 weeks prior to starting LDK378 treatment. 7. Major surgery (e.g., intra-thoracic, intra-abdominal or intra-pelvic) within 4 weeks prior (2 weeks for resection of brain metastases) to starting LDK378 treatment or who have not recovered from side effects of such procedures. Video-assisted thoracic surgery (VATS) and mediastinoscopy will not be counted as major surgery, and patients can be enrolled in the ETP ≥ 2 weeks after the procedure. 8. Presence or history of a malignant disease other than NSCLC that has been diagnosed and/or required therapy within the past 3 years. Exceptions to this exclusion include the following: completely resected basal cell and squamous cell skin cancers, and completely resected carcinoma in situ of any type. 9. Patients with known interstitial fibrosis or interstitial lung disease. 10. Patient has clinically significant, uncontrolled heart disease and/or recent cardiac event (within 6 months), such as: - unstable angina within 6 months prior to screening; - myocardial infarction within 6 months prior to screening; - history of documented congestive heart failure (New York Heart Association functional classification III-IV); - uncontrolled hypertension defined by a Systolic Blood Pressure (SBP) ≥ 160 mm Hg and/or Diastolic Blood Pressure (DBP) ≥ 100 mm Hg, with or without antihypertensive medication - - initiation or adjustment of antihypertensive medication(s) is allowed prior to screening; - ventricular arrhythmias; supraventricular and nodal arrhythmias not controlled with medication; - other cardiac arrhythmia not controlled with medication; - corrected QTc > 450 msec using Fridericia correction on the screening ECG 11. Impaired GI function or GI disease that may alter absorption of LDK378 or inability to swallow up to five LDK378 capsules daily 12. Ongoing ≥ grade 1 GI adverse events (e.g. nausea, vomiting, or diarrhea) at the start of the ETP 13. Receiving medications that meet one of the following criteria and that cannot be discontinued at least 1 week prior to the start of treatment with LDK378 and for the duration of the ETP participation (see Appendix 1: Tables 14-1, Table 14-2, Table 14-3, and Table 14-4): - Medication with a known risk of prolonging the QT interval or inducing Torsades de Pointes (please refer to http://www.azcert.org/medical-pros/drug-lists/drug-lists.cfm) - Strong inhibitors or strong inducers of CYP3A4/5 (please refer to http://medicine.iupui.edu/flockhart/table.htm or http://www.druginteractioninfo.org) - Medications with a low therapeutic index that are primarily metabolized by CYP3A4/5, CYP2C8 and/or CYP2C9 (please refer to http://medicine.iupui.edu/flockhart/table.htm or http://www.druginteractioninfo.org) - Therapeutic doses of warfarin sodium (Coumadin) or any other coumadin-derived anti-coagulant. Anticoagulants not derived from warfarin are allowed (eg, dabigatran, rivaroxaban, apixaban). - Unstable or increasing doses of corticosteroids - enzyme-inducing anticonvulsive agents - herbal supplements 14. Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test. 15. Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during dosing and for 3 months after the last dose of study treatment. In case of use of oral contraception, women should have been stable on the same pill for a minimum of 3 months before taking study treatment. Women are considered post-menopausal and not of child bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g., age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks prior to screening. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment is she considered not of child bearing potential. 16. Sexually active males unless they use a condom during intercourse while taking drug and for 3 months after the last dose of study treatment. Male patients for 3 months should not father a child in this period. A condom is required to be used also by vasectomized men in order to prevent delivery of the drug via seminal fluid.
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