Romanian Society of Pharmaceutical Sciences

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BREAST CANCER RESPONSE TO NEOADJUVANT CHEMOTHERAPY QUANTIFIED BY RESIDUAL CANCER BURDEN (RCB) SCORE

CRISTIAN NICOLAE POPA 1, RODICA DANIELA BÎRLĂ 1,2*, DANIELA ELENA DINU 1,2, CRISTINA IOSIF 3, EVELINA BOGASERIU 4, IOAN NICOLAE MATEȘ 1,2

1Department of General Surgery I, “Sf. Maria” Clinical Hospital, Bucharest, Romania
2“Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania
3Department of Pathology, “Sf. Maria” Clinical Hospital, Bucharest, Romania 4Department of Oncology, “Sf. Maria” Clinical Hospital, Bucharest, Romania

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Primary systemic therapy (PST) is the first weapon employed in fighting against breast cancer (BC) and the response to the numerous chemotherapy (ChT) regimens currently used is the key to the conservative surgical approach. The objective of this study was to analyse the efficiency of ChT by assessing the anatomopathological response on the surgical resection piece. 53 patients with BC have been investigated pre/post-PST within this retrospective study and the quantification of the tumour response was made using the Residual Cancer Burden Score (RCB). 6 patients achieved pathological complete response (pCR), and 13 patients presented a tumour < 2 cm. Except for the 4 patients with multiple tumours, the percentage of cases that could have benefited from post-PST conservative surgery (BCS) increased to 16.9% (9/53). 87.2% of the cases classified as RCB-III were ER+ (p = 0.005) and 82.1% PR+ (p = 0.014), while the utility of ChT in case of these BC subtypes is still in debate. The Paclitaxel (PTX) sequential administration following anthracycline-based regimens did not increase the PST response rate and was associated with significant residual disease (p = 0.027). The anthracycline-based regimens or the anti-HER2 therapy (trastuzumab) (p = 0.986) did not influence the pCR reach in a statistically significant manner. The BC low response rate to PST is associated with hormone receptor+ (HR+) subtypes with a weak response to ChT, but might also be due to malignant cells’ innate resistance to taxane therapy, presently considered as one of the cornerstones in BC treatment.