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Table 3 Characteristics of studies with quantitative analysis of BPE levels

From: Predictive value of background parenchymal enhancement on breast magnetic resonance imaging for pathological tumor response to neoadjuvant chemotherapy in breast cancers: a systematic review

Study ID

Analysis form

ROI for BPE segmentation

Calculation formula for BPE levels

Calculation formula for change in BPE

DCE phases for BPE analysis

DCE acquisition time points or temporal resolution

MRI follow-up time points

No. of readers

Blindness to clinical data

Major findings

You et al. 2017 [14]

Fully automated

All the fifibroglandular tissue

BPE = (the enhanced fibroglandular tissue volume / total fibroglandular tissue volume) × 100%

ΔBPE1/2/3 = (BPE2nd/4th/6th follow-up MRI – BPEbaseline MRI) / BPEbaseline MRI *100%

The subtraction image of pre- and post-contrast MRI scans

At 90, 180, 270, and 360 s after injection

Before and after the 2nd, 4th, 6th, and 8th cycle of NAC

NR

NR

Reduction of BPE at the early stage of NAC was positively associated with pCR, especially in HR-negative status

Rella et al. 2020 [15]

Semi-automated

All the fifibroglandular tissue

BPE = [(SI_post–SI_pre) / SI_pre] × 100%

The enhancement rate identified in the MRI after chemotherapy minus the enhancement rate identifified at the baseline MRI (total BPE change)

The pre- and first post-contrast acquisitions

NR

Before and after NAC (n = 101); Before NAC, after the 4th cycle of NAC and after NAC (n = 127)

2

NR

In the subgroup of patients with stages 3 and 4 breast cancers and who were diagnosed with a HER2-negative tumor phenotype, a significant association was found between early BPE change and pCR (P = 0.020)

Onishi et al. 2021 [19]

Fully automated

The central 50% of axial sections in the breast

BPE = [(SI_early post – SI_pre) / SI_pre] × 100%

Evaluated as suppressed if ΔBPE was less than 0

The pre- and early post-contrast acquisitions

80–100 s per dynamic acquisition

Before treatment (T0), early treatment (3 weeks after treatment initiation, T1), interregimen (T2), and before surgery (T3)

1

NR

The association between BPE nonsuppression and lower pCR rate was detected at T2 and T3 in the HR-positive cohort

Chen et al. 2015 [17]

Computer-based segmentation algorithm

All the fifibroglandular tissue

BPEi = ((SI_posti–SI_pre)/ SI_pre) × 100%; BPE = ∑BPEi / 12

NR

4 pre- and 12 post-contrast acquisitions

42 s per dynamic acquisition

Before NAC; After 1st cycle or 2ed cycle of AC; After 4th cycle of AC or 2ed cycle of AC + 3 weekly second-line taxane-based regimen

NR

NR

Compared to baseline, BPE at F/U-1 was significantly decreased in the pCR group but not in the non-pCR group

Arasu et al. 2020 [23]

Semi-automated

All the fifibroglandular tissue

BPE = (SI_early post – SI_pre) / SI_pre

%ΔBPE0_1 = (BPE_1 – BPE_0)/BPE_0

Pre-contrast (time 0) and the first post-contrast acquisition (time 1)

Continued for at least 8 min after injection

Before NAC (T0), after 3 weeks of NAC, or early treatment (T1), after 12 weeks of therapy, or inter-regimen (T2), and after NAC and prior to surgery, (T3)

NR

NR

Among women with HER2-negative cancer, BPE alone demonstrated association with pCR in women with HR-positive HER2-negative breast cancer

Moliere et al. 2019 [26]

Fully automated

All the fifibroglandular tissue

BPE20% = VBPE / VFGT × 100%

ΔBPE20% = (BPE20%post—BPE20%pre) / BPE20%pre

3 subtraction images of pre- and the three post-contrast sequences, respectively

90 s per dynamic acquisition; The late acquisition was centered at 6 min

Before and after NAC

2

Blinded to pathology data

There was no signifcant diference between complete responders and non-complete responders in term of pre- and post-therapeutic BPE

  1. NR Not reported
  2. Abbreviations: ROI Region of interest, HR Hormone receptor, BPE Background parenchymal enhancement, pCR Pathologic complete response, HER2 Human epidermal growth factor receptor 2, SI Signal strength, NAC Neoadjuvant chemotherapy