Safety, Feasibility, and Merits of Longitudinal Molecular Testing of Multiple Metastatic Sites to Inform mTNBC Patient Treatment in the Intensive Trial of Omics in Cancer

Author:

Burton Kimberly A.1234ORCID,Mahen Elisabeth256,Konnick Eric Quentin7ORCID,Blau Sibel23,Dorschner Michael O.8910,Ramirez Arturo B.11,Schmechel Stephen C.8ORCID,Song Chaozhong256,Parulkar Rahul12ORCID,Parker Stephanie34ORCID,Senecal Francis Mark34ORCID,Pritchard Colin C.7ORCID,Mecham Brigham H.13,Szeto Christopher12,Spilman Patricia14ORCID,Zhu Jingchun15ORCID,Gadi Vijayakrishna K.1617ORCID,Ronen Roy18,Stilwell Jackie11,Kaldjian Eric11,Dutkowski Janusz18,Benz Stephen Charles12ORCID,Rabizadeh Shahrooz14ORCID,Soon-Shiong Patrick1214ORCID,Blau C. Anthony25619ORCID

Affiliation:

1. Department of Medicine, University of Washington, Seattle, WA

2. Center for Cancer Innovation, University of Washington, Seattle, WA

3. Northwest Medical Specialties, Puyallup and Tacoma, WA

4. South Sound CARE Foundation, Seattle, WA

5. Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA

6. Department of Medicine/Hematology, University of Washington, Seattle, WA

7. Department of Laboratory Medicine, University of Washington, Seattle, WA

8. Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA

9. Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA

10. Center for Precision Diagnostics, University of Washington, Seattle, WA

11. Rarecyte Inc, Seattle, WA

12. NantHealth, Culver City, CA

13. Trialomics, Seattle, WA

14. ImmunityBio Inc, Culver City, CA

15. Computational Genomics Lab, University of California at Santa Cruz, Santa Cruz, CA

16. Department of Medicine, University of Illinois, Chicago, IL

17. Fred Hutchinson Cancer Research Center, Seattle, WA

18. Data4Cure Inc, La Jolla, CA

19. All4Cure Inc, Seattle, WA

Abstract

PURPOSE Patients with metastatic triple-negative breast cancer (mTNBC) have poor outcomes. The Intensive Trial of Omics in Cancer (ITOMIC) sought to determine the feasibility and potential efficacy of informing treatment decisions through multiple biopsies of mTNBC deposits longitudinally over time, accompanied by analysis using a distributed network of experts. METHODS Thirty-one subjects were enrolled and 432 postenrollment biopsies performed (clinical and study-directed) of which 332 were study-directed. Molecular profiling included whole-genome sequencing or whole-exome sequencing, cancer-associated gene panel sequencing, RNA-sequencing, and immunohistochemistry. To afford time for analysis, subjects were initially treated with cisplatin (19 subjects), or another treatment they had not received previously. The results were discussed at a multi-institutional ITOMIC Tumor Board, and a report transmitted to the subject's oncologist who arrived at the final treatment decision in conjunction with the subject. Assistance was provided to access treatments that were predicted to be effective. RESULTS Multiple biopsies in single settings and over time were safe, and comprehensive analysis was feasible. Two subjects were found to have lung cancer, one had carcinoma of unknown primary site, tumor samples from three subjects were estrogen receptor–positive and from two others, human epidermal growth factor receptor 2–positive. Two subjects withdrew. Thirty-four of 112 recommended treatments were accessed using approved drugs, clinical trials, and single-patient investigational new drugs. After excluding the three subjects with nonbreast cancers and the two subjects who withdrew, 22 of 26 subjects (84.6%) received at least one ITOMIC Tumor Board–recommended treatment. CONCLUSION Further exploration of this approach in patients with mTNBC is merited.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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