63MO Rechallenge of anlotinib in patients with advanced soft tissue sarcoma after progression on prior anlotinib treatment: A multicenter retrospective study

Background: NTRK gene fusions are oncogenic drivers in multiple tumour types.Larotrectinib (laro) is the first-in-class, highly selective TRK inhibitor approved for tumour-agnostic use in patients (pts) with TRK fusion cancer.Here, we report outcomes in paediatric pts with TRK fusion sarcomas who electively stopped laro while in response.Methods: Pts with TRK fusion cancer treated in the SCOUT trial (NCT02637687) were permitted to stop laro in the absence of on-treatment disease progression per investigator (INV) assessment (wait-and-see); pts who stopped laro were followed for progression.Pts who progressed were re-treated with laro and were reassessed by INV per RECIST v1.1.Most pts received laro 100 mg/m 2 (maximum dose: 100 mg) twice daily.Data cut-off date was 20 July 2023.

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Publication Details

Journal
ESMO Open
Published
2025-03-01
DOI
https://doi.org/10.1016/j.esmoop.2025.104377
Primary Topic
Lung Cancer Research Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

63MO Rechallenge of anlotinib in patients with advanced soft tissue sarcoma after progression on prior anlotinib treatment: A multicenter retrospective study

Tong Ye, Xiao Sun, Zeyu Luo, Jinfeng Wang et al.
ESMO Open
Lung Cancer Research Studies
article

63MO Rechallenge of anlotinib in patients with advanced soft tissue sarcoma after progression on prior anlotinib treatment: A multicenter retrospective study

Tong Ye, Xiao Sun, Zeyu Luo, Jinfeng Wang, Jinlong Chen
article en

Abstract

Background: NTRK gene fusions are oncogenic drivers in multiple tumour types.Larotrectinib (laro) is the first-in-class, highly selective TRK inhibitor approved for tumour-agnostic use in patients (pts) with TRK fusion cancer.Here, we report outcomes in paediatric pts with TRK fusion sarcomas who electively stopped laro while in response.Methods: Pts with TRK fusion cancer treated in the SCOUT trial (NCT02637687) were permitted to stop laro in the absence of on-treatment disease progression per investigator (INV) assessment (wait-and-see); pts who stopped laro were followed for progression.Pts who progressed were re-treated with laro and were reassessed by INV per RECIST v1.1.Most pts received laro 100 mg/m 2 (maximum dose: 100 mg) twice daily.Data cut-off date was 20 July 2023.

ESMO OpenVol. 10
Union Hospital (HK), Sun Yat-sen University (CN), Peking University (CN), Fudan University Shanghai Cancer Center (CN), Peking University People's Hospital (CN), Sun Yat-sen University Cancer Center (CN), Huazhong University of Science and Technology (CN)
Good health and well-being
Openalex Percentile: Top 92%
Lung Cancer Research Studies
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