Ceritinib in Mutation and Oncogene Directed Therapy in Thyroid Cancer
Status:
Withdrawn
Trial end date:
2019-01-01
Target enrollment:
Participant gender:
Summary
This is an, open-label, protocol designed to evaluate the activity of targeted therapy in
anaplastic/undifferentiated thyroid cancer. Arm A will evaluate ATC/UTC with mutations or
rearrangements detected in the ALK gene.
There is no effective treatment for anaplastic thyroid cancer in the locally recurrent or
metastatic setting. Ceritinib will be administered to the patient until disease progression
by RECIST 1.1, unacceptable toxicity, withdrawal of consent, or discontinuation of the trial
for any other reason.
The primary focus of this arm of the protocol is identifying ceritinib's activity in
anaplastic or undifferentiated thyroid cancer patients. Those patients with mutations
identified in their ALK gene by sequencing their tumor samples, or with the established ALK
abnormalities will be treated with ALK-inhibitors. These include the Ventana assay and Vysis
FISH probe, and patients with tumors positive by this assay will also be considered eligible
for therapy on the trial.
Therapeutic Portion:
ARM A: ALK Abnormality IND Ceritinib 750 mg orally daily on Day 1 Continue q4 weeks x 2
cycles
Primary Endpoint: The development of progression; new recurrence or distant metastasis, as
well as enlargement of an existing metastasis on radiographic imaging.
Secondary Endpoints:
1. Overall response rate for patients treated with ceritinib as part of the study.
2. Death of study participant due to any cause.