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A case of squamous cell carcinoma of the breast achieved a pathological complete response after dose-dense AC + dose-dense PTX
Surgical Case Reports volume 9, Article number: 137 (2023)
Abstract
Background
Squamous cell carcinoma (SCC) of the breast is a rare form of breast cancer, accounting for approximately 0.1% of all breast cancers. It is known for its rapid tumor growth and poor prognosis with no established treatment.
Case presentation
A 56-year-old woman was diagnosed with breast SCC with axillary, supraclavicular and internal thoracic lymph node metastases. She received neoadjuvant chemotherapy (NAC) with dose-dense doxorubicin and cyclophosphamide (AC) followed by dose-dense paclitaxel (PTX). This treatment resulted in a pathological complete response (pCR) after breast-conserving surgery. The patient was then treated with radiotherapy. She remained free of recurrence for three years postoperatively.
Conclusions
We report a rare case of breast SCC treated with preoperative dose-dense chemotherapy, resulting in pCR and allowing breast-conserving surgery.
Background
Squamous cell carcinoma (SCC) of the breast, classified as a metaplastic carcinoma by the World Health Organization (WHO) classification, is a rare form of breast cancer accounting for approximately 0.1% of all breast carcinomas [1].
It is characterized by rapid tumor growth and poor prognosis, with no established treatment. We present a case of squamous cell carcinoma treated with dose-dense doxorubicin and cyclophosphamide (AC) followed by dose-dense paclitaxel (PTX), resulting in a pathological complete response (pCR) after breast-conserving surgery.
Case presentation
A 56-year-old female with no significant medical or family history presented to our hospital with the chief complaint of a mass in the right breast. The Mammography, breast ultrasonography, CT, MRI and FDG-PET scans revealed a 35 mm mass in the right breast (Fig. 1). Core needle biopsy identified squamous cell carcinoma of the breast. The FDG-PET scan showed metastases in the axillary, supraclavicular and internal thoracic lymph nodes, giving a clinical stage of cT2N3M0, stage IIIC (Fig. 1).
Immunohistochemistry showed the tumor to be hormone receptor-negative, HER2-negative with a Ki-67 of 90% and triple negative (TN) breast cancer (Fig. 2).
The patient received 4 cycles of AC (doxorubicin 60 mg/m2 and cyclophosphamide 600 mg/m2) and 4 cycles of PTX (paclitaxel 175 mg/m2) with pegfilgrastim 3.6 mg as NAC. There were no serious adverse events. After NAC, the tumor was significantly reduced and showed ycT1N0M0 ycStage I on MRI (Fig. 1E). The patient underwent breast-conserving surgery and sentinel node biopsy, and postoperative histopathology showed no cancer cells.
After surgery, the patient received 50 Gy/25 fractions radiation to the residual breast and supraclavicular and internal thoracic lymph nodes and has remained free of recurrence for 3 years postoperatively.
Discussion
SCC of the breast, classified as a metaplastic carcinoma in the WHO classification system, is a rare form of breast cancer, accounting for 0.06–0.1% of all cases [1]. As a result, there is no established treatment strategy, and treatment is often determined by clinical features [2]. There have been several reports of SCC cases achieving pCR by NAC (Table 1). A significant number of these cases were treated with anthracycline/taxane therapy. These cases reported in Table 1 might be very limited cases because SCC breast cancer is too aggressive subtypes to be cured [2]. Also, there have been reports of poor efficacy of anthracycline in breast SCC [2]. On the other hand, the Japanese guideline recommends a dose-dense anthracycline/taxane regimen for the treatment of TN breast cancer [9]. The Norton-Simon hypothesis states that sensitivity to chemotherapy is increased when tumor volume is small. Dose-dense therapy shortens the repopulation period so that the next dose is given when tumor volume is small. This allows administration at a time when the tumor is more sensitive to chemotherapy and a greater anti-tumor effect can be expected [9]. Therefore, we chose a dose-dense anthracycline/taxane regimen. However, platinum-based regimens are also recommended for treating TN breast cancer. In neoadjuvant chemotherapy trials, platinum-based regimens prolonged OS and improved pCR rates in TN breast cancer patients [10,11,12]. This demonstrates the benefit of platinum-based drugs for treating TN breast cancer. Although the efficacy of platinum-based regimens would be expected in this case, the lack of insurance coverage in Japan makes their use difficult. Recently, the use of the platinum-based KEYNOTE-522 regimen is now a promising option [13]. The KEYNOTE-522 trial of pembrolizumab for NAC in TN breast cancer showed improved event-free survival and pCR rate compared with the standard treatment [13]. The use of immune-checkpoint inhibitors for the treatment of TN breast cancer, including special types, is likely to increase in the future. KEYNOTE-826 study also demonstrated the efficacy of pembrolizumab in advanced recurrent cervical cancer, including squamous cell carcinoma [14]. These results suggest that immune-checkpoint inhibitors may be considered for use in SCC of TN breast cancer. Further case series are expected in the future.
In this case, at least three sentinel lymph nodes were identified, including the previously diagnosed positive node prior to NAC, all of which were found to be negative for metastases; therefore, axillary dissection was not performed. Lymph node metastasis is an established poor prognostic factor in SCC of the breast, and axillary dissection has been commonly performed in previously reported cases [15]. However, in cases where a pCR was achieved in the primary tumor, all dissected axillary lymph nodes were found to be negative for metastases, resulting in a favorable prognosis. The incidence of lymph node metastasis has also been reported to be low in upfront surgery cases [16].
These findings suggest that sentinel lymph node biopsy or tailored axillary surgery may be appropriate for cases of SCC in which NAC has resulted in a significant reduction in the size of the primary tumor.
Regarding the surgical approach after NAC, mastectomy is often performed when the primary tumor is large. Total mastectomy was performed in all cases of breast SCC with pCR after NAC (Table 1), and no partial mastectomy was performed. If NAC leads to tumor shrinkage, Japanese guidelines also recommend breast-conserving therapy [3]. In this case, partial mastectomy was performed due to the significant reduction achieved with NAC.
There is also evidence that postoperative radiotherapy (PORT) significantly improves overall survival in SCC of the breast, regardless of surgical technique [16]. In the current case, radiotherapy was administered to the supraclavicular and internal thoracic lymph nodes that were preoperatively positive for metastases, in addition to the breast that was preserved postoperatively. The patient progressed without local recurrence. If a prominent reduction is obtained in NAC, partial mastectomy and PORT might be considered in breast SCC.
Conclusion
We encountered a case of squamous cell carcinoma of the breast where preoperative dose-dense chemotherapy was administered and breast-conserving surgery was possible. It was suggested that dose-dense therapy might be effective as NAC for breast SCC.
Availability of data and materials
The datasets of this case report are available from the corresponding author upon reasonable request.
Abbreviations
- SCC:
-
Squamous cell carcinoma
- NAC:
-
Neoadjuvant chemotherapy
- pCR:
-
Pathological complete response
- AC:
-
Doxorubicin and cyclophosphamide
- PTX:
-
Paclitaxel
- MRI:
-
Magnetic resonance imaging
- FDG-PET:
-
Fluorodeoxyglucose positron emission tomography
- TC:
-
Docetaxel and carboplatin
- EC:
-
Epirubicin and cyclophosphamide
- wPTX:
-
Weekly paclitaxel
- HP:
-
Trastuzumab and pertuzumab
- DTX:
-
Docetaxel
- CDDP + 5FU:
-
Cisplatinum + 5-fluorouracil
References
Benoist P, Mureau A, Joueidi Y, Arbion F, Vilde A, Body G, et al. Management and prognosis of pure primary squamous cell carcinoma of the breast. J Gynecol Obstet Hum Reprod. 2018;47(7):275–80. https://doi.org/10.1016/j.jogoh.2018.06.007.
Hennessy BT, Krishnamurthy S, Giordano S, Buchholz TA, Kau SW, Duan Z, et al. Squamous cell carcinoma of the breast. J Clin Oncol. 2005;23(31):7827–35. https://doi.org/10.1200/JCO.2004.00.9589.
Chen B, Jiang Y, Luo C, Bao Y, Tan N, Li T, et al. Significant efficacy of paclitaxel plus carboplatin (TP) as a neoadjuvant regimen for metaplastic squamous cell carcinoma of the breast: a rare case report and literature review. Transl Cancer Res. 2022;11(8):2953–9. https://doi.org/10.21037/tcr-22-484.
Alan O, Telli TA, Ercelep O, Hasanov R, Simsek ET, Mutis A, et al. A case of primary squamous cell carcinoma of the breast with pathologic complete response after neoadjuvant chemotherapy. Curr Probl Cancer. 2019;43(4):308–11. https://doi.org/10.1016/j.currproblcancer.2018.04.003.
Noro A, Ishitobi M, Hanamura N, Kashikura Y, Yamashita M, Kozuka Y, et al. A case of metaplastic squamous cell carcinoma of the breast that showed a pathological complete response after neoadjuvant chemotherapy with weekly paclitaxel. Am J Case Rep. 2022;23:e935035. https://doi.org/10.12659/AJCR.935035.
Usui Y, Matsunuma R, Yamaguchi K, Hayami R, Muramatsu A, Suzuki M, et al. Pathological complete response to neoadjuvant chemotherapy in a patient with HER2-positive squamous cell carcinoma of the breast. Case Rep Oncol. 2021;14(3):1536–41. https://doi.org/10.1159/000519746.
Sakuma T, Nomizu T, Matsuzaki M, Katagawa N, Sassa M, Kanke Y, et al. A case of triple-negative breast cancer with squamous metaplasia in which a pathologic complete response was achieved with neoadjuvant chemotherapy. Nihon Rinsho Geka Gakkai Zasshi (J Jpn Surg Assoc). 2015;76:478–83. https://doi.org/10.3919/jjsa.76.478.
Dejager D, Redlich PN, Dayer AM, Davis HL, Komorowski RA. Primary squamous cell carcinoma of the breast: sensitivity to cisplatinum-based chemotherapy. J Surg Oncol. 1995;59:199–203. https://doi.org/10.1002/jso.2930590313.
Breast Cancer Treatment Guidelines 1, Treatment Edition 2022, 5th edn. The Japanese Society of Breast Cancer: Kanehara; 2022. p. 95–98, p. 305–306.
Iwase M, Ando M, Aogi K, Aruga T, Inoue K, Shimomura A, et al. Long-term survival analysis of addition of carboplatin to neoadjuvant chemotherapy in HER2-negative breast cancer. Breast Cancer Res Treat. 2020;180(3):687–94. https://doi.org/10.1007/s10549-020-05580-y.
Ando M, Yamauchi H, Aogi K, Shimizu S, Iwata H, Masuda N, et al. Randomized phase II study of weekly paclitaxel with and without carboplatin followed by cyclophosphamide/epirubicin/5-fluorouracil as neoadjuvant chemotherapy for stage II/IIIA breast cancer without HER2 overexpression. Breast Cancer Res Treat. 2014;145(2):401–9. https://doi.org/10.1007/s10549-014-2947-1.
Sikov WM, Berry DA, Perou CM, Singh B, Cirrincione CT, Tolaney SM, et al. Impact of the addition of carboplatin and/or bevacizumab to neoadjuvant once-per-week paclitaxel followed by dose-dense doxorubicin and cyclophosphamide on pathologic complete response rates in stage II to III triple-negative breast cancer: CALGB 40603 (Alliance). J Clin Oncol. 2015;33(1):13–21. https://doi.org/10.1200/JCO.2014.57.0572.
Schmid P, Cortes J, Pusztai L, McArthur H, Kümmel S, Bergh J, et al. Pembrolizumab for early triple-negative breast cancer. N Engl J Med. 2020;382(9):810–21. https://doi.org/10.1056/NEJMoa1910549.
Colombo N, Dubot C, Lorusso D, Caceres MV, Hasegawa K, Shapira-Frommer R, et al. Pembrolizumab for persistent, recurrent, or metastatic cervical cancer. N Engl J Med. 2021;385(20):1856–67. https://doi.org/10.1056/NEJMoa2112435.
Soliman M. Squamous cell carcinoma of the breast: a retrospective study. J Cancer Res Ther. 2019;15(5):1057–61. https://doi.org/10.4103/jcrt.JCRT_303_17.
Wang X, Zhang L, Luo J, Jin K, Yang Z, Meng J, et al. Postoperative radiotherapy improves overall survival in patients with primary squamous cell carcinoma of the breast. Asia Pac J Clin Oncol. 2021;17(6):454–61. https://doi.org/10.1111/ajco.13466.
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MA and KM conceived and designed the case report and wrote the main body of the manuscript. KT evaluated the biopsy and resected specimens. EK, SS, SF, TW, TM, KH, TI, HT, KS, IH, SH, IY, TO, and TF participated in the patients’ care and critically reviewed the manuscript.
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Araki, M., Matsui, K., Takagi, K. et al. A case of squamous cell carcinoma of the breast achieved a pathological complete response after dose-dense AC + dose-dense PTX. surg case rep 9, 137 (2023). https://doi.org/10.1186/s40792-023-01719-3
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DOI: https://doi.org/10.1186/s40792-023-01719-3