Abstract. Background/Aim: Clinical response evaluation after neoadjuvant chemotherapy (NACT) for breast cancer could include various imaging methods, as well as clinical breast exam (CBE).Neoadjuvant chemotherapy (NACT) for early breast cancer is equivalent to adjuvant chemotherapy in terms of disease-free survival and overall survival (1). The major difference between NACT and adjuvant chemotherapy is the ability to directly observe the treatment effect on the tumor. Clinical response can be assessed throughout the administration of NACT, while pathologic response is revealed upon breast surgery after completion of NACT. A pathologic complete response (pCR) after NACT, defined as no residual invasive breast cancer, translates into an improved long-term prognosis (2, 3).The use of NACT also provides the opportunity to explore the potential value of response-guided therapy for early nonresponders (4-6). An improvement in disease-free survival for hormone receptor (HR)-positive breast cancer using a response-guided NACT regimen has been reported previously (4). On the other end of the spectrum, it could hypothetically be beneficial to identify early responders, who may have reached a complete remission after a shorter duration of therapy than planned. For these patients, completing NACT to the planned number of cycles could be unnecessary and potentially detrimental in terms of toxicity and cost.Routine clinical breast exam (CBE), as well as imaging modalities, such as mammography (MG), ultrasound (US) and magnetic resonance imaging (MRI), have been used to assess clinical response in an attempt to predict pathological response. A meta-analysis revealed that MRI most accurately predicts the amount of residual pathologic disease in nonsubtyped early breast cancer patients when compared to CBE, MG and US (7). Yet, there have been conflicting reports on whether MRI typically underestimates or overestimates the amount of residual disease after NACT (8,9). The routine use of MRI in clinical practice may at times be challenged by a patient's pre-existing conditions, technical feasibility and 5389