Impacts of Subtype on Clinical Feature and Outcome of Male Breast Cancer: Multicenter Study in Korea (KCSG BR16-09) (original) (raw)

Original Article
Breast cancer Impacts of Subtype on Clinical Feature and Outcome of Male Breast Cancer: Multicenter Study in Korea (KCSG BR16-09)

[Jieun Lee](/articles/search%5Fresult.php?term%5Ftype=authors&term=Jieun Lee)1, [Keun Seok Lee](/articles/search%5Fresult.php?term%5Ftype=authors&term=Keun Seok Lee)2, [Sung Hoon Sim](/articles/search%5Fresult.php?term%5Ftype=authors&term=Sung Hoon Sim)2, [Heejung Chae](/articles/search%5Fresult.php?term%5Ftype=authors&term=Heejung Chae)2, [Joohyuk Sohn](/articles/search%5Fresult.php?term%5Ftype=authors&term=Joohyuk Sohn)3, [Gun Min Kim](/articles/search%5Fresult.php?term%5Ftype=authors&term=Gun Min Kim)3, [Kyung-Hee Lee](/articles/search%5Fresult.php?term%5Ftype=authors&term=Kyung-Hee Lee)4, [Su Hwan Kang](/articles/search%5Fresult.php?term%5Ftype=authors&term=Su Hwan Kang)5, [Kyung Hae Jung](/articles/search%5Fresult.php?term%5Ftype=authors&term=Kyung Hae Jung)6, [Jae-ho Jeong](/articles/search%5Fresult.php?term%5Ftype=authors&term=Jae-ho Jeong)6, [Jae Ho Byun](/articles/search%5Fresult.php?term%5Ftype=authors&term=Jae Ho Byun)7, [Su-Jin Koh](/articles/search%5Fresult.php?term%5Ftype=authors&term=Su-Jin Koh)8, [Kyoung Eun Lee](/articles/search%5Fresult.php?term%5Ftype=authors&term=Kyoung Eun Lee)9, [Seungtaek Lim](/articles/search%5Fresult.php?term%5Ftype=authors&term=Seungtaek Lim)10, [Hee Jun Kim](/articles/search%5Fresult.php?term%5Ftype=authors&term=Hee Jun Kim)11, [Hye Sung Won](/articles/search%5Fresult.php?term%5Ftype=authors&term=Hye Sung Won)12, [Hyung Soon Park](/articles/search%5Fresult.php?term%5Ftype=authors&term=Hyung Soon Park)13, [Guk Jin Lee](/articles/search%5Fresult.php?term%5Ftype=authors&term=Guk Jin Lee)14, [Soojung Hong](/articles/search%5Fresult.php?term%5Ftype=authors&term=Soojung Hong)15, [Sun Kyung Baek](/articles/search%5Fresult.php?term%5Ftype=authors&term=Sun Kyung Baek)16, [Soon Il Lee](/articles/search%5Fresult.php?term%5Ftype=authors&term=Soon Il Lee)17, [Moon Young Choi](/articles/search%5Fresult.php?term%5Ftype=authors&term=Moon Young Choi)18, [In Sook Woo](/articles/search%5Fresult.php?term%5Ftype=authors&term=In Sook Woo)19

Cancer Research and Treatment : Official Journal of Korean Cancer Association 2023;55(1):123-135.
DOI: https://doi.org/10.4143/crt.2021.1561
Published online: March 24, 2022

1Division of Medical Oncology, Department of Internal Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

2Center for Breast Cancer, National Cancer Center, Goyang, Korea

3Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, College of Medicine, Yonsei University, Seoul, Korea

4Division of Oncology-Hematology, Department of Internal Medicine, Yeungnam University Medical Center, Yeungnam University College of Medicine, Daegu, Korea

5Department of Surgery, Yeungnam University Medical Center, Yeungnam University College of Medicine, Daegu, Korea

6Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

7Division of Medical Oncology, Department of Internal Medicine, Incheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

8Department of Internal Medicine, Ulsan University Hospital, Ulsan University College of Medicine, Ulsan, Korea

9Department of Hematology and Oncology, Ewha Womans University Hospital, Seoul, Korea

10Department of Hemato-Oncology, Wonju Severance Christian Hospital, Yonsei University Wonju College of Medicine, Wonju, Korea

11Division of Hematology–Oncology, Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Korea

12Division of Medical Oncology, Department of Internal Medicine, Uijeongbu St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

13Division of Medical Oncology, Department of Internal Medicine, St. Vincent’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

14Division of Medical Oncology, Department of Internal Medicine, Bucheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

15Department of Internal Medicine, National Health Insurance Service Ilsan Hospital, Goyang, Korea

16Division of Hematology and Oncology, Department of Internal Medicine, Kyung Hee University College of Medicine, Seoul, Korea

17Department of Internal Medicine, Dankook University College of Medicine, Cheonan, Korea

18Department of Internal Medicine, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea

19Division of Medical Oncology, Department of Internal Medicine, Yeouido St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea

Correspondence: In Sook Woo, Division of Medical Oncology, Department of Internal Medicine, Yeouido St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 10 63-ro, Yeongdeungpo-gu, Seoul 07345, Korea,
Tel: 82-2-3779-1574 Fax: 82-2-780-3132 E-mail: insookwoo@catholic.ac.kr

• Received: December 5, 2021 • Accepted: March 23, 2022

Copyright © 2023 by the Korean Cancer Association

This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Abstract

• Purpose
  The treatment of male breast cancer (MBC) has been extrapolated from female breast cancer (FBC) because of its rarity despite their different clinicopathologic characteristics. We aimed to investigate the distribution of intrinsic subtypes based on immunohistochemistry, their clinical impact, and treatment pattern in clinical practice through a multicenter study in Korea.
• Materials and Methods
  We retrospectively analyzed clinical data of 248 MBC patients from 18 institutions across the country from January 1995 to July 2016.
• Results
  The median age of MBC patients was 63 years (range, 25 to 102 years). Among 148 intrinsic subtype classified patients, 61 (41.2%), 44 (29.7%), 29 (19.5%), and 14 (9.5%) were luminal A, luminal B, human epidermal growth factor receptor 2, and triple-negative breast cancer, respectively. Luminal A subtype showed trends for superior survival compared to other subtypes. Most hormone receptor-positive patients (166 patients, 82.6%) received adjuvant endocrine treatment. Five-year completion of adjuvant endocrine treatment was associated with superior disease-free survival (DFS) in patients classified with an intrinsic subtype (hazard ratio [HR], 0.15; 95% confidence interval [CI], 0.04 to 0.49; p=0.002) and in all patients (HR, 0.16; 95% CI, 0.05 to 0.54; p=0.003).
• Conclusion
  Distribution of subtypes of MBC was similar to FBC and luminal type A was most common. Overall survival tended to be improved for luminal A subtype, although there was no statistical significance. Completion of adjuvant endocrine treatment was associated with prolonged DFS in intrinsic subtype classified patients. MBC patients tended to receive less treatment. MBC patients should receive standard treatment according to guidelines as FBC patients.
• Key words: Breast neoplasms, Male, Type, Prognosis, Asia

Introduction

Male breast cancer (MBC) is an orphan disease that accounts for 1% of all breast cancers [1]. In Korea, MBC accounts for approximately 0.36%–0.48% of all breast cancer cases [2,3], which is less frequent than that detected in the United States [1]. Until now, MBC patients have been alienated from various pivotal phase 3 trials due to their rarity in incidence. The treatment guidelines for MBC patients were extrapolated from female breast cancer (FBC) patients, but application of the newest treatment scheme to MBC patients was limited due to lack of evidence based on phase 3 trials that only included FBC patients.

Although the incidence of MBC is rare, it is on the rise [4,5], implying the need for focused studies in this specific population. The clinical and biological characteristics of MBC and FBC are similar in some ways, but there are also many distinct differences between the two disease categories [6]. Risk factors differ from those of FBC; for example, MBC patients tend to harbor BRCA2 mutations rather than BRCA1 mutations compared with FBC [7–10]. MBC tends to be diagnosed at an older age, with a higher incidence of hormone receptor–positive subtype and low incidence of human epidermal growth factor receptor 2 (HER2) compared with FBC [6,11]. Based on immunohistochemical markers or genomic profiling, subtypes of MBC have been previously analyzed in a few studies. Less than 10% of patients were classified as HER2 positive or triple-negative, and most cases were classified as luminal A or luminal B subtypes [11,12]. The distribution pattern and proportion of subtypes were different between MBC and FBC [13,14], and these biological differences may affect the differences in clinical outcomes between the two disease entities. However, the different biological behaviors of MBC were not reflected in the treatment due to the lack of clinical trials focusing on this patient subgroup.

In FBC, treatment is individualized according to the intrinsic subtype, and tailored management, such as anti-HER2 agents and immune-checkpoint inhibitors, has improved survival outcomes. However, as previously mentioned, the treatment of MBC patients is not based on unique biological features and extrapolated from clinical trials of FBC. There are growing efforts to gather data and establish the characteristics of biological features, treatment guidelines, and survival outcomes in MBC [15,16]. However, the studies are focused on the Western population, and the study design is mainly based on a review of previously collected databases that mainly provide basic clinical characteristics, but not sufficient data on pathologic characteristics and in-depth treatment patterns. Previously, we reported the clinical features, treatment patterns, and survival outcomes of MBC patients in seven institutions in Korea [17]. In previously published literature, we have reported that most MBC patients were diagnosed as hormone receptor-positive, and the latest hormonal agents and anti-HER2 treatments were relatively underutilized in these patients. A detailed analysis of the molecular subtype of the enrolled MBC patients was not feasible due to insufficient immunohistochemical surrogate markers, such as the Ki-67 index. Until now, the clinical characteristics and prognosis of Asian MBC patients according to intrinsic subtype have not been well analyzed due to the rarity of its incidence and absence of awareness of this cancer type.

In this study, we conducted a multicenter, retrospective analysis using patients’ baseline demographics and pathologic characteristics, including intrinsic subtype based on immunohistochemical stain, detailed treatment pattern, and clinical outcomes of MBC patients from 18 institutions in Korea during a 21-year period.

Materials and Methods

1. Patients

This retrospective, multicenter study was conducted by the Breast Cancer Division of the Korean Cancer Study Group (KCSG). From January 1995 to July 2016, the medical records of male patients with histologically confirmed breast cancer were retrospectively reviewed. Two-hundred and forty-eight patients primarily diagnosed as MBC were enrolled, and subtypes were able to be analyzed for 148 patients whose data of Ki-67 was available (Fig. 1).

2. Classification of subtype and stage

Estrogen receptor (ER) and progesterone receptor (PR) positivity was defined by American Society of Clinical Oncology/College of American Pathologists guideline (ASCO/CAP guideline) [18]. HER2-positive was defined as HER2 immunohistochemistry (IHC) 3+ or HER2 IHC 2+ with HER2 fluorescence or silver in situ hybridization positive based on ASCO/CAP guideline [19,20]. Before introduction of ASCO/CAP guideline, ER, PR, and HER2 positivity was interpreted based on in-house standards in each institution. Intrinsic subtype classification was based on 2015 St. Gallen Consensus Conference recommendations, categorized by IHC results of ER, PR, HER2, and Ki-67 index [21]. Luminal A subtype was defined as ER- and/or PR-positive and HER2-negative with Ki-67 ≤ 20%. Luminal B subtype was defined as ER- and/or PR-positive, HER2-negative with a Ki-67 index > 20%. HER2-enriched subtype was defined as HER2 positive based on IHC of fluorescence in situ hybridization, irrespective of the ER or PR status. Triple-negative breast cancer (TNBC) was defined as ER-, PR-, and HER2-negative. Tumor size and involved number of lymph nodes were collected based on each patient’s medical record. Tumor stage of each patient was redefined based on American Joint Committee on Cancer 7th staging manual [22].

3. Statistical analysis

Disease-free survival (DFS) was defined as the period from the time of primary treatment, such as surgical resection, to the date of disease recurrence or death from any cause. Overall survival (OS) was described as the period between the date of the first pathologic diagnosis and death or last follow-up. Continuous variables are presented as median values, and categorical variables are presented as percentages. Continuous variables were compared using the Mann-Whitney U test, while categorical variables were compared using the chi-square test and Fisher exact test. Survival analyses were performed using the Kaplan-Meier method and compared using the log-rank test. Hazard ratios for DFS and OS were estimated using the Cox proportional hazards model with a 95% confidence interval (CI). Two-sided p-values are presented for all analyses with p < 0.05, considered to be statistically significant. R ver. 3.6.3 (R Foundation for Statistical Computing, Vienna, Austria) was used for all statistical analyses.

Results

1. Patient characteristics

During the 21-year follow-up, 248 male patients with breast cancer were enrolled in the study. Baseline patient characteristics are described in Table 1. The median age of the patients was 63 years (range, 25 to 102 years), which was older than that of the Korean FBC patients [23]. Approximately half of the total number of patients were diagnosed before 2010. The number of study registrants tended to increase every 5 years from 1995 to 2016. Most patients (184 patients, 74.2%) complained of a palpable breast mass in the first diagnosis, with a median symptoms’ duration of 6 months (range, 0.2 months to 8 years). Forty percent of patients were diagnosed with stage II breast cancer, while less than 10% were initially diagnosed with stage IV MBC. Ten percent of patients had a family history of cancer (S1 Table), but BRCA mutation status was not assessed in most of them (225 patients, 90.7%). Of the 23 patients analyzed for BRCA mutational status, eight patients were shown to be BRCA mutants.

2. Histopathology of MBC

The histopathology and intrinsic subtype of enrolled patients were analyzed (Fig. 1). Similar to FBC patients, the most common histology of all 248 patients was invasive ductal carcinoma (192 patients, 77.4%). Most patients were diagnosed with hormone receptor–positive MBC (175 patients, 70.6%), with dual expression of the ER and PR (157 patients, 63.3%). Approximately 10% of patients were diagnosed with HER2-positive MBC, and 5% of them were diagnosed with TNBC. Among the 148 patients that underwent subtype classification, most of them were luminal A (61 patients, 41.2%) followed by 44 patients with luminal B disease (29.7%). The incidence of HER2-positive subtype was approximately 20% (29 patients, 19.5%), and TNBC was the least expressed subtype (14 patients, 9.5%) (Table 2).

3. Treatment for early and locally advanced breast cancer

Upfront surgery was performed without neoadjuvant chemotherapy in the majority of patients. Most patients underwent modified radical mastectomy (MRM; 165 patients, 72.1%) as surgical treatment. Anthracycline and taxane-based regimen was administered for patients who received neoadjuvant chemotherapy. Adjuvant chemotherapy was delivered to approximately half of the total surgically resected patients, which is a lower rate than that of FBC patients. Anthracycline-based adjuvant chemotherapy was most commonly administered, and approximately one-third of patients received taxane during adjuvant treatment. Few patients received trastuzumab as adjuvant treatment (Table 3). Patients who received adjuvant chemotherapy tended to be younger (median age, 59.5 vs. 70 years; p < 0.001), with good performance status. Adjuvant chemotherapy was mostly administered to patients with a higher tumor stage, histologic tumor grade, and nodal involvement. The adjuvant chemotherapy group tended to receive MRM with axillary node dissection and received adjuvant radiation therapy compared with patients who did not receive adjuvant chemotherapy (S2 Table).

Adjuvant radiation therapy was administered to fewer patients (24% of the 218 operable patients). When analyzed according to the administration of adjuvant radiation therapy, patients with nodal involvement and with higher histologic tumor grade received adjuvant radiation, similar to the adjuvant chemotherapy group. More patients underwent axillary lymph node dissection and neoadjuvant or adjuvant chemotherapy compared with patients who did not receive adjuvant radiation therapy (S3 Table).

Adjuvant endocrine treatment was administered to 166 patients of 200 patients (83%), and approximately 90% of patients received tamoxifen as adjuvant endocrine treatment (S2 Table). Although most hormone receptor–positive MBC patients initiated adjuvant endocrine treatment, approximately 40% of them were able to complete 5 years of adjuvant endocrine treatment (S2 Table).

4. Survival outcomes

Median OS of the total number of treated patients was 60.7 months (range, 1.2 to 230.4 months) and 5-year OS rate was 95.2% (95% CI, 0.921 to 0.984) (Fig. 2A). Older age (> 65 years) (Fig. 2B) and higher stage (Fig. 2C) were significantly associated with inferior survival, with the latter being compared with stage I. Although there were no statistical survival differences according to intrinsic subtype classification based on the Ki-67 index in the analysis, trends for superior OS were observed in luminal subtype compared to non-luminal subtypes (Fig. 3A), and in luminal A subtype when compared to luminal B subtype (Fig. 3B). Among operable hormone receptor-positive MBC patients, completion of adjuvant endocrine treatment was associated with superior DFS and OS compared with patients with incomplete endocrine treatment (median DFS, 13.73 years vs. 76.73 months; p < 0.001 [Fig. 4A]; median OS, 15.98 years vs. 13.88 years; p=0.072 [Fig. 4B]). Contrary to expectations, patients who received adjuvant chemotherapy or radiation therapy showed trends for inferior DFS and OS compared to patients who did not receive adjuvant chemotherapy or radiotherapy (S4 Fig.).

Cox regression analysis was performed for an in-depth analysis of the relationship between clinicopathological variables and survival outcomes (DFS and OS). Completion of adjuvant endocrine treatment was associated with prolonged DFS and OS in patients with MBC (hazard ratio [HR], 0.15; 95% CI, 0.07 to 0.33; p < 0.001; OS: HR, 0.32; 95% CI, 0.09 to 1.11; p=0.073) (Table 4). Older age was also associated with inferior OS (HR, 2.42; 95% CI, 1.13 to 5.16; p=0.023). When adjusted for stage, adjuvant systemic chemotherapy, and radiotherapy, completion of adjuvant endocrine therapy was still associated with prolonged DFS (HR, 0.16; 95% CI, 0.05 to 0.54; p=0.003). Completion of adjuvant endocrine treatment (HR, 0.16; 95% CI, 0.04 to 0.69; p=0.015) and older age (HR, 5.03; 95% CI, 1.13 to 22.4; p=0.034) were associated with OS when adjusted for administration of adjuvant systemic chemotherapy or radiation therapy (Table 4).

In 148 patients who were evaluable for intrinsic subtype classification, 5 years of adjuvant endocrine treatment was still associated with superior DFS (HR, 0.22; 95% CI, 0.07 to 0.63; p=0.004). When adjusted for stage, subtype, adjuvant chemotherapy, and radiotherapy, completion of adjuvant endocrine treatment remained to be associated with prolonged DFS in the group of patients that were classified according to the intrinsic subtype (HR, 0.15; 95% CI, 0.04 to 0.49; p=0.002) (Table 5).

5. Palliative treatment for recurrent, metastatic MBC

During a median follow-up of 59.6 months, 51 patients (22.2%) experienced disease recurrence. Nineteen patients (7.7%) were diagnosed with de novo stage IV MBC, and four patients (1.6%) were diagnosed with locally advanced disease at initial presentation. Among the 60 patients who were treated for recurrent or metastatic MBC, 43 (71.7%) received palliative treatment. The treatment patterns were analyzed based on the decade period. Although there were a small number of recurrent, metastatic HER2-positive patients (7 patients) in our study, anti-HER2 treatment, such as trastuzumab, pertuzumab, lapatinib, and trastuzumab emtansine were underutilized, and none of the patients received trastuzumab before 2010. During that period, patients received a combination of chemotherapy with taxane and anthracycline. After 2010, capecitabine was more frequently used in earlier settings, while monotherapy was utilized more often (S5 Table).

Among the 56 patients who were hormone receptor-positive, 35 (62.5%) received palliative endocrine treatment. Tamoxifen was the most frequently used endocrine treatment in MBC patients as a first-line treatment. Aromatase inhibitors were administered as first-line or above in patients, but few patients received concurrent gonadotropin-releasing hormone (GnRH) agonists during treatment. Although BOLERO-2 [24] enrolled postmenopausal women, three hormone receptor-positive MBC patients in our analysis used exemestane with everolimus for their treatment. However, GnRH agonists were not administered concurrently during treatment. None of the patients were treated with fulvestrant (S6 Table).

Discussion

In this study, we intensively reviewed the medical records of each enrolled patient from multiple tertiary medical centers who were qualified for breast cancer treatment. Based on the data collection over more than 20 years, we analyzed the clinicopathological characteristics, including intrinsic subtype, pattern of treatment during adjuvant and palliative setting, and survival outcome.

The median age of the total patient population was 63 years, similar to previous Korean Central Cancer Registry data and the Western registry data [3,25,26]. The median age of the enrolled patients was 10 years older than that of the FBC patients in Korea [23], suggesting possible characteristics of aging-associated disease of MBC compared with FBC [6]. Previous reports have proposed that the late onset of MBC may be due to delayed recognition and evaluation of symptoms and signs of breast cancer [27]. However, recent studies based on genomic profiling have suggested that the biological characteristics of MBC may differ from those of FBC [12,28]. Differences in genomic profiles may have affected the distinct clinicopathological characteristics between MBC and FBC. In our analysis, the proportion of hormone receptor–positive patients is higher and the incidence of TNBC is lower than that of FBC as previously reported [11]. Among intrinsic subtype classified patients, HER2-positive patients were higher than previously reported literature [11]. This discrepancy may be due to selection bias, considering that a certain portion of old archival tissue was not tested for HER2 and the Ki-67 index was not fully analyzed in all patients.

Considering that most patients with early-stage MBC are diagnosed as hormone receptor–positive, adjuvant endocrine treatment may have an important role in extending survival. In our study more than 80% of hormone receptor positive patients started adjuvant endocrine treatment but less than half of patients have completed 5 years of treatment. Considering the side effects of adjuvant endocrine treatment, long-term compliance has always been an issue in the treatment of MBC [29]. Previous studies have demonstrated that the use of adjuvant endocrine treatment is associated with improved survival [25], but treatment compliance has not been analyzed due to the limited assessment of medical records of each patient [26]. Completion of adjuvant endocrine treatment was significantly associated with prolonged DFS and OS, and still showed survival benefit when adjusted for other clinicopathological factors, such as tumor stage, history of adjuvant chemotherapy, or radiotherapy. Completion of adjuvant endocrine treatment was also associated with superior DFS in intrinsic subtype classified patients. Our analysis suggests that adherence to adjuvant endocrine treatment is the most important factor for prolonged survival in early-stage MBC, and adequate supportive care is also warranted to improve compliance with adjuvant endocrine treatment.

In MBC patients, neoadjuvant chemotherapy, adjuvant chemotherapy and adjuvant radiation treatment were not performed as often as in FBC. This result is in agreement with the Korea Central Cancer Registry data [3]. Compared with US data on MBC, a similar proportion of patients was treated with adjuvant chemotherapy, but fewer patients received adjuvant radiation therapy in our analysis [25,26]. No prospective randomized trials have evaluated the role of adjuvant chemotherapy or radiotherapy in MBC. Based on observational studies, adjuvant treatment is recommended, especially for node-positive disease [6]. However, MBC has been neglected and underestimated due to its rarity and this has influenced relative undertreatment in patient population. In our analysis, relatively young patients with good performance status diagnosed with more advanced stage received adjuvant chemotherapy or radiotherapy (S2 and S3 Tables). This limited assessment to adjuvant treatment might have influenced unexpected trends for inferior DFS or OS in patients who received adjuvant treatment.

Excluding MBC patients in various pivotal phase 3 trials has resulted in a relative lack of evidence when establishing treatment guidelines in various countries [6,26]. Therefore, the application of the latest treatment for MBC is frequently delayed due to regulatory issues in various countries. We showed that anti-HER2 agents were underutilized in HER2-positive MBC patients, and hormone receptor–positive patients had also limited assessment for fulvestrant and everolimus. Older drugs such as tamoxifen, taxane, anthracycline, and 5-fluorouracil were preferentially administered to patients in this study, while relatively few patients had the chance to receive novel anti-HER2 agents, such as trastuzumab, lapatinib, and trastuzumab emtansine. Considering most MBC patients were diagnosed as hormone receptor positive, treatment pattern in palliative endocrine regimen is quite important. Hormone positive MBC patients who were treated with aromatase inhibitor, exemestane with everolimus did not receive GnRH agonist, which might have reduced the treatment efficacy.

In our analysis, the 5-year OS was estimated to be over 90%, which is superior to previously published literature ranging from 77% to 87% [3,17,25,26]. The survival rate of MBC patients was comparable with that of patients with FBC [23]. There are conflicting reports about the survival of MBC compared with FBC [30,31]. Former literature has reported inferior OS of MBC may be due to the initial advanced stage, underlying comorbidity, and older age at diagnosis when compared with women [6]. However, there are incompatible report that MBC showed a superior survival rate compared with those with FBC when adjusted for stage, treatment, and demographic features [27]. Compared to other studies, higher proportion of adjuvant endocrine treated patient population might have influenced the better survival outcome in our study [25,26]. Considering completion of adjuvant endocrine treatment is also important in extending survival, this treatment pattern might have also influenced survival outcomes comparable with those of FBC.

The strength of this study is the long-term follow-up data that were collected in multiple institutions, spanning more than 20 years with detailed medical records of enrolled patients, although it was based on retrospective analysis. To the best of our knowledge, this is the first report analyzing the intrinsic subtype based on IHC for the Asian patients with MBC. Intrinsic subtype is originally defined after gene expression profiling, but the classification of intrinsic subtype was based only on IHC performed at each institution without central review. Gene expression profiling was not conducted due to lack of archival tumor tissues and poor quality of long-term stored formalin fixed paraffin embedded tissues. Although investigators have reviewed the medical records of each enrolled patient, pathological characteristics, such as Ki-67 index, were omitted or not analyzed in some patients that were diagnosed in the nineties or the early 2000s. Therefore, approximately half of the patients could not be classified for subtype analysis. Additionally, most patients did not undergo a germline BRCA1/BRCA2 mutation analysis, and their family cancer history or presence of secondary malignancies were omitted. Although BRCA mutation is a well-known contributing factor for the development of MBC, low recognition of clinicopathological characteristics of MBC and absence of national insurance coverage for laboratory analysis have influenced the lower detection rate of BRCA mutations in clinical settings. Nowadays, as there is a better understanding of the clinicopathological features of MBC, there is a growing rate of analysis of BRCA status and other genomic tests, such as Oncotype Dx and MammaPrint [32,33]. Analysis of the relationship between molecular profiles and germline mutations, such as BRCA mutations, with clinical characteristics and prognosis of MBC patients, may be warranted for future in-depth study.

To conclude, this was the first study analyzing subtypes of Korean MBC patients based on a multicenter study. The luminal A subtype was the most common, and completion of adjuvant endocrine treatment in patients that were classified based on the subtype was associated with prolonged DFS. Completion of adjuvant endocrine treatment was also the most important factor for prolonged DFS and OS in hormone receptor-positive MBC. Known prognostic factors were adjusted during analysis of relationship between prognostic factors and DFS or OS. Although statistically non-significant due to small number of patients, intrinsic subtype showed trend with improved survival for luminal A subtype. The incidence of MBC patients has increased recently, and appropriate treatment is this patient group is warranted. To improve survival of MBC patients, they should receive standard treatment according to guidelines as FBC patients.

Electronic Supplementary Material

Supplementary materials are available at Cancer Research and Treatment website (https://www.e-crt.org).

NOTES

Ethical Statement

This study was approved by the institutional review board of each participating institution. The requirement for informed consent was waived because of the retrospective nature of this study.

Author Contributions

Conceived and designed the analysis: Woo IS.

Collected the data: Lee J, Lee KS, Sim SH, Chae H, Sohn J, Kim GM, Lee KH, Kang SH, Jung KH, Jeong JH, Byun JH, Koh SJ, Lee KE, Lim S, Kim HJ, Park HS, Lee GJ, Hong S, Baek SK, Lee SI, Choi MY, Woo IS.

Contributed data or analysis tools: Lee J, Lee KS, Sim SH, Chae H, Sohn J, Kim GM, Lee KH, Kang SH, Jung KH, Jeong JH, Byun JH, Koh SJ, Lee KE, Lim S, Kim HJ, Won HS, Park HS, Lee GJ, Hong S, Baek SK, Lee SI, Choi MY, Woo IS.

Performed the analysis: Lee J.

Wrote the paper: Lee J, Woo IS.

Conflicts of Interest

Conflict of interest relevant to this article was not reported.

Fig. 1

Flow diagram of enrolled patients. HER2, human epidermal growth factor receptor 2.

Fig. 2

Survival outcomes in treated patients: (A) in all treated patients, (B) overall survival according to age, and (C) overall survival according to stage. CI, confidence interval; HR, hazard ratio; mOS, median overall survival; NA, not available; OS, overall survival.

Fig. 3

Survival outcomes according to subtypes. (A) Comparison of OS between luminal and non-luminal subtypes. (B) Comparison of OS between luminal A and other subtypes (n=148). CI, confidence interval; HR, hazard ratio; OS, overall survival.

Fig. 4

Survival outcomes according to completion of adjuvant endocrine treatment in hormone receptor–positive subgroup. (A) DFS according to completion of adjuvant endocrine treatment. (B) OS according to completion of adjuvant endocrine treatment. CI, confidence interval; DFS, disease-free survival; HR, hazard ratio; NA, not available; OS, overall survival.

Table 1

Baseline patient characteristics

| | No. (%) | | | ----------------------------------------------- | ------------- | | No. of patients | 248 | | Age (yr) | | | Median (range) | 63.0 (25–102) | | ≤ 65 | 134 (54.0) | | > 65 | 112 (45.2) | | Not assessed | 2 (0.8) | | Diagnosis period | | | 1995–1999 | 17 (6.9) | | 2000–2004 | 44 (17.7) | | 2005–2009 | 62 (25) | | 2010–2014 | 79 (31.9) | | 2015–2016 | 46 (18.5) | | Chief complaint | | | Palpable breast mass | 184 (74.2) | | Nipple discharge | 10 (4.0) | | Nipple retraction | 1 (0.4) | | Breast pain | 7 (2.8) | | Gynecomastia | 3 (1.2) | | Axillary mass | 6 (2.4) | | Chest wall mass | 1 (0.4) | | Bleeding | 3 (1.2) | | Skin ulceration | 3 (1.2) | | Back pain | 3 (1.2) | | Abnormal physical examination | 3 (1.2) | | Not assessed | 24 (9.7) | | Duration of symptom (mo) | | | Median (range) | 6.0 (0.2–96) | | Laterality | | | Unilateral, right | 113 (45.6) | | Unilateral, left | 115 (46.4) | | Bilateral | 1 (0.4) | | Not assessed | 19 (7.7) | | Multiplicity | | | No | 203 (81.9) | | Yes | 12 (4.8) | | Not assessed | 33 (13.3) | | ECOG PS | | | 0 | 81 (32.7) | | 1 | 115 (46.4) | | 2 | 5 (2.0) | | 3 | 2 (0.8) | | Not assessed | 45 (18.1) | | Overall TNM stage a) | | | I | 70 (28.2) | | II | 101 (40.7) | | III | 41 (16.5) | | IV | 19 (7.7) | | Not assessed | 17 (6.9) |

Table 2

Histopathologic characteristics of patient population

| | No. (%) (n=248) | | | -------------------------------------------- | ----------- | | Histology | | | Invasive ductal carcinoma | 192 (77.4) | | Invasive lobular carcinoma | 1 (0.4) | | Mucinous carcinoma | 9 (3.6) | | Papillary carcinoma | 13 (5.2) | | Cribriform carcinoma | 4 (1.6) | | Sarcoma | 4 (1.6) | | Carcinoma | 6 (2.4) | | Other | 5 (2.0) | | Not assessed | 14 (5.6) | | Histologic grade | | | Grade 1 | 36 (14.5) | | Grade 2 | 102 (41.1) | | Grade 3 | 39 (15.7) | | Not assessed | 71 (28.6) | | Lymphatic | | | No | 99 (39.9) | | Yes | 72 (29.0) | | Not assessed | 77 (31.0) | | Vascular | | | No | 125 (50.4) | | Yes | 44 (17.7) | | Not assessed | 79 (31.9) | | Perineural | | | No | 119 (48.0) | | Yes | 14 (5.6) | | Not assessed | 115 (46.4) | | Estrogen receptor | | | Negative | 18 (7.3) | | Positive | 200 (80.6) | | Not assessed | 30 (12.1) | | Progesterone receptor | | | Negative | 40 (16.1) | | Positive | 176 (71.0) | | Not assessed | 32 (12.9) | | HER2 receptor status | | | Negative | 184 (74.2) | | Positive | 29 (11.7) | | Not assessed | 35 (14.1) | | Subtype among evaluable patients (n=148) | | | Luminal A | 61 (41.2) | | Luminal B | 44 (29.7) | | HER2 enriched | 29 (19.6) | | TNBC | 14 (9.5) | | Ki-67, median (range) | 18.5 (2–80) |

Table 3

Treatment patterns in operable patients

| | No. (%) | | | ----------------------------------------------- | ------------- | | Operation (breast) | | | Modified radical mastectomy | 165 (72.1) | | Total mastectomy | 43 (18.9) | | Breast conserving surgery | 11 (4.8) | | Node excision | 2 (0.9) | | Not done | 6 (2.6) | | Not assessed | 1 (0.4) | | Operation (axilla) | | | ALND | 135 (61.1) | | SLNB | 53 (24.0) | | Not done | 16 (7.2) | | Not assessed | 17 (7.7) | | Neoadjuvant chemotherapy | | | No | 212 (95.9) | | Yes | 9 (4.1) | | AC followed by taxane | 5 (2.3) | | DA | 2 (0.9) | | Others | 2 (0.9) | | Adjuvant chemotherapy | | | Yes | 108 (48.6) | | AC followed by taxane | 32 (14.5) | | AC or EC | 30 (13.6) | | CMF | 14 (6.3) | | FAC or FEC | 13 (5.9) | | TAC | 4 (1.8) | | AC followed by taxane with trastuzumab | 3 (1.4) | | TC | 2 (0.9) | | AC followed by trastuzumab | 1 (0.5) | | Others | 7 (3.2) | | Not assessed | 2 (0.9) | | Completion of chemotherapy | | | Yes | 86 (38.9) | | No | 15 (6.8) | | Not assessed | 6 (2.7) | | No | 107 (48.2) | | Not assessed | 6 (3.2) | | Adjuvant endocrine treatment | | | Yes | 166 (83.0) | | Tamoxifen | 150 (75.0) | | Toremifen | 9 (4.5) | | Aromatase inhibitor | 2 (1.0) | | Others | 5 (2.5) | | Total duration of treatment, median (range, mo) | 48.5 (1.0–87) | | Completion of treatment | | | Yes | 68 (34.0) | | No | 63 (31.5) | | Ongoing | 23 (11.5) | | Not assessed | 12 (6.0) | | No | 25 (12.5) | | Not assessed | 9 (4.5) | | Adjuvant radiation treatment | | | No | 157 (71.9) | | Yes | 52 (24.0) | | Not assessed | 9 (4.1) |

Table 4

Univariate and multivariate Cox regression analysis for DFS and OS in total patient population

Table 5

Univariate and multivariate Cox regression analysis for DFS and OS in intrinsic subtype classified patients

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Figure & Data

REFERENCES

Citations

Citations to this article as recorded by

• Clinicopathologic Features and Prognoses of Male Patients With Breast Cancer
  Meiling Huang, Jingjing Xiao, Changjiao Yan, Rui Ling, Ting Wang
  American Journal of Men's Health.2024;[Epub] CrossRef

Impacts of Subtype on Clinical Feature and Outcome of Male Breast Cancer: Multicenter Study in Korea (KCSG BR16-09)

Fig. 1Flow diagram of enrolled patients. HER2, human epidermal growth factor receptor 2.

Fig. 2Survival outcomes in treated patients: (A) in all treated patients, (B) overall survival according to age, and (C) overall survival according to stage. CI, confidence interval; HR, hazard ratio; mOS, median overall survival; NA, not available; OS, overall survival.

Fig. 3Survival outcomes according to subtypes. (A) Comparison of OS between luminal and non-luminal subtypes. (B) Comparison of OS between luminal A and other subtypes (n=148). CI, confidence interval; HR, hazard ratio; OS, overall survival.

Fig. 4Survival outcomes according to completion of adjuvant endocrine treatment in hormone receptor–positive subgroup. (A) DFS according to completion of adjuvant endocrine treatment. (B) OS according to completion of adjuvant endocrine treatment. CI, confidence interval; DFS, disease-free survival; HR, hazard ratio; NA, not available; OS, overall survival.

Fig. 1

Fig. 2

Fig. 3

Fig. 4

Impacts of Subtype on Clinical Feature and Outcome of Male Breast Cancer: Multicenter Study in Korea (KCSG BR16-09)

Table 1

Baseline patient characteristics

| | No. (%) | | | ----------------------------- | ------------- | | No. of patients | 248 | | Age (yr) | | | Median (range) | 63.0 (25–102) | | ≤ 65 | 134 (54.0) | | > 65 | 112 (45.2) | | Not assessed | 2 (0.8) | | Diagnosis period | | | 1995–1999 | 17 (6.9) | | 2000–2004 | 44 (17.7) | | 2005–2009 | 62 (25) | | 2010–2014 | 79 (31.9) | | 2015–2016 | 46 (18.5) | | Chief complaint | | | Palpable breast mass | 184 (74.2) | | Nipple discharge | 10 (4.0) | | Nipple retraction | 1 (0.4) | | Breast pain | 7 (2.8) | | Gynecomastia | 3 (1.2) | | Axillary mass | 6 (2.4) | | Chest wall mass | 1 (0.4) | | Bleeding | 3 (1.2) | | Skin ulceration | 3 (1.2) | | Back pain | 3 (1.2) | | Abnormal physical examination | 3 (1.2) | | Not assessed | 24 (9.7) | | Duration of symptom (mo) | | | Median (range) | 6.0 (0.2–96) | | Laterality | | | Unilateral, right | 113 (45.6) | | Unilateral, left | 115 (46.4) | | Bilateral | 1 (0.4) | | Not assessed | 19 (7.7) | | Multiplicity | | | No | 203 (81.9) | | Yes | 12 (4.8) | | Not assessed | 33 (13.3) | | ECOG PS | | | 0 | 81 (32.7) | | 1 | 115 (46.4) | | 2 | 5 (2.0) | | 3 | 2 (0.8) | | Not assessed | 45 (18.1) | | Overall TNM stage a) | | | I | 70 (28.2) | | II | 101 (40.7) | | III | 41 (16.5) | | IV | 19 (7.7) | | Not assessed | 17 (6.9) |

ECOG PS, Eastern Cooperative Oncology Group performance status.

a)Based on American Joint Committee on Cancer 7th guideline.

Table 2

Histopathologic characteristics of patient population

| | No. (%) (n=248) | | | -------------------------------------------- | ----------- | | Histology | | | Invasive ductal carcinoma | 192 (77.4) | | Invasive lobular carcinoma | 1 (0.4) | | Mucinous carcinoma | 9 (3.6) | | Papillary carcinoma | 13 (5.2) | | Cribriform carcinoma | 4 (1.6) | | Sarcoma | 4 (1.6) | | Carcinoma | 6 (2.4) | | Other | 5 (2.0) | | Not assessed | 14 (5.6) | | Histologic grade | | | Grade 1 | 36 (14.5) | | Grade 2 | 102 (41.1) | | Grade 3 | 39 (15.7) | | Not assessed | 71 (28.6) | | Lymphatic | | | No | 99 (39.9) | | Yes | 72 (29.0) | | Not assessed | 77 (31.0) | | Vascular | | | No | 125 (50.4) | | Yes | 44 (17.7) | | Not assessed | 79 (31.9) | | Perineural | | | No | 119 (48.0) | | Yes | 14 (5.6) | | Not assessed | 115 (46.4) | | Estrogen receptor | | | Negative | 18 (7.3) | | Positive | 200 (80.6) | | Not assessed | 30 (12.1) | | Progesterone receptor | | | Negative | 40 (16.1) | | Positive | 176 (71.0) | | Not assessed | 32 (12.9) | | HER2 receptor status | | | Negative | 184 (74.2) | | Positive | 29 (11.7) | | Not assessed | 35 (14.1) | | Subtype among evaluable patients (n=148) | | | Luminal A | 61 (41.2) | | Luminal B | 44 (29.7) | | HER2 enriched | 29 (19.6) | | TNBC | 14 (9.5) | | Ki-67, median (range) | 18.5 (2–80) |

HER2, human epidermal growth factor receptor 2; TNBC, triple-negative breast cancer.

Table 3

Treatment patterns in operable patients

| | No. (%) | | | ----------------------------------------------- | ------------- | | Operation (breast) | | | Modified radical mastectomy | 165 (72.1) | | Total mastectomy | 43 (18.9) | | Breast conserving surgery | 11 (4.8) | | Node excision | 2 (0.9) | | Not done | 6 (2.6) | | Not assessed | 1 (0.4) | | Operation (axilla) | | | ALND | 135 (61.1) | | SLNB | 53 (24.0) | | Not done | 16 (7.2) | | Not assessed | 17 (7.7) | | Neoadjuvant chemotherapy | | | No | 212 (95.9) | | Yes | 9 (4.1) | | AC followed by taxane | 5 (2.3) | | DA | 2 (0.9) | | Others | 2 (0.9) | | Adjuvant chemotherapy | | | Yes | 108 (48.6) | | AC followed by taxane | 32 (14.5) | | AC or EC | 30 (13.6) | | CMF | 14 (6.3) | | FAC or FEC | 13 (5.9) | | TAC | 4 (1.8) | | AC followed by taxane with trastuzumab | 3 (1.4) | | TC | 2 (0.9) | | AC followed by trastuzumab | 1 (0.5) | | Others | 7 (3.2) | | Not assessed | 2 (0.9) | | Completion of chemotherapy | | | Yes | 86 (38.9) | | No | 15 (6.8) | | Not assessed | 6 (2.7) | | No | 107 (48.2) | | Not assessed | 6 (3.2) | | Adjuvant endocrine treatment | | | Yes | 166 (83.0) | | Tamoxifen | 150 (75.0) | | Toremifen | 9 (4.5) | | Aromatase inhibitor | 2 (1.0) | | Others | 5 (2.5) | | Total duration of treatment, median (range, mo) | 48.5 (1.0–87) | | Completion of treatment | | | Yes | 68 (34.0) | | No | 63 (31.5) | | Ongoing | 23 (11.5) | | Not assessed | 12 (6.0) | | No | 25 (12.5) | | Not assessed | 9 (4.5) | | Adjuvant radiation treatment | | | No | 157 (71.9) | | Yes | 52 (24.0) | | Not assessed | 9 (4.1) |

AC, adriamycin-cyclophosphamide; ALND, axillary lymph node dissection; CMF, cyclophosphamide-methotrexate-5-fluorouracil; DA, docetaxel-adriamycin; EC, epirubicin-cyclophosphamide; FAC, 5-fluorouracil-adriamycin-cyclophosphamide; FEC, 5-fluorouracil-epirubicin-cyclophosphamide; SLNB, sentinel lymph node biopsy; TAC, docetaxel-adriamycin-cyclophosphamide; TC, docetaxel-cyclophosphamide.

Table 4

Univariate and multivariate Cox regression analysis for DFS and OS in total patient population

CI, confidence interval; DFS, disease-free survival; HER2, human epidermal growth factor receptor 2; HR, hazard ratio; OS, overall survival; RT, radiation therapy; TNBC, triple-negative breast cancer.

Table 5

Univariate and multivariate Cox regression analysis for DFS and OS in intrinsic subtype classified patients

CI, confidence interval; DFS, disease-free survival; HER2, human epidermal growth factor receptor 2; HR, hazard ratio; LumA, luminal A; LumB, luminal B; OS, overall survival; RT, radiation therapy; TNBC, triple-negative breast cancer.

Table 1Baseline patient characteristics

ECOG PS, Eastern Cooperative Oncology Group performance status.

a)

Based on American Joint Committee on Cancer 7th guideline.

Table 2Histopathologic characteristics of patient population

HER2, human epidermal growth factor receptor 2; TNBC, triple-negative breast cancer.

Table 3Treatment patterns in operable patients

AC, adriamycin-cyclophosphamide; ALND, axillary lymph node dissection; CMF, cyclophosphamide-methotrexate-5-fluorouracil; DA, docetaxel-adriamycin; EC, epirubicin-cyclophosphamide; FAC, 5-fluorouracil-adriamycin-cyclophosphamide; FEC, 5-fluorouracil-epirubicin-cyclophosphamide; SLNB, sentinel lymph node biopsy; TAC, docetaxel-adriamycin-cyclophosphamide; TC, docetaxel-cyclophosphamide.

Table 4Univariate and multivariate Cox regression analysis for DFS and OS in total patient population

CI, confidence interval; DFS, disease-free survival; HER2, human epidermal growth factor receptor 2; HR, hazard ratio; OS, overall survival; RT, radiation therapy; TNBC, triple-negative breast cancer.

Table 5Univariate and multivariate Cox regression analysis for DFS and OS in intrinsic subtype classified patients

CI, confidence interval; DFS, disease-free survival; HER2, human epidermal growth factor receptor 2; HR, hazard ratio; LumA, luminal A; LumB, luminal B; OS, overall survival; RT, radiation therapy; TNBC, triple-negative breast cancer.

Table 1

Table 2

Table 3

Table 4

Table 5