Simultaneous Breast and Liver Surgery in a Patient with Stage IV Triple Positive Breast Cancer A Case Report

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Case Report Chirurgia (2017) 112: 165-171 No. 2, March - April Copyright Celsius http://dx.doi.org/10.21614/chirurgia.112.2.165 Simultaneous Breast and Liver Surgery in a Patient with Stage IV Triple Positive Breast Cancer A Case Report Alexandru Martiniuc 1, Traian Dumitraæcu 1, Mircea Pavel 1, Cezar Stroescu 1,2 1 Center of General Surgery and Liver Transplantation, Fundeni Clinical Institute, Bucharest, Romania 2 Carol Davila University of Medicine and Pharmacy, Bucharest, Romania Corresponding author: Alexandru Martiniuc, MD Center of General Surgery and Liver Transplantation, Fundeni Clinical Institute, Fundeni Street no 258, 022328, Bucharest, Romania E-mail: alex.martiniuc@gmail.com Received: 13.02.2017 Accepted: 28.03.2017 Rezumat Introducere: În contextul actual al strategiilor oncologice multimodale disponibile pacienţilor cu neoplazii în stadiu avansat, principiul clasic privind indicaţiile limitate ale chirurgiei devine din ce în ce mai puţin valabil. Cu toate că în majoritatea cazurilor un tratament cu viză curativă nu este posibil, totuşi, unii pacienţi cu boală sistemică limitată şi cu o biologie a tumorii favorabilă ar putea să beneficieze de un tratament agresiv, combinat, citotoxic şi chirurgical. Prezentare de caz: Pacientă în vârstă de 48 de ani a fost diagnosticată cu carcinom mamar ducal invaziv cu imunohistochimie pozitivă pentru receptorii de estrogeni, progesteron şi Her2 şi trei metastaze hepatice. După nouă şedinţe de chimioterapie s-a obiectivat un răspuns tumoral favorabil, atât la nivelul tumorii primare cât şi la nivel hepatic, prin dispariţia imagistică a două metastaze şi scăderea în dimensiuni a celei de-a treia. Pacienta a fost operată în clinica noastră, în aceeaşi intervenţie chirurgicală practicându-se sectorectomie mamară cu evidare ganglionară axilară şi hepatectomie atipică segment V. Concluzii: Un subgrup de pacienţi cu neoplasm mamar stadiul IV, cu metastaze hepatice rezecabile şi fără alte leziuni extrahepatice, ar putea să beneficieze de o strategie agresivă chimioterapică şi chirurgicală, cu rezultate bune privind supravieţuirea. Cuvinte cheie: neoplasm mamar, metastaze hepatice, rezecţii hepatice Chirurgia, 112 (2), 2017 165

A. Martiniuc et al Abstract Introduction: In the modern context of multimodal treatment strategies for cancer patients with systemic disease, the dogma that surgery has a limited role is becoming less and less valid. Although a curative approach is not possible for the majority of the cases, however, some patients with limited systemic disease and favorable tumor biology could benefit from an aggressive combined cytotoxic and surgical strategy. Case report: A 48-year-old patient was diagnosed with an invasive ductal carcinoma with the immunohistochemistry positive for estrogen and progesterone receptors, positive Her2 and three liver metastases. After nine cycles of chemotherapy, a favorable tumor response was identified at the level of the primary tumor as well as for the liver lesions: two of the metastases have disappeared, and the third one decreased in dimensions. The patient was operated in our unit, a lumpectomy together with a level II axillary lymph nodes dissection and a non-anatomic resection of the segment V of the liver was performed. Conclusions: A subgroup of patients with stage IV breast cancer with limited liver metastases and no extrahepatic disease might benefit from an aggressive combined cytotoxic and surgical strategy regarding disease control and overall survival. Key words: breast cancer, liver metastases, liver resection Introduction In the modern context of multimodal treatment strategies for cancer patients with systemic disease, the dogma that surgery has a limited role is becoming less and less valid. Although a curative approach is not possible for the majority of the cases, however, some patients with limited systemic disease and favorable tumor biology could benefit from an aggressive combined cytotoxic and surgical strategy (1). The liver is the third most common metastatic site for breast cancer after the skeleton and lungs. The median survival time for patients with untreated breast cancer liver metastases is only 4 8 months (2). Liver metastases are present in 15% of the patients newly diagnosed with metastatic breast cancer, and in one-third of these patients, the liver is the only distant site of the disease (3,4). Case report A 48-year-old woman was diagnosed in December 2014 with stage IV breast cancer. The physical examination revealed a 2 cm palpable tumor in the upper outer quadrant of the right breast and enlarged lymph nodes at the level of the right axillary region. A mammography was performed, and a BIRADS 5 lesion was detected (Fig. 1 A). The computed tomography (CT) confirmed the presence of the tumor in the right breast (Fig. 1 B). The tumor biopsy revealed an invasive ductal carcinoma with the immunohistochemistry positive for estrogen and progesterone receptors, positive Her2 and a Ki-67 index of 20%. The CA15-5 serum level was 69.5 U/ml (normal values: 0 5.8 U/ ml). The patient had no personal or familial history of breast cancer or other malignancies, and her major complaint was right breast pain. A full body contrast enhanced CT scan was performed in January 2015 which revealed only three liver nodular masses highly suggestive for metastatic lesions (Fig. 2). The first lesion has had 13 mm in diameter, and it was located in segment II, the second lesion was located in segment V and has had 44 mm, and the last one was located in segment VIII and measured 11 mm in diameter. The CT scan confirmed the enlarged lymph nodes only at the level of the right axilla. The medical oncologist decided a chemo- 166 Chirurgia, 112 (2), 2017

Simultaneous Breast and Liver Surgery in a Patient with Stage IV Triple Positive Breast Cancer A Case Report A B Figure 1. The breast tumor appearance at mammography (*) (A) and computed tomography (white arrow) (B) Figure 2. Liver metastases appearance before and after 4 cycles of chemotherapy. Chirurgia, 112 (2), 2017 167

A. Martiniuc et al therapy first approach based on docetaxel and epirubicin. Between January and July 2015 the patient received 9 cycles of chemotherapy with docetaxel and epirubicin. No major side effects occurred. After 4 cycles of chemotherapy, a CT scan was performed. An important morphological response was noted regarding the metastatic liver lesions. The lesion from segment II decreased from 13 mm to 5 mm, the lesion from segment VIII decreased from 11 mm to 6 mm, and the largest mass from segment V decreased from 44 mm to 26 mm. A pseudocyst like transformation was also noted for the segment V metastases (Fig. 2). After the 9 cycles of chemotherapy, a liver magnetic resonance imaging was performed describing only a single lesion, the one in segment V, measuring 14 mm (Fig. 3). The bone scan was negative for metastatic lesions. The patient was referred to the Department of Surgery. Because of the relatively young age, the good response to chemotherapy and the single site (liver) metastasis, simultaneously breast and liver surgery was proposed. The patient was discussed in our institution multidisciplinary oncological board. At presentation, the patient was in good health with normal laboratory testsexcept for a CA 15-3 serum level of 31.3 U/ ml(normal values: 0 5.8 U/ ml). The physical examination revealed no palpable tumor at the level of the upper outer right breast quadrant (where the tumor was initially described), most likely due tothe tumor shrinkage under chemotherapy and the relatively large breast. To perform a breast conservative surgery, a mammography with metallic harpoon placement was necessary (Fig. 4). Surgery was performed in August 2015: a right upper outer lumpectomy (guided by the metallic harpoon placed on the morning of the surgery) together with a level II axillary lymph nodes dissection. The liver surgery was performed through a subcostal incision; the intraoperative ultrasound confirmed the presence of a single lesion in segment V. The lesions from segment II and VIII were not detected. A non-anatomic (atypical) segment V Figure 3. Figure 4. Magnetic resonance imaging after 9 cycles of chemotherapy showing only the metastasis of the segment V of the liver Preoperative metallic harpoon marking of the breast tumor resection was performed under ultrasound guidance (Fig. 5). The postoperative course was uneventful. The pathology report of the lumpectomy confirmed a 15/11/12 mm fibrotic bed with groups of residual invasive ductal carcinoma G1 cells, with a partial post-therapeutic histopathological response. Two of the total 26 168 Chirurgia, 112 (2), 2017

Simultaneous Breast and Liver Surgery in a Patient with Stage IV Triple Positive Breast Cancer A Case Report Figure 5. Surgical approach of the primary breast tumor and liver metastasis axillary lymph nodes examined were positive. The resected liver parenchyma contained a 13 mm nodule with an important fibrotic stroma with metastatic breast tumor cells. (pt1cpn1a pm1-liver) The patient was referred for further oncologic treatment and continued with endocrine therapy. The follow-up CT (Fig. 6) and bone scans performed in January 2017 were negative. Chirurgia, 112 (2), 2017 169

A. Martiniuc et al Figure 6. Discussions The magnetic resonance imaging of the liver performed in January 2017 did not identify any signs of recurrence Metastatic breast cancer is widely considered an incurable disease. The treatment of stage IV breast cancer is directed towards symptom control, prevention of complications and maintenance of the quality of live by minimizing toxicity. The natural history of stage IV breast cancer has been and continues to change, especially because the diagnosis is made when the disease burden is lower and better drugs translate into better survivals. The better understanding of the molecular biology of the breast cancer has led to important improvements in overall survival and mortality rates. For example, in a 2016 US estimation of cancer-related deaths, pancreatic cancer mortality has moved from the fourth leading cause of cancer-related deaths to the third, surpassing breast cancer (5,6). Because of the heterogeneous stage IV breast cancer population, no current guidelines offer the optimal management of these patients and it is emphasized the importance of centralization of patients in centers with high volume, experience, and important resources. Classically, surgery for stage IV disease was indicated only in the setting of palliation of symptoms. International consensus guidelines now recognize that surgery can be recommended in a subgroup of patients (7,8). The advances made in the treatment of colorectal and neuroendocrine liver metastases led to the idea of identification of a subset of patients with breast cancer and limited liver disease that might be considered candidates for an aggressive combined cytotoxic and surgical strategy (9). Several centers have published their experience with breast cancer liver metastases resection (10). Promising results have emerged over the years, while identification of some prognostic factors that could influence survival appears to be the key to the effectiveness of surgery (11). An aggressive cytotoxic therapy and surgery were associated with median survival times of 15 91 months and 5-year survival rates of 11% 61% (12). Disappearing liver metastases are defined as a disappearance of liver metastases on crosssectional imaging after administration of chemotherapy. The phenomenon was intensely reported for colorectal cancer liver metastases, and it occurs between 5 38% of the patients (13). Several authors recommend that in the case of preoperative administration of chemotherapy for respectable liver disease, chemotherapy should be given for a short fixed period to avoid overtreatment (13). Data in the literature regarding disappearing breast cancer liver metastases are scares. If we extrapolate from the experience of colorectal liver metastases, complete clinical response following chemotherapy does not mean cure of the disease and complete pathological response (14).The complete pathological response was observed in only 4% of the patients with resected colorectal liver metastases and preoperative chemotherapy (15). Initially, the reported patient has had 3 liver metastases. After 9 cycles of chemotherapy two of them disappeared; these liver lesions could not be objectified on the preoperative magnetic resonance or intraoperative ultrasound. An objective response could be seen only after 4 cycles of chemo. Although the scientific data regarding the timing of surgery is scarce, one might question if the same principle used for colorectal liver metastases treated with neoadjuvant chemotherapy can be applied for this subgroup of patients with breast cancer and resectable liver disease, to avoid the issue of disappearing liver metastases. 170 Chirurgia, 112 (2), 2017

Simultaneous Breast and Liver Surgery in a Patient with Stage IV Triple Positive Breast Cancer A Case Report Conclusions A subgroup of patients with stage IV breast cancer with limited liver metastases and no extrahepatic disease might benefit from an aggressive combined cytotoxic and surgical strategy regarding disease control and overall survival. Although many problems have not yet been answered, the indication of surgery should be done in the multidisciplinary context in hepato-biliary centers. No funding and no conflict of interests. References 1. Ruiz A, Castro-Benitez C, Sebagh M, Giacchetti S, Castro-Santa E, Wicherts DA, et al. Repeat Hepatectomy for Breast Cancer Liver Metastases. 2015;22(S3):1057-66. 2. Adam R, Aloia T, Krissat J, Bralet M-P, Paule B, Giacchetti S, et al. Is Liver Resection Justified for Patients With Hepatic Metastases From Breast Cancer? Annals of Surgery. 2006;244(6):897-908. 3. Clark GM, Sledge GW, Osborne CK, McGuire WL. Survival from first recurrence: relative importance of prognostic factors in 1,015 breast cancer patients. J Clin Oncol. 1987;5(1):55-61. 4. Insa A, Lluch A, Prosper F, Marugan I, Martinez-Agullo A, Garcia- Conde J. Prognostic factors predicting survival from first recurrence in patients with metastatic breast cancer: analysis of 439 patients. Breast Cancer Res Treat. 1999;56(1):67 78. 5. Pancreatic cancer facts. Pancreatic Cancer Action Network. 2016. https://www.pancan.org/wp-content/uploads/2016/02/2016-gaa- PC-Facts.pdf. 6. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2016. CA Cancer J Clin. 3rd ed. 2016;66(1):7 30. 7. Cardoso F, Harbeck N, Fallowfield L, Kyriakides S, Senkus E. Locally recurrent or metastatic breast cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. Oxford University Press; 2012;23(suppl_7):vii11 9. 8. Cardoso F, Costa A, Norton L, Senkus E, Aapro M, André F, et al. ESO-ESMO 2nd international consensus guidelines for advanced breast cancer (ABC2). Elsevier; 2014. p. 489 502. 9. Golse N, Adam R. Liver Metastases From Breast Cancer: What Role for Surgery? Indications and Results. Clinical Breast Cancer. Elsevier; 2017. 10. Bacalbasa N, Dima SO, Purtan-Purnichescu R, Herlea V, Popescu I. Role of surgical treatment in breast cancer liver metastases: a single center experience. Anticancer Res. 2014;34(10):5563-8. 11. Bacalbasa N, Balescu I, Dima S, Popescu I. Long-term survivors after liver resection for breast cancer liver metastases. Anticancer Res. 2015;35(12):6913 7. 12. Nickkholgh A, Mehrabi A. Liver Metastases from Breast Cancer. In: Noncolorectal, Nonneuroendocrine Liver Metastases. Cham: Springer International Publishing; 2014. p. 15-31. 13. Zendel A, Lahat E, Dreznik Y, Zakai BB, Eshkenazy R, Ariche A. Vanishing liver metastases - A real challenge for liver surgeons. Hepatobiliary Surg Nutr. 2014;3(5):295-302. 14. Benoist S, Brouquet A, Penna C, Julié C, Hajjam El M, Chagnon S, et al. Complete response of colorectal liver metastases after chemotherapy: does it mean cure? J Clin Oncol. 2006;24(24):3939-45. 15. Adam R, Wicherts DA, de Haas RJ, Aloia T, Lévi F, Paule B, et al. Complete pathologic response after preoperative chemotherapy for colorectal liver metastases: myth or reality? J Clin Oncol. American Society of Clinical Oncology; 2008;26(10):1635-41. Chirurgia, 112 (2), 2017 171