Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster display session: Basic science, Endocrine tumours, Gastrointestinal tumours - colorectal & non-colorectal, Head and neck cancer (excluding thyroid), Melanoma and other skin tumours, Neuroendocrine tumours, Thyroid cancer, Tumour biology & pathology

3781 - Phase 1b/2 study of the combination of SD-101 and pembrolizumab in patients with advanced melanoma who had progressive disease on or after prior anti-PD-1 therapy

Date

21 Oct 2018

Session

Poster display session: Basic science, Endocrine tumours, Gastrointestinal tumours - colorectal & non-colorectal, Head and neck cancer (excluding thyroid), Melanoma and other skin tumours, Neuroendocrine tumours, Thyroid cancer, Tumour biology & pathology

Topics

Clinical Research;  Immunotherapy

Tumour Site

Melanoma

Presenters

Antoni Ribas

Citation

Annals of Oncology (2018) 29 (suppl_8): viii442-viii466. 10.1093/annonc/mdy289

Authors

A. Ribas1, I. Mehmi2, T. Medina3, C. Lao4, S. Kummar5, A. Amin6, S. Deva7, A.K. Salama8, T. Tueting9, M. Milhem10, C.J. Hoimes11, G. Daniels12, M. Shaheen13, S. Jang14, M. Barve15, A. Powell16, S. Chandra17, E.V. Schmidt18, R. Janssen19, G.V. Long20

Author affiliations

  • 1 Department Of Medicine, Jonsson Comprehensive Cancer Center at UCLA, 90095-1781 - Los Angeles/US
  • 2 Mary Babb Randolph Cancer Center, West Virginia University, Morgantown/US
  • 3 Medicine/medical Oncology, University of Colorado Cancer Center, Aurora/US
  • 4 Medicine, University of Michigan Health System, Ann Arbor/US
  • 5 Medical Oncology, Stanford University School of Medicine, 94305 - Stanford/US
  • 6 Medical Oncology, Levine Cancer Institute, NC 28204 - Charlotte/US
  • 7 Medical Oncology, Auckland City Hospital, Auckland/NZ
  • 8 Oncology, Duke University, Durham/US
  • 9 Dermatology, University Hospital Madgeburg, Madgeburg/DE
  • 10 Medicine, University of Iowa, Iowa City/US
  • 11 Hematology And Oncology, Case Western Reserve University, Cleveland/US
  • 12 Medicine, University of California, San Diego, San Diego/US
  • 13 Medicine, University of Arizona Cancer Center North, Tucson/US
  • 14 Melanoma And Skin Cancer Center, Inova Schar Cancer Institute, Fairfax/US
  • 15 Oncology, Mary Crowley Cancer Research, 75230 - Dallas/US
  • 16 Oncology, Affinity Research, Nedlands/AU
  • 17 Medicine, Northwestern University, Chicago/US
  • 18 Early Oncology, Clinical Development, Merck & Co Inc, 19454 - North Wales/US
  • 19 Clinical Development, Dynavax Technologies Corporation, 94710 - Berkeley/US
  • 20 Medical Oncology, Melanoma Institute Australia, University of Sydney, 2060 - North Sydney/AU

Resources

Login to access the resources on OncologyPRO.

If you do not have an ESMO account, please create one for free.

Abstract 3781

Background

SD-101 is a synthetic CpG-ODN agonist of TLR9. Pembrolizumab is an antibody to PD-1. DV3-MEL-01 (SYNERGY-001) assesses the safety and preliminary efficacy of the combination of SD-101 and pembrolizumab in stage IIIC-IV melanoma.

Methods

Phase 1b evaluated SD-101 at multiple doses injected in a single tumor Q1W x 4 then Q3W x 7 in combination with a fixed dose of pembrolizumab (200 mg IV Q3W). Phase 2 is evaluating SD-101 at 8 mg in 1 lesion and 2 mg/lesion in 1-4 lesions. Patients were eligible if their tumor progressed on or after prior anti-PD-1 therapy. Scans are performed every 64 days. Per-protocol overall responses (ORR) were assessed per investigator using RECIST v1.1/irRECIST. The modified intent-to-treat (mITT) population included all patients except those on study who had not reached the Day 64 scan. PFS rate was calculated using the mITT population. The per-protocol population comprised patients who received at least 1 dose of each drug and had ≥1 post baseline scan.

Results

38 patients enrolled: median age 64 years; male 74%; ECOG PS 0 58%; Stage IIIC 32%, IVM1a/b 13%, Stage IVM1c/d 50%; LDH > ULN 39%. SD-101 safety profile consists of transient, mild-to-moderate flu-like symptoms and injection-site reactions. Grade 3-4 treatment-related AEs = 32%. Immune-related AEs (irAEs) = 5%. ORR (mITT) = 16% (6/37) (CR 3%/PR 14%/SD 30% [DCR = 46%]/PD 38%/NE 16%). Evaluable ORR =19% (6/31). 7 pts were not evaluable: on study but no Day 64 scan yet (n = 1), AE (n = 1), clinical PD (n = 2), withdrew consent/unknown (n = 3). 2 of 8 patients who began combination therapy within 3 months of starting anti-PD-1 therapy had responses including 1 CR. Median DOR not reached (range 9 weeks, 45 weeks). Median follow up = 13 weeks (range 6, 45 weeks). 6 month PFS rate = 16%. One third of the patients currently have biomarker assessments demonstrating a broad increase in TILs in patients with responses with ≥ 3 fold increase in T cells.

Conclusions

The combination of SD-101 and pembrolizumab induced responses in some patients who developed progressive disease on or after prior anti-PD-1 therapy. The combination is well tolerated with no evidence of an increased rate of irAEs.

Clinical trial identification

NCT02521870.

Legal entity responsible for the study

Dynavax Technologies Corporation.

Funding

Dynavax Technologies Corporation.

Editorial Acknowledgement

Disclosure

A. Ribas: Consulting fees: Dynavax Technologies. C. Lao: Research funding: Merck. A. Amin: Honoraria, Speaker’s bureau: Merck & Co. M. Milhem: Advisory board: Blueprint Medicines GIST. S. Chandra: Membership on advisory boards and/or Speaker's Bureau Member: EMD Serono, Bristol-Myers Squibb, Array BioPharma, Regeneron. E.V. Schmidt: Employee: Merck. R. Janssen: Employee: Dynavax Technologies Corporation; Shareholder: Dynavax and Merck stock. All other authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.