Invasive ductal carcinoma in a fatty breast
Interventional radiology
Case TypeClinical Cases
AuthorsPY Marcy, A Chaturvedi, C Bailet, JM Gaillochon, PY Bondiau
Patient81 years, female
The patient underwent hormonotherapy (Letozole: 2.5mg daily) for three months, before radiofrequency ablation (RFA), allowing a decrease in tumour size from 24mm x 17mm to 18mm x 15mm, on high frequency ultrasound. MRI (Fig. 2) and conventional mammograms (Fig. 6b) were performed before the RFA procedure.
Percutaneous radiofrequency lumpectomy was performed after written informed consent, under sedo-analgesia, using US guidance. RF was applied between a large neutral electrode, leading to a high electric field line density in the region of the needle tip, and the 1.5mm x 1.1mm non-insulated needle tip ablation electrode. Thermal lesions were produced with RF power 30 Watts, at a frequency of 500KHz, for an application time of 12 minutes (Elektrotom 104HF Thermo- Berchtold Medizinelektronik Gmbh, Tuttlingen Germany). Controlled interstitial needle perfusion of isotonic sterile saline solution (0.9% NaCl) was applied using an infusion pump (Perfusor Secura FT, BRAUN). The current flowed from the uninsulated perfused electrode implanted in the tumour to a grounding pad applied externally to the skin. A feedback system controlling RF power application and saline infusion of the needle maintained power delivery.
The axillary needle (= RFA probe), penetrating the 18mm hypoechogenic breast tumour is shown in Figure 3, its long axis staying parallel to the overlying skin. Ablation zones are visualised as cone-shaped hyperechogenic areas around the needle tip, experiencing the temperature increase (Fig. 4a). The increase reflexivity is due to the development of microbubbles due to boiling fluid, and the increase in US velocity.
Follow-up was as follows. The patient underwent conventional radiation therapy of the breast (35Gy + superimpression on the nipple area). Clinical examination disclosed a 35mm x 45mm painless firm treatment mass in the upper right breast within the first six months. Breast imaging (MRI, US, mammogram) was performed at 24h, 1 month, 3 months and every 3 months during the first year (Figs 4b,5,6,8). At three months, US-guided percutaneous biopsy of the RF-treated breast and fine needle aspiration cytology of the oil cyst were performed, showing no evidence of tumour persistance or recurrence (Fig. 7).
The patient was still free of disease at 8 months follow-up (Fig. 8). The CA15-3 level has decreased steadily from 42 units to 35 units and then to 31 units (Normal <25 units).
Radiotherapy (50Gy) prevents local recurrence of breast cancer after breast-conserving surgery. In patients who receive an additional dose of 16Gy of radiation to the tumour bed, the risk of local recurrence is further reduced, especially in patients younger than 50 years of age. The incidence of tumoral recurrence after lumpectomy without radiation seems to be directly correlated to the size of the tumour, but also decreases with advancing age.
In elderly women (>70 years old) the disease is at stage I-II in 92% of cases. Comorbid conditions that may influence treatment planning are reported in up to 50% of the patients. Rates of locoregional recurrence decline with age, indicating that the benefit of radiation therapy would be more limited. The locoregional recurrence at 4-years median follow-up is 5%, and occurs almost exclusively at the original tumoral bed.
The rate of distant metastases is 11% (mainly in the lung), and the 5-year and 10-year disease specific survival rates are 96% and 91%.
Because of the increasing use of screening mammography, most women with breast cancer now present with small tumours that can be removed with surgical or percutaneous minimally invasive procedures (1), which preserve the breast and the woman's body image, as well as allowing rapid recovery.
As the sentinel lymph node mapping procedure, rather than routine axillary node dissection, becomes the standard of care, the challenge for interventional radiologists is to treat the primary tumour without surgery, with a minimally invasive percutaneous treatment.
Alternatives to traditional surgery and radioguided surgery that are currently being explored include different approaches; their goal is either to excise the primary tumour percutaneously (Mammotome, MIBB, ABBI, site select system), cool it (cryotherapy), heat it with focused ultrasound, laser interstitial therapy or RFA, or focally deliver radiation therapy via the Mammotome.
Böhm et al. (2) explored the in vitro feasibility of saline-enhanced RFA for the treatment of breast tumours. Interstitial perfusion is important to improve the electrical conditions for ablation by the spread of hot liquid. The irregular expansion of RF lesions may be due to the inhomogeneous tissue impedance resulting in electrical inhomogeneities and irregular heating; the presence of multiple ductal structures, which may result in possible propagation of the hot emulsion into the surrounding tissue; or a high infusion rate of interstitial saline solution. The authors concluded that percutaneous thermolysis is feasible with a better control of lesioning with a low saline interstitial infusion rate. Optimal NaCl concentration (38.5% saturated solution) of the interstitial saline solution may increase energy deposition, tissue heating and induced coagulation.
We think that the problems of irregularity in thermolysis/RFA tend to reduced in fatty breast tissue ("oven effect" and rare ductal structures) and in the early-stage neoplastic nodules (size <30mm) without microcalcifications found in older women.
Invasive lobular carcinoma may not be treated under US monitoring because of discrepancies between imaging and histogical spread.
The first study of feasibility of RFA in human breast tumours was reported in 1999 by Jeffrey et al., who treated five women with locally advanced breast cancer (4-7cm). In four patients, complete ablation was found in an area of 8-18mm diameter; the tumour in the fifth patient had a small area of viable cells lining a cyst. The authors concluded that PRA may be most effective for the treatment of cancers smaller than 30mm (3).
Izzo et al. reported a 96% complete necrosis rate in tumours less than 30mm, under US control of T1 and T2 breast carcinomas (4). One patient had a microscopic focus of viable tumour adjacent to the needle shaft site. The only complication was a full thickness burn in one patient whose tumour was immediately beneath the skin.
Tumour recurrence may be detected by clinical examination and multimodal imaging (US, Mammogram, core biopsy and MRI). Particular attention should be paid to the original tumour bed, and along the needle tract (as described in patients with RFA-treated hepatocellular carcinomas).
An increase in the size of the lesion on mammogram/US/MRI or nodular enhancing areas on MRI may suggest tumour recurrence at follow-up (5). Percutaneous biopsy may give histological proof.
MRI is very sensitive to tissue-water mobility and distribution; and the temperature dependence of MR relaxation parameters such as T1 relaxation times and diffusion coefficients make it particularly suitable for the demonstration of thermal energy deposition in breast tissue. Potentially, the use of real-time MR imaging to monitor RFA in breast carcinomas, and the availability of open-access breast coils may facilitate complete tumour ablation with MR-compatible needles, in the future. Moreover, MRI may depict any further recurrence as well as US/Mammogram/clinical examination (5).
KEY POINTS
1. Definitive RFA should never be undertaken without histological confirmation of malignancy.
2. The objective of RFA ablation is clearance of the local disease with a margin of clear tissue, and to achieve an acceptable cosmetic outcome, in elderly patients with early stage breast cancer T1-2N0M0.
3. For successful RFA treatment, the breast carcinoma needs to be of the invasive ductal type, a centrally located solid mass without any microcalcifications, less than 30mm in diameter, and distant to the skin and the pectoralis muscle.
4. RFA may be an alternative treatment option to lumpectomy in elderly patients with comorbid conditions, who fear surgery. The procedure is cheaper and much less invasive than surgery (no scar).
5. Typically, percutaneous RFA-lumpectomy under US/MRI guidance is given as an outpatient procedure, with the patient lightly sedated. That point is of utmost importance for elderly women, handicapped by mobility and/or transportation problems, who fear surgery.
[1] 1. Hall-Craggs MA. Interventional MRI of the breast: minimally invasive therapy. Eur Radiol 2000;10:59-62. (PMID: 10663718)
[2] 2. B怀hm T, Hilger I, Müller W, Reichenbach JR, Fleck M, Kaiser WA. Saline- enhanced radiofrequency ablation of the breast tissue. An in vitro feasibility study. Investigate Radiology 2000;35:149-57. (PMID: 10719824)
[3] 3. Jeffrey SS, Birdwell RL, Ikeda DM, Daniel BL, Nowels KW, Dirbas FM, Griffey SM. Radiofrequency ablation of breast cancer: first report of an emerging technology. Arch Surg 1999;134;1064-8. (PMID: 10522847)
[4] 4. Izzo F, Thomas R, Delrio P, Rinaldo M, Vallone P, De Chiara A, Botti G, D'Aiuto G, Cortino P, Curley SA. RFA in patients with primary breast carcinoma: a pilot study in 26 patients. Cancer 2001;92(8):2036-44. (PMID: 11596017)
[5] 5. Ralleigh G, Walker AE, Hall-Craggs MA, Lakhani SR, Saunders C. MR imaging of the skin and nipple of the breast: differentiation between tumour recurrence and post-treatment change. Eur Radiol 2001;11(9):1651-8. (PMID: 11511886)
URL: | https://www.eurorad.org/case/1774 |
DOI: | 10.1594/EURORAD/CASE.1774 |
ISSN: | 1563-4086 |