The use of larotrectinib in the management of locally advanced pediatric NTRK-fusion sarcoma

Similar documents
A pediatric phase 1 study of larotrectinib, a highly selective inhibitor of the tropomyosin receptor kinase (TRK) family: an updated analysis

Efficacy of larotrectinib in adolescents and young adults with TRK fusion cancer

Larotrectinib efficacy and safety in TRK fusion cancer: an expanded clinical dataset showing consistency in an age and tumor agnostic approach

Development of LOXO-101 in Adult and Pediatric Patients With Cancer

Activity of larotrectinib in patients with TRK fusion GI malignancies

Characterization of TRK fusions and therapeutic response to TRK inhibition in hematologic malignancies

RXDX-101 & RXDX-102. Justin Gainor, MD February 20 th, 2014

SCOUTing a Path to NAVIGATE Expedited Pediatric Development

PLX7486 Background Information October Candidate for CRUK Combinations Alliance

RARE TUMORS OF INFANCY. RAJKUMAR VENKATRAMANI, MD, MS Director, Rare Tumors Program, Texas Children s Hospital

Clinical response to entrectinib in a patient with NTRK1-rearranged non-small cell lung cancer (NSCLC)

Supplementary appendix

Efficacy of Larotrectinib in TRK Fusion Positive Cancers in Adults and Children

Bayer and Loxo Oncology to develop and commercialize two novel oncology therapies selectively targeting genetic drivers of cancer

Phase 1 study of AG-881, an inhibitor of mutant IDH1/IDH2, in patients with advanced IDH mutant solid tumors, including glioma

REWRITING CANCER TREATMENT THROUGH EPIGENETIC MEDICINES

Effective local and systemic therapy is necessary for the cure of Ewing tumor Most chemotherapy regimens are a combination of cyclophosphamide,

FEASIBILITY OF PRE- OPERATIVE mtor INHIBITOR SIROLIMUS IN CHILDREN AND YOUNG ADULTS WITH DESMOID TUMOR

Case 1. Clinical history

Innovazioni Terapeutiche In Oncologia Dott. Massimo Ghiani A USL N 8 Ospedale A. Businco Oncologia Medica III. Tarceva TM

Index. Note: Page numbers of article titles are in boldface type.

All India Institute of Medical Sciences, New Delhi, INDIA. Department of Pediatric Surgery, Medical Oncology, and Radiology

Repurposed RET Inhibitors : poor RET coverage in humans MKI Approved Dose Toxicities

Randomized trial of irinotecan and cetuximab with or without vemurafenib in BRAF-mutant metastatic colorectal cancer (SWOG S1406)

DOSAGE FORMS AND STRENGTHS Capsules: 25 mg, 100 mg (3) Oral Solution: 20 mg/ml (3)

ONT-380 and HER2+ Breast Cancer

Scientific Perspectives of Olaratumab Beyond the Approval Indication

VITRAKVI (larotrectinib) Sample Letter of Appeal

Study Rationale. Reference: Chanan-Khan, A., et al., ASH 2010, Abstract#1962. Reference: Whiteman, K., et al, AACR, 2009, Abstract#2799

EFFICACY AND SAFETY OF TABELECLEUCEL IN PATIENTS WITH EPSTEIN-BARR VIRUS-ASSOCIATED LEIOMYOSARCOMAS (EBV + LMS)

Solid organ transplant after treatment for childhood cancer: A report from the Childhood Cancer Survivor Study.

A Phase 1 Study of Tazemetostat (EPZ-6438), an Enhancer of Zeste-Homolog 2 (EZH2) Inhibitor: Preliminary Activity in INI1-Negative Tumors

Pediatric Liver Tumors and Transplantation. Northwest Regional Pediatric Live Disease Symposium, Seattle WA, April 12, 2008

Making the TRK to Precision Medicine in Cancer The Promise of Targeting TRK Fusions in Lung, Breast, GI, and Other Tumors

Protocol Abstract and Schema

Abstract and Schema. Phase 1 and Pharmacokinetic Study of AZD6244 for Recurrent or Refractory Pediatric Low Grade Glioma

Presenter Disclosure Information

Lab Approach for Basket Trials in Advanced Tumors. Mohamed Salama M.D. Professor of Pathology, University of Utah

ALCHEMIST. Adjuvant Lung Cancer Enrichment Marker Identification And Sequencing Trials

The 2010 Gastrointestinal Cancers Symposium Oral Abstract Session: Cancers of the Pancreas, Small Bowel and Hepatobilliary Tract

Other Driver Mutations: cmet, B-RAF, RET, NTRK

No Other Company Discloses Higher Transplant Survival Rate. Infusions For Emerging Treatments. Date of Use. Recipient Age (yrs)

2010 ASCO Annual Meeting Chicago, IL June 4 - June 8, 2010

Oncolytic Viruses: Reovirus

Molecular characterization of cancers with NTRK gene fusions

Molecular Imaging in the Development of Cancer Therapeutics. Johannes Czernin

Contemporary Chemotherapy-Based Strategies for First-Line Metastatic Breast Cancer

Selumetinib (AZD6244; ARRY ) Pediatric MATCH. George Kirk June 2016

New Biological and Immunological Therapies for Cancer

B Kahl 1, M Hamadani 2, P Caimi 3, E Reid 4, K Havenith 5, S He 6, JM Feingold 6, O O Connor 7

Original Articles. The World Health Organization Classification of Skeletal Muscle Tumors in Pediatric Rhabdomyosarcoma

Update on new agents in Gastrointestinal Tumor (GIST)

Dennis J Slamon, MD, PhD

Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea

Phase 1 study of AG-881, an inhibitor of mutant IDH1 and IDH2: results from the recurrent/progressive glioma population

2018 National Oncologists Workforce Study OCTOBER 2018

Evening Specialty Conference: Cytopathology

Local Therapy for Ewing Sarcoma: Current Concepts and Opportunities for Improvement

UPDATE ON RADIOTHERAPY

Financial assistance for genetic diagnostic testing may be available for eligible patients with NTRK gene fusion

Fusion Analysis of Solid Tumors Reveals Novel Rearrangements in Breast Carcinomas

Clinical activity of BLU-285, a highly potent and selective KIT/PDGFRα inhibitor designed to treat gastrointestinal stromal tumor (GIST)

Bone HDR brachytherapy in a patient with recurrent Ewing s sarcoma of the acetabulum: Alternative to aggressive surgery

Immunotherapy for the Treatment of Head and Neck Cancers. Robert F. Taylor, MD Aurora Health Care

ASCO Annual Meeting 2013, May 31 June , Chicago, IL

LIBRETTO-001: A phase 1 study of LOXO-292, a potent and highly selective RET inhibitor, in patients with RET-altered cancers

ICONIC: Biologic and clinical activity of first in class ICOS agonist antibody JTX /- nivolumab (nivo) in patients with advanced cancers

Soft Tissue Sarcoma. Presley Regional Trauma Center Department of Surgery University of Tennessee Health Science Center Memphis, Tennessee

Abstract and Schema. Phase 1 and Pharmacokinetic Study of AZD6244 for Recurrent or Refractory Pediatric Low Grade Glioma

Adaptive Design of Affordable Clinical Trials Using Master Protocols in the Era of Precision Medicine

Wilms Tumor Outcomes at a Single Institution and Review of Current Management Recommendations

Survival of Pediatric Patients After Relapsed Osteosarcoma: The St. Jude Children s Research Hospital Experience

HDAC Inhibitors and PARP inhibitors. Suresh Ramalingam, MD Associate Professor Chief of Thoracic Oncology Emory University School of Medicine

The clinical trial information provided in this public disclosure synopsis is supplied for informational purposes only.

The clinical trial information provided in this public disclosure synopsis is supplied for informational purposes only.

Desmoid tumor trial using a gamma secretase inhibitor PF

A Phase 2 Study of Glembatumumab Vedotin, an Antibody Drug Conjugate Targeting gpnmb, in Advanced Melanoma

A randomized phase 2 trial of CRLX101 in combination with bevacizumab in patients with metastatic renal cell carcinoma (mrcc) vs standard of care

This clinical study synopsis is provided in line with Boehringer Ingelheim s Policy on Transparency and Publication of Clinical Study Data.

DCC-2618, a novel pan-kit and PDGFR

Long-term safety and efficacy of vismodegib in patients with advanced basal cell carcinoma (BCC): 24-month update of the pivotal ERIVANCE BCC study

Single Agent Activity of ZW25, a HER2-Targeted Bispecific Antibody, in Heavily Pretreated HER2-Expressing Cancers

A phase II study of weekly paclitaxel and cisplatin followed by radical hysterectomy in stages IB2 and IIA2 cervical cancer AGOG14-001/TGOG1008

PHASE 1 CLINICAL TRIALS: DESIGNS AND CONSIDERATIONS. Sarit Assouline, MD, MSc, FRCPC Associate professor, McGill University Jewish General Hospital

Cohort D Xentuzumab + abemaciclib + fulvestrant (500 mg/month) Key exclusion criteria RP2D-4 NSCLC. Cohort F Xentuzumab + abemaciclib + fulvestrant

ORIGINAL ARTICLE CHEMOTHERAPY ALONE FOR ORGAN PRESERVATION IN ADVANCED LARYNGEAL CANCER

Safety and Efficacy of Venetoclax Plus Low-Dose Cytarabine in Treatment-Naïve Patients Aged 65 Years With Acute Myeloid Leukemia

Clinical Trials for Adult Brain Tumors - the Imaging Perspective

Basket trial of TRK inhibitors demonstrates efficacy in TRK fusion-positive cancers

Pediatric Preclinical Testing Program (PPTP) evaluation of the Bcl-2 inhibitor ABT-263

GIST: imatinib and beyond

ACTR-46. Presented at the Society for Neuro-Oncology Annual Scientific Meeting, November 16-19, 2017; San Francisco, CA, USA

State of the art: CAR-T cell therapy in lymphoma

Case Conference. Craig Morgenthal Department of Surgery Long Island College Hospital

Avapritinib is Highly Active and Well-tolerated in Patients With Advanced GIST Driven by a Diverse Variety of Oncogenic Mutations in KIT and PDGFRA

ACCME/Disclosures ALK FUSION-POSITIVE MESENCHYMAL TUMORS. Tumor types with ALK rearrangements. Anaplastic Lymphoma Kinase. Jason L.

Breast Cancer: Weight and Exercise. Anne McTiernan, MD, PhD. Fred Hutchinson Cancer Research Center Seattle, WA

Announce Expected Initiation of an Investigator-Initiated, Randomized, Phase 2, Multicenter Trial of Ficlatuzumab and Cetuximab in HNSCC in 2H 2017

Transcription:

The use of larotrectinib in the management of locally advanced pediatric NTRK-fusion sarcoma DuBois SG, 1 Laetsch TW, 2 Federman N, 3 Albert CM, 4 Turpin B, 5 Nagasubramanian R, 6 Reynolds M, 7 Cruickshank S, 7 Cox MC, 7 Hawkins DS, 4 Mascarenhas L, 8 Pappo AS 9 1 Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA; 2 University of Texas Southwestern/Children s Health, Dallas, TX; 3 UCLA David Geffen School of Medicine, Los Angeles, CA; 4 Seattle Children s Hospital, University of Washington, Fred Hutchinson Cancer Research Center, Seattle, WA; 5 Cincinnati Children's Hospital Medical Center, Cincinnati, OH; 6 Nemours Children's Hospital, Orlando, FL; 7 Loxo Oncology, Inc., South San Francisco, CA; 8 Children s Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, CA; 9 St. Jude Children's Research Hospital, Memphis, TN 1

Disclosures Prior consultation for Loxo Oncology: DuBois and Laetsch Employees of Loxo Oncology: Reynolds, Cruickshank, and Cox Larotrectinib is an investigational agent 2

Role of TRK in normal biology and cancer Neurotrophin family of receptors TRK fusions TRKA (NTRK1) TRKB (NTRK2) TRKC (NTRK3) Pain, thermoregulation Movement, memory, mood, appetite, body weight Proprioception Ligand binding domain (LBD) replaced by 5 fusion partner Drives overexpression and ligand-independent activation NTRK1/2/3 Promoter 5 partner LBD kinase domain Tyr Tyr 5 partner NTRK kinase domain ERK Tyr Tyr Tyr Tyr 5 partner NTRK kinase domain 5 partner NTRK kinase domain AKT TRK uncommonly expressed in normal tissues or cancer Fusion drives abnormally high expression and activation of TRK kinase domain 3

TRK fusions seen in diverse range of pediatric tumors Gliomas Thyroid cancer Secretory breast carcinoma Infantile fibrosarcoma (IFS) Spitz nevi Congenital mesoblastic nephroma Various sarcomas 4

TRK fusions seen in diverse range of pediatric tumors Gliomas Thyroid cancer Secretory breast carcinoma Infantile fibrosarcoma (IFS) Spitz nevi Congenital mesoblastic nephroma Various sarcomas 5

Larotrectinib (LOXO-101) Larotrectinib is the first and only selective pan-trk inhibitor in clinical development TRKA/B/C Highly potent against TRKA, TRKB, TRKC (5 11 nm IC 50 in cellular assays) Highly selective High response rate in adult and pediatric patients with TRK fusions Recommended phase 2 dose in adults is 100 mg BID continuously and 100mg/m2 BID in pediatrics (100mg BID maximum) Liquid formulation for pediatric patients 6

Design of pediatric phase I trial (SCOUT) Eligibility 1 month 21 years of age Relapsed/refractory solid tumor (including CNS) or locally advanced IFS Patients with locally advanced disease who had not undergone definitive surgery were eligible Evaluable or measurable disease by RECIST v1.1 Karnofsky/Lansky status 50 Adequate organ function n=17 TRK fusion patients n=7 non-fusion patients Objectives Safety, including dose-limiting toxicities (DLTs) Pharmacokinetics Maximum tolerated dose (MTD) Antitumor activity Modified rolling 6 design Patients with TRK fusions continue to enroll to current dose level during DLT evaluation Intrapatient dose escalation allowed Target AUC 0 24 50% of adults at RP2D TRK fusion status determined by local CLIA (or similarly accredited) laboratories 7

Patient and disease characteristics for SCOUT Characteristic Age group, n (%) <1 year 1 2 years 2 12 years >12 years Total (N=24) 5 (21) 2 (8) 10 (42) 7 (29) Median age (range), years 4.5 (0.1 18.0) Female, n (%) 12 (50) Extent of disease at study enrollment, n (%) Locally advanced Metastatic No. of prior systemic therapies, n (%) 0 1 2 14 (58) 10 (42) 7 (29) 6 (25) 11 (46) Data cutoff: 17 April 2017 Laetsch et al. Proc ASCO 2017 8

Efficacy in children with TRK fusions (ASCO 2017) Non-TRK fusion TRK fusion Maximum change in tumor size (%) 50 40 30 20 10 0-10 -20-30 -40-50 -60-70 -80-90 -100 91.9 *Locally advanced patients who underwent surgery Note: 3 Non-NTRK fusion patients not shown due to clinical disease progression without post-baseline tumor measurements 4 TRK fusion patients not shown due to having non-measurable disease (n=2) or no disease assessments yet/continuing treatment (n=2) Data cutoff: 17 April 2017 * Laetsch et al. Proc ASCO 2017 * * * * IFS Soft tissue sarcoma 9

Current report Detailed description of children with sarcoma who underwent surgical resection after treatment with larotrectinib in phase 1 Pathologic responses following larotrectinib Surgical outcomes, including margins and wound complications Patients were restaged following surgery according to UICC restaging: R0 = complete tumor resection with free margins R1 = macroscopic resection with invaded margins R2 = macroscopic residual tumor Clinical course after recovery from surgery UICC (1987) TNM Classification of Malignant Tumours 10

Clinical characteristics of surgical patients Characteristic Age group, n (%) <1 year 1 <2 years 2 <12 years >12 years Total (N=5) 1 (20) 0 (0) 3 (60) 1 (20) Median age (range), years 2 (0.4 12) Female, n (%) 2 (40) Extent of disease at study enrollment, n (%) Locally advanced Metastatic No. of prior systemic therapies, n (%) 0 1 2 5 (100) 0 (0) 1 (20) 1 (20) 3 (60) Data cutoff: 17 July 2017 11

Case 1: 2 yo with progressive ETV6-NTRK3 IFS 2 yo girl with infantile fibrosarcoma 2 cycles of vincristine/ actinomycin- D/ cyclophosphamide progression amputation was only alternative --------------------------------------------- 4 cycles larotrectinib PR referred for surgery Pathologic complete response with clear margins (R0 resection); >98% necrosis Baseline Start of Cycle 3 No functional deficit post-surgery Off larotrectinib x 8 months and no evidence of disease Data cutoff: 17 July 2017 Courtesy of L. Mascarenhas, CHLA 12

Case 2: 5 mo with progressive ETV6-NTRK3 IFS 5 mo boy with infantile fibrosarcoma 2 cycles of vincristine/ actinomycin-d progression vincristine / actinomycin-d / cyclophosphamide inadequate response --------------------------------------------- 6 cycles larotrectinib PR referred for surgery Pathologic complete response with clear margins (R0 resection) Baseline Data cutoff: 17 July 2017 Pre-operative Courtesy of N. Federman, UCLA No functional deficit post-surgery Off larotrectinib x 6 months and no evidence of disease 13

Case 3: 12 yo with TPM3-NTRK1 sarcoma 12 yo boy with poorly classified spindle cell sarcoma No standard therapy option --------------------------------------------- 9 cycles larotrectinib PR referred for surgery Uncomplicated R0 resection No viable tumor Baseline Pre-operative Surgery occurred at data cut-off date; follow-up off larotrectinib ongoing Data cutoff: 17 July 2017 14

Case 4: 2 yo with PDE4DIP-NTRK1 IFS (1 of 2) 2 yo boy with infintile fibrosarcoma One cycle vincristine / actinomycin- D / cyclophosphamide / ifosfamide /doxorubicin surgery progression --------------------------------------------- 6 cycles larotrectinib PR referred for surgery Baseline Pre-operative Uncomplicated R1 resection Viable tumor seen at margin Data cutoff: 17 July 2017 Courtesy of A. Pappo, St Jude 15

Case 4: 2 yo with PDE4DIP-NTRK1 IFS (2 of 2) While waiting to restart larotrectinib, patient progressed Re-started, 7 cycles larotrectinib Second PR referred for surgery Second uncomplicated R1 resection Viable tumor seen at margin Recurrence after surgery with positive margins Second PR Adjuvant radiotherapy followed by larotrectinib, ongoing 11 months on study Data cutoff: 17 July 2017 Courtesy of A. Pappo, St Jude 16

Case 5: 2 yo with SQSTM1-NTRK1 IFS (1 of 2) 2yo girl with infantile fibrosarcoma 3 cycles of vincristine/ actinomycin- D / cyclophosphamide surgery recurrence 4 cycles VAC surgery recurrence 2 cycles ifosfamide/etoposide --------------------------------------------- 5 cycles larotrectinib Partial Response Baseline After 5 cycles Data cutoff: 17 July 2017 Courtesy of B. Turpin, Cincinnati 17

Case 5: 2 yo with SQSTM1-NTRK1 IFS (2 of 2) Uncomplicated R1 resection Viable tumor without necrosis Continues on adjuvant larotrectinib 13 months on study Data cutoff: 17 July 2017 Courtesy of B. Turpin, Cincinnati 18

Larotrectinib may facilitate resection of previously unresectable pediatric sarcomas Promising early experience demonstrates: 1. Pediatric patients with TRK-fusion advanced sarcomas are able to proceed to surgical resection following pre-surgical larotrectinib, in settings where amputation and/or grossly morbid surgery was the only other alternative 2. Extensive necrosis on histopathology 3. No postoperative complications or wound healing issues to date 4. Potential for clean margins without recurrence 5. Potential use of adjuvant larotrectinib 19

Next steps Phase 2 portion of SCOUT trial ongoing surgical resection allowed for patients with sarcoma use of larotrectinib in adjuvant setting allowed Considering pediatric frontline trial 20

Acknowledgements The authors would like to thank: Patients and their families Research staff Funded by Loxo Oncology, Inc 21