Abbreviated magnetic resonance imaging in breast cancer: A systematic review of literature.

BACKGROUND: : magnetic resonance imaging (MRI) has been increasingly used to study breast cancer for screening high-risk cases, pre-operative staging, and problem-solving because of its high sensitivity. However, its cost-effectiveness is still debated. Thus, the concept of abbreviated MRI (ABB-MRI) protocols was proposed as a possible solution for reducing MRI costs.
PURPOSE: : to investigate the role of the abbreviated MRI protocols in detecting and staging breast cancer.
METHODS: : a systematic search of the literature was carried out in the bibliographic databases: Scopus, PubMed, Medline, and Science Direct.
RESULTS: : forty-one articles were included, which described results of the assessment of fifty-three abbreviated protocols for screening, staging, recurrence assessing, and problem-solving or clarification.
CONCLUSIONS: : the use of ABB-MRI protocols allows reducing the acquisition and reading times, maintaining a high concordance with the final interpretation, in comparison to a complete protocol. However, larger prospective and multicentre trials are necessary to validate the performance in specific clinical environments.

Introduction

Breast cancer is one of the leading causes of death in the world and the leading cause of death by cancer among women around the world [1]. In 2018, the World Health Organisation (WHO) reported more than 2 million new cases and 626,679 deaths by this disease [2]. Early detection continues to be the best strategy to improve the prognosis of breast cancer, and mammography remains the standard screening method for detection in women over 40 years, with a sensitivity of 70% and a specificity of 92% in the general population [3]. Different studies have shown that screening with mammography has an effect on mortality by breast cancer [4].

Despite this, mammography has shown poor performance in the detection of cancer in patients with dense breasts [5], [3]. It is also not indicated in young patients because of the possible effect of radiation exposure. To counteract this problem, other imaging modalities have been proposed, such as tomosynthesis, a variation of mammography that generates three-dimensional images but whose performance is not significantly greater; breast ultrasound, which is useful as a complementary study, but with a low-positive predictive value [6], and magnetic resonance imaging (MRI), and specifically the Dynamic Contrast-Enhanced MRI, which is currently considered the most sensitive method for detecting breast cancer without the use of ionizing radiation and is proposed as an effective screening alternative in high-risk population [7].

The usefulness of breast magnetic resonance imaging not only includes an initial diagnosis and detection of breast cancer, but it is also recommended for preoperative staging, problem-solving, follow-up of treatment response, among others. A great benefit of MRI is its high detection sensitivity of breast cancer and its usefulness for finding subtle tumors in mammograms, ultrasounds, and physical examination [8]. Particularly, breast cancer screening with MRI alone or combined with ultrasound or mammography has shown variable cost-effectiveness regarding the objective population. Studies have shown that MRI is cost-effective for high-risk patients [9], [10]. In fact, in the last years has been a generalised agreement among the main European and American radiology associations (the European Society of Breast Cancer Specialists - EUSOMA, European Society of Breast Imaging-EUSOBI, Society of Breast Imaging-SBI, American College of Radiology-ACR, and American Cancer Society -ACS) regarding to recommendations for annual screening with MRI and mammography for women with a risk of [11], [12], [13], [14], [15], [16], which includes women with BRCA1 or BRCA2 mutation, women with relatives of first degree of consanguinity with a BRCA mutation, clinical history of thoracic radiation, and Li-Fraumeni, Cowden or Bannayan-Riley-Ruvalcaba syndrome [9]. However, its use as a screening method in the general population or with an intermediate or lower risk of life is hindered due to the cost associated with the study acquisition and the radiology time interpretation. Thus, although recent studies have estimated that screening with MRI alone in women whose only risk factor is dense breasts is economically feasible [17], [18], none of the current guidelines recommend MRI as a screening imaging technique in those cases.

In 2014, Cristiane Kuhl [19] introduced the concept of an abbreviated protocol for breast MRI (ABB-MRI) for breast cancer screening, which required the acquisition of only two sequences, i.e., T1-weighted, acquired before and immediately after the application of gadolinium; from them, two derived images, i.e., the First contrast-enhanced Acquisition SubTracted (FAST) and maximum-intensity projection (MIP) were used for interpretation. This study, which included women with increased risk of developing the disease, allowed establishing the absence of cancer with a negative predictive value of and a diagnostic accuracy equivalent to that obtained by a complete protocol but reducing the acquisition and interpretation times to 3 minutes and fewer than 30 seconds, respectively. From this study, the research into the use of abbreviated protocols for the detection, characterization, and staging of lesions in breast magnetic resonance has become a relevant topic due to the feasibility of substantially reducing the image acquisition and reading times.

Other review articles have described some of the abbreviated protocols published in the literature [20], [21], [22], [23], [24], [25], [26], [27], [28], [29], [30]; however, none of them performed a comprehensive systematic review. Recently, Baxter et al [31] presented a systematic review and meta-analysis of published ABB-MRI studies but focused on screening only cohorts and enriched cohorts separately. Additionally, the search was carried out in August 2019, which implies the exclusion of recent works. Similarly, Geach et al. [32] presented a systematic review and meta-analysis of ABB-MRI for breast cancer screening that included the FAST sequence; the search was performed in November 2019.

This document presents the results of a comprehensive systematic review of literature on abbreviated protocols for breast cancer study, including screening, follow-up, staging, among other applications. We analyze the configuration of the proposed protocols, its performance, and the effect produced by the acquisition and interpretation times.

Materials and methods

Sources consulted and search strategy

A search of published documents was carried out using the following equation: (MRI AND “breast cancer” AND (abbreviated OR accelerated OR fast)), in the databases PubMed (134), Medline (124), Science Direct (27) and Scopus (253). The search was restricted to metadata title, abstract, and keywords. It was also limited to the period between January 1, 2013, and July 31, 2020.

Eligibility criteria

For this review, full-text availability articles published in a peer-reviewed journal (abstracts and conference proceedings were excluded) and written in English were considered. Studies that include a reduced number of MRI sequences for the detection, staging, and/or follow-up of breast cancer were evaluated. A comparison concerning a referenced standard (complete protocol interpretation, biopsy, or imaging follow-up) was also required.

Data extraction

Data extraction was performed by one of three reviewers and confirmed by two other reviewers. Study details (imaging use, study design, number of cases, age range, ABB-MRI protocol, acquisition and reading times, summary findings) were extracted from the included full-text articles and recorded on a database (Excel, Microsoft, Redmond WA, USA).

Results and discussion

Fig. 1 illustrates the flow of searching, selection, and inclusion/exclusion performed in this systematic literature review [33]. The initial search yielded 538 documents, with 280 duplicated documents, which implied a final recovery of 258 documents. Each of these articles was independently reviewed by one of the three of the researchers, based on the reading of the title and abstract, in order to establish if its content did or did not describe the use of abbreviated protocols for the study of breast cancer, discarding articles that did not include this aspect. Then, a more detailed review determined if the articles that were maintained in the previous step presented evaluations for the implementation of ABB-MRI, according to the criteria defined above. Three researchers carried out this review, and in case of disagreement, some articles were included for full-text review. Therefore, documents were excluded, of them because not reporting abbreviated protocols, for being reviews or technical notes, either of general aspects of the use of magnetic resonance in the diagnosis of breast cancer or specifically on abbreviated protocols for breast cancer [20], [21], [22], [23], [24], [25], [26], [27], [28], [29], [30], [32], [31], seven documents that corresponded to editorials, letters or erratum, two documents because the full text was not available in the English language, three more there was no full-text availability, and two documents that studied animal specimens. After the previous process, articles were maintained for full-text review, which reported breast ABB-MRI protocols.

Fig. 1

Flow diagram for study searching, selection and inclusion. A total of 41 articles that reported 53 ABB-MRI protocols were included.

The main technical specifications of the studies included in this review are presented in Table 1. A total of articles reviewed in full text, were published between and , and were published between and , demonstrating a growing interest in this subject area the last years. In studies, patients were retrospectively identified from consecutive breast MRI studies performed for many clinical indications such as preoperative staging for patients with known malignant lesions, screening for high-risk patients, problem-solving, among others, which entails a potential selection bias. At the same time, in the other articles, all data were prospectively acquired, the largest being the multicentre, cross-sectional EA1141 randomized trial [34], which was conducted at institutions in the United States and one institution in Germany. This study compared the diagnostic performance of ABB-MRI and Digital Breast Tomosynthesis (DBT) for screening average-risk women with dense breasts. Study results showed a significantly higher rate of invasive breast cancer detection.

Table 1

Technical specifications of included ABB-MRI studies.

Study	Year	Purpose	Design	Field strength	Population	Subjects	Age range	MRI protocol	Acquisition time (minutes)	Reading time (minutes)
Kuhl et al. [19]	2014	Screening: detection	Prospective	1.5T	Women at low to moderate risk	443	54.225−73	T1W 1st post-contrast subtracted + MIP	3.06	0.46(20−68 seg)
Grimm et al. [35]	2015	Screening: detection	Retrospective	1.5T−3T	Women at high risk of breast cancer	48	49.1−	T2W FST1W pre and 1st post-contrast	6−8	2.98
								T2W FS, Pre, 1st and 2nd post-contrast.	8	NR
Mango et al. [45]	2015	Screening: detection	Retrospective	1.5T−3T	Women with biopsy proven unicentric breast carcinoma visualized on MRI	100	5228−84	T1W pre and 1st post-contrastsubtraction and MIP	10−15	0.73
Harvey et al. [46]	2016	Screening: detection	Retrospective	NR	Women at high risk of breast cancer	505	53.224−81	Axial T1W-FS pre and 1st post-contrastSubtraction + MIP	1.91	1.55
Heacock et al. [47]	2016	Screening: detection	Retrospective	3T	Women who had undergone breast MRI	107	5533−83	T1W post-contrast	12	−−
								T1W post-contrast with prior imaging	4.5	−−
								T2W, T1W post-contrast with prior imaging	12	1−2
Moschetta et al. [36]	2016	Screening: detection	Retrospective	1.5T	Women with a family history of cancer and dense glandular structure	470	53.2±8.928−77	STIR - T2W - THRIVEpre and 1st post-contrastTHRIVE	10	2±1.2
Bickelhaupt et al. [69]	2017	Screening clarification	Retrospective	1.5T	Women with suspicious breast lesions detected in x-ray screening (BIRADS 4-5)	50	57.550−70	T2W, DWI with background suppression	NR	0.48±0.17
Bickelhaupt et al. [70]	2017	Screening clarification	Retrospective	1.5T	Asymptomatic women with suspicious breast lesions detected in x-ray screening (BIRADS 4)	115	5750−69	T2W, maximum intensity breast diffusion (MIBD)	7	0.5
Chen et al. [48]	2017	Screening with dense breast tissue	Retrospective	3T	Women with dense breast tissue and negative previous results who had undergone routine breast MRI	478	49.330−71	1st post-contrastsubtracted + MIP	3	0.7±0.3
Chen et al. [49]	2017	Screening of dense breast tissue	Retrospective	3T	Women with dense breast tissue who had undergone routine breast MRI	356	48.2±4.730−75	1st post-contrast subtracted + MIP	3	0.61
								1st post-contrast1st subtraction + MIP, DWI	3.2	0.9
Jain et al. [37]	2017	Screening: detection	Retrospective	1.5T−3T	Women with a personal or family history of cancer	591	44.2521−74	T1W pre and 1st post-contrast, 1st subtraction	NR	NR
Kang et al. [71]	2017	Screening: detection	Retrospective	3T	Women with a personal history of breast cancer	358	46.3426−74	T1W-FS and Non FS, DWI1st and 5th post-contrast	5	NR
Machida et al. [64]	2017	Screening: detection	Retrospective	3T	Women who had undergone breast MRI	88	54.531−78	Coronal VIBE pre-contrast and coronal TWIST post-contrast	4.29	NR
Oldrini et al. [38]	2017	Screening: detection and characterization	Retrospective	1.5T	Women who had undergone breast MRI	70	5324−77	1st T1W post-contrast + MIP	NR	NR
								1st T1W post-contrast, subtraction and T2W	5.8	1.8
								TRICKS + MIP	1.34	NR
								1st T1W post-contrast, subtraction, T2W and TRICKS + MIP	7.2	3.5
Panigrahi et al. [50]	2017	Screening: detection	Prospective	1.5T−3T	Women at high risk of breast cancer	1052	53.119−86	T1W-FS1st subtraction + MIP	3	2.4±1.8
Petrillo et al. [51]	2017	Screening: detection and characterization	Retrospective	1.5T	Women who had undergone breast MRI	508	46.414−75	T1W 1st subtraction + MIP	10−15	0.73
Romeo et al. [39]	2017	Screening: detection and characterization	Retrospective	1.5T	Women at high risk of breast cancer with previous screening	98	5030−73	T1W FS pre-contrast, 1st, 2nd, 3th subtractions	5.58	0.63
Strahle et al. [40]	2017	Screening	Prospective	1.5T	Asymptomatic women with a negative mammogram	671	55.740−80	T1W pre and 1st post-contrast, T2, 6th post-contrast	7.5	NR
Choi et al. [52]	2018	Recurrent breast cancer diagnosis	Prospective	1.5T−3T	Women with a history of breast cancer surgery	725	5126−84	Sagittal T2W-FS, sagittal T1W pre and 1st post-contrast, subtraction + MIP	8.5	NR
Dogan et al. [63]	2018	Screening (Quality image evaluation)	Prospective	3T	Patients at increased breast cancer risk	23	5738−72	T2W FSE Triple-Echo Dixon T2W, 3D Dual-Echo FSPGR Dixon (DCE)	9.42±0.81	13.92±4.28
Oldrini et al. [41]	2018	Screening: detection, time	Retrospective	3T	Women who had undergone breast MRI	90	50.427−76	Sagittal T1W pre and 1st post-contrast subtraction	3	1−4.11
Seppala et al. [53]	2018	Screening: detection	Retrospective	1.5T	Women at high risk of breast cancer	100	NR30−69	T1W sagittal pre and first post-contrast subtraction + MIP	4.58	2.5
Zelst et al. [65]	2018	Screening: detection	Prospective	3T	Women at high risk	201	42.720−74	TWIST	1.42	1.09
Yamada et al. [54]	2018	Screening: detection	Retrospective	1.5T	Women who had undergone breast MRI with breast cancer <2 cm	87	NR	T2W FS,DWI, MIP-DWI	9	0.22−0.47
								T2W FS, 2nd subtraction + MIP	NR	0.23−0.58
Borthakur et al. [42]	2019	Comparing time to Screening	Retrospective	1.5T	Women who had undergone breast MRI as part of their scheduled clinical examinations	736	55.3±0.8	Axial T2W STIR, Axial T1W pre and 1st post-contrast	17.5±0.5	NR
Dialani et al. [55]	2019	Screening: detection	Retrospective	1.5T	Women at high risk who had a negative mammogram in the previous year	259	5226−78	T2W MIP post-contrast	−−	−−
								T2W MIP post-contrast, T1W pre and 1st post-contrast	3	−−
								T2W MIP post-contrast, T1W Pre and 1st postcontrast, T2W	8	2.4
Girometti et al. [74]	2019	Detection of additional disease in breast cancer staging.	Retrospective	1.5T	Women with a histological diagnosis of breast cancer	87	5630−79	FLASH T pre-contrast, 1st post-contrast + MIP	3	NR
Goto et al. [66]	2019	Screening: detection and classification	Prospective	3T	Women with a history of chemotherapy	200	5735−84	TWIST-VIBE	1.78	NR
Ha et al. [43]	2019	Screening: detection	Retrospective	1.5T−3T	Women with a history of breast cancer	2310	50±8	T2W-FS T1W-FS 1st post-contrast	1.5	NR
Jones et al. [56]	2019	Screening performed by mammogram readers	Prospective	3T	Women at high risk	125	4028−61	1st post-contrast-subtracted images+MIP	NR	0.56−1.28
Lee-Felker et al. [57]	2019	Estimating extent of disease in diagnosed breast cancer	Retrospective	3T	Women with breast cancer newly diagnosed	81	5632−92	T1W FS pre and 1st post-contrast, subtraction + MIP	3.5	1 to 4
Milon et al. [27]	2019	Screening: detection and characterization	Retrospective	1.5T	Women who had undergone breast MRI	120	5528−88	T1W, T2W, T1W-FS 1st post-contrast	7.8	NR
								T1W, T2W, T1W-FS 1st post-contrast, HTR DCE	8.35	NR
An et al. [58]	2020	Screening: detection	Retrospective	3T	Women with a personal history of cancer and post-surgical mammography and ultrasound testing	763	5523−89	T2W, T1W pre- and 1st post-contrast, subtraction and MIP.	8.3	NR
Comstock et al. [34]	2020	Screening of dense breast tissue	Prospective	1.5T−3T	Women with heterogeneously dense or extremely dense breasts	1444	5440−75	T2W and T1W pre and post-contrast	7.9	NR
Choudhery et al. [67]	2020	Comparing kinetic parameters of the RAMP MRI protocol Vs. DCE	Retrospective	1.5T−3T	Women with tissue diagnoses of suspicious MRI lesions	162	51.6±11.1	Rapid Abridged Multiphase (RAMP)	3	NR
Kwon et al. [44]	2020	Screening: detection	Retrospective	1.5T−3T	Women with previously treated cancer	973	5026−84	T2, 1st and 2nd post-contrast	10−11	3
Marquina et al. [59]	2020	Screening: detection	Retrospective	1.5T	Women at high risk of breast cancer	82	46.84±11.23	T1W pre and 1st post-contrast + MIP	NR	NR
Mori et al. [68]	2020	Comparing kinetic parameters of the Ultrafast MRI protocol Vs. DCE	Retrospective	3T	Patients with histologic diagnosis of NMEs made by core biopsy or clinically confirmed benign NME.	77	5223−81	T1W pre-contrast, Ultrafast (8 series) post-contrast	1.1	NR
Park et al. [60]	2020	Recurrent breast cancer diagnosis	Retrospective	1.5T−3T	Women with a personal history of breast cancer	656	50.4±9.1	T2W, T1W pre, 1st and 2nd post-contrast, subtractions, Axial and Sagital MIP	3	0.73−1.55
Shiraishi et al. [61]	2020	Estimating extent of disease in diagnosed breast cancer	Retrospective	1.5T	Patients with pathologically proven DCIS who underwent preoperative breast MRI	164	5419−81	T1W pre and 1st post-contrast + MIP	NR	NR
Scoggins et al. [62]	2020	Screening: detection and categoriztion	Prospective	3T	Women at high risk of breast cancer	73	53.526−75	Subtraction MIPs	NR	5.92
								Non-subtraction and subtraction DCE	NR	26.44
								Non subtraction, subtraction DCE + MIP, T2W-FSE Dixon, 3D dual-echo Dixon	9.63	21.68

Another aspect that stands out from the included studies is the variation in the field strength of the scanners. Thus, studies acquired images using a scanner of 1.5T, used scanners of 3T, and in studies, both 1.5T and 3T scanners were used, respectively.

Abbreviated protocols specification

Varying versions of the abbreviated protocols have been reported in the literature. The selection of the sequences that make them up is apparently heuristic, with a general tendency using a non-contrast T1-weighted (T1W) or T2-weighted (T2W) acquisition plus at least one contrast-enhanced sequence [35], [36], [37], [38], [39], [40], [41], [42], [43], [27], [34], [44]. This is to improve the specificity, including information that allows greater discrimination between benign and malignant lesions and make it possible to evaluate the tumor uptake. Other studies explicitly incorporate the use of maximum intensity projection (MIP) images of post-contrast examinations as part of the reading protocol [19], [45], [46], [47], [48], [49], [50], [51], [52], [53], [54], [55], [56], [57], [58], [59], [60], [61], [62]. This derivated image highlights maximum enhancement areas such as tumor or lymph nodes, and allows for the assessment of the relationship among arteries, veins, and blood vessels.

Some studies have focused on determining the effect by including the T2W sequence in an ABB-protocol [47], [40]. Strahle et al. [40] developed an evaluation of the conspicuity of lesions in each sequence to determine those that could contribute better to the detection of suspicious lesions of malignancy. In this study, the authors request each radiologist to assign a conspicuous value for each observed lesion, that is, the intensity relative to the surrounding tissue, on the hypothesis that acquisitions that present greater conspicuity in the intensity of the signal improves the morphological characterization of the lesions, and consequently the ability to differentiate benign from malignant lesions. As a result, the proposed protocol contained the sequences T1W pre and post-contrast T2W post-contrast (taken at one and a half minutes), and T1 postcontrast at minute 6. This protocol has not been evaluated with respect to a complete protocol, and neither follow-up period was part of the study, which does not allow for calculation of sensitivity, specificity, and negative predictive values. The assessment of conspicuity has also been included as a variable of analysis in the study of Heacock et al. [47]; the authors demonstrated that the T2W sequence does not affect the performance detection of lesions using an abbreviated protocol and is better than the T1W sequence. Thus, T2W sequence has been incorporated in several ABB-MRI protocols such as [35], [36], [38], [52], [63], [54], [42], [55], [43], [27], [58], [34], [44], [60], [62]. Dixon sequence has also been proposed in [63] and [62] to form up an ABB-MRI protocol for screening patients with high and increased risk. These sequences generate both water-only and fat-only series in a single acquisition, reducing the study acquisition time significantly while minimizes false-positive rates with no impact on cancer detection.

Incorporating ultrafast DCE MRI sequences has also been proposed as an alternative for reducing the acquisition time on dynamic contrast enhanced studies. Ultrafast contrast-enhanced sequence refers to a new technique that allows capturing early contrast material wash-in at high temporal resolution, obtaining a series of images that describe the path of the contrast bolus within the first 2 minutes after contrast injection. Time-resolved angiography with interleaved stochastic trajectories (TWIST) by Siemens, Time-Resolved Imaging of Contrast Kinetics (TRICKS) and Differential Subsampling with Cartesian Ordering (DISCO) by GE, are the sequences used in the included studies [64], [38], [65], [66], [27]. In particular, Zelst et al. [65] proposed to use TWIST as a single-sequence in an ultrafast breast MRI protocol (UBMP) with an acquisition time of 1 minute and 42 seconds. Reported results indicated that this protocol is at least as accurate as a complete protocol. Additionally, Choudhery et al. [67] found no significant difference between the rapid abridged multiphase (RAMP) ACR-accredited breast MRI protocol and one standard DCE-MRI for discriminating benign from malignant lesions, based on delayed-phase percentage washout, predominant curve type, or worst curve type. Similar results were found by Mori et al. [68] but only for non-mass enhancement lesions. Unfortunately, specific MRI coil and sequence requirements are needed to achieve diagnostic spatial resolution at the high temporal resolution; it is because ultrafast imaging is not readily feasible with all available scanners.

On the other hand, there is a growing interest in the development of contrast-agent free protocols by using the acquisition of diffusion-weighted images (DWI) and their respective Apparent diffusion coefficient (ADC) maps [69], [70], [49], [71], [72], [54], especially because gadolinium deposition in the brain has been described recently [73]. Bickelhaupt et al. [69], [70] proposed to use diffusion-weighted imaging with background suppression (DWIBS) for defining an ABB-MRI protocol and clarify mammogram based screening findings. The proposed protocol is composed of the DWIBS, TW2, and the fusion of both images. With this protocol, the false-positive rate of non-invasive measures decreased from 64% to 19%, whereas preserving the sensitivity. In a similar way, Kang et al. [71] proposed an abbreviated protocol consisted of fused DWI and unenhanced T1W images, and the DWI-MIP for screening patients with a personal history of breast cancer, which diagnostic performance was similar to a complete protocol. Chen et al. [49] showed that adding the diffusion to a protocol based on the first post-contrast sequence and MIP, significantly improves the performance of the protocol. Likewise, in 2018, Kul et al. [72] conducted a study that seeks to establish the viability of using the acquisition of diffusion-weighted images and ADC map for describing the cellularity of masses detected in the breasts and to establish the contribution of this evaluation for its characterization. From the reported results, the diffusion images showed a high to moderate concordance during breast masses description respect to dynamic contrast-enhanced (DCE) study. In addition, the diagnostic accuracy achieved with the morphological evaluation was slightly lower in comparison with the DCE. Furthermore, this study showed that the combination of DWI and ADC acquisitions could achieve even better performance than the DCE. Chen et al. [49] showed that adding the diffusion imaging to a protocol based on the first post-contrast sequence and MIP significantly improves the performance of the protocol. Moreover, Yamada et al. [54] reported that the detectability of the unenhanced abbreviated protocol based on DWI would be comparable to that abbreviated protocol based on postcontrast. According to the above, abbreviated unenhanced MRI based on DWI seems to have the potential for screening breast MRI.

Study purpose and population

Several included articles varied in both the study purpose and population, respectively. articles studied the ABB-MRI protocols in breast cancer screening from both screening only and enriched cohorts with known cancers. In two others, the evaluation of recurrency was addressed [52], [60]. Two of the articles evaluating the use of ABB-MRI for the extent of the disease assessing [57], [61], and the other one for detecting additional lesions in confirmed breast cancer patients [74].

A total of breast MRI studies were evaluated in the includes studies, of which were acquired prospectively. In four articles, MRI studies corresponded to subjects reported in another study; therefore, they were counted only once. The total number of subjects by study vary between and in retrospective studies; and between and in the prospective studies. Age ranges were between 14 and 92 years, with a mean of .

From the set of retrospective studies, included women who had undergone breast MRI by currently accepted indications, such as preoperative breast staging, problem-solving, follow-up for previous non-surgical breast intervention, and probably benign findings detected on previous studies, among others [47], [48], [49], [64], [38], [51], [41], [54], [42], [27]; two of them were specifically oriented to the detection of lesions in women with heterogeneously or extremely dense breasts [48], [49], according to ACR categorization, and another one in to detect lesions in pathologically proven breast cancer studies [45]. Six aimed to evaluate the feasibility of using abbreviated protocols to screening high risk women [35], [46], [59], [39], [53], [55]; and others, to women with a personal or family history of breast cancer [71], [36], [43], [37], [58], [44], [60]. Additionally, studies established as inclusion criteria to present lesions previously identified by another imaging modality [69], [70], [67]; and the other , focused on pathologically proven breast cancer studies [74], [57], [68], [61].

On the other hand, from the subset of articles that studied subjects prospectively enrolled: studied feasibility of ABB-AP for screening patients at high-risk of breast cancer [50], [65], [56], [62]; two analyzed studies of women who carried a mildly or moderately increased risk, either because of dense breast tissue, mild or moderate family history, or personal history of breast cancer [19], [63]; and two more, women with a personal history of breast cancer [52], [66]. Another one, studied asymptomatic women with a negative mammogram, which did not have a personal history of breast cancer or prior chest radiation therapy [40]. Additionally, as was depicted above, Comstock et al. [34] studied clinically asymptomatic women with heterogeneously dense or extremely dense breasts.

From the foregoing, although the abbreviated magnetic resonance protocols are presented to the scientific and healthcare community as an alternative for screening of breast cancer, few studies are oriented to assess their feasibility in the general population or in women with moderate risk. Additionally, given the advantages of magnetic resonance imaging, there does not seem to be any restriction to include women in a wide range of ages. Thus, the inclusion of young women with a moderate or high risk of developing the disease could be one of the main advantages of this type of studies.

Acquisition and interpretation times

From the studies that reported acquisition and interpretation times, we can conclude that there is evidence of a substantial reduction in an abbreviated protocol compared to the conventional complete MRI protocol. The average acquisition time of the includes studies was minutes ( minutes - minutes), and the interpretation time of minutes ( seconds - minutes). It should be noted that the times to review the medical history, the previous studies (mammograms or comparison ultrasounds), time to load images in the PACS system, or the time to report the findings, which consume an important part of the interpretation process, were not included. In this regard, Borthakur et al. [42] analyzed the activity times from ABB-MRI and complete protocols for the examination, scan, and technologist activity, included both scan-related and non-scan-related activities. They found that the scan-related activities, such as creating post-processing images and injecting contrast, are performed during the long and idle times, which are more frequently available during the longer scan sequences of the complete protocol. That is to say, those times are absorbed by the longer imaging acquisition times during the complete protocol, offsetting some of the gains from performing the ABB-MRI protocol. Consequently, the implementation of an ABB-MRI increased only at the patient flow rate, which was less than the that was anticipated based on expected scan times.

Diagnostic performance

Despite the variability of the protocol designs, the included results consistently report non-significant differences in the diagnostic performance between Abbreviated and complete breast MRI protocols. Table 2, Table 3, Table 4, Table 5, Table 6, Table 7 summarize the main performance measures reported in the included studies: Sensitivity (Sens.), Specificity (Spec.), Predictive Positive Value (PPV), Predictive Negative Value (PNV), and Inter-observer agreement (Agree). Overall ABB-MRI protocols used biopsy or follow-up imaging results as standard of reference. Additionally, the varied inclusion/exclusion criteria for each study makes the enrolled subject cohorts differ greatly regarding cancer frequency and alter the diagnostic performance. Thus, articles were grouped according to their purpose and study population for readability. No larger differences were found in performance measures reported for each subset, although, as was expected, PPV was higher in studies with a larger prevalence of cancer.

Table 2

Performance of ABB-MRI protocols in screening settings to women who had undergone breast MRI for varied indications.

Study	Lesions	Cancers/ Subjects	Reference	Readers	Exper. (years)	Sens.	Spec.	PPV	PNV	Agree.
Mango et al. [45]	100	100/100	Biopsy	4	5−18	96	92.9	−−	−−	−−
Heacock et al. [47]	107	107/107	Biopsy	3	2−6	96.3100	−−	−−	−−	−−
						98.1100	−−	−−	−−	−−
						98.1100	−−	−−	−−	−−
Chen et al. [48]	41	16/478	Biopsy/ follow-up	2	10	93.8	88.3	21.7	99.8	−−
Chen et al. [49]	67	14/356	Biopsy/ follow-up	3	10−15	92.9	86.5	22	99.7	−−
						100	95	45.2	100	−−
Machida et al. [64]	53	31/88	Biopsy/ follow-up	2	6−13	90.3	87.55	61.95	97.7	0.56
Oldrini et al. [38]	106	58/70	Biopsy	2	5−6	93.95	25	60.25	77.5	−−
						93.1	60.4	74	87.9	0.8
						89.7	60.4	73.25	82.85	−−
						93.1	77.05	83.25	90.2	0.87
Petrillo et al. [51]	295	207/508	Biopsy/ follow-up	2	20	99.5	75.4	73.5	99.6	0.99
Oldrini et al. [41]	26	26/90	Biopsy/ follow-up	2	0.5−6	100	93.3	−−	−−	−−
Yamada et al. [54]	89	89/87	Biopsy	2	8−15	89.995.5	97.694.1	−−	−−	0.45
						95.598.9	90.694.1	−−	−−	0.56
Milon et al. [27]	179	110/120	Biopsy	2	2−6	92	27	63	72	0.8
						95	45	70	87	0.89

Table 3

Performance of ABB-MRI protocols in screening settings for women at high-risk of breast cancer.

Study	Lesions	Cancers/ Subjects	Reference	Readers	Exper. (years)	Sens.	Spec.	PPV	PNV	Agree.
Grimm et al. [35]	24	12/48	Biopsy/ follow-up	3	7−14	86	86	−−	−−	−−
Harvey et al. [46]	−−	7/505	Biopsy	−−	1−22	89	45	−−	−−	−−
Panigrahi et al. [50]	49	14/1052	Biopsy	10	1−22	81.8	97.2	30.4	−−	0.94
Romeo et al. [39]	180	64/98	Biopsy/ follow-up	2	8−16	97	95	95	98	−−
Seppala et al. [53]	56	23/100	Biopsy	3	6−22	69.6	77.9	−−	−−	0.540.53
Zelst et al. [65]	85	31/100	Biopsy/ follow-up	7	6−15	84	82	45	−−	0.73
Dialani et al. [55]	7/259	7/259	Biopsy/ follow-up	5	4−28	77	81	−−	−−	−−
						91	76	−−	−−	−−
						91	89	−−	−−	−−
Jones et al. [56]	56	56/125	Biopsy/ follow-up	8	2−28	88	87	−−	−−	0.660.63
Marquina et al. [59]	12	11/82	Biopsy/ follow-up	1	>10	100	91.43	47.83	100	−−
Scoggins et al. [62]	20	6/73	Biopsy/ follow-up	16	1−27	100	73.6	5	100	0.68
						100	77.8	5.9	100	0.51
						100	93	16.7	100	0.37

Table 4

Performance of ABB-MRI protocols in screening settings for women at middle or moderate risk of breast cancer because of personal or familiar history.

Study	Lesions	Cancers/ Subjects	Reference	Readers	Exper. (years)	Sens.	Spec.	PPV	PNV	Agree.
Kuhl et al. [19]	34	11/443	Biopsy/ follow-up	2	6−18	100	94,3	24,4	100	−−
Moschetta et al. [36]	185	75/470	Biopsy	2	NR	89	91	64	98	−−
Jain et al. [37]	40	10/591	Biopsy	2	NR	100	95.17	28.2	100	−−
Kang et al. [71]	358	9/358	Biopsy	3	4−10	92.6	94.4	30.3	99.7	0.69
Choi et al. [52]	97	12/725	Biopsy	2	7−12	100	89.2	61.5	−−	−−
Goto et al. [66]	215	106/200	Biopsy	2	6−12	100	56.840.9	−−	−−	0.74
Ha et al. [43]	149	51/2310	Biopsy	2	8−15	94.192.2	97.698.6	34.547.5	99.9299.89	−−
An et al. [58]	32	21/763	Biopsy/ follow-up	3	9−16	95.2	98	57.1	99.9	−−
Kwon et al. [44]	29	10/973	Biopsy	5	NR	71.4	98.2	50	99.6	−−

Table 5

Performance of ABB-MRI protocols in screening clarification settings.

Study	Lesions	Cancers/ Subjects	Reference	Readers	Exper. (years)	Sens.	Spec.	PPV	PNV	Agree.
Bickelhaupt et al. [69]	50	22/50	Biopsy	2	2−6	−−	89.3	87.6	96.1	0.92
Bickelhaupt et al. [70]	115	42/115	Biopsy	2	<1−6	95.12	89.19	−−	−−	0.82

Table 6

Performance of ABB-MRI protocols in screening settings for asymptomatic or health women.

Study	Lesions	Cancers/ Subjects	Reference	Readers	Exper. (years)	Sens.	Spec.	PPV	PNV	Agree.
Strahle et al. [40]	435	6/671	Biopsy	4	6−12	−−	−−	41.2	−−	−−
Comstock et al. [34]	126	22/1444	Biopsy	2	NR	95.7	86.7	19.6	−−	−−

Table 7

Performance of ABB-MRI protocols in recurrence, disease extension and staging settings.

Study	Lesions	Cancers/ Subjects	Reference	Readers	Exper. (years)	Sens.	Spec.	PPV	PNV	Agree.
Girometti et al. [74]	36	36/87	Biopsy	4	1.5−20	86100	−−	76.284.6	−−	−−
Lee-Felker et al. [57]	116	81/81	Biopsy or follow-up	8	1−25	99	97	98	95	0.83
Park et al. [60]	20	10/656	Biopsy/ follow-up	1	NR	70	98	35	99.5	−−

Although Girometti et al. [74] reported that less experienced radiologists induced more false-positive findings than experienced ones, no large differences were reported between them for interpreting the ABB-MRI protocols. However, most studies were performed by experienced readers, which could bias the interobserver agreement that was reported between moderate and perfect in most of the cases when this measure was computed.

Some articles were excluded from these tables because they non focused on diagnostic or categorization tasks [63], [67], [68], [61]. However, the reported results are mostly consistent with the feasibility of using abbreviated protocols for breast cancer. In [42], activity times of an ABB-MRI were compared with the complete-protocol examination, but no diagnostic comparison was made. Dogan et al. [63] showed that an abbreviated protocol comprising a T2W and a 3D dual-echo fast spoiled gradient echo two-point Dixon sequences, not shown significantly image quality differences to that of a standard-of-care MRI protocol. Choudhery et al. [67] demonstrates comparable kinetic characteristics for discriminating benign from malignant lesions between the ACR-accredited rapid abridged multiphase (RAMP) MRI protocol and a complete DCE MRI protocol. Likewise, the kinetic characteristics of ultrafast DCE-MRI allow differentiating benign from malignant non-mass enhancements as a standard DCE MRI protocol [68].

Finally, it is important to mention the results reported by Shiraishi et al. [61], who evaluated the feasibility of using an ABB-MRI protocol for preoperative assessment of the tumor extent in patients with pure DCIS. The ABB-MRI protocol was comprised of a pre-contrast and 60 seg post-contrast T1W images with MIP.

The performance was assessed by the rate of concordance between pathology and the extent estimated by image interpretation. In this case, the rate of concordance for the complete protocol was higher than for the ABB-MRI. However, variation in measurements between readers tended to be slightly lower for the ABB-MRI than the complete protocol.

Cost-effectiveness

The potential cost and time savings of the abbreviated protocols have been indicated in all of the studies included in this review; however, none of them evaluated the cost-effectiveness of abbreviated breast MRI relative to other imaging techniques. These analyzes are required to advance in the incorporation of the use of these protocols for screening low and intermediate risk patients in both current guidelines and clinical settings. For cost-effectiveness analyses of abbreviated MRI protocols, it is important to realize that time saving must consider both scan-related and non-scan-related activities, in order to compute the real value of an abbreviated MRI study.

Conclusions

Several studies in the literature have proposed the use of abbreviated MRI protocols for breast cancer. Most of them were assessed for screening purposes; however, the most recent publications have considered other diagnostic tasks, such as recurrence, staging, screening clarification, and disease extension. Overall, the abbreviated protocols have diagnostic performances comparable to that of the standard breast MRI protocol, except for the tumor extent estimation, when the concordance rate between the extent estimated by image interpretation and pathological results was higher for the complete protocol than ABB-MRI. Moreover, abbreviated MRI has also been shown to have superior cancer yield to that of digital breast tomosynthesis (DBT).

Abbreviated protocols were initially comprised of a subset of sequences of the standard complete protocol. However, at last times, the use of ultrafast o high temporal resolution (HTR) sequences has been introduced in both standalone and added to abbreviated MRI schemes. Ultrafast MRI sequences seem to be a really viable alternative since they allow a kinetic analysis of the contrast enhancement uptake of the lesions. On the other hand, unenhanced or free contrast MRI techniques such as diffusion-weighted imaging (DWI) are also being investigated because gadolinium deposition in the brain recently described. These have shown a larger cancer detectability of mammography but slightly inferior to DCE based MRI protocols.

In summary, shorter imaging times achieved with the abbreviated MRI protocols have the potential to increase efficiency in breast imaging practice, which would be expected to improve their cost-effectively even for the screening of increased-risk women such as women with dense breast tissue. However, further studies about the effect on clinical outcomes, physicians and patients acceptability, and cost-effectiveness compared with other technologies such as ABUS or CES are also required.

Author contributions

This work was developed with the substantial contribution of all the authors. G.D. and M.L.H. conceived and designed the study and searching strategy. S.O., K.F. and A.O carried out the searching and selection of articles and the information extraction, which was confirmed by G.D. and M.L.H. All authors have contributed to the preparation of the paper, the discussing of the searching results and the reviewing of the content of this article, and have approved the manuscript.

Ethical statement

Authors confirm that the manuscript has been read and approved by all named authors and that there are no other persons who satisfied authorship criteria. Authors further confirm that all have approved the order of authors listed in the manuscript. Additionally, authors declare that this manuscript is original, has not been published before, and is not currently being considered for publication elsewhere.

Funding

This work was funded by MinCiencias (Colombia), Instituto Tecnológico Metropolitano, and Ayudas Diagnósticas Sura. Project RC 740-2017.

Conflicts of interest

The authors declare no conflict of interest.