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Association details:
Evidence:
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Matching Adjusted Indirect Comparison (MAIC) in RET-Mutation Positive Medullary Thyroid Cancer (MTC)

Published date:
04/12/2021
Excerpt:
RET M918T mutation status...In both a naïve comparison and an unanchored MAIC, selpercatinib demonstrated a significant improvement in PFS and OS versus cabozatinib and versus placebo.
Evidence Level:
Sensitive: C3 – Early Trials
Title:

SUN-LB75 The Anti-Tumor Activity of the Selective Ret Inhibitor Selpercatinib (LOXO-292) in Medullary Thyroid Cancer Is Independent of the Specific RET Mutation

Published date:
05/08/2020
Excerpt:
In a first-in-human, phase 1/2 clinical trial (LIBRETTO-001, NCT03157128), selpercatinib (LOXO-292)...Here, we evaluated investigator-assessed ORR per RECIST 1.1 and clinical benefit rate (CBR) in this previously treated patient population by RET alteration and by germline or somatic testing used for enrollment. The CBR remained consistent across subgroups with RET M918T (88%, 95% CI 71.8-96.6, n=29/33), V804M/L gatekeeper mutations (80%, 95% CI 28.4-99.5, n=4/5), extracellular cysteine mutations (71%, 95% CI 29.0-96.3, n=5/7), other mutations (100%, 95% CI 69.2-100.0, n=10/10), and germline (75%, 95% CI 19.4-99.4, n=3/4) or somatic (88%, 95% CI 76.1-95.6, n=45/51) testing.
DOI:
10.1210/jendso/bvaa046.2223
Evidence Level:
Sensitive: C3 – Early Trials
New
Source:
Title:

Selective RET kinase inhibition for patients with RET-altered cancers

Excerpt:
A patient with RET M918T-mutant medullary thyroid cancer metastatic to the liver and an acquired RET V804M gatekeeper resistance mutation, previously treated with six MKI regimens, experienced rapid reductions in tumor calcitonin, CEA and cell-free DNA, resolution of painful hepatomegaly and tumor-related diarrhea and a confirmed tumor response.
DOI:
10.1093/annonc/mdy137