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Article

Prognosis of Subcutaneous Mastectomy for Special Types of Breast Cancer

1
Department of Breast Surgery, Tokyo Medical and Dental University, Tokyo 1138519, Japan
2
Department of Plastic Surgery, Tokyo Medical and Dental University, Tokyo 1138519, Japan
3
Department of Pathology, Tokyo Medical and Dental University, Tokyo 1138519, Japan
4
Department of Radiology, Tokyo Medical and Dental University, Tokyo 1138519, Japan
5
Department of Specialized Surgeries, Graduated School, Tokyo Medical and Dental University, Tokyo 1138519, Japan
*
Author to whom correspondence should be addressed.
Medicina 2022, 58(1), 112; https://doi.org/10.3390/medicina58010112
Submission received: 8 December 2021 / Revised: 5 January 2022 / Accepted: 6 January 2022 / Published: 12 January 2022
(This article belongs to the Section Surgery)

Abstract

:
Background and objectives: In the treatment of the special type of breast cancer (STBC), the choice of chemotherapeutic agents is often based on the characteristic features of the histological type. On the other hand, the surgical strategy is usually determined by the tumor size and presence of lymph node metastasis, and the indication for immediate reconstruction is rarely discussed based on the histological type. The prognoses of STBC and invasive ductal carcinoma of the breast (IDC) patients who underwent subcutaneous mastectomy (SCM) with immediate reconstruction at our institution were compared. Materials and Methods: A total of 254 patients with SCM with immediate reconstruction from 1998 to 2018 were included; their tumor diameter or induration was less than 25 mm, and it was not in close proximity to the skin. Preoperative chemotherapy and non-invasive cancer cases were excluded. Results: The number of patients was 166 for skin-sparing mastectomy (SSM) and 88 for nipple-sparing mastectomy (NSM). The reconstructive techniques were deep inferior epigastric artery perforator flap (DIEP) reconstruction in 43 cases, latissimus dorsi flap reconstruction (LDflap) in 63 cases, tissue expander (TE) in 117 cases, and transverse rectus abdominis myocutaneous flap/vertical rectus abdominis myocutaneous flap (TRAM/VRAM) reconstruction in 31 cases. The histological types of breast cancer were 211 IDC and 43 STBC; 17 were mucinous carcinoma (MUC), 17 were invasive lobular carcinoma (ILC), 6 were apocrine carcinoma, 1 was tubular carcinoma, and 2 were invasive micropapillary carcinoma. There was no difference in local recurrence or disease-free survival (LRFS, DFS) between IDC and STBC, and overall survival (OS) was significantly longer in STBC. OS was better in the STBC group because SCM with immediate reconstruction was performed for STBC, which is a histological type with a relatively good prognosis. Highly malignant histological types, such as squamous cell carcinoma or metaplastic carcinoma, were totally absent in this study. Conclusions: The indications for SCM with immediate reconstruction for relatively common STBCs such as MUC and ILC can be the same as for IDC.

1. Introduction

Subcutaneous mastectomy (SCM) is a method of breast cancer surgery performed for breast reconstruction and is classified as skin-sparing mastectomy (SSM) or nipple-sparing mastectomy (NSM) [1,2,3,4]. In both cases, the skin just above the tumor is preserved, which makes it difficult to perform for advanced breast cancer. When performing breast cancer surgery, the surgical method is mainly determined by the preoperative tumor diameter and the presence of lymph node metastasis. Special type of breast cancer (STBC) refers to breast cancer other than ductal carcinoma, and there are various histological types [5]. The most common types of STBC are mucinous carcinoma (MUC) and invasive lobular carcinoma (ILC) [5]. It is difficult to diagnose the extent of ILC spread preoperatively, and when partial resections are performed, additional resection is often required after partial resection for ILC [6,7]. Highly malignant histological types of breast cancer, such as squamous cell carcinoma and metaplastic carcinoma, are often not early-stage breast cancer at the time of diagnosis, and breast reconstruction may not be indicated in the primary setting [8,9,10]. The indications and prognosis of SCM with immediate reconstruction for STBC have not been widely discussed. In this study, the prognoses of IDC and STBC cases treated with SCM were compared, and the oncological safety of the procedure was investigated retrospectively. These were evaluated by DFS, OS, and LRFS. MUC and ILC, which are more frequent in STBC, were also compared.

2. Methods

2.1. Patient Population and Surgical Treatment

A total of 363 patients underwent SCM (231 SSM and 132 NSM) with immediate reconstruction at Tokyo Medical and Dental University from 1998 to 2018. Invasive breast cancer with an invasive component of 1 mm or more was included in the study, but cases with preoperative chemotherapy and non-invasive ductal carcinoma were excluded. Under the exclusion criteria, 254 cases (166 SSM and 88 NSM) were included in the study. SCM was indicated for patients with tumors less than 25 mm in diameter and not in close proximity to the skin or pectoral muscles on preoperative imaging. NSM was indicated for patients with a nipple–tumor distance of at least 1 cm. These indication criteria were defined in 1998. There was no nipple areola necrosis in NSM, and no additional nipple areola excision was performed for positive nipple side margins. Reconstruction techniques included autograft reconstruction or artificial reconstruction, and the patient chose the reconstruction method. Deep inferior epigastric artery perforator flap (DIEP) reconstruction was started in 2008, and SSM was performed in all DIEP cases. This is because microvascular anastomosis is necessary. Sentinel lymph node biopsy (SNB) was introduced in 2004. All cases before that time were treated with axillary lymph node dissection.

2.2. Pathological Analysis

Histopathological examination was performed according to the International Union Against Cancer Tumor-Node-Metastasis classification criteria [11]. Blood vessel invasion and lymphatic vessel invasion were also evaluated. The nuclear grade was defined according to the Japan National Surgical Adjuvant Study of Breast Cancer (NSAS-BC) protocol [12]. Biological features, including estrogen receptor (ER) and c-erbB-2 (HER2), were evaluated by immunohistochemistry.

2.3. Follow-Up

All patients were followed-up by physical examination every 6 months and mammography with breast ultrasonography annually. Chest and abdominal computed tomography, liver ultrasonography, bone scan, and other investigations were performed in symptomatic cases or whenever clinically indicated. Adjuvant chemotherapy and hormonal therapy were performed according to the contemporary recommendations. Post-mastectomy radiotherapy (PMRT) was carried out according to the pathological findings of each case. Although local recurrence usually includes recurrence in the regional lymph nodes, only local recurrence in the anterior chest wall was considered in this study.

2.4. Statistical Analysis

The χ2 test and Fisher’s exact test were used to examine the relationships between factors. Median follow-up time was calculated as the median observation time of all patients. Local recurrence-free survival (LRFS) and disease-free survival (DFS) were measured from the date of surgery to the date of first local or distant recurrence. Overall survival (OS) was measured from the date of surgery to the date of death. The actuarial rates of LRFS, DFS, and OS were calculated according to the Kaplan–Meier method. A p-value < 0.05 was considered significant. These statistical analyses of clinicopathological and biological factors were carried out using EZR (Saitama Medical Center, Jichi Medical University, Saitama, Japan), which is a graphical user interface for R (The R Foundation for Statistical Computing, Vienna, Austria) [13]. More precisely, it is a modified version of R commander designed to add statistical functions frequently used in biostatistics.

3. Results

3.1. Comparison of Prognosis between IDC and STBC

The patients’ background characteristics are listed in Table 1. The mean patient age was 46 years (range 26–72 years). The patients had a median follow-up time of 135 months (range 4–280 months). There were 211 cases of IDC and 43 cases of STBC. The special types included 17 cases of MUC, 17 cases of ILC, 6 cases of apocrine carcinoma, 1 case of tubular carcinoma, and 2 cases of invasive micropapillary carcinoma. The nuclear grade of the STBC group was significantly lower, and the tumor diameter tended to be larger.
There were no differences in DFS and LRFS (Figure 1A,B). There were no deaths in the STBC group, and there was a significant difference in OS (Figure 1C).

3.2. Comparison of Prognosis between MUC and ILC

The background characteristics of MUC and ILC patients are shown in Table 2. Ten cases of MUC and five cases of ILC had an IDC component. The tumor size of the ILC group was significantly larger. ILC had five pT3 cases, two of which were treated with PMRT.
There were many cases in which NSM was performed in the MUC group. There were no distant recurrences, deaths, or local recurrences of ILC. There were no significant differences between MUC and ILC in DFS, OS, and LRFS (Figure 2A–C).

4. Discussion

In general, SCM with immediate reconstruction is indicated for relatively early-stage breast cancer [1,2,3,4]. Therefore, the indication for SCM often depends on tumor size and the presence of lymph node metastasis. Of course, if the patient has advanced cancer, the appropriateness of SCM after preoperative chemotherapy will be considered [14,15].
There are few cases where the indication for SCM is considered based on the histological type of breast cancer. The appropriateness of SCM for STBC has rarely been discussed. In the present study, the prognosis of patients who underwent SCM for STBC was reviewed. However, there is no similarity in the biological behavior of breast cancers that are not IDC [5]. STBC includes squamous cell carcinoma and metaplastic carcinoma, which have very poor prognoses, as well as tubular carcinoma and MUC, which have relatively good prognoses [8,9,10,16,17]. As expected, squamous cell carcinoma or metaplastic carcinoma were totally absent in this study. All of the histological types of the SCMs performed at our institution for STBC were histological types that are considered to have a relatively good prognosis. This may be the most important reason for the better OS of STBC.
In STBC, ILC is the most common histological type that is considered for surgical treatment. ILC accounts for about 5% of primary breast cancers and has increased in recent years. The frequency of hormone receptor expression is high, endocrine therapy is effective, and the prognosis is relatively good [18,19]. On the other hand, the appropriateness of partial mastectomy has often been discussed, and various imaging studies have reported difficulties in diagnosing spread within the breast [6,7]. Additional resection is often required after partial resection for ILC. However, there were no cases of local recurrence in the present study because the whole mammary gland is usually excised when immediate reconstruction is performed. However, ILC cases in which SCM was performed were significantly more likely to have larger tumor diameters, and pT3 cases were relatively common. It may make sense to perform SCM with immediate reconstruction for ILC if the patient is not concerned about partial resection.
MUC accounts for about 3% of primary breast cancers, and pure MUC has a relatively good prognosis [20]. The prognosis of the mixed type of MUC, which are MUCs with an IDC component, is similar to that of normal IDC [21]. In the present study, there were significantly more cases in which NSM was indicated for MUC. This may be because the preoperative imaging often shows that there is little intraductal extension and the tumor is localized. Local recurrence occurred in two MUC cases: one case was a mixed type, and local recurrence occurred through the needle tract at the time of core needle biopsy. In the cases of NSM performed for MUC, fortunately, no local recurrence occurred on the nipple areola complex. In particular, when NSM is performed for Asian patients with small breasts who have mucinous carcinoma with a large vertical diameter, it is necessary to be very careful even if an experienced surgeon is performing NSM, because the field of view of NSM is poor, and cutting into the tumor itself may cause dissemination. Thus, MUC with a large tumor size may increase the possibility of local dissemination, and a total mastectomy should be performed rather than SCM.
This study is limited by the small number of cases at a single institution. A multi-institutional study will be necessary to accumulate cases of SCM for various STBCs, including histological types with poor prognoses. In addition, this study has more limitations, such as the retrospective nature of the study and the included relatively new cases with different follow-up periods.

5. Conclusions

The cases of SCM for STBC were limited to histological types with a relatively good prognosis. The indications for SCM with immediate reconstruction for relatively common STBCs such as MUC and ILC can be the same as for IDC.

Author Contributions

Conceptualization, T.N.; methodology, T.N.; software, T.N.; validation, T.N.; formal analysis, T.N.; investigation, T.N.; resources, T.N., G.O., H.M., N.U., I.O., N.S., T.F., M.M. and K.K.; data curation, T.N., G.O., H.M., N.U., I.O., N.S., T.F., M.M. and K.K.; writing—original draft preparation, T.N.; writing—review and editing, T.N.; visualization, T.N.; supervision, K.O., T.I. and H.U.; project administration, T.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Ethics Committee of Tokyo Medical and Dental University, Tokyo, Japan (M2019-137, date of approval: 19 September 2019).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study. Written informed consent has been obtained from the patients to publish this paper.

Data Availability Statement

The datasets analyzed in the present study are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Comparison of prognosis between IDC and STBC. (A) DFS: There was no significant difference in DFS between the IDC and STBC groups. (B) OS: There were no deaths in the STBC group, and OS was significantly longer in the STBC group (p = 0.0266). (C) LRFS: There was no significant difference in LRFS between the IDC and STBC groups.
Figure 1. Comparison of prognosis between IDC and STBC. (A) DFS: There was no significant difference in DFS between the IDC and STBC groups. (B) OS: There were no deaths in the STBC group, and OS was significantly longer in the STBC group (p = 0.0266). (C) LRFS: There was no significant difference in LRFS between the IDC and STBC groups.
Medicina 58 00112 g001
Figure 2. Comparison of prognosis between MUC and ILC. (A) DFS, (B) OS, (C) LRFS. There were no statistically significant differences in DFS, OS, or LRFS between the MUC and ILC groups.
Figure 2. Comparison of prognosis between MUC and ILC. (A) DFS, (B) OS, (C) LRFS. There were no statistically significant differences in DFS, OS, or LRFS between the MUC and ILC groups.
Medicina 58 00112 g002
Table 1. Background characteristics of all patients.
Table 1. Background characteristics of all patients.
CharacteristicsTotal (254)IDC (211)STBC (43)p
Age (Mean) 26–72 (46)26–72 (45)31–64 (48)
Type of subcutaneous mastectomySkin sparing mastectomy166145211
Nipple sparing mastectomy887513
Operation on axillary lymph nodesSentinel Lymph node biopsy129113160.493
Sentinel Lymph node biopsy → Axillary lymph node dissection45378
Axillary lymph node dissection807010
Reconstruction methodTRAM/VRAM312650.623
DIEP43385
LD63549
TE11710215
Post mastectomy irradiationNo247215320.338
Yes752
Histological typeInvasive ductal carcinoma211211--
Special type43-43
Mucinous carcinoma17-17
Invasive lobular carcinoma17-17
Apocrine carcinoma6-6
Tubular carcinoma1-1
Invasive micropapillary carcinoma2-2
Tumor size1150137130.0651
2947816
31055
Lymph node metastasisNo179155240.856
Yes756510
Nuclear grade1143113300.0004
259554
352520
Estrogen receptorPositive223192310.441
Negative31283
HER2Positive201911
Negative23420133
Lymphatic vessel invasionPositive363240.811
Negative21818830
Blood vessel invasionPositive171610.32
Negative23720433
Adjuvant chemotherapyNo191164271
Yes63567
Distant MetastasisNo228197310.586
Yes26233
SurvivalAlive233199340.03
Dead21210
Local RecurrenceNo237205320.745
Yes17152
Table 2. Background characteristics of patients with MUC and ILC.
Table 2. Background characteristics of patients with MUC and ILC.
CharacteristicsTotal (34)Mucinous Carcinoma (17)Invasive Lobular Carcinoma (17)p
Age (Mean) 31–64 (48)31–62 (45)38–64 (50)-
Type of subcutaneous mastectomySkin sparing mastectomy217140.0324
Nipple sparing mastectomy13103
Operation on axillary lymph nodesSentinel Lymph node biopsy16880.18
Sentinel Lymph node biopsy → Axillary lymph node dissection826
Axillary lymph node dissection1073
Reconstruction methodTRAM/VRAM5230.223
DIEP514
LD972
TE1578
Post mastectomy irradiationNo3217150.485
Yes202
Pure/Mixed typePure197120.166
Mixed15105
Tumor size113670.0262
216115
3505
Lymph node metastasisNo2414100.259
Yes1037
Nuclear grade13015151
2422
3000
Estrogen receptorPositive3114170.227
Negative330
HER2Positive1101
Negative331617
Lymphatic vessel invasionPositive4221
Negative301515
Blood vessel invasionPositive1011
Negative331716
Adjuvant chemotherapyNo2716110.0854
Yes716
Distant MetastasisNo3114170.227
Yes330
SurvivalAlive3417171
Dead000
Local RecurrenceNo3215170.485
Yes220
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MDPI and ACS Style

Nakagawa, T.; Oda, G.; Mori, H.; Uemura, N.; Onishi, I.; Sagawa, N.; Fujioka, T.; Mori, M.; Kubota, K.; Ishikawa, T.; et al. Prognosis of Subcutaneous Mastectomy for Special Types of Breast Cancer. Medicina 2022, 58, 112. https://doi.org/10.3390/medicina58010112

AMA Style

Nakagawa T, Oda G, Mori H, Uemura N, Onishi I, Sagawa N, Fujioka T, Mori M, Kubota K, Ishikawa T, et al. Prognosis of Subcutaneous Mastectomy for Special Types of Breast Cancer. Medicina. 2022; 58(1):112. https://doi.org/10.3390/medicina58010112

Chicago/Turabian Style

Nakagawa, Tsuyoshi, Goshi Oda, Hiroki Mori, Noriko Uemura, Iichiro Onishi, Noriko Sagawa, Tomoyuki Fujioka, Mio Mori, Kazunori Kubota, Toshiaki Ishikawa, and et al. 2022. "Prognosis of Subcutaneous Mastectomy for Special Types of Breast Cancer" Medicina 58, no. 1: 112. https://doi.org/10.3390/medicina58010112

APA Style

Nakagawa, T., Oda, G., Mori, H., Uemura, N., Onishi, I., Sagawa, N., Fujioka, T., Mori, M., Kubota, K., Ishikawa, T., Okamoto, K., & Uetake, H. (2022). Prognosis of Subcutaneous Mastectomy for Special Types of Breast Cancer. Medicina, 58(1), 112. https://doi.org/10.3390/medicina58010112

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