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Identifying novel oncogenic RET mutations and characterising their sensitivity to RET-specific inhibitors.

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J Med Genet2020PMID 32284345stubpubmedProvenance
Source
PubMed
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-CIVIC-20260908-000001
Published

Abstract

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Linked entities

Linked entities (5)

How each link was made (MeSH, dictionary, registry reference, curation…) and whether it has been validated. Candidate links are not counted in entity statistics.

Validated 5

Curated evidence

Evidence citing this paper (11)

civicProvenance
Source
CIViC — Clinical Interpretation of Variants in Cancer
Dataset
CIViC evidence items
Version
civic-2026-09-08
Retrieved
Sep 8, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Evidence
expert curation
License
CC0 1.0
PMID
32284345
Run
ING-CIVIC-20260908-000001
Open at source
CuratedShowing 1–11 of 11 evidence items · levels, directions and significance as curated at the source; each row links to its CIViC record.
TherapyCancerTypeLevelDirection · significanceRating (1–5)StatusEvidenceSource
RET D898_E901del2
(oncogenic)Malignant NeoplasmALIASOncogenicDSupports Oncogenicity4submitted
EID11865

To assess recurrent somatic mutations in the RET kinase domain (T930K/M/P and D898_E901del) that were identified in a large study of 37,056 Chinese cancer patients, in vitro functional tests were run … (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
Pralsetinib + SelpercatinibSubstitutesMalignant NeoplasmALIASPredictiveDSupports Sensitivity Response4submitted
EID11870

Ba/F3 transformed cells harboring RET D898_E901del, T930K, T930P, or M918T mutations were shown to be sensitive to the highly selective RET inhibitors selpercatinib (LOXO-292) and pralsetinib (BLU-667… (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
RET M918T2
(oncogenic)Malignant NeoplasmALIASOncogenicDSupports Oncogenicity4accepted
EID11723

Recurrent somatic mutations within or near the RET kinase domain (T930K/M/P and D898_E901del) were identified in a large study of 37,056 East Asian cancer patients. After excluding RET mutations with … (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
Pralsetinib + SelpercatinibSubstitutesMalignant NeoplasmALIASPredictiveDSupports Sensitivity Response4accepted
EID11867

Ba/F3 transformed cells harboring RET D898_E901del, T930K, T930P, or M918T mutations were shown to be sensitive to the highly selective RET inhibitors selpercatinib (LOXO-292) and pralsetinib (BLU-667… (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
RET T930K2
(oncogenic)Malignant NeoplasmALIASOncogenicDSupports Oncogenicity3submitted
EID11864

To assess recurrent somatic mutations in the RET kinase domain (T930K/M/P and D898_E901del) that were identified in a large study of 37,056 Chinese cancer patients, in vitro functional tests were run … (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
Pralsetinib + SelpercatinibSubstitutesMalignant NeoplasmALIASPredictiveDSupports Sensitivity Response3submitted
EID11869

Ba/F3 transformed cells harboring RET D898_E901del, T930K, T930P, or M918T mutations were shown to be sensitive to the highly selective RET inhibitors selpercatinib (LOXO-292) and pralsetinib (BLU-667… (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
RET T930M1
(oncogenic)Malignant NeoplasmALIASOncogenicDDoes Not Support Oncogenicity2submitted
EID11866

To assess recurrent somatic mutations in the RET kinase domain (T930K/M/P and D898_E901del) that were identified in a large study of 37,056 Chinese cancer patients, in vitro functional tests were run … (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
RET T930P2
(oncogenic)Malignant NeoplasmALIASOncogenicDSupports Oncogenicity3submitted
EID11863

To assess recurrent somatic mutations in the RET kinase domain (T930K/M/P and D898_E901del) that were identified in a large study of 37,056 Chinese cancer patients, in vitro functional tests were run … (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
Pralsetinib + SelpercatinibSubstitutesMalignant NeoplasmALIASPredictiveDSupports Sensitivity Response3submitted
EID11868

Ba/F3 transformed cells harboring RET D898_E901del, T930K, T930P, or M918T mutations were shown to be sensitive to the highly selective RET inhibitors selpercatinib (LOXO-292) and pralsetinib (BLU-667… (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
RET CLD1 Mutation1
(oncogenic)Solid NeoplasmCURATED_BROADEROncogenicBSupports Oncogenicity1submitted
EID11722

560 of 37,056 patients from hospitals across China were found to contain RET mutations with the prevalence highest in thyroid cancer (6.45%), mediastinal tumor (7.69%), uterine cancer (3.94%), urinary… (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic
RET TKD Mutation1
(oncogenic)Solid NeoplasmCURATED_BROADEROncogenicBSupports Oncogenicity2submitted
EID11721

560 of 37,056 patients from hospitals across China were found to contain RET mutations with the prevalence highest in thyroid cancer (6.45%), mediastinal tumor (7.69%), uterine cancer (3.94%), urinary… (full text at CIViC)

PMID 32284345 · Zhao et al., 2020 · Open in CIViC

civic