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Poster Display session

136P - Efficacy and safety of larotrectinib (laro) as first-line treatment for paediatric (paed) patients (pts) with TRK fusion cancer

Date

15 Mar 2024

Session

Poster Display session

Presenters

Daniel Orbach

Citation

Annals of Oncology (2024) 9 (suppl_2): 1-32. 10.1016/esmoop/esmoop102441

Authors

D. Orbach1, C..M. Zwaan2, C.M. Albert3, N. Federman4, A. Pappo5, V. Bernard-Gauthier6, N. Neu7, E.A. De La Cuesta8, T. Laetsch9, Y. Zhang10

Author affiliations

  • 1 Siredo Oncology Center (care, Innovation And Research For Children And Aya With Cancer), Institut Curie, 75005 - Paris/FR
  • 2 Department Of Pediatric Oncology And Hematology, Prinses Máxima Centrum, Utrecht/NL
  • 3 Hematology Oncology And Bone Marrow Transplant Department, Seattle Children’s Hospital and University of Washington School of Medicine, Seattle/US
  • 4 Pediatric Hematology Oncology Department, David Geffen School of Medicine, University of California, Los Angeles/US
  • 5 Department Of Global Pediatric Medicine, St. Jude Children's Research Hospital, Memphis/US
  • 6 Medical Affairs Oncology, Bayer Pharmaceuticals, Inc., Toronto/CA
  • 7 Department Of Medical Affairs, Chrestos Concept GmbH & Co. KG, Essen/DE
  • 8 Late Stage Development, Bayer Pharmaceuticals, Inc., Toronto/CA
  • 9 Department Of Oncology, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia/US
  • 10 Pediatric Oncology, Sun Yat-sen University Cancer Center, Guangzhou/CN

Resources

This content is available to ESMO members and event participants.

Abstract 136P

Background

Laro is the first-in-class, highly selective, central nervous system (CNS)-active TRK inhibitor approved for tumour-agnostic use in pts with TRK fusion cancer based on a robust and durable overall response rate (ORR) in both adult and paed pts with various tumour types. Here, we report data on paed pts with TRK fusion cancer treated in the first line.

Methods

Pts with treatment-naïve non-primary CNS TRK fusion cancer were included. Responses were independent review committee (IRC)-assessed (RECIST v1.1). Pts were permitted to stop laro in the absence of on-treatment progression (wait-and-see).

Results

As of July 2022, 37 paed pts were eligible for efficacy analyses by IRC. There were 5 tumour types: infantile fibrosarcoma (n=18; 49%), soft tissue sarcoma (n=14; 38%), congenital mesoblastic nephroma (n=2; 5%), thyroid cancer (n=2; 5%) and breast cancer (n=1; 3%). Median age was 2.1 years (range 0–17). NTRK gene fusions were identified by NGS, FISH and RT-PCR in 24, 7 and 6 pts, respectively. ORR was 89% (95% CI 75–97); best overall responses were 26 (70%) complete response (CR; including 5 pathologic CR), 7 (19%) partial response, 3 (8%) stable disease and 1 (3%) not evaluable. Median time to first response was 1.8 months. Medians for duration of response, progression-free survival and overall survival (OS) were 38.4 months (95% CI 23.4–not estimable [NE]), 40.2 months (95% CI 25.5–NE) and not reached, at median follow-ups of 28.6, 30.3 and 37.8 months, respectively. The 48-month OS rate was 95% (95% CI 87–100). Treatment duration was 1–64+ months (median 31.2 months). At data cut-off, 22 (59%) pts had participated in wait-and-see. Treatment-related adverse events (TRAEs) were mainly Grade 1/2. Grade 3/4 TRAEs occurred in 15 (41%) pts; 2 pts discontinued due to a TRAE (malaise and hypoventilation occurred in one pt each).

Conclusions

Laro demonstrated rapid and durable responses, extended survival and had a favourable safety profile in paed pts without prior systemic therapy. This supports the use of laro in a first-line setting and the wider adoption of next-generation sequencing panels that include NTRK gene fusions to identify paed pts who may benefit from targeted treatment.

Clinical trial identification

NCT02637687, NCT02576431.

Editorial acknowledgement

Medical writing assistance was provided by Patricia Badia Folgado, MSc, and editorial assistance was provided by Melissa Ward, BA, both of Scion (a division of Prime, London, UK).

Legal entity responsible for the study

Bayer HealthCare Pharmaceuticals, Inc.

Funding

Bayer HealthCare Pharmaceuticals, Inc.

Disclosure

D. Orbach: Financial Interests, Personal, Other, Consultancy: Bayer, Roche; Financial Interests, Personal, Funding: Bayer. C..M. Zwaan: Financial Interests, Institutional, Funding: Pfizer, Takeda, Kura Oncology, Daiichi Sankyo, Jazz Pharmaceuticals, AbbVie; Financial Interests, Personal, Other, Consultancy: Novartis, Takeda, Sanofi, Roche, Incyte. N. Federman: Financial Interests, Personal, Stocks/Shares: Genmab, Moderna, Reata Pharmaceuticals, BlueBird Bio; Financial Interests, Personal, Other, Consulting/Advisory: Bayer, Fennec, SpringWorks; Financial Interests, Personal, Invited Speaker: Bayer, Fennec Pharma; Financial Interests, Personal, Other, Patents/Royalties: NanoValent Ltd. A. Pappo: Financial Interests, Personal, Other, Personal fees: Bayer. V. Bernard-Gauthier, E.A. De La Cuesta: Financial Interests, Personal, Full or part-time Employment: Bayer. N. Neu: Financial Interests, Personal, Full or part-time Employment, External employee: Bayer. T. Laetsch: Financial Interests, Personal, Other, Consultancy: Novartis, Cellectis, Bayer, Loxo Oncology, Lilly, Deciphera, Jumo Health, Y-mAbs Therapeutics; Financial Interests, Personal, Funding: Pfizer, Novartis, Bayer, Loxo Oncology, AbbVie, Amgen, Atara, Biotherapeutics, BMS, Lilly, Epizyme, GSK, Janssen, Jubilant Pharmaceuticals, Novella Clinical, Servier. All other authors have declared no conflicts of interest.

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