Circulating tumor cells (CTCs) detection and isolation in different subtypes of early-stage breast cancer patients from Bangladesh.

Authors

null

Shakera Ahmed

Chittagong Medical College & Hospital, Chittagong, Bangladesh

Shakera Ahmed , Atul Bharde , Muhammad Mosaraf Hossain , Ramendu Parial , Nusrat Jahan Nayeema , Manisha Das , Mizanur Rahman , Abu Shadat Mohammod Noman , S.M. Sabbir Alam , Sayali Gosavi , Meghana Garbhe , Gourishankar Aland , Sreeja Jayant , Jayant Khandare

Organizations

Chittagong Medical College & Hospital, Chittagong, Bangladesh, OneCell Dx, Pune, India, University of Chittagong, Bangladesh and EuGEF Research Foundation, Kotwali, Bangladesh, University of Chittagong and EuGEF Research Foundation, Chittagong, Bangladesh, EuGEF Research Foundation, Chattogram, Chattogram, Bangladesh, University of Chittagong, Bangladesh, Chittagong, Bangladesh, University of Chittagong, Chattogram and EuGEF Research Foundation, Chattogram, Chattogram, Bangladesh, Actorius Innovations and Research, Pune, India, Actorius Innovations and Research Pvt. Ltd, Pune, India

Research Funding

Other
EuGEF research group

Background: Breast cancer is a highly heterogeneous pathophysiology characterized by poor outcomes. Due to the increasing incidence and disease progression rates and undefined relapse periods, reliable disease monitoring is a challenge and has remained an unmet need. Advancements in liquid biopsy have significantly enhanced our understanding of clinical oncology. CTC-based liquid biopsy is emerging as a reliable prognostic tool to predict various clinical indicators. Although extensively investigated in metastatic breast cancers, little is known about CTCs in early-stage breast cancers. CTCs with respect to different molecular subtypes of breast cancer in early-stage breast cancer patients is evaluated. Methods: In this prospective clinical trial (CMC 59.27.0000.013.19 PG.009.2022/262) 40 early-stage patients with luminal (A +B, 33.33%), HER 2 positive (12.8%), triple-negative (12.8%) and undetermined (41.07%) subtype were recruited. CTCs were isolated in 1.5 ml blood using the Drug Controller General of India approved OncoDiscover CTC test. This platform contains affinity-based magnetic nanoparticles to mediate EpCAM-based CTC isolation. CTCs were detected as CK18+, DAPI+, and CD45- cells using a fluorescence detection-based automated digital imaging platform. Results: CTCs were detected in 60 % of patients with a mean CTC count of 1 cell / 1.5ml blood. Among total positive patients, the luminal subtype was the least positive (46 %), followed by TNBC (60 %) and undetermined (62.5 %) subgroup, while all HER2-positive patients showed the presence of CTCs. Besides individual cells, CTC clusters were detected in 12.5 % of patients and they were equally distributed in luminal and HER2-positive subpopulations. When analyzed on the scale of tumor grade, grade I patients did not show the presence of CTC, while 58.33 % of grade II patients had ≥ 1 CTC. All grade III patients showed the presence of ≥ 1 CTC. CTC count was high among CTC-positive grade II patients (average 2 CTCs) and correlated well with the presence of CTC clusters in these patients. Patients who had surgical intervention had a low CTC burden compared to patients who did not have a surgical resection. 75 % of treatment naïve patients showed the presence of CTC while 58 % of patients receiving chemotherapy alone showed the presence of 1 CTC. 50 % of patients who had surgery followed by CT+RT showed the presence of 1 CTC. Conclusions: The presence of CTCs may suggest for biological progression of disease in early-stage BC patients. CTC detected in all HER2-positive patients suggested the high shedding nature of these tumors, which correlates well with their reported migratory tendency. The presence of CTCs did not show a clear correlation with the treatment regimen. However, this data is based on a single time point and needs longitudinal correlation with CTC on a larger sample size. Clinical trial information: 59.27.0000.013.19 PG.009.2022/262.

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Abstract Details

Meeting

2023 ASCO Annual Meeting

Session Type

Publication Only

Session Title

Publication Only: Breast Cancer—Local/Regional/Adjuvant

Track

Breast Cancer

Sub Track

Adjuvant Therapy

Clinical Trial Registration Number

59.27.0000.013.19 PG.009.2022/262

Citation

J Clin Oncol 41, 2023 (suppl 16; abstr e12529)

DOI

10.1200/JCO.2023.41.16_suppl.e12529

Abstract #

e12529

Abstract Disclosures

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