1. Introduction
Long-term follow-up data from several randomized controlled trials undertaken to compare the efficacy of mastectomy with that of breast-conserving therapy (BCT) consisting of lumpectomy or quadrantectomy followed by postoperative radiotherapy showed no differences in terms of disease-free survival (DFS), distant-disease-free survival, and overall survival (OS) among the treatment groups [
1,
2,
3,
4,
5]. The trials, conducted in the 1970s and 1980s, paved the way for the increased utilization of BCT for patients with stage I-II breast cancer [
6]. Retrospective studies based on the analysis of large patient populations with early-stage breast cancer (EBC) treated in modern contexts indicate that BCT is at least comparable or even better in terms of breast-cancer-specific survival (BCSS) and OS compared to mastectomy without radiation therapy for early-stage breast cancer [
7,
8,
9,
10,
11,
12,
13]. Improved DFS and OS rates were recently confirmed in smaller cohort studies [
14,
15,
16,
17,
18,
19,
20] and were also observed in young women with EBC [
21,
22,
23]. Based on older research, local recurrence is considered to be more common after BCT than after mastectomy. However, over the last 20 years, local recurrence rates after BCT have decreased substantially and are now shown to be as low as after mastectomy, most likely due to better understanding of breast cancer heterogeneity and consequently tailored systemic and radiation treatments [
24,
25].
For patients with breast cancer who are potentially suitable for both local treatments, BCT is suggested as the evidence-based primary local treatment [
26]. Breast-conserving surgery is one of the major advances in the management of breast cancer. Nevertheless, breast-conserving surgery rates, as commonly reported, have reached a plateau in the last decade. In 2010–2011, breast-conserving surgery rates for the general population with unilateral EBC were 64.5–69% in the US [
27,
28,
29], 73.3% in Europe [
30], and 36.5–49.4% for patients younger than 50 years [
28,
31]. However, in some countries, the overall rate of breast-conserving surgery is lower than 50% [
32,
33].
The aim of BCT, as compared to mastectomy, is to achieve oncological safety with less extensive surgery, minimizing the psychosocial sequelae, and to obtain favorable cosmetic results with the use of oncoplastic techniques whenever possible. Most women feel negatively impacted by the scars resulting from breast cancer surgery, a consequence that particularly affects patients undergoing mastectomy [
34]. When comparing long-term quality of life amongst patients treated with BCT or mastectomy, significantly lower scores for body image, role, and physical and sexual functioning, and more lifestyle disruptions were found for those treated with mastectomy. Conversely, psychosocial functioning slowly increased over time for women who underwent BCT, regardless of their age [
35,
36]. For patients undergoing mastectomy, access to breast reconstruction procedures is essential to increase positive body image and overall satisfaction and to maintain health-related quality of life [
26,
37]. However, barriers to immediate or delayed breast reconstruction exist on many levels, depending on the type of hospital (teaching vs. private), geographic location, reimbursement by insurance companies, lack of patient awareness, and the acceptability of the procedures by both physicians and patients [
38]. In the past decade, the use of breast reconstruction has increased globally together with the indications for the use of postmastectomy irradiation for EBC [
39,
40]. It has been documented that the use of postmastectomy radiation therapy may be a negative outcome predictor for breast reconstruction [
39]. On the other hand, opting for breast reconstruction may also influence clinical decision making in recommending postoperative radiation therapy due to the impact of radiation on long-term cosmetic results [
39,
41].
In the current study, we aimed to compare the outcomes of BCT and mastectomy-only treatment performed in the modern era in patients with stage I-IIA breast cancer, whose tumors are typically suitable for either BCT or mastectomy. The primary outcomes were DFS and OS, and secondary outcomes included any breast cancer recurrence (local, regional, and/or distant).
3. Results
In total, 1360 patients with stage I-IIA breast cancer treated with either BCT (
n = 1021, 75.1%) or mastectomy only (
n = 339, 24.9%) were included in the study. The median age at breast cancer diagnosis was 61 years in both groups (BCT range 23–87 and mastectomy range 27–91). The majority of breast tumors were sized ≤2 cm (
n = 1100, 81.5%) and had positive estrogen or progesterone receptors (
n = 1241, 92.3%). More than half of the patients had left-sided breast cancer (
n = 729; 54.2%). Compared with patients receiving mastectomy only as local therapy, patients undergoing BCT were less likely to be younger than 50 or older than 70 years, less likely to have had more extensive axillary surgery, and more likely to have stage I breast cancer. We observed no differences in the two groups with respect to tumor grade, intrinsic subtype, and administration of endocrine or targeted therapy. However, more patients in the mastectomy group received adjuvant chemotherapy (
Table 1).
3.1. Surgery
Most patients received a limited axillary surgery (n = 1360, 81.3%). Data regarding breast reconstruction were known for 557 (41.0%) patients. Among the 62 patients receiving breast reconstruction, 4 had stage IA, 31 had stage IB, and 27 had stage IIA breast cancer.
3.2. Radiation Therapy
Out of the 1021 patients receiving radiotherapy, all following breast-conserving surgery, 495 (48.5%) were treated with conventional fractionation (median dose 50 Gy; range 28–50.4 Gy), 489 (47.9%) with moderate hypofractionated schedules (median dose 45 Gy; range 34.5–47.5), and 37 (3.6%) received one of the ultra-hypofractionated schedules (median dose 31.5 Gy; range 20–50 Gy). Additional dose to the tumor bed was received by 661 (64.7%) patients. Almost all patients received whole-breast radiotherapy only, excluding axillary or supraclavicular nodal volumes (n = 1014; 99.3%).
3.3. Systemic Treatment
Timing (preoperative versus postoperative) and type of systemic treatment are presented separately for both groups in
Table 2. The receipt of taxane-based chemotherapy was more frequently observed in the mastectomy group, as compared to the BCT group (32.8% versus 24.7%;
p < 0.0005).
In total, 578 (45.1%) evaluated patients received endocrine therapy with aromatase inhibitors, 539 (42.0%) with tamoxifen, and 122 (12.9%) with treatment combinations (i.e., tamoxifen and aromatase inhibitors). Compared with patients treated with mastectomy only, patients undergoing BCT more often received adjuvant endocrine therapy with aromatase inhibitors (n = 141; 40.3% versus n = 437; 46.9%) and were less likely to receive adjuvant therapy with tamoxifen (152; 43.4% versus 387; 41.5%). The observed differences were statistically significant (p < 0.0005).
3.4. Outcome
Median follow-up for DFS and OS was 6.9 years (range: 0.3–15.9) and 7.5 years (range: 0.2–25.9), respectively. Overall, 86 (6.3%) patients experienced local (LR), regional (RR), or distant recurrence. We observed statistically meaningful differences across all recurrence types (
Table 3). The cumulative incidences of 5-year LR and 10-year LR were 2.0% and 3.0% for the whole group, respectively. For the BCT group, the cumulative incidences of 5-year and 10-year LR were 1.0% and 3.0%; the corresponding cumulative incidences for the mastectomy group were 4% for both observed intervals. Observed absolute differences in cumulative incidence of recurrences between BCT and mastectomy groups were small, although statistically significant.
For the whole cohort, the estimated 5-year and 10-year DFS were 96% and 95%, respectively. After stratification according to the type of local treatment, the estimated 5-year and 10-year DFS for the BCT group were 97% and 96%, and the estimated 5-year and 10-year DFS for the mastectomy-only group were 91% and 90% (log-rank;
p < 0.001). In a univariate analysis, the following factors were associated with a decreased DFS: not receiving BCT, age > 70 years, tumor size ≥ 2 cm, stage IIA, tumor grade ≥ 2, and omission of endocrine adjuvant therapy. Upon multivariate Cox analysis, type of local treatment and tumor grade maintained statistical significance (
Table 4).
The estimated 5-year and 10-year OS, calculated for the whole cohort, were 97% and 92%, respectively. Among patients treated with BCT, 5-year and 10-year OS estimates were 97% and 93%, and for those treated with mastectomy-only, 95% and 89%, respectively (log-rank;
p = 0.045). Univariate and multivariate analyses were performed to analyze factors associated with worse survival outcomes. The use of mastectomy as the only local treatment was found to be correlated with worse OS in univariate analysis, but this finding was not confirmed in the multivariate Cox regression analysis (
Table 5).
High tumor grade and the omission of systemic chemotherapy were the only two factors associated with poorer OS. The type of local treatment was not associated with improved OS using multivariable Cox regression. Kaplan–Meier survival curves for all included patients representing DFS and OS with respect to breast cancer stage group are presented in
Figure 1.
After IPTW matching based on confounding variables (age at diagnosis, pathological tumor and nodal stage, overall breast cancer stage group, tumor grade, type of axillary surgery, and the receipt of chemotherapy or endocrine therapy), and after excluding study subjects with extreme weights, 1343 patients were available for the analysis. Mastectomy was associated with worse DFS (HR 2.839, 95% CI 1.760–4.579, p < 0.0001). This finding was not confirmed for OS (HR 1.455, 95% CI 0.844–2.511, p = 0.177).
4. Discussion
In our patient cohort treated in the contemporary era, we evaluated the therapeutic outcomes in patients with stage I-IIA breast cancer treated with either conservative surgery combined with postoperative radiation therapy or with mastectomy alone. We demonstrated an outcome improvement associated with BCT in terms of both 5-year DFS and 5-year OS, with absolute differences of 6% and 2%, respectively. The observed differences were also consistent at 10 years. However, using multivariable Cox regression and after IPTW matching, the only outcome that was found to be significantly impacted by the type of local treatment (BCT compared to mastectomy) was DFS.
In our study, we observed very low LR, RR, and distant metastasis rates within the whole cohort. The cumulative in-breast/chest-wall failure rates at 10 years after treatment were 3.0% for the BCT group and 4.0% for the mastectomy group. Compared to historical series, reporting approximately 5–10% in-breast failures after 10 years from treatment, our results compare favorably [
46,
47]. This finding is in agreement with the reports of other studies, which are all convincing and uniformly show DFS and/or OS benefits for BCT compared to mastectomy in patients with stage I-II breast cancer (
Table 6). Equivalent or improved outcomes with BCT as compared with mastectomy in terms of locoregional control, BCSS, DFS, or OS have been reported regardless of age [
14,
15], intrinsic breast cancer subtype [
48,
49,
50,
51], pathological tumor stage [
11,
14,
15,
51], overall breast cancer stage [
52], and grade [
51]. Recently, a Swedish cohort study using prospectively collected data of women with stage T1-2 N0-2 breast cancer confirmed better survival with BCT vs. mastectomy (irrespective of radiation therapy) even when taking into account comorbidity and socioeconomic status in both node-negative and node-positive disease, pointing out that offering more extensive surgery to patients who are suitable for either breast-conserving surgery or mastectomy is not saving lives [
51].
Improved survival rates in patients with breast cancer over the past couple of decades are largely attributable to the use of breast cancer screening and better imaging, predictive biomarkers, and better understanding of breast cancer heterogeneity. New advances in the field of systemic treatments, including molecularly targeted therapies, endocrine therapy, taxane-based chemotherapy, and bisphosphonates have all effectively contributed to reduce the risk of distant and local breast cancer recurrence. Consequently, breast cancer mortality rates have declined in recent decades even in patients with a low risk of recurrence at baseline [
53]. However, the contributions of a particular type of local treatment and new developments related to both surgical techniques and modern radiation therapy are frequently overlooked [
54]. It is well known that prevention of locoregional recurrence reduces the risk of breast-cancer-specific death and is related to improvements in OS [
55,
56]. Many possible reasons for the better outcomes observed for patients with breast cancer undergoing lumpectomy combined with postoperative radiotherapy compared with mastectomy have been already elucidated [
46,
54,
57,
58]. Surgery does provide superior local control within resected tissue; however, with tangential radiotherapy techniques, the treated volume is larger (as compared to simple mastectomy) and typically includes unoperated breast tissue in its entirety, part of the muscle, regional lymphatics, draining lymphatics towards the axillary region, subcutaneous lymphatic plexus, and skin [
46]. Incidental irradiation may potentially sterilize microscopic disease outside the breast tissue as it covers approximately 85% of axillary level I lymph nodes if the patient is treated in a supine position [
59]. At the same time, radiotherapy techniques have improved in the past years, with three-dimensional treatment planning and heart-sparing techniques, including deep-inspiration breath-hold, prone-positioning, and partial breast irradiation substantially decreasing the dose to the heart and subsequently reducing mortality rate from the cardiac events [
60].
The possibility of an anticancer immune response that can be elicited by radiotherapy outside of the radiation field, targeting micro- or macro-metastases, is also one of the postulated mechanisms of action. Abscopal effects have been demonstrated not only at higher doses per fraction but also at the lower dose per fraction (2.0–2.5 Gy) typically used in breast cancer postoperative radiotherapy [
61]. Moreover, it is well known that postoperative radiotherapy not only reduces local recurrence, but also diminishes the risk of any recurrence type, including distant relapse, which could be explained by mechanisms such as the abscopal effect [
62].
Omitting postoperative radiation therapy after mastectomy in patients undergoing breast reconstruction or in those with N1 disease may be a partial culprit of higher disease recurrence in these patients. In our study, 17.6% of patients had pathological N1 disease and the percentage of patients with pathological N1 disease did not differ between the groups. None of the patients with pathological N1 disease in the mastectomy group received postoperative radiation therapy. In a study by Sun et al., the authors analyzed the treatment outcomes of 4262 patients with clinical stage T1-2N1M0 breast cancer, and 832 (21.6%) of them received mastectomy and postoperative radiation therapy. In multivariate and propensity-score matching analyses, radiation therapy, but not type of surgical treatment, appeared to be an independent prognostic factor for improved OS, DFS, and loco-regional recurrence [
19]. Although results from the meta-analysis of individual patient data clearly demonstrated a benefit in reducing both recurrence and breast cancer mortality in women with one to three positive lymph nodes, postmastectomy radiotherapy is less often routinely recommended than radiotherapy following breast-conserving surgery in patients with pathological N1 disease [
46,
62]. Patients who require post-mastectomy radiation therapy following immediate breast reconstruction are exposed to a detectably higher risk of post-reconstruction complications, including infection, implant removal, and capsular contracture in patients receiving implant-based reconstruction, and fat necrosis in those receiving autologous-tissue-based reconstruction [
63]. Factors influencing the final cosmetic outcome and patients’ preferences may all affect the final decision to undergo postoperative chest-wall radiation therapy.
Despite the many benefits observed with BCT, the rates of unilateral or bilateral mastectomies for patients with unilateral breast cancer, who are candidates for BCT, are on the rise [
29,
64]. Perceived risks such as a fear of developing a second breast cancer, a historical belief that mastectomy is a safer option, possible avoidance of long-term breast cancer surveillance imaging, and the inconvenience of daily radiotherapy treatments may all have contributed to increasing mastectomy rates, which is of concern [
53,
65,
66,
67]. Nevertheless, it is important to note that different mastectomy and reconstruction techniques may lead to various amounts of remaining breast glandular tissue, potentially increasing the risk of breast cancer residual disease or recurrence [
68].
As pointed out by Dodwell et al., women with screen-detected breast cancer are more likely to undergo BCT and mammographic screening confers a survival advantage compared to symptomatic presentation [
69]. In our study, in which two-thirds of patients were aged between 50 and 70 years (
n = 880, 64.7%) and a similar proportion had stage I disease (
n = 891, 65.5%), individual data regarding screening status were missing.
The strengths of our study include a large patient cohort and thorough analysis with adjustments for confounding factors. Nevertheless, we acknowledge the limitations of our study and the difficulties in bias elimination in observational research. Our results may have been influenced by the retrospective nature of the study, as the quality of our data depend on reliable data collection. Additionally, follow-up was short and some of the data were not available at the time of the analysis. In our study, the impact of specific patient and tumor characteristics (e.g., age, tumor grade or size, lymph node status, and the receipt of endocrine therapy and systemic therapy) were adjusted with the use of a rigorous approach to reduce the effects of confounding in the estimation of the type of local treatment effect. However, we acknowledge the limitations of the propensity score analysis and IPTW-matching method, especially that there was no adjustment for the impact of all baseline characteristics [
45]. In addition, a comparison of the results of patients with stage I-IIA EBC and treated with mastectomy followed by postoperative radiation therapy would certainly add value to our research.