Intraoperative radiotherapy boost as part of breast-conservation therapy for breast cancer: a single-institution retrospective analysis

Following breast-conserving surgery (BCS), radiotherapy (RT) reduces local recurrence and breast cancer mortality [1]. There is an additional reduction in local recurrence with the delivery of a focal RT boost to the tumor bed following whole-breast irradiation (WBI) [2]. External-beam RT is the most commonly used technique for adjuvant treatment of breast cancer; however, other modalities have been increasingly explored.

Intraoperative RT (IORT) is one such modality that has been used as a substitute for both WBI as well as in the boost setting [3, 4]. Randomized data for the former setting include the TARGIT‑A and ELIOT trials [5, 6], and the accruing TARGIT‑B (NCT01792726) and recently published HIOB (NCT01343459) [7] trials. IORT is delivered by means of electrons or 50-kV X‑ray therapy as a single fraction during the course of BCS.

IORT has been primarily analyzed for patients with low-risk features. The sole use of IORT as a substitute for WBI was critically questioned. The current data demonstrate a tendency for higher local recurrence rates; therefore, the authors recommend critical patient selection for the use of IORT alone when omitting WBI [8].

IORT has several theoretical advantages, in particular “same-day approach” settings in addition to increased patient convenience [9]. IORT allows for increased skin sparing and avoids potential tumor repopulation between the completion of surgery and initiation of WBI. It also allows for a more accurate assessment of the dimensions of the operative tumor bed and, hence, potentially reduces irradiated volumes. In comparison to the scar boost using electrons, the risk of a potential target miss due to problems with identification of the tumor bed can be avoided. Notably, current guidelines allow a safe and reproducible boost definition even after the oncoplastic surgical procedures [10].

In the absence of published data from randomized trials of IORT as a boost, reporting institutional experiences is necessary. The goal of this single-institutional retrospective study was to describe outcomes and toxicities of IORT boost using 50-kV X‑rays for early breast cancer.

Altogether, 214 patients were analyzed for this investigation. Table 1 displays clinical characteristics of this population. Most patients had T1 disease (n = 124) and were clinically node negative. Only few patients had high-grade and/or triple-negative disease.

Table 2 shows treatment-related parameters. The vast majority of patients underwent sentinel node biopsy and 32 (15%) required re-resection for initially positive margins. Re-resection for R+ was performed as part of the first surgery in 13 patients. The remaining 19 patients underwent a second procedure with re-resection. IORT was performed as part of the first surgery in each case.

After re-resection, all tumor bed margins were clear. Nine (4.2%) and 48 (22.4%) patients underwent neoadjuvant and adjuvant chemotherapy, respectively. The vast majority (n = 187, 87.4%) received conventionally fractionated WBI, and the median time from BCS to WBI was 54.5 (range 21-325) days. IORT was successfully delivered in all cases, to a median dose of 20 Gy using applicator surface median 35 mm (range 20–50 mm). WBI was applied using standard tangential treatment portals in most cases (94.2%). Only 12 patients (5.7%) received WBI using IMRT/VMAT. The median WBI dose was 50 Gy (range 29.4–50.4 Gy); 2 (0.9%) did not receive WBI. These patients renounced WBI explicitly due to own request or advanced age, while guaranteeing a close clinical follow-up and adjuvant systemic therapy. All patients with pN2a (n = 3) and 8 patients with pN1a (since 2017) received normofractionated RT to the regional lymph node levels with 50.4 Gy in 28 fractions.

Table 3 demonstrates the toxicity profile of the study population. No patients experienced grade 4 events, and grade 3 toxicities after WBI were limited to 17 (8%) cases of radiation dermatitis. Postoperative toxicities occurring before WBI were mild, no case of grade 2 seroma/hematoma occurred. Late toxicities were also mild, with just one case of a late grade ≥ 2 event.

With 28 months (range 2–59 months) median follow-up, two recurrences in the tumor bed and one contralateral breast event have occurred. The 3‑year ipsilateral breast recurrence rate (IBRT) and contralateral breast recurrence (CBE) rate were 1.8% (95% CI 99.5–92.7%) and 0.6% (95% CI 99.9–95.9%), respectively. The 3‑year DMFS and OS rates were 96.8% (95% CI 98.8–91.6%) and 98.7% (95% CI 99.7–94.7%), respectively (Figs. 1 and 2).

Lastly, binary correlation analysis did not reveal statistically significant associations between any particular variables (in particular applicator size, systemic therapy, neoadjuvant chemotherapy) and the risk of acute and chronic toxicity. Only hypofractionated WBI (Spearman rank correlation r_s = −0.197, p = 0.004, Cohen’s effect size: weak to moderate) was significantly correlated with increased occurrence of acute dermatitis.

This single-institutional retrospective investigation demonstrates preliminary results on IORT boost with 50-kV photons regarding the feasibility, mild toxicities, and association with appropriate early oncological outcomes for breast cancer.

There are few reports on the use of IORT as a tumor bed boost. Wenz et al. reported a clear correlation between breast volume, applicator size, and degree of fibrosis with comparable techniques [11]. The long-term analysis from the same institution after 78 months in 400 patients demonstrated on the one hand low in-breast and axillary node recurrence rates and on the other hand, few high-grade adverse events, mostly fibrosis and pain. The majority of late side effects occurred during the first 3 years after IORT and WBI [12]. In light of this, given the short follow-up time in our collective with median 28 months, chronic toxicity may be underrepresented. Furthermore Wenz et al. reported the development of higher-grade fibrosis grade II–III after a median of 36 months as an effect of a possibly shorter interval (< 30 days) between IORT and WBI [13]. These findings and recommendations to keep an interval between IORT and WBI of about 5–6 weeks were integrated into our clinical routine early on. In our cohort only 4.2% (n = 9) of patients had an interval of < 30 days and 12.7% (n = 27) of patients had a cumulative interval of < 35 days with a median interval of 54 days between IORT and WBI.

The largest experience is available for the IORT using electrons (IOERT) prescribed such a boost [14]. IOERT also offers satisfactory oncological outcomes in groups with a high risk for local relapse, like TNBC [15]. In a retrospective analysis comparing IOERT as an anticipated boost to patients treated with conventional percutaneous boost, improved local and locoregional control could also be shown in locally advanced stages (initial clinical stages II and III) after neoadjuvant chemotherapy [16].

When considering local antitumor efficacy, it is important to consider that the IORT boost with a single dose of 20 Gy at the surface of the IORT applicator using 50-kV photons is attenuated to 5 Gy at 1 cm from the edge of the excision cavity. Analyses of wound fluid from patients treated with IORT suggest that IORT has a positive effect on the tumor microenvironment. Noteworthily, a high single IORT dose elicits impact beyond the direct killing of residual tumor cells, because of influencing the microenvironment in the wound fluid through the interruption of the proliferative cytokine cascade and downregulation of the local expression of epidermal growth factor [17, 18]. Taking into account the limited spatial range and significant dose attenuation to 5 Gy at 1 cm depth from the edge of the excision cavity, it is questionable what effect level and efficacy would be expected.

The comprehensive adoption of a reconstructive approach during breast-conserving surgery is mostly termed oncoplastic surgery. This concept has been introduced to allow wide excision for BCS and simultaneously minimize cosmetic impairment [19]. Notwithstanding clip marking of the tumor bed, postoperative delineation of the tumor bed after oncoplastic surgery can be challenging and represents a risk for geographic miss [20, 21]. IO(E)RT is commonly performed prior to the reconstruction and/or remodeling procedure and enables precise and accurate dose delivery to the tumor bed.

On the basis of a low α/β ratio for breast cancer in the range of 3.5 to 4 [22‐24], hypofractionation has been studied by a number of prospective phase III trials [25‐31]. In our analysis, only 11.7% (n = 25) of patients received hypofractionated WBI. The use of IOERT boost (11.1 Gy) and hypofractionated WBI (40.5 Gy in 15 fractions) was studied within the non-randomized HIOB study [7]. The HIOB trial demonstrated an excellent acute and late toxicity profile without cosmetic impairment after 3 years of follow-up [7]. Grade II–III fibrosis in the tumor bed occurred in 6% (range 3–8.9) of patients [7]. In comparison, in our cohort, hypofractionated WBI was significantly correlated only with acute dermatitis. Another non-randomized phase II study evaluated hypofractionated WBI of 36.63 Gy in 11 fractions, followed by a sequential percutaneous boost of 13.32 Gy in 4 fractions [32]. The estimated 5‑year locoregional and distant control rates were 98% in each case. Secondary endpoints were acute and late toxicity, which were assessed with grade II–III in 30%/10% and 1%/3%, respectively [32]. Another approach to shorten overall treatment time is to use a simultaneous integrated boost (SIB). Data from three randomized controlled trials comparing normofractionated WBI with a SIB to normofractionated WBI with sequential boost have been published recently [33‐35]. Oncological outcomes were comparable, and two of the three trials showed reduced acute toxicity with the SIB approach [33, 35].

Our findings are similar to those of existing data using IORT as a boost, demonstrating a 5-year IBTR rate of ≤ 5%, along with a similar rate of acute grade ≥ 3 and late grade ≥ 2 toxicities [36‐43]. The rate of postoperative complications was also low in this study and numerically comparable to existing data, corroborating that IORT is safe from this standpoint as well. Our data compare favorably in terms of chronic toxicity with no case of fibrosis grade ≥ II (Table 3).

Despite these encouraging results, limitations of this investigation should be acknowledged. This first relates to the single-institutional and retrospective nature of this study, including careful patient selection for IORT, thus limiting applicability to other patient populations. Additionally, newer data have now provided more detailed information about the limited benefit/risk ratio for applying boost treatments to low-risk patients. Additionally, the short follow-up of this study limits the light shed onto toxicity events and recurrences/survival that occur in the long term. To this extent, obtaining longer-term results from this and other cohorts is essential. An important potential limitation of single-shot IORT is the ability to sufficiently cover adequate target volumes with adequate doses.

In summary, this investigation provides preliminary corroborative data for the use of IORT in the boost setting. Along with a substantially low rate of postoperative complications, there were altogether few higher-grade toxicities along with appropriate outcomes for early breast cancer. These results should be corroborated by the eventual publication of randomized studies such as TARGIT‑B.