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ePoster Display

232P - Longitudinal circulating tumor DNA (ctDNA) analysis in the phase 1b MONALEESASIA study of ribociclib (RIB) + endocrine therapy (ET) in Asian patients (pts) with hormone receptor–positive (HR+)/human epidermal growth factor receptor 2–negative (HER2–) advanced breast cancer (ABC)

Date

16 Sep 2021

Session

ePoster Display

Topics

Translational Research

Tumour Site

Breast Cancer

Presenters

Yoon Sim Yap

Citation

Annals of Oncology (2021) 32 (suppl_5): S457-S515. 10.1016/annonc/annonc689

Authors

Y.S. Yap1, F. Su2, M. Joshi3, J. Chiu4, N. Masuda5, Y. Ito6, T. Ishikawa7, T. Aruga8, S.J. Kim9, U. Deore2, N. Babbar2, A. Balbin3

Author affiliations

  • 1 Medical Oncology, NCCS - National Cancer Centre Singapore, 169610 - Singapore/SG
  • 2 Oncology, Novartis Pharmaceuticals Corporation, 07936 - East Hanover/US
  • 3 Oncology, Novartis Institutes for BioMedical Research, 02139 - Cambridge/US
  • 4 Oncology, Queen Mary Hospital, Pok Fu Lam/HK
  • 5 Department Of Surgery, Breast Oncology, NHO Osaka National Hospital, 540-0006 - Osaka/JP
  • 6 Oncology, Cancer Institute Hospital of JFCR, 113-8602 - Tokyo/JP
  • 7 Oncology, Tokyo Medical University Hospital, 160-0023 - Tokyo/JP
  • 8 Department Of Breast Surgery, Tokyo Metropolitan Cancer and Infectious diseases Center Komagome Hospital, 113-8677 - Tokyo/JP
  • 9 Oncology, Osaka University Hospital, 565-0871 - Osaka/JP

Resources

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Abstract 232P

Background

The phase 1b MONALEESASIA (NCT02333370) study is assessing Asian pts with HR+/HER2– ABC treated with RIB plus ET. We report the results of a longitudinal analysis of ctDNA in this trial.

Methods

MONALEESASIA included dose-escalation and -expansion phases and enrolled premenopausal and postmenopausal Japanese pts and postmenopausal Asian non-Japanese pts. In the dose-escalation phase, all pts received RIB + letrozole (LET). In the dose-expansion phase, all Asian non-Japanese pts received RIB + LET, whereas Japanese pts received RIB + LET or fulvestrant (for postmenopausal pts) or RIB + TAM + goserelin (for premenopausal pts). Cell-free DNA (cfDNA) samples were collected from pts at baseline (BL), during treatment, and at end of treatment (EOT). ctDNA was evaluated with a targeted NGS panel comprising ≈ 600 cancer-related genes. ctDNA levels were evaluated throughout treatment by best overall response (BOR).

Results

86 pts were included in this analysis, and 574 cfDNA samples were tested. Some of the most frequently altered genes were PIK3CA, TP53, and ESR1. The alteration frequency for PIK3CA and TP53 was similar from BL to EOT but was numerically higher at EOT for ESR1. There was a consistent trend of lower BL ctDNA levels in pts with partial response (PR) or stable disease (SD) vs pts with progressive disease; however, there was no difference in ctDNA levels at on-treatment time points and EOT by BOR. In all treatment arms, pts with PR and SD had a decrease in ctDNA levels at the first collected on-treatment time point vs BL. Three categories of case studies will be presented: (1) ctDNA was detectable at BL and became undetectable on treatment; (2) ctDNA increased before tumor progression; (3) ctDNA was not detectable throughout treatment.

Conclusions

ctDNA levels were dynamic throughout treatment in Asian pts with HR+/HER2– ABC in MONALEESASIA. These findings suggest that on-treatment ctDNA levels may help identify pts at risk of progression.

Clinical trial identification

NCT02333370.

Editorial acknowledgement

Medical editorial assistance was provided by Casey Nielsen, PhD, of MediTech Media, and was financially supported by Novartis Pharmaceuticals Corporation.

Legal entity responsible for the study

Novartis Pharmaceuticals Corporation.

Funding

Novartis Pharmaceuticals Corporation.

Disclosure

Y.S. Yap: Financial Interests, Personal, Invited Speaker, Received honoraria/travel support: Novartis; Financial Interests, Personal, Invited Speaker, Received honoraria/travel support: Pfizer; Financial Interests, Personal, Invited Speaker, Received honoraria/travel support: Lilly; Financial Interests, Personal, Invited Speaker, Received honoraria/travel support: AstraZeneca; Financial Interests, Personal, Invited Speaker, Received honoraria/travel support: Roche; Financial Interests, Personal, Invited Speaker, Received honoraria/travel support: Eisai; Financial Interests, Personal, Invited Speaker, Received honoraria/travel support: MSD; Financial Interests, Personal, Invited Speaker, Received honoraria/travel support: Inivata. F. Su: Financial Interests, Personal and Institutional, Full or part-time Employment: Novartis; Financial Interests, Personal and Institutional, Stocks/Shares: Novartis. N. Masuda: Financial Interests, Personal, Other, Honoraria for lecture, Research funding to institution: Chugai; Financial Interests, Personal and Institutional, Other, Honoraria for lecture, Research funding to institution: AstraZeneca; Financial Interests, Personal and Institutional, Other, Honoraria for lecture, Research funding to institution: Pfizer; Financial Interests, Personal and Institutional, Other, Honoraria for lecture, Research funding to institution: Eli Lilly; Financial Interests, Personal, Other, Honoraria for lecture, Research funding to institution: Eisai; Financial Interests, Personal, Invited Speaker, Honoraria for lecture: Takeda; Financial Interests, Personal and Institutional, Other, Honoraria for lecture, Research funding to institution: Kyowa-Kirin; Financial Interests, Personal and Institutional, Other, Honoraria for lecture, Research funding to institution: Novartis; Non-Financial Interests, Institutional, Funding, Research funding to institution: MSD; Financial Interests, Personal and Institutional, Other, Honoraria for lecture, Research funding to institution: Daiichi Sankyo; Non-Financial Interests, Institutional, Funding, Research funding to institution: Nippon-Kayaku; Financial Interests, Institutional, Research Grant, Honoraria for lecture, Research funding to institution: Chugai; Financial Interests, Institutional, Research Grant, Honoraria for lecture, Research funding to institution: Eisai. Y. Ito: Financial Interests, Institutional, Research Grant: Daiichi Sankyo; Financial Interests, Institutional, Research Grant: Chugai; Financial Interests, Institutional, Research Grant: Novartis; Financial Interests, Institutional, Research Grant: Parexel; Financial Interests, Institutional, Research Grant: EPS; Financial Interests, Institutional, Research Grant: MSD; Financial Interests, Institutional, Research Grant: AstraZeneca; Financial Interests, Institutional, Research Grant: Eli Lilly; Financial Interests, Institutional, Research Grant: Kyowa Kirin; Financial Interests, Institutional, Research Grant: Covance; Financial Interests, Institutional, Research Grant: Taiho; Financial Interests, Institutional, Research Grant: A2 Healthcare; Financial Interests, Institutional, Research Grant: QVIA services Japan; Financial Interests, Institutional, Research Grant: Eisai. T. Aruga: Financial Interests, Personal, Other: Eisai; Financial Interests, Personal, Other: Pfizer; Financial Interests, Personal, Other: Chugai. U. Deore: Financial Interests, Personal and Institutional, Full or part-time Employment: Novartis; Financial Interests, Personal and Institutional, Stocks/Shares: Novartis. N. Babbar: Financial Interests, Personal and Institutional, Full or part-time Employment: Novartis; Financial Interests, Personal and Institutional, Stocks/Shares: Novartis. All other authors have declared no conflicts of interest.

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