Discussion
In this study, we evaluated the clinical characteristics and histopathological features of giant breast sarcoma and malignant phyllodes tumor (GBPS) in one institution. To our knowledge, GBPS are rare entities and impair the quality of life seriously. There are only no more than 20 cases reports of giant breast sarcoma or malignant phyllodes tumors in the PubMed when sorting with ‘giant breast tumor’, ‘giant breast sarcoma’ and ‘giant phyllodes tumor’. There is limited information available on the diagnosis, prognosis, and treatment of GBPS because of rarity with only 1% of all cancers [
5]. Our cohort from a real-world study proved a mastectomy is meaningful, but the LR rate is still as high as 30%. The 5-year DFS and OS in our study is relatively 60% and 90% by Kaplan–Meier method. It is meaningful to explore the proper treatment and risk factors of GBPS.
The incidence of GBPS in women without metastases was found to be around 0.07% (4/6000) in this investigation. Previous study reported that duration for the GBPS to grow ranges from 2 to 10 months, with an average of 4.75 months, partially with pain and bleeding [
21]. To obtain a wide and clear margin, total mastectomy has traditionally been considered the gold standard surgical therapy for breast sarcoma, especially for tumors larger than 10 cm. In our cohort all the GBPS undergone mastectomy instead of operation with wide margins, that is significantly different with BPS(
p < 0.05). Of note, 50% of the participants had enlarged lymph nodes at the time of preoperative examination, no lymphatic metastases were found in the final pathology report. Even though the management of the axilla is still unclear, some subtypes of sarcoma are suspect of having the capacity to disseminate lymphogenously [
75]. There are reports of lymphogenous spread in angiosarcoma, rhabdomyosarcoma, and epithelioid sarcoma
1. Many previous researches perform axillary lymph node biopsy or dissection for breast sarcoma or malignant phyllodes tumors [
22]. Lee JS, et al. reported 25% of BS had lymphatic metastases if imaging suggested lymphadenopathy [
23]. As a preventative measure against undiscovered early lymph node metastases, we therefore performed axillary lymph nodes dissection (ALND) or sentinel lymph node biopsy (SLNB) in according to the enlarged lymph nodes revealed by imaging, that pathologically diagnosed no metastasis. Malignant PTs (MPT) have a metastasis rate of about 22% and can spread to the pancreas, lung, kidney, and duodenum [
18,
24]. With only three examples of PTs spreading to the stomach and causing anemia, MPT metastasizing to the gastrointestinal tract is rare [
25‐
27]. The most severe case in our cohort, which had a similar prognosis to those previously reported, passed away 3 months after surgery from a large tumor with 17 cm diameter and skin ulceration. In this case, the abdomen and lung were examined using a contrast-enhanced CT scan; no metastases were discovered. However, due of the tumor's enormous size and quick metastasis, we did not have the chance to give a molecular or genomic test to predict tumor behavior.
The GBPS is uncommon cancer subtype with distinct heterogeneity. The distinction between GBS and MPT is made by residual epithelial tissue and malignant mesenchymal components, but with a similar treatment and prognosis. In a retrospective analysis that ranged from the years 1991 to 2014, BS can be divided as undifferentiated pleomorphic sarcoma (70.6%), angiosarcoma (17.6%), osteosarcoma (5.9%), chondrosarcoma (5.9%), fibrosarcoma (0.1%), and liposarcoma (0.1%) [
28]. In a separate investigation of 991 BS cases, spindle cell, leiomyosarcoma, and giant cell sarcomas were all reported to be 13.4%, 11.7%, and 10.1%, respectively [
7]. GBS has tumor-specific differentiation in the stromal nuclear pleomorphism but neither squamous differentiation nor epithelial cells [
76]. Histologically, undifferentiated pleomorphic sarcoma has a storiform, fascicular structure with a high level of cellular atypia and pleomorphism, whereas liposarcoma has variable adipocytic differentiation and heterogeneous shape embedded in a vascularized stroma. In addition, decisive immunohistochemistry markers for undifferentiated pleomorphic sarcoma include S100/SOX10, smooth muscle actin (SMA), and desmin [
29,
30]. All GBPS in this study—two fibrosarcomas and two liposarcomas—showed adipocytic pleomorphism and a significant amount of cellular atypia with mitosis. Two cases of fibrosarcoma composed of spindle cell and bleeding with inflammatory infiltration which manifested poor prognosis. The majority of GBPS includes the specific hallmarks, including mitoses, pleomorphism, necrosis, and inflammatory infiltration, as this study demonstrates (Table
2). Previous studies demonstrated characteristics in GBPS as improved stromal cellularity, stromal nuclear pleomorphism, stromal overgrowth, more than 10 mitoses per 10 HPF, and an infiltrative boundary [
18].
We used a variety of immunohistochemical stains to corroborate the final diagnosis, however only three gave strong or positive results, as indicated below (Supplement
1): S-100 (-), Bcl-2 (-), Stat6 (-), MelanA (-), EMA (-), Calponin (-), CD10 (-), CD34 (-), CK (-), Desmin (-), HMB-45 (-), P63 (-), and β-catenin (-) were all negative. However, Ki67 (40–90% +), SMA (weak +), and Vimentin ( +) were positive in GBS. Due to the markers SMA (weak +), CK (-), and Desmin, the relationship between the metabolic mechanism of the islet cell and giant sarcoma is not as strong (-). Immunohistochemistry findings of diffuse cytokeratin (-) and p63 (-), which support a diagnosis of non-metaplastic carcinoma, must be separated from metaplastic carcinoma to identify BS. The relative risk of mortality is 5.12 (
p = 0.0022), which is unsatisfactory and indicates that 32.2% of patients have a poor prognosis [
31]. There may be focal expression of CKs and P63 as supporting markers in MPT, but none do in this example [
32]. Vimentin, a classic marker for aggressive and invasive mesenchymal cells, most likely predicted the rapid development and early relapse of the giant sarcoma [
33]. For GBPS, a previous study investigated the large tumor size with skin ulceration had significant poor prognosis [
77], which is proved in our cohort. GBPS has a poor prognosis due to high mitoses (ten or more per 10 HPF), infiltrative borders, stromal atypia, marked stromal cellularity, and overwhelmed stromal development [
34‐
36].
Although they remain unidentified, the genetic variations of GBPS are being carefully examined. In PT stromal cells, there is a unique CD34 activity that is associated with benign histology and is recognized as being negative in MPT differentiation [
37]. A few indicators, including bcl-2 and CD117, have been identified as sarcoma-specific chromosomal abnormalities and have increased molecular adjunction in MPT [
37‐
40].
With the expression of pluripotency factors such as OCT3/4, NANOG, KLF4 and SOX2 [
41‐
43], stemness in sarcoma is a variable condition. By investigating genetic alterations in p53, Ki67, CD117, EGFR, p16, and VEGF, numerous research have sought to improve MPT categorization and prognosis; however, only p53 expression and the Ki67 index have been proven to be significantly linked with DFS and OS [
44‐
46]. Recently, it was found that MED12 is commonly changed in the initial phases of PT [
47]. Notably, genetic mutations in FLNA (28%), SETD2 (21%), and KMT2 (9%) were exclusively found in PT, indicating that it is a distinct component from BS. The aggressive biologic behavior in PT was discovered to be caused by mutations in p53, RB1, and NF1, as well as genetic amplification of EGFR and IGF1R, suggesting EGFR could be a therapeutic target for MPT. P53, on the other hand, has been identified as mutated in 15% of sarcomas, which can be targeted or regulated in an early stage of clinical trial by blocking the interaction of p53-MDM. In 4.2% of pleomorphic liposarcomas and about 10% of leiomyosarcomas, RB1 mutations have been reported. Isocitrate dehydrogenase (IDH) is a particular enzyme that takes part in the oxidation of NAPDH throughout the metabolic process in sarcomas. IDH was found to have a mutation in early research, supporting its status as a prospective target for the differential diagnosis and therapy of BS, but no antibody approvement in clinic. The literature highlights the possibility of targeting the extracellular region of EGFR as a potential approach for anti-EGFR drug discovery. Currently, monoclonal antibodies like cetuximab and panitumumab are used to target EGFR in certain cancer types, but there is no specific mention of these antibodies being approved for GBPS [
48]. Curcuma has been used as an adjuvant treatment for osteosarcoma as a target of EGFR, but not available for breast sarcoma. Clinical trials and research studies are continuously exploring potential treatment options to improve patient outcome for GBPS.
The prognosis of GBPS is influenced by its clinicopathological characteristics, including tumor size greater than 5 cm, high-grade nucleus, stromal atypical cells, and positive resection margins [
49]. According to official statistics, the median 5-year overall survival rate for sarcoma is 63.5% [
50], which is similar to our results of GBPS (5-year DFS 60%). In contrast to other forms of breast malignancies, breast sarcomas are often staged and treated differently. In a meta-analysis of 10 retrospective studies that included 9 reports of local recurrence rates, 4 reports of distant metastasis, and 4 reports of survival, Thind A. et al. found that tumor size (
p = 0.03) and a surgical margin of at least 1 cm did not significantly affect local control (
p = 0.33,
n = 456), distant metastasis (RR 1.93, 95% CI 0.35—10.63;
p = 0.45,
n = 72), or overall survival (RR 1.93, 95% CI 0.42—8.77;
p = 0.40,
n = 58) [
51]. The local recurrence and metastatic rates of MPT range from 15 to 40% and 9% to 27%, respectively. Once metastasis occurs, the prognosis is dismal, with death occurring within the next two years [
14,
52,
53]. According to the current study's findings, GBPS has a recurrence rate of 30% and an early metastasis rate of 20%, which is higher than that of MPT or BS. In our cohort we concluded a similar result as LR of 30%(
n = 3) of GBPS, as well as that of 20.6%(
n = 26) of BPS.
Regarding adjuvant therapy for GBPS, there is a lack of consensus. Adjuvant radiation for MPT remains controversial (category 2B), according to the National Comprehensive Cancer Network (NCCN) guidelines for the treatment of PTs (version 4, 2022) [
54]. However, the use of radiotherapy has lately increased due to the substantial risk of recurrence in several reported cases [
55]. A retrospective study of 59 individuals with soft tissue sarcoma over a 43-year follow-up found that 4 of 16 patients received radiation after segmental resection and 13 of 38 patients received radiation after mastectomy. Local recurrence occurred in 13% of patients who underwent mastectomy and radiation, compared to 13 individuals (34%) who underwent mastectomy alone. Without adjuvant radiation, local failure occurred in 60% of instances with positive surgical margins, while local recurrences affected more than 75% of patients who underwent surgery alone [
56]. Radiotherapy was successful in treating high-grade GBS according to Johnstone et al., who studied mastectomy and postoperative radiotherapy in ten patients over the course of 99 months [
9]. Adjuvant radiation therapy is recommended for borderline and malignant PTs with a tumor-free margin of 1 cm or greater [
57]. Adjuvant radiation is recommended after R1 resection and indicated after R0 resection for high-risk malignant tumors (higher grade, size > 5 cm) [
58]. Radiation-induced secondary sarcoma limits the clinical application of radiotherapy. Palta et al. advised hyper fractionated and accelerated radiotherapy (HART) for radiation-induced breast angiosarcomas, and they found that 14 patients who received HART had a 64% 5-year disease-free survival rate [
59]. In a median follow-up of 76 months (range: 7–216 months), postoperative radiation had no impact on cancer-specific survival, regardless of mastectomy or breast conserving surgery [
60,
61]. According to a multivariate Kaplan–Meier curves and Cox proportional hazards analysis of 1353 MPT patients with a follow-up of 99 months (range: 0–331 months), adjuvant radiation does not increase overall survival [
52]. There were limited studies specifically addressing the effect of site and radiation dose (in Gray, GY) on the OS and DFS of patients with malignant phyllodes tumors receiving adjuvant radiotherapy. The impact of radiation dose and site (field) on OS and DFS can vary depending on several factors, including the extent of tumor spread, patient characteristics, and the overall treatment plan. Previous studies reported the inclusion of all relevant lymphatic drainage sites in the radiation volumes seemed to result in the best therapeutic effect [
62]. It is essential to consider that higher radiation doses may increase the likelihood of achieving local tumor control but also carry the potential risk of radiation-related side effects. The radiation field (site) will depend on the extent of the original tumor and the surgical procedure performed. McGowan et al. [
2] reported that the cause-specific survival, which received over 48 Gy radiation dose comparing with the group of no or less than 48 Gy radiation dose, was 91% and 50%, respectively. However, to determine the specific impact of site and radiation dose on OS and DFS in malignant phyllodes tumor patients, larger clinical studies with sufficient follow-up and comprehensive patient data are required.
Adjuvant radiotherapy is still under consideration for its fear of the potential late effects of cumulatively high radiation dose, including rib fractures, lung fibrosis and cardiomyopathy. In addition, radiotherapy is limited in treatment of GBPS due of the rarity of radiation-induced breast sarcomas (RIBS), which accounts for less than 1% of all initial breast malignancies. Angiosarcoma is the most frequent subtype of RIBS, which makes up around one-third of all BS cases with presented at 5
th or 6
th decade of life [
63]. Radiation-induced breast angiosarcoma (RIBA) exhibited an incidence of 0.1% after breast-conserving therapy, which derives from the dermis of irradiated breast. Surgery with negative margins is the main treatment for localized disease [
64]. According to earlier investigations, RIBS had a mastectomy as a strong recommendation in most series. HART, or hyper-fractionated accelerated RT, may be very helpful for RIBS [
65]. However, tumor margins are technically difficult to be assessed for GBPS to ensure clear margins, due to infiltrative margins and multifocality. Adjuvant radiotherapy is proposed by some groups for GBPS [
66].
Chemotherapy for BPS is reported infrequently and with uncertainty. In this study, chemotherapy was advised for two cases. Some studies on adjuvant chemotherapy in BS yielded inconclusive results [
7,
67,
68]. Zer A, et al. performed a comprehensive review and meta-analysis of 5044 cases reported between 1974 and April 2016 to evaluate the advantages and disadvantages of multi-agent chemotherapy in advanced soft tissue sarcoma. Multi-agent chemotherapy was shown to be linked with a marginally significant increase in overall survival (HR:0.79,
p = 0.02) and a marginally significant increase in progression-free survival (PFS) (HR:0.86,
p = 0.05) [
69]. Adjuvant treatment was shown by Gutman et al. to be associated with longer DFS in patients from the MD Anderson Cancer Center with breast sarcoma. An ifosfamide + doxorubicin regimen gave a minor improvement in soft tissue sarcomas with respect to OS, LR, and metastasis, according to a comprehensive assessment that included 22 trials and 1953 participants. A Japanese patient was given neoadjuvant chemotherapy and a mastectomy for a 10 cm leiomyosarcoma with a 12-month follow-up. According to the findings of the study, neoadjuvant chemotherapy for aggressive high-grade lesions is a viable therapeutic approach with promising outcomes [
70]. Neoadjuvant chemotherapy's future, however, is still up in the air due to the rarity and lack of clarity surrounding the measurement of sarcoma regression.
The genetic target therapy is recommended in some series with GBPS. Receptor tyrosine kinases (RTK), including as PDGFR, have been demonstrated to be expressed or elevated at the mRNA level in certain BS in addition to VEGF/VEGFR. Pazopanib, a tiny multi-targeted tyrosine kinase inhibitor (TKI) against VEGFR1, VEGFR2, VEGFR3, and PDGFR, has been given the green light for the treatment of metastatic BS following anthracycline-based chemotherapy or as a first line of therapy for patients who are ineligible for this treatment [
78]. Pazopanib, a tiny multi-targeted tyrosine kinase inhibitor (TKI) against VEGFR1, VEGFR2, VEGFR3, and PDGFR, has been given the green light for the treatment of metastatic BS following anthracycline-based chemotherapy or as a first line of therapy for patients who are ineligible. Another multikinase inhibitor, sorafenib, targets the kinases Raf, PDGF, VEGFR2, VEGFR3, and c-Kit, was only proven to be effective against angiosarcoma in a phase 2 trial, with 5/37 patients exhibiting at least a partial response. Though no RECIST responses were identified in the phase II S050 study of sorafenib in selected sarcoma histotypes, including five angiosarcomas, the majority of angiosarcoma showed a clinical benefit. A limited investigation of RIBS, including RIBA, showed a positive marker for Kit RTK by IHC that is not coupled with exon 11 mutations, that provides a rationale for imatinib usage in RIBS. A novel weapon is immunotherapy (IO) conjugated with chemotherapy as a systematic regimen. Compared to other cancer types, primary breast angiosarcomas had a higher mutational rate, along with a 45% positive for PD-1/PD-L1 and tumor-infiltrating lymphocytes [
71]. There are totally 20 clinical trials of PD-1/L1 inhibitors plus chemotherapy registered in clinicaltrials.gov in the treatment of sarcomas. The effective prediction of IO, including high PD-L1 expression, microsatellite instable-high/mismatch repair deficient phenotype, tumor mutation burden-high status, are proposed without solid evidence in evaluating prognosis. Obviously, the combination therapy is a promising treatment for BS, which needs further exploration.
In this study, the median 5-year DFS and OS of GBPS are 60% and 90%, respectively. A recent study found that a quickly progressing tumor with significant skin invasion and ulceration ultimately led to tumor lysis and death [
72]. There was no statistically significant difference in survival rates between GBS and MPT according to several studies. In comparison to the 5-year OS, which was 86.5 and 78.5%, the 5-year DFS for BS and MPT was 59.1% and 57.4%, respectively (
p = 0.816) [
28]. Both BS and MPT diagnosed at department of pathology in Singapore General Hospital from January 1991 to December 2014 have a poor prognosis in the median follow-up of 37.86 months (range: 0.13–272.82 months) when it comes to multifocality (
p = 0.019), histological subtype (
p = 0.014), the presence of malignant heterologous elements (
p = 0.001), and surgical margin (
p = 0.023) [
28]. The 5-year retrospective investigation of Asian patients' Kaplan–Meier curves revealed no appreciable difference in 5-year DFS and OS in 35 cases of BS and 70 cases of MPT [
73]. According to published studies, BS has a poorer prognosis than breast cancer. The 5-year DFS and OS were 44% and 55%, respectively, according to a retrospective study of 103 breast sarcomas with a median size of 4.45 cm (range: 0.8–22 cm) [
68]. The prognosis is not affected by pathological differentiation of GBS and MPT, in this case, our GBPS and BPS cohorts are reasonable. The 5-year OS was verified to be 67% (83% for tumor size 5 cm and 42% for tumor size > 5 cm) in another retrospective analysis involving 13 instances of primary BS with mastectomy. Tumor size (> 5 cm), residual tumor and margin, cellular pleomorphism, and angiosarcoma were proved to be prognostic factors for survival rate [
23,
74]. Age and histopathological stromal atypia are independent predictors of local recurrence rate in our cohort by Cox proportional analysis. In addition, mitoses and giant sarcoma with the broken skin barrier are associated with exceptionally high death and recurrence rates in this study. This study fills in the knowledge gaps in our understanding of GBPS and encourages further investigation of the underlying principles.
Limitation
The retrospective study conducted has certain limitations. It involved a systematic investigation of the rare Giant Breast Sarcoma (GBPS) by comparing 136 cases of breast malignancies (GBPS vs. BPS: 10 vs. 126) from a single institution, potentially introducing selection bias. While two co-authors collected the data together to minimize bias, the sample's representativeness remains questionable due to its sole source from one institution. The small sample size and rarity of GBPS pose challenges in drawing definitive conclusions. However, in an effort to understand its characteristics better, we divided the cases into the giant group and normal group, ensuring a balanced representation. Despite this approach, the limited comprehension and uncertain prognosis of GBPS call for further investigations to shed light on this uncommon and diverse condition.
Our research contributes to filling the existing knowledge gap surrounding GBPS and emphasizes the need for greater attention and consolidation of efforts to study this rare and complex medical condition.