Ceritinib Rare Indications Study in ALK+ Tumors

Novartis

Status and phase: Terminated; Phase 2

Conditions: Tumors With Aberrations in ALK; Glioblastoma; Inflammatory Myofibroblastic Tumor; Anaplastic Large Cell Lymphoma

Treatments: Drug: Ceritinib (LDK378)

Study type: Interventional

Funder types: Industry

Identifiers

NCT02465528

CLDK378A2407

Details and patient eligibility

About

This is Proof-of-Concept (POC) study to assess the preliminary antitumor activity and safety and tolerablity using ceritinib (LDK378) in the treatment of life threatening tumors that are characterized by ALK genetic alteration (and/or overexpression in some diseases).

Enrollment: 22 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient has a histologically or cytologically confirmed diagnosis of ALK positive (ALK+) tumor other than Non-Small Cell Lung Cancer (NSCLC).

• Patient must provide an archival or fresh tumor tissue before the first dose of the study drug for ALK testing at a Novartis designated central laboratory.

• Patient has WHO Performance Status (PS) ≤ 2

• Patient must have received at least one line of prior systemic treatment for recurrent, locally advanced and/or metastatic disease, and may have discontinued for:

  • Disease progression as defined by RECIST 1.1 for solid tumors; by RANO for GBM and by Cheson assessment criteria for lymphoma, or
  • Intolerance described as any discontinuation due to an AE of any grade despite appropriate supportive treatment

• Patient has at least one measurable lesion as defined by appropriate guidelines. A lesion at a previously irradiated site may only be counted as a target lesion if there is clear sign of progression since the irradiation.

• Patient has received no chemotherapy, immunotherapy or stem cell therapy at least 4 weeks before starting ceritinib

• Radiotherapy and prior ALK inhibitors must be stopped at least 1 week prior to starting ceritinib

• Recovered from all toxicities related to prior anticancer therapies to grade ≤ 1 (Common Terminology Criteria for Adverse Events [CTCAE] v4.03).

Exclusion criteria

• Patient has ALK+lung cancer
• Patient with symptomatic CNS metastases who are neurologically unstable or have required increasing doses of steroids within the 2 weeks prior to study entry to manage CNS symptoms.
• Patient with acute or chronic GI disease that may significantly alter the absorption of ceritinib.
• Patient with a history of pancreatitis or history of increased amylase or lipase that was due to pancreatic disease.
• Patient has history of interstitial lung disease or interstitial pneumonitis, including clinically significant radiation pneumonitis.
• Patient has clinically significant, uncontrolled heart disease and/or recent cardiac event (within 6 months).
• Patient has evidence of active viral hepatitis, including Hepatitis A, B or C (testing for viral hepatitis is not mandatory).
• Patient has known diagnosis of human immunodeficiency virus (HIV) infection (HIV testing is not mandatory).

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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22 participants in 4 patient groups

Inflammatory myofibroblastic tumor (IMT)

Experimental group

Description:

Patients diagnosed with IMT with a confirmed translocation involving the ALK gene

Treatment:

Drug: Ceritinib (LDK378)

Anaplastic large cell lymphoma (ALCL)

Experimental group

Description:

Patients with a diagnosis of ALCL histologically or cytologically confirmed to be ALK-positive

Treatment:

Drug: Ceritinib (LDK378)

Glioblastoma (GBM)

Experimental group

Description:

Patients with GBM with a translocation involving the ALK gene

Treatment:

Drug: Ceritinib (LDK378)

Any other ALK-positive tumor

Experimental group

Description:

Patients with any other ALK-positive tumor. Patients in this arm included adenocarcinoma (n= 2), sarcoma (1) and other (2).

Treatment:

Drug: Ceritinib (LDK378)