Skip to main content

Imaging surveillance for the detection of ipsilateral local tumor recurrence in patients who underwent oncoplastic breast-conserving surgery with acellular dermal matrix: abbreviated MRI versus conventional mammography and ultrasonography

Abstract

Background

To evaluate the usefulness of surveillance-abbreviated magnetic resonance imaging (AB-MRI) for the detection of ipsilateral local tumor recurrence (LTR) in patients who underwent oncoplastic breast-conserving surgery (BCS) with acellular dermal matrix (ADM) by comparing its diagnostic performance with that of mammography (MG) and ultrasonography (US).

Methods

The postoperative MG, US, and AB-MRI findings of the ipsilateral breast and pathological results of 324 patients who underwent oncoplastic BCS using ADM were reviewed. The cancer detection rate (CDR), sensitivity, specificity, positive predictive value (PPV) for biopsy, accuracy, and area under the curve (AUC) for each imaging modality were calculated.

Results

A total of 8 ipsilateral LTRs were diagnosed, and most cancers (87.5%) were stage 0 or 1 (median size of invasive cancer, 1.44 cm; range, 0.7–2 cm). The CDRs of MG, US, MG + US, and AB-MRI were 0.009, 0.012, 0.015, and 0.025 per woman, respectively. Three cancers were detectable on only AB-MRI, and the additional CDR of AB-MRI was 0.010. The sensitivity and specificity of MG, US, MG + US, and AB-MRI were 37.5%, 50%, 62.5%, and 100% and 99.7%, 98.4%, 98.1%, and 97.8%, respectively. The PPVs for biopsy were 75%, 44.4%, 45.5%, and 53.3%, respectively. The AUC was significantly higher for AB-MRI (0.989) than for MG alone (0.686, P = 0.0009), US alone (0.742, P = 0.009), and MG + US (0.803, P = 0.04). A total of 66.7% of cancers visible on only AB-MRI were located at the deep posterior portion of the excision cavity, which might have been missed with MG or MG + US due to masking by the ADM filler.

Conclusion

AB-MRI can improve the detection of ipsilateral LTR despite postoperative changes caused by ADM fillers compared to conventional MG and US. Patients who undergo BCS with ADM can be candidates for AB-MRI surveillance considering improved cancer detection and high sensitivity.

Background

Breast-conserving surgery (BCS) combined with postoperative radiotherapy has been established as a standard treatment for early-stage breast cancer [1]. The goal of BCS is to remove breast cancer completely with an adequate resection margin and without compromising cosmetic outcomes [2, 3]. Achieving both goals may be challenging, and approximately 30% of patients who undergo BCS are known to be unsatisfied with their cosmetic outcome [4, 5]. In particular, large-volume resection during BCS can result in unsatisfactory cosmetic outcomes in women with small- to medium-sized breasts [6,7,8,9]. In recent years, oncoplastic surgery has been introduced to overcome the cosmetic disadvantage of conventional BCS and has increasingly gained acceptance among both surgeons and patients [2]. Oncoplastic surgery is a combination of tumor removal and breast reconstruction and is divided into two broad techniques: volume displacement and volume replacement. In patients with relatively small breasts, the volume replacement technique has shown better cosmetic results than the volume displacement technique [6,7,8,9].

Acellular dermal matrices (ADMs) are well-known biological scaffolds of human, bovine, or porcine origin and do not evoke an immune response. ADMs are widely used in burn care and breast reconstruction surgery [10,11,12]. In breast surgery, ADM is used in more than 75% of immediate tissue expander reconstruction procedures to support the implant [13]. ADMs are increasingly utilized in BCS for volume replacement, and recent reports show satisfactory results regarding their safety and cosmetic outcome over a short-term follow-up period [14,15,16]. However, concern still exists regarding the influence of postoperative changes by ADM on monitoring local tumor recurrence (LTR) on postoperative imaging surveillance [16, 17]. The ADM-filled cavity presents as a high-density mass-like lesion on mammography (MG) and an echogenic mass with posterior shadowing on ultrasonography (US) [14, 16, 17] (Fig. 1). ADM can cause difficulties in image interpretation using conventional imaging, such as MG and US, during the follow-up period [14, 16, 17]. To date, whether ADM inserted in the excision cavity interferes with the early diagnosis of ipsilateral LTR has not yet been reported.

Fig. 1
figure 1

Follow-up imaging after 24 months of a 49-year-old woman who underwent oncoplastic BCS with ADM. The ADM was observed as A a circumscribed high-density mass on mammography and B a heterogeneous echogenic mass with posterior acoustic shadowing. The evaluation of the deep posterior margin of the excision cavity was limited by shadowing. The ADM showed low signal intensity on T2-weighted imaging and no enhancement on contrast-enhanced T1-weighted imaging (C)

Breast magnetic resonance imaging (MRI) is the most sensitive imaging method for detecting breast cancer and offers the highest cancer detection rate (CDR) of all breast imaging modalities. Since the introduction of the abbreviated MRI (AB-MRI) protocol by Kuhl et al. [18, 19], it has competed with MG or US as a screening tool by reducing the complexity and cost of breast MRI with a short scan time and improving access to breast MRI [20]. Currently, the use of AB-MRI as a screening tool is being actively investigated at different risk levels. We hypothesize that AB-MRI can improve the detection of ipsilateral LTR despite postoperative findings with ADM insertion compared to conventional MG or US. Therefore, the purpose of this study is to compare the diagnostic performance of AB-MRI to that of MG and US for the detection of ipsilateral LTR and to evaluate the clinical value of AB-MRI in the postoperative surveillance of patients who underwent oncoplastic BCS with ADM.

Materials and methods

Study population

This retrospective study was approved by the Catholic Medical Center Office of the Human Research Protection Program (CMC-OHRP) Institutional Review Board (Approval No. VC21RISI0105), and the requirement for informed consent was waived. In a retrospective search of our medical database between August 2017 and June 2020, we identified 329 patients with stage 0 to III breast cancer who underwent BCS and immediate volume replacement with the crosslinked human ADM (MegaDerm; L&C BIO, Seongnam, Korea) derived from donated human skin in the USA tissue banks following the guidelines of the American Association of Tissue Banks and the US Food and Drug Administration. Our study included patients who underwent postoperative imaging surveillance using MG, US, and AB-MRI and were followed-up for at least 1 year. Five patients were excluded due to follow-up loss within 1 year (n = 5). A total of 324 patients with a median follow-up of 22.8 months (12–38 months) were included in this study. The patients ranged in age from 22 to 83 years, and the mean age was 53.9 years. We reviewed the medical records, including the clinical, radiological, and pathological characteristics of breast cancer of the study population.

Definition

An ipsilateral LTR was defined as a recurrent invasive carcinoma or ductal carcinoma in situ (DCIS) that occurred in either the parenchyma and/or skin of the treated breast. An ipsilateral LTR was confirmed by histopathologic evaluation of the tumor. The interval was calculated from the date of the first oncoplastic BCS procedure with ADM to the date of pathologic confirmation.

Postoperative imaging surveillance

After breast cancer surgery, all patients underwent follow-up examinations with MG and US every 6 months for the first 2 years and annually thereafter. All mammographic imaging data were acquired by using a full-field digital mammography (DM) unit with integrated digital breast tomosynthesis (DBT) acquisition (Selenia Dimensions, Hologic). Standard DM followed by DBT acquisition was performed during the same breast compression and included two bilateral view mammograms (craniocaudal and mediolateral oblique views). Whole-breast US examinations were obtained by using an Aplio i800 system (Canon Medical System) equipped with a matrix linear transducer with a bandwidth of 5 to 18 MHz. With a 3 T scanner (Verio, Siemens Medical Solutions, Erlangen, Germany) equipped with a dedicated breast coil, AB-MRI was performed by using the following protocols: (a) axial fat-suppressed T2-weighted imaging, (b) pre- and postcontrast axial T1-weighted imaging before and immediately after gadoterate meglumine injection (0.1 mmol per kilogram body weight, Dotarem; Guerbet, Anlnay-Sous-Bois, France), (c) subtraction from postcontrast T1-weighted imaging, and (d) reformatting with a maximum intensity projection. The total acquisition time was only 8.3 min. AB-MRI was performed along with MG and US examinations on the same day or around the same time.

Postoperative imaging interpretation

Two board-certified radiologists specializing in breast imaging with 17 years of experience who were blinded to the results of the other studies independently reviewed MG, US, and AB-MRI follow-up studies. Because we aimed to evaluate the influence of ADM on ipsilateral LTR, we analyzed imaging studies in the treated breast only. All imaging studies were interpreted according to the 5th edition of the Breast Imaging Reporting and Data System (BI-RADS) classification. BI-RADS category 4 or 5 was considered a positive result, and tissue diagnosis was recommended. For lesions categorized as BI-RADS category 3, short-interval follow-up (6–12 months) was recommended. If lesions were stable during the follow-up period, they were downgraded to BI-RADS category 2. If any changes occurred, the lesions were upgraded to BI-RADS category 4, and biopsy was recommended. If a suspicious lesion was visible on MG or US, MG-guided or US-guided biopsy was performed. If a suspicious lesion was detected on only AB-MRI, a second-look US was first performed. If a correlate was present on second-look US, US-guided biopsy was performed. If there was no correlation, MR-guided biopsy was recommended, but none of the patients in this study were diagnosed by this modality.

Outcome measures and statistical analysis

We used the tissue diagnosis results at biopsy and at the clinical follow-up within 1 year as the reference standard to assess imaging surveillance for the detection of ipsilateral LTR. A true positive was defined as a case with positive results on MG, US, the combination of MG and US (MG + US), and AB-MRI followed by tissue confirmation. A true negative was defined as a case with negative imaging findings and the absence of cancer at the 1-year surveillance imaging. A false positive was defined as a case with positive imaging findings and with no detection of cancer within 1 year. A false negative was defined as a case with negative imaging findings and a tissue confirmation of cancer within 1 year.

We calculated the CDR, positive predictive value (PPV) for biopsy, sensitivity, specificity, diagnostic accuracy, and area under the curve (AUC) of MG, US, MG + US, and AB-MRI surveillance. Additionally, we compared the diagnostic performance outcomes of MG, MG + US, and AB-MRI surveillance by using receiver operating characteristic (ROC) analysis. The CDR was defined as the number of detected malignancies per woman for each group.

The clinicopathological characteristics of primary breast cancer patients with and without ipsilateral LTR were compared using the independent samples t test or Fisher’s exact test for continuous and categorical variables. Statistical analyses were performed using SAS version 9.4 (SAS Institute, Cary, NC, USA) and MedCalc ver. 16.1 (MedCalc software, Mariakerke, Belgium). Statistical significance was set at P value < 0.05.

Results

The demographic details of the patients in this study and the characteristics of the patients with ipsilateral LTR detected on imaging surveillance are summarized in Table 1. A total of 8 ipsilateral LTRs were diagnosed, and the frequency of LTR was 2.5% (8 of 324 women) in this study. Tumor subtype was significantly different between patients with and without ipsilateral LTR. HER2 (+) breast cancer and triple-negative breast cancer, not luminal-type breast cancer, were significantly associated with ipsilateral LTR (P = 0.03). The other findings were not significantly different.

Table 1 Characteristics of 324 patients included in this study

The types and biological profiles of ipsilateral LTR are summarized in Table 2. Of 324 patients, 15 patients had suspicious malignant lesions categorized as BI-RADS 4 or 5, and biopsies were performed. The biopsy recommendation rates of MG, US, and AB-MRI were 1.2% (4 of 324), 2.8% (9 of 324), and 4.6% (15 of 324), respectively. Of these 15 suspicious lesions, 8 were malignant (6 invasive, 2 ductal carcinoma in situ) and 7 were benign. Most of the detected cancers were stage 0 or 1 (87.5%, 7 of 8), and the median size of invasive cancer was 1.44 cm (range 0.7–2 cm). A total of 62.5% (5 of 8) were high-grade tumors, and 25% (2 of 8) showed multifocalities. One patient had clinically detected skin lesions, and invasive cancer was diagnosed by skin punch biopsy. After mastectomy, cancer invading into the dermis/epidermis with skin ulceration (T4b) was confirmed in the specimen. The remaining 7 patients were clinically asymptomatic, and imaging detected cancers. As summarized in Table 2, MG detected 3 cancers, US detected 4 cancers, and AB-MRI detected all 8 cancers. AB-MRI detected 3 additional cancers compared to MG + US. Overall, the CDRs of MG, USG, MG + US, and AB-MRI were 0.009, 0.012, 0.015, and 0.025 per woman, respectively. The additional CDR of AB-MRI was 0.010 per woman. Of the 3 cases visible only on AB-MRI, two cancers were observed at the medio-basal margin and at the basal margin of the original tumor bed (deep posterior portion of ADM filled cavity), so recurrent tumors were partially and completely obscured by ADM filling on both MG and US (Fig. 2) and missed on initial US exam. One lesion was identified on second-look US and confirmed by US-guided biopsy, but another lesion was not identified on second-look US, so ADM removal and surgical excision were performed. One patient had clinically detected skin lesions (reddish patches on skin), which were obscured by radiation treatment-related skin edema on both MG and US. Tumor infiltration presented as overlying skin enhancement and scattered small foci of remaining breast parenchyma (less than 0.3 cm) on AB-MRI.

Table 2 Characteristics of 8 ipsilateral LTRs detected on imaging studies
Fig. 2
figure 2

Follow-up imaging after 6 months of a 56-year-old woman who underwent oncoplastic BCS with ADM. A, B Post-surveillance mammogram and ultrasonogram were negative. C AB-MRI showed an irregular enhancing mass (block arrow) at the deep margin of the excision cavity filled with ADM (arrows). Second-look ultrasonography was performed, but the lesion at the deep portion was not identified due to shadowing. At surgery, a 0.7-cm-sized invasive cancer was confirmed

A comparison of the diagnostic performance of each imaging modality for the detection of ipsilateral LTR is summarized in Table 3, and the corresponding ROC curve is shown in Fig. 3. The sensitivity and specificity of MG, US, MG + US, and AB-MRI were 37.5%, 50%, 62.5%, and 100% and 99.7%, 98.4%, 98.1%, and 97.8%, respectively. The PPVs for biopsy were 75%, 44.4%, 45.5%, and 53.3%, respectively. The AUC was significantly higher for AB-MRI (0.989, 95% CI 0.971–0.997) than MG alone (0.686, 95% CI 0.632–0.736; P = 0.0009), US alone (0.742, 95% CI 0.691–0.789; P = 0.009), and MG + US (0.803, 95% CI 0.755–0.845; P = 0.04). There were no statistically significant differences in the AUC values between MG and US, MG, and MG + US, or US and MG + US.

Table 3 Diagnostic performances of each imaging modalities
Fig. 3
figure 3

Comparison of ROC curves (AB-MRI ~ MG + US, P = 0.04; AB-MRI ~ MG, P = 0.0009; AB-MRI ~ US, P = 0.009)

Discussion

The aim of surveillance in breast cancer survivors is to detect second breast cancers in the asymptomatic phase, which allows interventions that may lead to improved survival and quality of life. Because the early detection of tumor recurrence can result in a better prognosis, careful clinical and imaging surveillance are needed for patients who undergo BCS. Although there is no standard protocol for posttreatment imaging surveillance, annual MG with or without US is currently used in women who underwent BCS [21,22,23].

In patients who underwent oncoplastic BCS with ADM, ipsilateral LTR is an important issue because it is associated with distant metastasis and poor prognosis and is directly related to remnant tumor cells within the remaining breast tissue. However, there are concerns that the fibrogenetic action induced by ADM and its partial reabsorption may lead to misdiagnosis during follow-up [17]. Biomaterials such as ADM or regenerated oxidized cellulose show similar peculiar imaging findings, which are well-circumscribed masses that are similar in density and echogenicity to fibroglandular tissue on both MG and US [14, 16, 24, 25]. Thus, the early and accurate diagnosis of ipsilateral LTR using only conventional imaging modalities such as MG and US can be problematic in women who undergo oncoplastic BCS with ADM.

MRI is often used as a part of postoperative surveillance in the clinical setting and is considered the most sensitive imaging modality compared with conventional imaging methods such as MG and US in discriminating between postoperative scarring and tumor recurrence [26, 27]. Current data also support MRI as a postoperative surveillance modality with high diagnostic yield, sensitivity, and specificity for detecting recurrent cancer [26, 28,29,30,31,32]. More recently, the American College of Radiology has broadened its stance to also recommend supplemental screening MRI in women with a personal history of breast cancer [33]. The reason that most guidelines do not support the use of breast MRI for postoperative surveillance is its comparative effectiveness [34,35,36,37]. However, the use of the AB-MRI protocol with a short examination time is more cost-effective [19]. AB-MRI also showed equivalent diagnostic accuracy compared to full diagnostic MRI protocols [18], which has led to the consideration of using AB-MRI as a screening modality in patients with a personal history of breast cancer.

In our study, the ipsilateral LTR rate was 2.5% in patients who underwent oncoplastic BCS with ADM, which was similar to the previously reported rate in patients who underwent conventional BCS (2%) [38, 39]. Tumor subtype was different between patients with and without LTR. HER2 (+) type cancer and triple-negative type cancer were significantly associated with ipsilateral LTR in univariate analysis, although multivariate analysis was not performed. Regarding the performance of AB-MRI in the detection of LTR, AB-MRI demonstrated a significantly higher invasive CDR than other imaging modalities. AB-MRI detected 15 more cancers per 1000 women than MG alone and 9 more cancers per 1000 women than MG + US. Most detected cancers on AB-MRI were stage 0 or 1 (87.5%, 7 of 8), except for only 1 cancer with skin metastasis (T4b, stage IIIC), which was comparable to previous results indicating that MRI could detect biologically relevant breast cancer in high-risk patients [20, 40,41,42,43,44]. In addition to improved CDR, AB-MRI showed the highest sensitivity and negative predictive value (NPV) of 100% without sacrificing specificity for detecting LTR, and its AUC value was higher than that of other surveillance modalities (0.989 for AB-MRI vs. 0.686 for MG, 0.742 for US, and 0.803 for MG + US), which was consistent with previous data that MRI had a higher cancer detection yield, high sensitivity and specificity, and acceptable PPV for biopsy [28,29,30, 36, 45,46,47,48,49,50,51].

Despite the high sensitivity and CDR of AB-MRI, its high false positive rate (25%) and biopsy recommendation rate (4.6%) are the main drawbacks of its use in surveillance. However, 62.5% of cancers (5 of 8) might have been missed with mammography alone, and 37.5% (3 of 8) might have been missed with MG + US. In particular, 66.7% (2 of 3) of cancers visible on only AB-MRI were located at the basal margin of the excision cavity, which were obscured partially and completely by the ADM filler on conventional imaging. 50% (1 of 2) of cancers at the basal margin of the excision cavity were still not identified on a second-look US exam due to masking by the ADM filler. Therefore, we believe that AB-MRI surveillance could be a useful screening tool for the detection of ipsilateral LTR without delayed diagnosis despite postoperative changes with ADM filler in these patients. If informed patients choose AB-MRI for surveillance considering the harm caused by false negative cases, the false positive cases resulting from AB-MRI might be acceptable. In our study, the addition of US to MG increased its sensitivity from 37.5 to 62.5%; therefore, MG + US might be considered another surveillance option if patients are unable to undergo AB-MRI due to cost or accessibility [34, 52]. However, there is still the possibility of delayed diagnosis of ipsilateral LTR caused by the ADM filler, especially in the case of LTR at the basal margin of the original tumor bed. Our study results can inform patient and clinician decision making regarding postoperative surveillance methods and be used to develop personalized screening guidelines and recommendations in these populations.

In our study, AB-MRI required less than 10 min for examination (mean, 8.5 min), which is comparable to the MG examination time. AB-MRI showed the highest sensitivity for the detection of breast cancer irrespective of breast density. However, there is no radiation exposure or breast compression during MG examination and no reproducibility issue for US examination. If AB-MRI is reimbursable for patients with a personal history of breast cancer, it can be a good screening test with a short examination time, low cost, low harm, and wide availability. However, gadolinium deposition within the basal ganglia by intravenous contrast injection is still a concern with frequent, repeated AB-MRI examinations.

Our study had several limitations. First, it was limited by its retrospective design with small populations. The CDR of our study might be overestimated due to the selection bias of our retrospective study from a single medical center. Second, the follow-up period of this study was relatively short (12–38 months), which could have affected the diagnostic performance of each modality. Third, we did not evaluate the appropriate interval and frequency of AB-MRI surveillance. In addition, studies on the cost-effectiveness and survival benefit of AB-MRI are needed for the wide application of this surveillance method. Our study indicates that a continued larger, prospective, multicenter study is needed to validate the benefit of AB-MRI surveillance in this population.

Conclusions

In patients who underwent BCS with ADM volume replacement, AB-MRI showed an advantage for the detection of ipsilateral LTR despite postoperative changes. AB-MRI can be a useful postoperative surveillance tool for ipsilateral LTR considering its improved cancer detection and high diagnostic performance compared with MG and US.

Availability of data and materials

Please contact the corresponding author with requests for data.

Abbreviations

BCS:

Breast-conserving surgery

ADM:

Acellular dermal matrix

LTR:

Local tumor recurrence

MG:

Mammography

US:

Ultrasonography

MRI:

Magnetic resonance imaging

CDR:

Cancer detection rate

AB-MRI:

Abbreviated MRI

BI-RADS:

Breast Imaging Reporting and Data System

PPV:

Positive predictive value

AUC:

Area under the curve

ROC:

Receiver operating characteristic

References

  1. Association of Breast Surgery at B. Surgical guidelines for the management of breast cancer. Eur J Surg Oncol. 2009;35 Suppl 1:1–22.

  2. Clough KB, Kaufman GJ, Nos C, Buccimazza I, Sarfati IM. Improving breast cancer surgery: a classification and quadrant per quadrant atlas for oncoplastic surgery. Ann Surg Oncol. 2010;17(5):1375–91.

    Article  PubMed  Google Scholar 

  3. Rainsbury RM. Surgery insight: oncoplastic breast-conserving reconstruction--indications, benefits, choices and outcomes. Nat Clin Pract Oncol. 2007;4(11):657–64.

    Article  PubMed  Google Scholar 

  4. Shin ES, Kim HI, Song SY, Lew DH, Lee DW. Selection of oncoplastic surgical technique in Asian breast cancer patients. Arch Plast Surg. 2018;45(1):37–44.

    Article  PubMed  Google Scholar 

  5. Urban C, Lima R, Schunemann E, Spautz C, Rabinovich I, Anselmi K. Oncoplastic principles in breast conserving surgery. Breast. 2011;20(Suppl 3):S92–5.

    Article  PubMed  Google Scholar 

  6. Noguchi M, Yokoi-Noguchi M, Ohno Y, Morioka E, Nakano Y, Kosaka T, et al. Oncoplastic breast conserving surgery: volume replacement vs. volume displacement. Eur J Surg Oncol. 2016;42(7):926–34.

    Article  CAS  PubMed  Google Scholar 

  7. Ogawa T. Usefulness of breast-conserving surgery using the round block technique or modified round block technique in Japanese females. Asian J Surg. 2014;37(1):8–14.

    Article  PubMed  Google Scholar 

  8. Yang JD, Bae SG, Chung HY, Cho BC, Park HY, Jung JH. The usefulness of oncoplastic volume displacement techniques in the superiorly located breast cancers for Korean patients with small to moderate-sized breasts. Ann Plast Surg. 2011;67(5):474–80.

    Article  CAS  PubMed  Google Scholar 

  9. Yang JD, Lee JW, Kim WW, Jung JH, Park HY. Oncoplastic surgical techniques for personalized breast conserving surgery in breast cancer patient with small to moderate sized breast. J Breast Cancer. 2011;14(4):253–61.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Baek WY, Byun IH, Kim YS, Lew DH, Jeong J, Roh TS. Patient satisfaction with implant based breast reconstruction associated with implant volume and mastectomy specimen weight ratio. J Breast Cancer. 2017;20(1):98–103.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Bloemen MC, van Leeuwen MC, van Vucht NE, van Zuijlen PP, Middelkoop E. Dermal substitution in acute burns and reconstructive surgery: a 12-year follow-up. Plast Reconstr Surg. 2010;125(5):1450–9.

    Article  CAS  PubMed  Google Scholar 

  12. Lee JH, Kim HG, Lee WJ. Characterization and tissue incorporation of cross-linked human acellular dermal matrix. Biomaterials. 2015;44:195–205.

    Article  CAS  PubMed  Google Scholar 

  13. Sorkin M, Qi J, Kim HM, Hamill JB, Kozlow JH, Pusic AL, et al. Acellular dermal matrix in immediate expander/implant breast reconstruction: a multicenter assessment of risks and benefits. Plast Reconstr Surg. 2017;140(6):1091–100.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Gwak H, Jeon YW, Lim ST, Park SY, Suh YJ. Volume replacement with diced acellular dermal matrix in oncoplastic breast-conserving surgery: a prospective single-center experience. World J Surg Oncol. 2020;18(1):60.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Jung W, Kim K, Paik NS. Displacement of surgical clips in patients with human acellular dermal matrix in the excision cavity during whole breast irradiation following breast-conserving surgery. Cancer Res Treat. 2020;52(2):388–95.

    Article  PubMed  Google Scholar 

  16. Lee J, Yang JD, Lee JW, Li J, Jung JH, Kim WW, et al. Acellular dermal matrix combined with oxidized regenerated cellulose for partial breast reconstruction: two case reports. Medicine (Baltimore). 2020;99(31):e21217.

    Article  Google Scholar 

  17. Franceschini G, Masetti R. Acellular dermal matrix as filler in breast-conserving surgery: warnings for a careful use. World J Surg Oncol. 2021;19(1):1.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Kuhl CK. Abbreviated magnetic resonance imaging (MRI) for breast cancer screening: rationale, concept, and transfer to clinical practice. Annu Rev Med. 2019;70:501–19.

    Article  CAS  PubMed  Google Scholar 

  19. Kuhl CK, Schrading S, Strobel K, Schild HH, Hilgers RD, Bieling HB. Abbreviated breast magnetic resonance imaging (MRI): first postcontrast subtracted images and maximum-intensity projection-a novel approach to breast cancer screening with MRI. J Clin Oncol. 2014;32(22):2304–10.

    Article  PubMed  Google Scholar 

  20. Kuhl C, Weigel S, Schrading S, Arand B, Bieling H, Konig R, et al. Prospective multicenter cohort study to refine management recommendations for women at elevated familial risk of breast cancer: the EVA trial. J Clin Oncol. 2010;28(9):1450–7.

    Article  PubMed  Google Scholar 

  21. Khatcheressian JL, Hurley P, Bantug E, Esserman LJ, Grunfeld E, Halberg F, et al. Breast cancer follow-up and management after primary treatment: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol. 2013;31(7):961–5.

    Article  CAS  PubMed  Google Scholar 

  22. Senkus E, Kyriakides S, Ohno S, Penault-Llorca F, Poortmans P, Rutgers E, et al. Primary breast cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2015;26(Suppl 5):v8–30.

    Article  PubMed  Google Scholar 

  23. Runowicz CD, Leach CR, Henry NL, Henry KS, Mackey HT, Cowens-Alvarado RL, et al. American Cancer Society/American Society of Clinical Oncology Breast Cancer Survivorship Care Guideline. J Clin Oncol. 2016;34(6):611–35.

    Article  CAS  PubMed  Google Scholar 

  24. Franceschini G. Internal surgical use of biodegradable carbohydrate polymers. Warning for a conscious and proper use of oxidized regenerated cellulose. Carbohydr Polym. 2019;216:213–6.

    Article  CAS  PubMed  Google Scholar 

  25. Franceschini G, Visconti G, Sanchez AM, Di Leone A, Salgarello M, Masetti R. Oxidized regenerated cellulose in breast surgery: experimental model. J Surg Res. 2015;198(1):237–44.

    Article  CAS  PubMed  Google Scholar 

  26. Belli P, Costantini M, Romani M, Marano P, Pastore G. Magnetic resonance imaging in breast cancer recurrence. Breast Cancer Res Treat. 2002;73(3):223–35.

    Article  CAS  PubMed  Google Scholar 

  27. Preda L, Villa G, Rizzo S, Bazzi L, Origgi D, Cassano E, et al. Magnetic resonance mammography in the evaluation of recurrence at the prior lumpectomy site after conservative surgery and radiotherapy. Breast Cancer Res. 2006;8(5):R53.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Giess CS, Poole PS, Chikarmane SA, Sippo DA, Birdwell RL. Screening breast MRI in patients previously treated for breast cancer: diagnostic yield for cancer and abnormal interpretation rate. Acad Radiol. 2015;22(11):1331–7.

    Article  PubMed  Google Scholar 

  29. Gweon HM, Cho N, Han W, Yi A, Moon HG, Noh DY, et al. Breast MR imaging screening in women with a history of breast conservation therapy. Radiology. 2014;272(2):366–73.

    Article  PubMed  Google Scholar 

  30. Lehman CD, Lee JM, DeMartini WB, Hippe DS, Rendi MH, Kalish G, et al. Screening MRI in women with a personal history of breast cancer. J Natl Cancer Inst. 2016;108(3).

  31. Vardanian AJ, Clayton JL, Roostaeian J, Shirvanian V, Da Lio A, Lipa JE, et al. Comparison of implant-based immediate breast reconstruction with and without acellular dermal matrix. Plast Reconstr Surg. 2011;128(5):403e-10e.

  32. Morris EA, Liberman L, Ballon DJ, Robson M, Abramson AF, Heerdt A, et al. MRI of occult breast carcinoma in a high-risk population. AJR Am J Roentgenol. 2003;181(3):619–26.

    Article  PubMed  Google Scholar 

  33. Monticciolo DL, Newell MS, Moy L, Niell B, Monsees B, Sickles EA. Breast cancer screening in women at higher-than-average risk: recommendations from the ACR. J Am Coll Radiol. 2018;15(3 Pt A):408–14.

  34. Berg WA, Zhang Z, Lehrer D, Jong RA, Pisano ED, Barr RG, et al. Detection of breast cancer with addition of annual screening ultrasound or a single screening MRI to mammography in women with elevated breast cancer risk. JAMA. 2012;307(13):1394–404.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Kim SJ, Chung SY, Chang JM, Cho N, Han W, Moon WK. Ultrasound screening of contralateral breast after surgery for breast cancer. Eur J Radiol. 2015;84(1):54–60.

    Article  PubMed  Google Scholar 

  36. Schacht DV, Yamaguchi K, Lai J, Kulkarni K, Sennett CA, Abe H. Importance of a personal history of breast cancer as a risk factor for the development of subsequent breast cancer: results from screening breast MRI. AJR Am J Roentgenol. 2014;202(2):289–92.

    Article  PubMed  Google Scholar 

  37. Wernli KJ, DeMartini WB, Ichikawa L, Lehman CD, Onega T, Kerlikowske K, et al. Patterns of breast magnetic resonance imaging use in community practice. JAMA Intern Med. 2014;174(1):125–32.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Fisher B, Anderson S, Bryant J, Margolese RG, Deutsch M, Fisher ER, et al. Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation for the treatment of invasive breast cancer. N Engl J Med. 2002;347(16):1233–41.

    Article  PubMed  Google Scholar 

  39. Veronesi U, Cascinelli N, Mariani L, Greco M, Saccozzi R, Luini A, et al. Twenty-year follow-up of a randomized study comparing breast-conserving surgery with radical mastectomy for early breast cancer. N Engl J Med. 2002;347(16):1227–32.

    Article  PubMed  Google Scholar 

  40. Kriege M, Brekelmans CT, Boetes C, Besnard PE, Zonderland HM, Obdeijn IM, et al. Efficacy of MRI and mammography for breast-cancer screening in women with a familial or genetic predisposition. N Engl J Med. 2004;351(5):427–37.

    Article  CAS  PubMed  Google Scholar 

  41. Sardanelli F, Podo F, D'Agnolo G, Verdecchia A, Santaquilani M, Musumeci R, et al. Multicenter comparative multimodality surveillance of women at genetic-familial high risk for breast cancer (HIBCRIT study): interim results. Radiology. 2007;242(3):698–715.

    Article  PubMed  Google Scholar 

  42. Warner E, Hill K, Causer P, Plewes D, Jong R, Yaffe M, et al. Prospective study of breast cancer incidence in women with a BRCA1 or BRCA2 mutation under surveillance with and without magnetic resonance imaging. J Clin Oncol. 2011;29(13):1664–9.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Weinstein SP, Localio AR, Conant EF, Rosen M, Thomas KM, Schnall MD. Multimodality screening of high-risk women: a prospective cohort study. J Clin Oncol. 2009;27(36):6124–8.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Sung JS, Stamler S, Brooks J, Kaplan J, Huang T, Dershaw DD, et al. Breast cancers detected at screening MR imaging and mammography in patients at high risk: method of detection reflects tumor histopathologic results. Radiology. 2016;280(3):716–22.

    Article  PubMed  Google Scholar 

  45. Alderman A, Gutowski K, Ahuja A, Gray D, Postmastectomy ExpanderImplant breast reconstruction guideline work G. ASPS clinical practice guideline summary on breast reconstruction with expanders and implants. Plast Reconstr Surg. 2014;134(4):648e-55e.

  46. Brennan S, Liberman L, Dershaw DD, Morris E. Breast MRI screening of women with a personal history of breast cancer. AJR Am J Roentgenol. 2010;195(2):510–6.

    Article  PubMed  Google Scholar 

  47. An YY, Kim SH, Kang BJ, Suh YJ, Jeon YW. Feasibility of abbreviated magnetic resonance imaging (AB-MRI) screening in women with a personal history (PH) of breast cancer. PLoS One. 2020;15(3):e0230347.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Cho N, Han W, Han BK, Bae MS, Ko ES, Nam SJ, et al. Breast cancer screening with mammography plus ultrasonography or magnetic resonance imaging in women 50 years or younger at diagnosis and treated with breast conservation therapy. JAMA Oncol. 2017;3(11):1495–502.

    Article  PubMed  PubMed Central  Google Scholar 

  49. Choi BH, Choi N, Kim MY, Yang JH, Yoo YB, Jung HK. Usefulness of abbreviated breast MRI screening for women with a history of breast cancer surgery. Breast Cancer Res Treat. 2018;167(2):495–502.

    Article  PubMed  Google Scholar 

  50. Park VY, Kim EK, Kim MJ, Moon HJ, Yoon JH. Breast magnetic resonance imaging for surveillance of women with a personal history of breast cancer: outcomes stratified by interval between definitive surgery and surveillance MR imaging. BMC Cancer. 2018;18(1):91.

    Article  PubMed  PubMed Central  Google Scholar 

  51. Weinstock C, Campassi C, Goloubeva O, Wooten K, Kesmodel S, Bellevance E, et al. Breast magnetic resonance imaging (MRI) surveillance in breast cancer survivors. Springerplus. 2015;4:459.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Berg WA, Blume JD, Adams AM, Jong RA, Barr RG, Lehrer DE, et al. Reasons women at elevated risk of breast cancer refuse breast MR imaging screening: ACRIN 6666. Radiology. 2010;254(1):79–87.

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

Not applicable.

Funding

Grant No. 5–2020-B0001–00274; Initial of author who received grant: Y. Y An; Funder’s full name: The Catholic Medical Center Research Foundation, College of Medicine, The Catholic University of Korea (author’s institution, internal grant); Website URL of sponsor: http://www.cukrnd-iacf.ac.kr/index.jsp; None of the authors received salary or other funding from commercial companies. The funder had no role in the study design.

Author information

Authors and Affiliations

Authors

Contributions

YYA contributed to the study conception and design. MYK contributed to the data acquisition and quality control. YYA and MYK contributed to the data analysis and interpretation. All authors contributed to the manuscript preparation and editing. The authors read and approved the final manuscript.

Corresponding author

Correspondence to Yeong Yi An.

Ethics declarations

Ethics approval and consent to participate

This was approved by the Catholic Medical Center Office of the Human Research Protection Program (CMC-OHRP)/Institutional Review Board (Approval No. VC21RISI0105).

Consent for publication

The Catholic Medical Center Office of the Human Research Protection Program (CMC-OHRP)/Institutional Review Board (Approval No. VC21RISI0105) approved the future publication of this study.

Competing interests

The authors declare that they have no conflict of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kim, M.Y., Suh, Y. & An, Y.Y. Imaging surveillance for the detection of ipsilateral local tumor recurrence in patients who underwent oncoplastic breast-conserving surgery with acellular dermal matrix: abbreviated MRI versus conventional mammography and ultrasonography. World J Surg Onc 19, 290 (2021). https://doi.org/10.1186/s12957-021-02403-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12957-021-02403-2

Keywords