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Larotrectinib efficacy and safety in adult patients with tropomyosin receptor kinase fusion sarcomas.
Kummar, Shivaani; Shen, Lin; Hong, David S; McDermott, Ray; Keedy, Vicki L; Casanova, Michela; Demetri, George D; Dowlati, Afshin; Melcón, Soledad Gallego; Lassen, Ulrik N; Leyvraz, Serge; Liu, Tianshu; Moreno, Victor; Patel, Jyoti; Patil, Tejas; Mallick, Atrayee Basu; Sousa, Nuno; Tahara, Makoto; Ziegler, David S; Norenberg, Ricarda; Arvis, Pierre; Brega, Nicoletta; Drilon, Alexander; Tan, Daniel S W.
Afiliação
  • Kummar S; Stanford Cancer Center, Stanford University, Palo Alto, California, USA.
  • Shen L; Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
  • Hong DS; The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • McDermott R; St. Vincent's University Hospital and Cancer Trials Ireland, Dublin, Ireland.
  • Keedy VL; Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Casanova M; Paediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Demetri GD; Dana-Farber Cancer Institute and Ludwig Center at Harvard Medical School, Boston, Massachusetts, USA.
  • Dowlati A; University Hospitals Ahuja Medical Center, Beachwood, Ohio, USA.
  • Melcón SG; Pediatric Oncology and Hematology, Vall d'Hebron Children's Hospital, Barcelona, Spain.
  • Lassen UN; Department of Oncology, Rigshospitalet, Copenhagen, Denmark.
  • Leyvraz S; Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Liu T; Zhongshan Hospital-Fudan University, Shanghai, China.
  • Moreno V; START MADRID-FJD, Hospital Fundación Jiménez Díaz, Madrid, Spain.
  • Patel J; Northwestern University, Chicago, Illinois, USA.
  • Patil T; Department of Medicine, Division of Medical Oncology, University of Colorado, Aurora, Colorado, USA.
  • Mallick AB; Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
  • Sousa N; Instituto Portugues de Oncologia do Porto Francisco Gentil, Porto, Portugal.
  • Tahara M; National Cancer Center Hospital East, Kashiwa, Japan.
  • Ziegler DS; Sydney Children's Hospital, Randwick, New South Wales, Australia.
  • Norenberg R; Australia and School of Women's and Children's Health, University of New South Wales Sydney, Sydney, New South Wales, Australia.
  • Arvis P; Chrestos Concept GmbH & Co. KG, Essen, Germany.
  • Brega N; Bayer Pharmaceuticals, Loos, France.
  • Drilon A; Bayer Pharmaceuticals, Milan, Italy.
  • Tan DSW; Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Cancer ; 129(23): 3772-3782, 2023 12 01.
Article em En | MEDLINE | ID: mdl-37769113
ABSTRACT

BACKGROUND:

Larotrectinib, a first-in-class, highly selective tropomyosin receptor kinase (TRK) inhibitor, has demonstrated efficacy in adult and pediatric patients with various solid tumors harboring NTRK gene fusions. This subset analysis focuses on the efficacy and safety of larotrectinib in an expanded cohort of adult patients with TRK fusion sarcomas.

METHODS:

Patients (≥18 years old) with sarcomas harboring NTRK gene fusions were identified from three clinical trials. Patients received larotrectinib 100 mg orally twice daily. Response was investigator-assessed per RECIST v1.1. Data cutoff was July 20, 2021.

RESULTS:

At the data cutoff, 36 adult patients with TRK fusion sarcomas had initiated larotrectinib therapy two (6%) patients had bone sarcomas, four (11%) had gastrointestinal stromal tumors, and 30 (83%) had soft tissue sarcomas. All patients were evaluable for response and demonstrated an objective response rate of 58% (95% confidence interval, 41-74). Patients responded well to larotrectinib regardless of number of prior lines of therapy. Adverse events (AEs) were mostly grade 1/2. Grade 3 treatment-emergent AEs (TEAEs) occurred in 15 (42%) patients. There were no grade 4 TEAEs. Two grade 5 TEAEs were reported, neither of which were considered related to larotrectinib. Four (11%) patients permanently discontinued treatment due to TEAEs.

CONCLUSIONS:

Larotrectinib demonstrated robust and durable responses, extended survival benefit, and a favorable safety profile in adult patients with TRK fusion sarcomas with longer follow-up. These results continue to demonstrate that testing for NTRK gene fusions should be incorporated into the clinical management of adult patients with various types of sarcomas. PLAIN LANGUAGE

SUMMARY:

Tropomyosin receptor kinase (TRK) fusion proteins result from translocations involving the NTRK gene and cause cancer in a range of tumor types. Larotrectinib is an agent that specifically targets TRK fusion proteins and is approved for the treatment of patients with TRK fusion cancer. This study looked at how well larotrectinib worked in adult patients with sarcomas caused by TRK fusion proteins. Over half of patients had a durable response to larotrectinib, with no unexpected side effects. These results show that larotrectinib is safe and effective in adult patients with TRK fusion sarcomas.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma / Neoplasias de Tecidos Moles / Neoplasias Ósseas / Neoplasias Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoma / Neoplasias de Tecidos Moles / Neoplasias Ósseas / Neoplasias Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos