Management and Outcomes of Metastatic and Recurrent Malignant Phyllodes Tumors of the Breast: A Systematic Literature Review
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Systematic Reviewes
P: 191-200
July 2023

Management and Outcomes of Metastatic and Recurrent Malignant Phyllodes Tumors of the Breast: A Systematic Literature Review

Eur J Breast Health 2023;19(3):191-200
1. Faculty of Medicine, University of Geneva, Geneva, Switzerland
2. Department of Gynecology and Obstetrics, Valais Hospital, Sion, Switzerland
3. Department of Pediatrics, Gynecology and Obstetrics, Geneva University Hospitals, Geneva, Switzerland
No information available.
No information available
Received Date: 06.03.2023
Accepted Date: 30.03.2023
Publish Date: 03.07.2023
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ABSTRACT

To summarize the evidence on the current management and outcomes for metastatic and recurrent malignant phyllodes tumors (MPTs) of the breast. A systematic literature review of all cases of metastatic or recurrent MPTs of the breast published between 2010 and 2021 was performed. In total, 66 patients from 63 articles were included. Fifty-two (78.8%) had distant metastatic disease (DMD subgroup), and 21 (31.8%) showed locoregional recurrent/progressive disease (LRPR subgroup). Locoregional recurrences in patients with no distant metastases were treated with surgical excision in all cases. Radiotherapy was administered in 8/21 cases (38.1%) and was combined with chemotherapy in 2/21 cases (9.5%). Metastatic disease was managed through metastases surgical excision, chemotherapy, radiotherapy, or a combination of these three in 84.6% of cases, while the remaining patients received no oncological treatments. Chemotherapy was proposed in 75.0% of cases. Anthracycline and alkylating agent-based combination regimens were most frequently administered. The median survival time was 24 (2.0–152.0) months, and 72.0 (2.5–98.5) months in the DMD and LRPR subgroups, respectively. Management of recurrent or metastatic MPTs is challenging. Surgery is the fundamental approach, but the use of adjuvant radio- and chemo-therapy remains controversial due to the lack of scientific evidence. Further studies and international registers are needed to implement new and more efficient treatment strategies.

Keywords:
Phyllodes tumor, breast cancer, recurrence, local relapse, metastatic, adjuvant treatment

Key Points

• Evidence and guidelines concerning the management of malignant phyllodes tumors (MPTs) of the breast are limited, especially in the case of recurrent or metastatic disease.

• This study reports current trends in managing MPTs, confirming inconsistent management approaches and a lack of evidence supporting treatment plans.

• Further studies and international registers are needed to implement new and more efficient treatment strategies.

Introduction

Phyllodes tumors of the breast are rare fibroepithelial neoplasms, representing less than 1% of all breast tumors (1). They are classified into benign, borderline, and malignant phyllodes tumors (MPTs) based on histologic characteristics (2). The rarity of this malignancy contributes to the difficulty in defining the most appropriate treatment. This uncertainty is even more marked for recurrent and metastatic MPTs, for which prognosis is significantly affected, and evidence is limited concerning their optimal management. In this study, all cases of metastatic and/or recurrent MPTs published in the last decade were reviewed to give an overall view of their current management and outcomes.

Materials and Methods

Results

In total, 66 patients from 63 series/case reports were included in the analysis. Fifty-two (78.8%) presented with a distant metastatic disease (DMD subgroup), and 21 (31.8%) showed locoregional recurrent/progressive disease (the LRPR subgroup). Seven patients first presented with locoregional progressions/recurrences with no distant lesions and later developed metastatic disease. These patients were analyzed in both the DMD and LRPR subgroups.

The median age was 50 (26–82) years in the DMD subgroup and 45 (18–82) years in the LRPR subgroup. The median tumor size was 100 (22–430) mm and 90 (30–300) mm in the DMD and LRPR subgroups, respectively. All except one patient (62/63, 94.4%) received primary breast surgery by mastectomy (51/63, 81.0%) or a lumpectomy (11/63, 17.5%). Histological characteristics, including surgical margin status, were reported in 25 patients (37.9%) and are summarized in Table 1. Following primary surgery, systemic chemotherapy was administered in 6/13 patients (46.2%) with distant metastasis at diagnosis and in 3/60 patients (5.0%) with no initial sign of metastatic disease. Chemotherapy was given as an adjuvant treatment except in one patient, who received neoadjuvant doxorubicin and cyclophosphamide before mastectomy for mass reduction (45). Adjuvant radiotherapy was administered in 1/13 patients (7.7%) with distant metastases at diagnosis and in 12/60 patients (20.0%) with no initial sign of metastases. Complementary data concerning initial observations and management are reported in Table 1.

Table 1

Discussion and Conclusion

MPTs of the breast constitute an uncommon condition and represent 0.03–0.3% of all breast cancers, with an annual incidence of about 2/1,000,000 (1). Surgery is the management of choice for the primary treatment of localized MPTs. However, due to its rarity, little is known about appropriate management in the case of metastatic or locally recurrent MPTs. In this study, we systematically reviewed all cases of metastatic and/or recurrent MPTs published in the last 10 years to give an overall view of their current management and outcomes.

The national cancer center network (NCCN) recommends treating primary MPTs with lumpectomy or mastectomy in cases of impossibility to adequately obtain 1 cm margins or for cosmetic reasons (67). Mastectomy did not prove superior to wide excision in terms of survival and, therefore, should not be routinely performed (68). Nodal involvement is very rare, and sentinel lymph node biopsy or axillary lymph node dissection are not indicated unless there is suspicion of lymph nodal metastases (67, 69). Adjuvant radiotherapy, chemotherapy, and hormonotherapy are not recommended for the primary treatment of localized MPTs (67).

Locoregional recurrences are common complications of MPTs and are observed in about 12–65% of cases (70, 71). In this systematic review locoregional recurrences were observed within a median time of 8.9 (1.0–36.0) months (70, 71). Positive surgical margins and large tumor size seem to be the main risk factors for locoregional recurrences (70, 72). In this review, these characteristics were found in about 2/3 of patients presenting with a locoregional recurrence.

Although adjuvant radiotherapy following primary surgery is not routinely indicated, in the case of locoregional recurrence, the NCCN recommends considering local irradiation following tumor excision (67). Adjuvant radiotherapy following primary surgery seems to reduce locoregional relapses but with no proven effect on overall survival, regardless of the surgical margin status (73, 74, 75, 76, 77). The role and impact of adjuvant radiotherapy for locoregional relapses are unclear due to limited evidence. In our review, 100% of tumor recurrences were surgically excised, while adjuvant radiotherapy was administered in just over a third of cases. Our review showed no survival differences in locoregional relapsing patients treated with or without adjuvant radiotherapy. No validated guidelines exist for radiation treatment for recurrent MPTs, and in our review, radiotherapy modalities were rarely reported, and no general agreement was found. Combined radio- and chemotherapy seem not indicated and have been reported only twice (22, 61). Multiple recurrences were rarely reported, and except for surgical excision, no consistent trends were observed in their adjuvant treatment. Surgical excision of the local lesion at each relapse seems appropriate (39), associated with a single course of radiotherapy. However, the role of adjuvant chemotherapy for multiple local recurrences is unclear and currently not indicated unless concomitant distant metastases are observed.

As previously observed (70), we found locoregional recurrence to be a strong predictor of distant metastases, with 42.9% of patients developing distant disease after a median time of 2.0 (0.5–14.0) months from their first locoregional recurrence. Yet, the relationship between local relapses and distant metastatic spread is unclear and often debated by authors (78). In our review, survival in patients with locoregional recurrent MPTs was similar to the reported overall survival in the case of MPTs (2, 70, 78, 79). However, the observed 5-year survival rate of 50.0% reduced dramatically to 18.2% in those patients who subsequently developed distant metastases. This highlights the relative controllability of localized MPTs and their locoregional recurrences but the difficulty in managing a distant metastatic spread.

Around 1.5% of MPTs present with metastatic disease at diagnosis, and 10–25% are associated with distant metastatic recurrences, with predominant hematogenous spread and lesions observed in nearly all organs but predominantly in lungs and bones (1, 70, 79, 80, 81, 82). In our review, metastatic recurrences were observed within a median time of 9.0 (1.0–60.0) months. Similar to other studies, the intervals between primary treatment and metastatic recurrences vary widely, from a few weeks to several years (70, 71). The main risk factors associated with the development of distant disease are large tumor size, infiltrative surgical margins, marked stromal overgrowth or cellularity, >5 mitoses per 10 high-power fields, and tumor necrosis (70, 79). In our study, these features were observed in about 3/4 of patients presenting with distant metastases. The presence of heterologous sarcomatous elements could predispose to the development of distant metastases (83), but this association was not universally shared (78). In our study, patients with metastatic recurrences presented with osteosarcomatous and/or chondrosarcomatous heterologous elements in about 70% of cases. However, the small sample size limits any possible suggestions of the relation between these histological features and metastatic MPTs. Patients with metastatic disease, whether at diagnosis or for relapses, should be treated in accordance with the guidelines for metastatic soft tissue sarcomas, as recommended by the NCCN (67). However, these patients frequently do not respond to chemotherapy and often have poor survival (84). In our review, chemotherapy was proposed in around 3/4 of cases with distant metastases, and a wide range of chemotherapy regimens was administered. Anthracycline and alkylating agent-based combination regimens were most frequently administered, and the combination of doxorubicin-ifosfamide was administered in more than one-third of cases. Protocols varied between 6–8 cycles with doxorubicin 25 or 30 mg/m2 days 1-2, and ifosfamide 2 or 7.5 g/m2. Due to limited data, there was no superiority in a specific treatment regimen over the others, as reported in earlier studies. Currently, there are no randomized clinical trials assessing the role of adjuvant chemotherapy in MPTs, and its role remains undefined (78, 79, 82). This uncertainty was highlighted by the fact that, in our review, more than 1/3 of patients with distant metastases were not offered or considered for chemotherapy. In part of these cases, metastases were managed through surgical excision and/or radiotherapy, but more than 20% of patients received no oncological treatments.

Overall, patients with MPTs have a 5-year survival rate of around 65% (2, 70, 78, 79), which, from our results, reduces to approximately 20% in case of metastatic disease. Conversely, patients with localized disease present a 10-year survival rate as high as 90% (85). In addition to distant metastases, survival seems to be affected by the tumor size, the surgical margin status, the stromal overgrowth and differentiation, and the presence of osteosarcomatous or chondrosarcomatous histological features (70, 86, 87, 88, 89). Due to the limited sample size, we could not assess these features in this review. Characteristics predisposing to locoregional relapses, metastatic disease, and poor prognosis should be studied carefully in future research to identify possible indications for primary adjuvant chemo- and/or radiotherapy. In addition, due to the relative uncertainty and confusion around the optimal management of MPTs, more specific international and local guidelines for the management of MPTs are needed.

The main limitation of this study was its small sample size. In addition, analyzed data were extrapolated from case reports and small case series, which were rarely oriented toward metastatic or recurrent MPT, and which frequently reported only limited and incomplete data. This may have resulted in selection and information bias. However, to our knowledge, this study represents the only review of metastatic or recurrent MPT and could improve the general knowledge about the current trends in managing this rare condition.

Search Strategy and Selection Process

This systematic literature review was conducted using a structured search protocol based on the PRISMA criteria (3). To find all cases of metastatic or recurrent MPTs of the breast reported over the last decade, PubMed, Embase, and Web of Science were searched using the terms “malignant phyllode/malignant phyllodes,” “tumor/tumors,” and “breast” for all articles published from 1st January 2010 and 31st December 2021. We included all articles in English or French reporting metastatic or recurrent phyllodes tumors of the breast. We excluded articles reporting benign or borderline phyllodes tumors, patients aged <18 years, phyllodes tumors in men, studies or case series without individual data, and articles with unavailable full text. Sixty-three articles were selected and analyzed (4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66). The literature search protocol design is summarized in Figure 1.

Figure 1

Data Collection Process and Analysis

Two authors performed data extraction independently, results were compared, and any conflict was discussed with a third party. For each patient, any relevant demographic and oncological data concerning the initial treatment, follow-up, management, and outcomes in cases of metastatic or recurrent phyllodes tumors of the breast was extracted. When possible, corresponding authors were contacted to obtain missing or updated information.

SPSS, v20 (IBM Corp., Armonk, NY, USA) was used for statistical analysis. Data were analyzed for the subgroups of patients presenting distant metastases at the time of diagnosis or as a progression/recurrence, designated the distant metastatic disease (DMD) subgroup and for those with locoregional progressive or recurrent disease, designated the locoregional progressive/recurrent (LRPR) subgroup. Since the difference between progression and recurrence was frequently difficult to clarify, these two entities were analyzed together. LRPR disease was considered to consist of lesions limited to the initially involved breast, skin, surgical scar, surrounding soft tissues, and ipsilateral thoracic wall (e.g., pectoral muscles), axillary and internal mammary lymph nodes, without any sign of distant metastases. DMD was considered in all cases presenting with lesions in any other location, with or without a concomitant LRPR disease. Patients who first presented with a locoregional progression/recurrence with no distant lesions that lately developed a metastatic disease were analyzed in both the LRPR and DMD subgroups. Continuous variables are presented as median with minimum and maximum values, and categorical variables as numbers and percentages (%). All missing information was considered as such, and no assumptions were made. Patients with missing data for a specific variable were not included in the statistical analysis. The Kaplan-Meier statistical method was applied for survival analysis, and the log-rank test was used to compare survival curves. Comparison between subgroups was not the objective of this study, but when reported, differences were compared using ANOVA, the Kruskal-Wallis test, or Fisher’s exact test. A p-value <0.05 was considered statistically significant.

Management of Locoregional Progressions/Recurrences

Locoregional progression/recurrence was observed in 21/21 patients (100%) in the LRPR subgroup and in 18/52 patients (34.6%) in the DMD subgroup. Overall, the median time after the initial breast surgery and the first locoregional progression/recurrence was 8.9 (1.0–36.0) months. No differences were observed between patients operated on by mastectomy or lumpectomy or relating to surgical margins status.

Locoregional progressions/recurrences in patients with no distant metastases were treated with surgical excision in all cases (21/21, 100%). Adjuvant radiotherapy was administered in 8/21 cases (38.1%) and was combined with chemotherapy in 2/21 cases (9.5%). In patients with associated distant metastases, locoregional lesions were surgically excised in 14/18 patients (77.8%). Adjuvant radiotherapy was given in 9/18 patients (50.0%) and was associated with adjuvant chemotherapy in 3/18 cases (16.7%).

Patients with initially limited locoregional recurrences/progressions (LRPR subgroup) subsequently developed distant metastases in 9/21 patients (42.9%) with a median interval between first local progression/recurrence and distant relapse of 2.0 (0.5–14.0) months.

Overall, multiple local progressions/recurrences were observed in 10 patients (15.9%), 4 patients (6.3%) presented with two progressions/recurrences, and 4 patients (7.9%) presented with more than two progressions/recurrences. The median interval between the first and the second and between the second and the third locoregional recurrences/progressions was 3.5 (0.5–40) months and 4 (0.5–14) months, respectively. All patients except three developed concomitant distant metastases and died of their disease in a median interval of 2 (0.5–34.5) months from the last locoregional recurrence/progression.

The three patients with multiple recurrences without distant metastases were treated with surgical excision in all cases (3/3, 100%) for both the second and third progressions/recurrences. Radiotherapy was also given in 1/3 of patients (33.3%), and chemotherapy was administered in 1/3 of cases (33.3%) for the second and third progression/recurrence, respectively. Median survival was 70.3 (68.5–72) months for these patients. Additional data concerning the management and outcomes of locoregional progressions/recurrences are reported in Tables 2 and 3.

Table 2
Table 3

Management in Metastatic MPTs

Distant metastases were observed at the time of diagnosis in 13 patients. They were localized in the lungs (11/13, 84.6%), liver (1/13, 7.7%), brain (1/13, 7.7%), soft tissues in the lumbar region (1/13, 7.7%), and in the abdominal wall (1/13, 7.7%). Subsequent progressions/recurrences in other locations were observed in six cases (6/13, 46.2%) within a median interval of 2.0 (1.0–9.0) months. Lesions were observed in bones (1/13, 7.7%), brain (2/13, 15.4%), mediastinal lymph nodes (1/13, 7.7%), adrenal glands (1/13 7.7%), and in the oral cavity (2/13, 15.4%). Distant metastatic progressions/recurrences were observed in 39 patients within 9.0 (1.0–60.0) months from the initial diagnosis of locoregionally-confined disease. Metastases were more frequently observed in the lungs (29/39, 74.4%), the bones (10/39, 25.6%), and the brain (7/39, 17.9%). Data concerning all metastases localizations are summarized in Table 2.

Table 2

Patients with distant metastases at the time of diagnosis received breast surgery in all cases but one (12/13, 92.3%), who was deemed a non-surgical candidate, given multiple sites of metastases and no local pain or open wounds (38). Operated patients received a mastectomy in all the cases reporting the type of surgery, with associated axillary lymph node dissection in 5/12 cases (41.7%). Distant metastases were surgically excised in two patients (2/13, 15.4%) through partial pulmonary thoracoscopic resection (1/13, 7.7%) and cerebral metastatic excision (1/13, 7.7%). Systemic chemotherapy was administered in 6/13 cases (46.2%) and was proposed but refused by the patient in one additional case (1/13, 7.7%). Chemotherapy was administered as adjuvant treatment in all cases but one (1/13, 7.7%), in which neoadjuvant paclitaxel was given before mastectomy (35). A combination of systemic chemotherapy and radiotherapy of the chest wall was reported in one case (1/13, 7.7%) (49).

Metastatic progressions/recurrences in patients with no distant lesions at diagnosis were treated through metastases surgical excision in 13/39 cases (33.3%), which in most cases represented partial pulmonary resections (6/39, 15.4%). Excisions of bowel, kidney, adrenal gland, and heart metastases were also reported. Chemotherapy was proposed in 32/39 cases (82.1%), administered in 26/39 cases (66.7%), and refused by 6/39 patients (15.4%). Combined radiotherapy was reported in 12/39 cases (30.8%), which was mainly used to irradiate the chest wall and axilla for concomitant locoregional progressions/recurrences (6/39, 15.4%). However, radiotherapy was also reported for irradiation of scalp, pancreatic, bone, and parotid metastases. Additional data concerning the management and outcomes of metastatic MPT are reported in Tables 2 and 3.

Table 2
Table 3

Overall, metastatic MPTs were managed through surgical excision, chemotherapy, radiotherapy, or a combination of these three in 84.6% of cases, and chemotherapy was proposed in 75.0% of cases. In 15.4% of cases, patients received no oncological treatments. Reasons for this decision, such as patient refusal, poor general conditions, and no expected benefits, were rarely reported.

Chemotherapeutic Agents

The type of chemotherapeutic agents used was reported in 32/38 cases (84.2%), and details concerning dosages, intervals, and the number of cycles were reported in 9/38 patients (23.7%). The most frequently used chemotherapeutic agents were doxorubicin and ifosfamide (14/38, 36.8%). Protocols comprised 6-8 cycles with doxorubicin 25 or 30 mg/m2 days 1-2, and ifosfamide 2 or 7.5 g/m2 days 1–5. Other chemotherapeutic agent combinations were only reported in one or two cases and comprised a vast heterogeneity of treatments summarized in Table 4. No differences were observed in survival between patients who received different chemotherapeutic agents. Chemotherapy was always administered as adjuvant treatment, except in two cases where chemotherapy was given before breast surgery (35, 45). Chemotherapeutic agents were always administered systemically, except in one case where epirubicin was injected as chemoembolization for breast mass reduction (62).

Table 4

Radiotherapy

Radiotherapy was used to treat locoregional as well as distant progressions/recurrences. Information concerning the location, doses, and fractions was reported in 13/38 cases (34.2%). Locoregional radiotherapy on the remaining breast and/or chest wall was administered with a median dose of 60 (50–84) Gray and a median number of fractions of 28 (10–30). Locoregional radiotherapy was administered as adjuvant treatment following local excisions in all cases except one, in which neoadjuvant radiotherapy was administered before the excision of the lesion (33). Details concerning radiotherapy in other localization were only reported for single disparate cases and are not reported.

Long-Term Outcomes

In the DMD subgroup, data concerning outcomes were available in 51/52 patients (98.1%), and the median follow-up was 14.5 (2.0–152.0) months. At the last control, 18/51 patients (35.3%) were alive with the disease, and 33/51 (64.7%) died of the disease. The median survival time was 24.0 (2.0–152.0) months. The 2-year and 5-year survival rates were 48.7% and 21.2%, respectively.

In the LRPR subgroup, data were available in all patients, and the median follow-up was 13.0 (2.5–98.5) months. At last control, 8/21 patients (38.1%) presented with no evidence of disease, 4/21 patients (19.0%) were alive with the disease, and 9/21 (42.9%) died of the disease. The median survival time was 72.0 (2.5–98.5) months. The 2-year and 5-year survival rates were 60.0% and 50.0%, respectively. Patients in the LRPR subgroup who presented subsequent distant metastatic lesions had a 2-year and 5-year survival rate of 27.3% and 18.2%, respectively.

The 5-year survival rate in the DMD subgroup was lower than the LRPR subgroup, although not significant (21.2% vs. 50.0%, p = 0.07). Comparisons concerning survival time and the 2-year survival rate between subgroups were not significant.

No survival differences were observed between patients managed with different therapeutic strategies in either subgroup. Data concerning outcomes are summarized in Table 3, and Kaplan-Meier survival curves are presented in Figure 2.

Table 3
Figure 2

Clinical and Research Consequences

Due to limited data and inconsistent results, this study carries no clinical consequences. However, we see an urgent need to create international registers and perform specific trials to improve evidence about treatment strategies for recurrent or metastatic MPTs of the breast.

Management of recurrent and metastatic MPTs is a challenge. Surgery remains the fundamental approach, but the role of adjuvant radio- and chemotherapy remains controversial due to the lack of evidence of their positive impact on survival. This study reports the current trends in managing MPTs, confirming inconsistent approaches and a lack of evidence supporting the superiority of one or some treatment options. Further trials and international registers are needed to gather evidence about treatment options, therapy response, and patient-reported outcomes to implement new management strategies.

References

1
Bernstein L, Deapen D, Ross RK. The descriptive epidemiology of malignant cystosarcoma phyllodes tumors of the breast. Cancer 1993; 71: 3020-3024. (PMID: 8387873)
2
Lakhani SR, Ellis IO, Schnitt SJ, Tan PH, van de Vijver MJ. World health organization classification of tumours of the breast. Vol. 4. Lyon: Iarc Press; 2012.
3
Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The prisma 2020 statement: An updated guideline for reporting systematic reviews. BMJ 2021;372:n71.
4
Yamamoto S, Yamagishi S, Kohno T, Tajiri R, Gondo T, Yoshimoto N, et al. Effective Treatment of a Malignant Breast Phyllodes Tumor with Doxorubicin-Ifosfamide Therapy. Case Rep Oncol Med 2019; 2019: 2759650. (PMID: 31316848)
5
Sanchez AM, Franceschini G, Di Giorgio D, Masetti R. Metastatic giant malignant phyllodes tumor of the breast. Breast J 2018; 24: 416-417. (PMID: 29139587)
6
Amir RA, Rabah RS, Sheikh SS. Malignant Phyllodes Tumor of the Breast with Metastasis to the Pancreas: A Case Report and Review of Literature. Case Rep Oncol Med 2018; 2018: 6491675. (PMID: 30050709)
7
Su CC, Chen CJ, Kuo SJ. Effect of Lipodox in combination with bevacizumab in a patient with a metastatic malignant phyllodes breast tumor: A case report. Oncol Lett 2017; 14: 6685-6689. (PMID: 29344119)
8
Wang Q, Su J, Lei Y. Recurrent malignant phyllodes tumor of the breast: A case report. Medicine (Baltimore) 2017; 96: e9069. (PMID: 29245318)
9
Tiwari V, Mandloi V, Ghori H. Malignant phyllodes tumor of the breast with isolated brain metastasis: A case report of an intriguing aggressive subtype. Clin Cancer Investig J 2017; 6: 167-170.
10
Yoshiba S, Saotome T, Mikogami T, Shirota T. Metastasis of Mammary Gland Malignant Phyllodes Tumor to the Mandibular Region: A Case Report and Review of the Literature. J Oral Maxillofac Surg 2017; 75: 440.e1-440.e9. (PMID: 27765548)
11
Sera T, Kashiwagi S, Takashima T, Asano Y, Goto W, Iimori N, et al. Multiple metastatic malignant phyllodes tumor of the breast with tonsillar metastasis: a case report. BMC Res Notes 2017; 10: 55. (PMID: 28103951)
12
Johnson ED, Gulbahce E, McNally J, Buys SS. Malignant Phyllodes Tumor Presenting in Bone, Brain, Lungs, and Lymph Nodes. Case Rep Oncol 2016; 9: 861-868. (PMID: 28203179)
13
Sato T, Muto I, Sakai T. Coexistence of malignant phyllodes tumor and her2-positive locally advanced breast cancer in distinct breasts: A case report. Int J Surg Case Rep 2016; 19: 163-167. (PMID: 26773878)
14
Shan J, Zhang S, Wang Z, Fu Y, Li L, Wang X. Breast malignant phyllodes tumor with rare pelvic metastases and long-term overall survival: A case report and literature review. Medicine (Baltimore) 2016; 95: e4942. (PMID: 27661051)
15
Rowe JJ, Prayson RA. Metastatic malignant phyllodes tumor involving the cerebellum. J Clin Neurosci 2015; 22: 226-227. (PMID: 25449208)
16
Roberts N, Runk DM. Aggressive malignant phyllodes tumor. Int J Surg Case Rep 2015; 8C: 161-165. (PMID: 25697402)
17
Al-Rabiy FN, Ali RH. Malignant phyllodes tumor with osteosarcomatous differentiation metastasizing to small bowel and causing intestinal obstruction. Diagnostic Histopathology 2015; 21: 165-168.
18
Augustyn A, Sahoo S, Wooldridge RD. Large Malignant Phyllodes Tumor of the Breast with Metastases to the Lungs. Rare Tumors 2015; 7: 5684. (PMID: 26266007)
19
Karczmarek-Borowska B, Bukala A, Syrek-Kaplita K, Ksiazek M, Filipowska J, Gradalska-Lampart M. A Rare Case of Breast Malignant Phyllodes Tumor With Metastases to the Kidney: Case Report. Medicine (Baltimore) 2015; 94: e1312. (PMID: 26287414)
20
Jhawar SS, Upadhyay S, Mahajan A, Grewal SS. Malignant phyllodes tumor of the breast with isolated intracranial metastases: A report. Neurol India 2015; 63: 963-965. (PMID: 26588634)
21
Farias-Eisner GT, Small K, Swistel A, Ozerdem U, Talmor M. Immediate implant breast reconstruction with acellular dermal matrix for treatment of a large recurrent malignant phyllodes tumor. Aesthetic Plast Surg 2014; 38: 373-378. (PMID: 24570179)
22
Shin YD, Lee SK, Kim KS, Park MJ, Kim JH, Yim HS, et al. Collision tumor with inflammatory breast carcinoma and malignant phyllodes tumor: a case report and literature review. World J Surg Oncol 2014; 12: 5. (PMID: 24400686)
23
Sano R, Sato E, Watanabe T, Oshima H, Ando A, Masaki M, et al. Phyllodes tumor metastasis to the tonsil with synchronous undifferentiated carcinoma. Int J Surg Case Rep 2014; 5: 290-293. (PMID: 24747756)
24
Mačák J, Hurník P, Dvořáčková J, Mačáková J. An isolated metastasis to the heart from a malignant phyllodes tumor with osteosarcomatous differentiation. Cesk Patol 2014; 50: 146-149. (PMID: 25418902)
25
Yukawa M, Watatani M, Isono S, Shiono H, Hasegawa H, Okajima K, et al. Pancreatic metastasis from phyllodes tumor presenting initially as acute retroperitoneal hemorrhage. Int Canc Conf J 2013; 2: 238-242.
26
Singer A, Tresley J, Velazquez-Vega J, Yepes M. Unusual aggressive breast cancer: metastatic malignant phyllodes tumor. J Radiol Case Rep 2013; 7: 24-37. (PMID: 23705037)
27
Bilen MA, Laucirica R, Rimawi MF, Nangia JR, Cyprus GS. Jejunal intussusception due to malignant phyllodes tumor of the breast. Clin Breast Cancer 2012; 12: 219-221. (PMID: 22381472)
28
Al-Zoubaidi M, Qiu S, Bonnen M, Joyner M, Roehl K, Silva C, et al. Malignant phyllodes tumor of the breast: A case report. The Open Breast Cancer Journal 2011; 3: 45-48.
29
Sadatomo A, Hozumi Y, Shiozawa M, Hirashima Y, Koinuma K, Kurihara K. Spontaneous regression of pulmonary metastases from a malignant phyllodes tumor. Jpn J Clin Oncol 2011; 41: 915-917. (PMID: 21527411)
30
Ito T, Ito K, Okada T, Murayama K, Hanamura T, Kanai T, et al. Full-thickness chest-wall resection followed by thorax reconstruction for recurrent malignant phyllodes tumor. Int J Clin Oncol 2011; 16: 156-160. (PMID: 20721595)
31
Nakatsu T, Koshiji T, Sakakibara Y, Hagio K, Ishigami M, Arima Y, et al. Pulmonary artery obstruction due to a metastatic malignant phyllodes tumor of the breast. Gen Thorac Cardiovasc Surg 2010; 58: 423-426. (PMID: 20703865)
32
Suzuki-Uematsu S, Shiraishi K, Ito T, Adachi N, Inage Y, Taeda Y, et al. Malignant phyllodes tumor composed almost exclusively of a fibrosarcomatous component: a case report and review of malignant phyllodes tumors with metastases. Breast Cancer 2010; 17: 218-224. (PMID: 19350353)
33
Yeh R, Chong LN, Hughes TM. Malignant phyllodes: excellent response to neoadjuvant radiotherapy. ANZ J Surg 2019; 89: 1668-1670. (PMID: 30208507)
34
Tokoyoda M, Adachi S, Ishida Y, Yamazaki K. Osteosarcoma mimic in the breast: A recurrent malignant phyllodes tumour harbouring MED12 and hTERT mutations. Cytopathology 2018; 29: 383-385. (PMID: 29633481)
35
Yeong J, Thike AA, Young Ng CC, Md Nasir ND, Loh K, Teh BT, et al. A genetic mutation panel for differentiating malignant phyllodes tumour from metaplastic breast carcinoma. Pathology 2017; 49: 786-789. (PMID: 29066183)
36
Goh CH, Lim YP, Su JW, Khoo KS, Thomas A, Sittampalam K, et al. Cardiopulmonary thromboembolism of epithelioid angiosarcoma arising from malignant phyllodes tumour of the breast. J Clin Pathol 2014; 67: 450-454. (PMID: 24399035)
37
Goel A, Insa R, Gaur MK, Garg PK. Palliative Surgery for Metastatic Fungating Phyllodes Tumors: A Series of Two Cases. Perm J 2018; 22: 17-100. (PMID: 30010535)
38
Ruiz-Flores L, Ebuoma LO, Benveniste MF, Nagi C, OrtizPerez T, Benveniste AP. Case Report: Metastatic Phyllodes Tumor. Semin Ultrasound CT MR 2018; 39: 122-126. (PMID: 29317034)
39
Iimori N, Kashiwagi S, Ishikawa T, Kawajiri H, Takashima T, Ohsawa M, et al. Mammary phyllodes tumor with six episodes of a relapse: a case report. J Med Case Rep 2017; 11: 261. (PMID: 28911335)
40
Arai H, Nobusawa S, Kawabata-Iwakawa R, Rokudai S, Higuchi T, Yamazaki T, et al. Myeloid sarcoma arising in malignant phyllodes tumour: clonal relationships revealed by comparative genome-wide analyses. Br J Haematol 2018; 181: 255-259. (PMID: 28211578)
41
Morcos BB, Baker B, Hashem SA. Ileocaecal intussusception secondary to metastatic phyllodes tumour of the breast. Ann R Coll Surg Engl 2010; 92: W29-W30. (PMID: 20573310)
42
Choi DI, Chi HS, Lee SH, Kwon Y, Park SY, Sim SH, et al. A Rare Case of Phyllodes Tumor Metastasis to the Stomach Presenting as Anemia. Cancer Res Treat 2017; 49: 846-849. (PMID: 27586673)
43
Renard E, Langbour-Remy C, Klein M, Le Bouc Y, Weryha G, Cuny T. Severe hypoglycemia with “Big”-IGF-2 oversecretion by a giant phyllode tumor of the breast: a rare case of non-islet cell tumor-induced hypoglycemia (NICTH). Ann Endocrinol (Paris) 2012; 73: 488-491. (PMID: 22867750)
44
El Ochi MR, Toreis M, Benchekroun M, Benkerroum Z, Allaoui M, Ichou M, et al. Bone metastasis from malignant phyllodes breast tumor: report of two cases. BMC Clin Pathol 2016; 16: 4. (PMID: 26933383)
45
Chang YW, Kim HS, Kim DW, Son GS. Fulminant course in a case of malignant phyllodes tumor. Ann Surg Treat Res 2017; 92: 110-112. (PMID: 28203559)
46
Morioka E, Noguchi M, Noguchi M, Inokuchi M, Shimada KI, Shioya A, et al. A case of recurrent malignant phyllodes tumor undergoing nipple-sparing mastectomy with immediate breast reconstruction. Surg Case Rep 2020; 6: 297. (PMID: 33237380)
47
Yoshidaya F, Hayashi N, Takahashi K, Suzuki K, Akiyama F, Ishiyama M, et al. Malignant phyllodes tumor metastasized to the right ventricle: a case report. Surg Case Rep 2015; 1: 121. (PMID: 26943445)
48
Nasri S, Hamila F, Bourigua R, Mestiri S, Elghali MA. Pancreatic metastases and first reported gallbladder metastasis from phyllodes tumor of the breast. Rare Tumors 2020; 12: 2036361320972866. (PMID: 33282161)
49
Koukourakis IM, Zygogianni A, Kouloulias V, Koukourakis MI. Successful Treatment of a Locally Recurrent and Metastatic Malignant Phyllodes Tumor with Accelerated Radiotherapy and Nab-Paclitaxel, Cisplatin, and Liposomal Doxorubicin Chemotherapy. Chemotherapy 2021; 66: 82-86. (PMID: 34233328)
50
Strzępek Ł, Ciesielska P, Karakiewicz-Krawczyk K, Czerw A. Malignant phyllodes tumor of the breast: Case report, tumor characteristics, treatment approach. Breast Cancer Management 2021; 10: BMT58.
51
Tada Y, Yasunaga M, Tomonobe H, Yamada Y, Hori E, Okugawa K, et al. A Case of Malignant Phyllodes Tumor of the Breast Metastasizing to the Ovary. Int J Surg Pathol 2022; 30: 427-431. (PMID: 34761702)
52
Wang X, Xie L, Hu W, Yan J, Qian X, Zhu L. Apatinib treatment is effective for metastatic malignant phyllodes tumors of the breast: a case report. BMC Womens Health 2021; 21: 218. (PMID: 34022875)
53
Reinisch M, Kuemmel S, Breit E, Theuerkauf I, Harrach H, Schindowski D, et al. Two progressed malignant phyllodes tumors of the breast harbor alterations in genes frequently involved in other advanced cancers. Orphanet J Rare Dis 2021; 16: 363. (PMID: 34399808)
54
Morisaki T, Noda S, Ishihara S, Asano Y, Kashiwagi S, Takashima T, et al. A Case of a Malignant Phyllodes Tumor in the Breast with Lymph Node Metastasis. Gan To Kagaku Ryoho 2021; 48: 437-439. (PMID: 33790180)
55
Nakamura S, Goto T, Nara S, Kawahara Y, Yashiro S, Kano S, et al. Pure ground glass opacity (GGO) on chest CT: a rare presentation of lung metastasis of Malignant Phyllodes Tumor. Breast Cancer 2020; 27: 1187-1190. (PMID: 32578005)
56
Liu HP, Chang WY, Hsu CW, Chien ST, Huang ZY, Kung WC, et al. A giant malignant phyllodes tumor of breast post mastectomy with metastasis to stomach manifesting as anemia: A case report and review of literature. BMC Surg 2020; 20: 187. (PMID: 32799838)
57
Bachert SE, Stewart RL, Samayoa L, Massarweh SA. Malignant phyllodes tumor metastatic to pancreas. Breast J 2020; 26: 1627-1628. (PMID: 32720379)
58
Lee HJ, Lim HS, Ki SY, Lee JE, Lee JS, Park MH. Cutaneous Scalp Metastases of Malignant Phyllodes Tumor of the Breast. J Breast Cancer 2020; 23: 320-325. (PMID: 32595994)
59
Conduit C, Luen S, Xu H, Byrne D, Fox S, Desai J, et al. Using Genomic Sequencing to Explain an Exceptional Response to Therapy in a Malignant Phyllodes Tumor. JCO Precis Oncol 2020; 4: 1263-1266. (PMID: 35050785)
60
Wu H, Li L, Yang J, Guo C, Zhang W, Wang H. Radiotherapy with apatinib for recurrence of malignant phyllodes tumor of the breast: A case report. Medicine (Baltimore) 2020; 99: e18808. (PMID: 32011486)
61
Andring L, Tawil A, Deraniyagala R. A rare case of a malignant phyllodes tumor of the breast associated with secretion of beta-human chorionic gonadotropin. Breast J 2019; 25: 984-985. (PMID: 31192485)
62
Kuo CY, Lin SH, Lee KD, Cheng SJ, Chu JS, Tu SH. Transcatheter arterial chemoembolization improves the resectability of malignant breast phyllodes tumor with angiosarcoma component: a case report. BMC Surg 2019; 19: 100. (PMID: 31351458)
63
Li JJX, Chan WC, Chau HHL, Wu C, Tse GM. Cytologic diagnosis of metastatic malignant phyllodes tumor of the breast in pleural effusion. Diagn Cytopathol 2019; 47: 599-602. (PMID: 30829462)
64
Fang CL, Hsu CH, Tu CW. Malignant Phyllodes Tumor Recurrence in the Pleural Cavity via the Deep Inferior Epigastric Perforator Flap and Internal Mammary Vessel Bundle: A Case Report. Ann Plast Surg 2019; 82: 618-621. (PMID: 30882414)
65
Moon SH, Jung JH, Lee J, Kim WW, Park HY, Lee JW, et al. Complete remission of giant malignant phyllodes tumor with lung metastasis: A case report. Medicine (Baltimore) 2019; 98: e15762. (PMID: 31145295)
66
Kim  S, Oh HY, Ryu Y. Benign phyllodes tumor of the breast recurring as a rapidly growing recurrent malignant phyllodes tumor: A case report. Iran J Radiol 2019; 16: e13062.
67
Gradishar WJ, Moran MS, Abraham J, Aft R, Agnese D, Allison KH, et al. NCCN Guidelines® Insights: Breast Cancer, Version 4.2021. J Natl Compr Canc Netw 2021; 19: 484-493. (PMID: 34794122)
68
Macdonald OK, Lee CM, Tward JD, Chappel CD, Gaffney DK. Malignant phyllodes tumor of the female breast: association of primary therapy with cause-specific survival from the Surveillance, Epidemiology, and End Results (SEER) program. Cancer 2006; 107: 2127-2133. (PMID: 16998937)
69
Adesoye T, Neuman HB, Wilke LG, Schumacher JR, Steiman J, Greenberg CC. Current Trends in the Management of Phyllodes Tumors of the Breast. Ann Surg Oncol 2016; 23: 3199-3205. (PMID: 27334214)
70
Kapiris I, Nasiri N, A’Hern R, Healy V, Gui GP. Outcome and predictive factors of local recurrence and distant metastases following primary surgical treatment of high-grade malignant phyllodes tumours of the breast. Eur J Surg Oncol 2001; 27: 723-730. (PMID: 11735168)
71
Barth RJ Jr. Histologic features predict local recurrence after breast conserving therapy of phyllodes tumors. Breast Cancer Res Treat 1999; 57: 291-295. (PMID: 10617306)
72
Lu Y, Chen Y, Zhu L, Cartwright P, Song E, Jacobs L, et al. Local Recurrence of Benign, Borderline, and Malignant Phyllodes Tumors of the Breast: A Systematic Review and Meta-analysis. Ann Surg Oncol 2019; 26: 1263-1275. (PMID: 30617873)
73
Belkacémi Y, Bousquet G, Marsiglia H, Ray-Coquard I, Magné N, Malard Y, et al. Phyllodes tumor of the breast. Int J Radiat Oncol Biol Phys 2008; 70: 492-500. (PMID: 17931796)
74
Gnerlich JL, Williams RT, Yao K, Jaskowiak N, Kulkarni SA. Utilization of radiotherapy for malignant phyllodes tumors: analysis of the National Cancer Data Base, 1998-2009. Ann Surg Oncol 2014; 21: 1222-1230. (PMID: 24306659)
75
Zhao W, Tian Q, Zhao A, Wang B, Yang J, Wang L, et al. The role of adjuvant radiotherapy in patients with malignant phyllodes tumor of the breast: a propensity-score matching analysis. Breast Cancer 2021; 28: 110-118. (PMID: 32748225)
76
Kim YJ, Kim K. Radiation therapy for malignant phyllodes tumor of the breast: An analysis of seer data. Breast 2017; 32: 26-32. (PMID: 28013032)
77
Mituś J, Reinfuss M, Mituś JW, Jakubowicz J, Blecharz P, Wysocki WM, et al. Malignant phyllodes tumor of the breast: treatment and prognosis. Breast J 2014; 20: 639-644. (PMID: 25227987)
78
Papas Y, Asmar AE, Ghandour F, Hajj I. Malignant phyllodes tumors of the breast: A comprehensive literature review. Breast J 2020; 26: 240-244. (PMID: 31478587)
79
Lissidini G, Mulè A, Santoro A, Papa G, Nicosia L, Cassano E, et al. Malignant phyllodes tumor of the breast: a systematic review. Pathologica 2022; 114: 111-120. (PMID: 35414723)
80
Tan PH, Ellis I, Allison K, Brogi E, Fox SB, Lakhani S, et al. The 2019 World Health Organization classification of tumours of the breast. Histopathology 2020; 77: 181-185. (PMID: 32056259)
81
Tse GM, Lee CS, Kung FY, Scolyer RA, Law BK, Lau TS, et al. Hormonal receptors expression in epithelial cells of mammary phyllodes tumors correlates with pathologic grade of the tumor: a multicenter study of 143 cases. Am J Clin Pathol 2002; 118: 522-526. (PMID: 12375638)
82
Tan BY, Acs G, Apple SK, Badve S, Bleiweiss IJ, Brogi E, et al. Phyllodes tumours of the breast: a consensus review. Histopathology 2016; 68: 5-21. (PMID: 26768026)
83
Fede ÂBS, Pereira Souza R, Doi M, De Brot M, Aparecida Bueno de Toledo Osorio C, Rocha Melo Gondim G, et al. Malignant Phyllodes Tumor of the Breast: A Practice Review. Clin Pract 2021; 11: 205-215. (PMID: 33917271)
84
Zhang Y, Kleer CG. Phyllodes Tumor of the Breast: Histopathologic Features, Differential Diagnosis, and Molecular/Genetic Updates. Arch Pathol Lab Med 2016; 140: 665-671. (PMID: 27362571)
85
Grabowski J, Salzstein SL, Sadler GR, Blair SL. Malignant phyllodes tumors: a review of 752 cases. Am Surg 2007; 73: 967-969. (PMID: 17983058)
86
Hines JR, Murad TM, Beal JM. Prognostic indicators in cystosarcoma phylloides. Am J Surg 1987; 153: 276-280. (PMID: 3030151)
87
Norris HJ, Taylor HB. Relationship of histologic features to behavior of cystosarcoma phyllodes. Analysis of ninety-four cases. Cancer 1967; 20: 2090-2099. (PMID: 4294565)
88
Pietruszka M, Barnes L. Cystosarcoma phyllodes: a clinicopathologic analysis of 42 cases. Cancer 1978; 41: 1974-1983. (PMID: 206344)
89
Contarini O, Urdaneta LF, Hagan W, Stephenson SE Jr. Cystosarcoma phylloides of the breast: a new therapeutic proposal. Am Surg 1982; 48: 157-166. (PMID: 6282155)