Introduction

Despite technological and biological advances in malignant disease management, loco-regional failure remains a frequent challenge after primary radio-(chemo)therapy as recent studies have shown for different entities [1–5]. The locoregional failure rate is 41.7% at three years after concomitant radiochemotherapy for locally advanced head and neck squamous-cell carcinoma (HNSCC) [2]. Locoregional recurrences are reported in up to 85% of the patients after radiochemotherapy for locally advanced non-small cell lung cancer (NSCLC) [6, 7]. The locoregional recurrence rate in women treated with radiochemotherapy for cervical cancer was 35% in a met-analysis of 13 trials over all stages (Ia – IVa) [8].

The intention of treatment for locoregional recurrences is manifold and depends on factors like disease type, extent of initial disease and recurrence, metastatic status, primary treatment, interval to locoregional recurrence, performance status, age of the patients and symptoms of the recurrent disease. Consequently, the goal of re-treatment ranges between palliative symptom control, prevention of symptoms due to progressive disease and curative treatment in the absence of metastatic spread.

Locoregional recurrences are a major challenge because therapeutic options are limited in many tumor sites after both primary surgical and radiotherapy treatment. The overall frequency of re-irradiation for locoregional recurrences is unknown. Even in a palliative setting of spinal metastases, re-irradiation is practiced in few patients only [9]. One important reason might be the fear or risk of normal tissue toxicity in the re-irradiation situation.

Normal tissue tolerance in the re-irradiation situation

Whereas useful guidelines do exist for normal tissue tolerance in the primary situation [10] information in the re-irradiation situation seem to be limited as only few systematic clinical analyses have been performed. Animal models have been used for many decades to evaluate normal tissue tolerance in the re-irradiation situation. While providing the opportunities of systematic study protocols, the transfer of the results from such animal studies into clinical practice must be performed with caution [11]: The simulation of previous oncological and non-oncological therapies or co-morbidities is not possible in animal studies. Due to multimodal therapies many patients e.g. receive chemotherapy before, during or after radiotherapy or are referred to a surgical resection. Combination of different treatment modalities can lead to increased toxicity. Also long-term follow-up is difficult in animal models. Less severe or more subtle toxicity cannot be evaluated in animal studies but might be of clinical relevance. Uniform dose distributions, which are most frequently used in animal studies, are not representative for modern intensity-modulated radiation therapy (IMRT) / SBRT. Lastly, small sample numbers lead to wide confidence intervals especially at the low-risk part of the normal tissue complication probability (NTCP) curve.

Regarding re-irradiation tolerance of acute responding tissue, clinical studies have shown an almost complete recovery within a few months. After full dose re-irradiation in 169 patients with unresectable head and neck cancer, De Crevoisier et al. showed that the incidence of grade 3 mucositis and dermatitis was not significantly different during the first and the second radiotherapy course [12]. In a hyper-fractionated re-irradiation series of 13 patients with recurrent or metastatic abdominal malignancies, only one patient developed grade 3 acute toxicity (abdominal pain and gastro-intestinal bleeding) requiring hospitalization [13].

With regard to re-irradiation of late responding tissue, tolerance is depending on the specific organ at risk. For epithelial and mesenchymal tissues, animal studies suggest almost complete recovery of dermal structures [14]. However clinical data show increased rates of severe toxicity and some studies have shown a dose and volume effect [15, 16]. No valid normal tissue complication probability model (NTCP) has been found. Another late-responding tissue complication is osteonecrosis. No clear dose and volume effect has been reported. In an analysis of 115 reirradiated head and neck cancer patients, Salama et al. reported a 11% osteoradionecrosis rate of the mandible after a median lifetime radiation dose of 135 Gy [17]; patients in this study had been treated with a three-dimensional conformal radiation therapy (3D-CRT). Later studies using IMRT showed that sparing of the mandible seems to reduce the rate of osteonecrosis [18, 19].

Concerning lung toxicity, good recovery was found in animal models for the acute pneumonitis phase. Recovery took place in 1–3 months and was best for treatment doses less than 75% of the tolerance dose [20]. In contrast, recovery is smaller for late pulmonary fibrosis. For clinical practice this implicates, that re-irradiation in the pulmonary region should be practiced primarily in palliative situations with short life expectancy unless sparing of the lungs is possible. No recovery has been observed in animal studies for the heart, bladder or kidney nor are there any systematic clinical analyses available. Sparing of these organs seems to be of importance.

With respect to spinal cord tolerance in the re-irradiation situation, again animal models have been used for systematic examination of spinal cord damage and recovery. Ang et al. reported a re-irradiation series to the spinal cord in 56 rhesus monkeys: only 4 of 45 animals developed myeloparesis after a first course of 44 Gy followed by re-irradiation course with 57.2 Gy after 1 and 2 years or with 66 Gy after 2 and 3 years, respectively. Recovery of the spinal cord was modelled in two ways: an optimistic model described spinal cord recovery by 76%, 85% and 101% of the initial 44 Gy dose after 1, 2 and 3 years. A pessimistic model described the overall recovery equivalent by 61% [21]. The spinal cord tolerance after re-irradiation with a single fraction radiosurgery was examined in 23 female Yucatan minipigs by Medin et al. [22]. After a uniform dose of 30 Gy in 10 fractions to the spinal cord, the minipigs were re-irradiated with single-fraction radiosurgery and the dose was positioned laterally to the spinal cord resulting in an inhomogeneous dose distribution to the spinal cord (effective dose 50 (ED50) of 19.7 Gy). Identical spinal cord tolerance for radiosurgery was observed whether or not a prior conventionally fractionated radiotherapy had been performed, which indicates full recovery of 30 Gy after 1 year.

Clinical data support the hypothesis of relevant spinal recovery. Analysing the clinical data of 40 patients retreated with conventional fractionation published in 8 different series, Nieder et al. came to the conclusion that the risk of myelopathy is low if cumulative doses to the spinal cord do not exceed 70-75 Gy (2 Gy-fractionated equivalent dose, α/β = 2 (EQD2/2)), single course doses do not exceed 50 Gy (EQD 2/2) and the interval between the two courses is not shorter than 6 months [23]. In case of re-irradiation to the spinal cord with hypo-fractionated stereotactic body radiotherapy, Sahgal et al. performed a case–control study and reported similar results to Nieder et al. [24]: the risk of RM seems to be low if the initial course does not exceed 50 Gy (EQD 2/2), the SBRT-course does not exceed 25 Gy (EQD 2/2) and the interval between the two courses is not shorter than 5 months.

Rational for using SBRT in the re-irradiation situation

To limit normal tissue toxicity in the reirradiation situation, the target volume is confined to the recurrent macroscopic tumor in most clinical situations without elective nodal irradiation or coverage of larger areas of potential microscopic spread: imaging technologies like FDG-PET are helpful in differentiation of recurrent tumor and post-surgical or radiation induced fibrosis. Highly conformal treatment planning by the use of IMRT or volumetric-modulated arc therapy (VMAT) reduces incidental exposure of normal tissue especially to high irradiation doses; however, a larger low-dose volume needs to be considered. To further reduce irradiation of normal tissue, tight safety margins around the recurrent tumor are vital and can today be realized by the use of daily image-guidance. Effective immobilization of the patient or active motion management strategies need to be applied to minimize intra-fractional uncertainties. Adaptive re-planning might be required in the situation of clinically relevant tumor regression or other anatomical changes during the treatment course.

In this context, stereotactic body radiotherapy needs to be interpreted as a combination of all above-described technologies aiming at best possible accuracy of the whole radiotherapy workflow. Also the short treatment time due to hypo-fractionated delivery of SBRT is to be considered as re-treatment often takes place in a palliative intention.

SBRT re-irradiation for spinal metastases

Radiotherapy is an essential treatment modality in the management of symptomatic vertebral metastases either for pain palliation, the prevention or control of neurological symptoms or pathological fractures. By using conventionally fractionated radiation protocols with low irradiation doses of 8 – 40Gy in 1 – 20 fractions, good pain response has been reported in the literature [25–27]. However, the achieved duration of pain control is short with a median of 3–6 months [9]. As overall survival has improved substantially in many cancer sites due to modern systemic approaches, re-treatment with conventionally fractionated RT has been used and achieves pain control in approximately 60% of the patients [28] but is performed in only few patients due to the fear of radiation induced myelopathy.

Therefore, several studies investigating SBRT for spinal metastases in preirradiated areas have been performed in the last decade summarized in Table 1[29–37]. All studies used either IMRT, a robotic stereotactic radiosurgery system or tomotherapy for highly conformal dose distributions and daily image-guidance was performed in all studies. However, substantial variability in the reirradiation doses, fractionation and assumed spinal cord recovery is seen in the literature. The median total dose (TD) of the first radiation course ranged from 30–39.2 Gy and the interval between the first course and the SBRT-retreatment ranged between 11–25 months. Median TD for re-irradiation was 30 Gy in most of the trials given in approximately 5 fractions (median 3–22). The accumulated spinal cord dose ranged between 48–83.4 Gy EQD2, indicating no consensus about spinal cord recovery.

Table 1 SBRT reirradiation for spinal metastases
Full size table

Overall, a very low incidence of myelopathy was observed. In the study conducted by Choi et al. one patient of 42 (incidence 2%) developed a grade 4 spinal cord neurotoxicity. This patient had received a spinal cord total dose of 40 Gy for metastatic breast cancer in the first course and a stereotactic radiation surgery for a 10.5 cm3 T5 recurrence with 20 Gy in 2 fractions. Dose was prescribed to the 80% isodose line. The maximal spinal cord dose in the SBRT course was 19.25 Gy [30].

Garg et al. observed 2 of 59 patients (incidence 3.3%) with grade 3 neurological toxicity related to nerve damage without loss of independent ambulatory function [32]. Mahadevan et al. described 4 patients of 60 (6.7%) with persistent or even worsening neurological symptoms, yet all of them having corresponding radiological progression [33]. There were no cases of myelopathy in the other studies.

Local control (LC) ranged from 63% to 100% and therefore seems to be very promising (details see Table 1). Damast et al. analysed the largest study population: 97 tumor sites were retreated with image-guided IMRT, resulting in a local control rate of 66% at one year. Patients in this study were either re-irradiated with 5 × 4 Gy or 5 × 6 Gy. The comparison between the two dose groups showed a significant difference in cumulative local failure after one year: 26% for the 30 Gy group and 45% for the 20 Gy group [31]. Milker-Zabel et al. reported a local control rate of 94.7% after a median follow-up of 12.3 months in 18 patients (19 lesions) re-treated with either fractionated stereotactic conformal RT or IMRT [35]. No local recurrences at the time of follow-up were observed in the analyses by Mahan et al., but only eight patients were re-treated in this study of whom one died of distant disease briefly after treatment and one 11 months after treatment [34]. Mahadevan et al. reported SBRT for patients with progressive epidural disease: at a median follow-up time of 12 months they observed a 93% rate of stable or improved epidural disease, results equally to surgery in this situation [33]. Some studies examined pain control as an endpoint: Damast et al. reported a significant, mild or no pain relief in 46%, 31% and 23% of the patients, respectively [31]. Pain relief occurred in 13 of 16 patients (81%) in the analysis of Milker-Zabel et al. [35]. Sterzing et al. reported a reduction of tumor-related pain on a visual analogue scale (0 – 10, 0 = no pain; 10 – worst imaginable pain) from a median value of 7 down to a median value of 3 after 6 weeks (p = 0.0046) [37].

In conclusion, these findings suggest that SBRT is a safe and effective treatment modality in the re-treatment situation when conventional radiotherapy is unable to be within spinal dose tolerance. However, further knowledge about spinal recovery and spinal cord tolerance to inhomogeneous SBRT dose distributions is required.

SBRT re-irradiation for lung tumors (NSCLC)

In locally advanced lung cancer, locoregional recurrence remains high in up to 85% of patients [6, 7]. Intrathoracic relapse in previously irradiated areas of patients is a frequent challenge in clinical routine. However, re-irradiation of NSCLC is performed in only 1.5% to 8.1% of all patients [7, 38, 39].

In 2011 Jeremic et al. reviewed 11 studies (two of them prospective) of conventionally fractionated external beam radiation therapy (EBRT) re-irradiation for recurrent NSCLC. The analyses showed an improved overall survival (OS) after retreatment with higher doses compared to low-dose retreatments accompanied by increased rates of grade 2–3 pneumonitis and esophagitis [40]. The rational for SBRT therefore is safely escalating the irradiation dose while minimising toxicity (Table 2).

Table 2 SBRT reirradiation for lung cancer
Full size table

Poltinnikov et al. examined the outcome and dosimetric predictors of acute esophagitis in 17 NSCLC patients receiving re-irradiation using a stereotactic body frame (SBF) [41]. Hypofractionated 3-dimensional RT was used with a median RT dose of 32 Gy (range, 4 – 42 Gy) and a median fraction size of 4 Gy (2.5 – 4.2 Gy). Multiple noncoplanar RT fields (median 6) were used in each patient to minimize spinal cord exposure. In this study re-irradiation was defined as treatment of areas that had received a full RT of 50 Gy or more 13 patients had symptoms as pain or shortness of breath. After re-treatment, 11 of these 13 symptomatic patients had improved or even complete disappearance of symptoms. Grade 1 and 2 acute esophagitis was observed in 7 patients, however symptoms disappeared within 3 months after RT. One patient suffered from pneumonitis grade 2. Notably, no grade 3 toxicities and no bronchial or vascular toxicities were observed. Radiologic response rates before death or at the time of last follow-up showed one patient with complete response, 4 patients with partial response and 5 patients with stable disease whereas 7 patients had disease progression. Median overall survival time was 5.5 months (2.5 – 30 months).

In an analysis of 51 NSCLC patients treated with the Cyberknife Radiosurgery Robotic System Coon et al. evaluated the role of positron-emission tomography in the planning and evaluation of RT treatment response. Among these patients 12 patients with recurrent disease after definitive treatment were described [42]. Re-treatment doses in these patients were three fractions of 20 Gy whereas no information was given about the initial radiation doses or treatment intervals. Treating volumes were substantially smaller compared to the study of Poltinnikov et al. with a median gross tumor volume of 14.3 cm3 compared to a median field size of 95 cm2, respectively. Local control rates and overall survival rates one year after reirradiation were 92% and 67%, respectively. Similar to the study mentioned above no G3 toxicities occurred.

Kelly et al. retrospectively reviewed the medical records of 36 patients treated with SBRT for relapse of NSCLC who had been previously irradiated to the chest [43]. In-field relapse was defined as a recurrence in an area that had received an initial dose of more than 30 Gy in the first EBRT course. The median tumor size was 1.7 cm for SBRT re-irradiation and most of the patients received 50 Gy in 4 fractions. The median initial EBRT dose was 62 Gy and the median interval between EBRT and SBRT 22 months. The median follow-up time after SBRT was 15 months in this study. The overall 2-year survival was 59% and 2-year progression-free survival was 26%: the most frequent site of failure was intrathoracic. However, only 13.6% (3 patients of 22) of these intrathoracic relapses occurred inside the SBRT field and the authors mention that planning target volume (PTV) dose coverage and/or total dose and fractionation was suboptimal in two of the three patients. At least one form of late grade 3 toxicity was observed in 12 patients (33%). Grade 3 pneumonitis was experienced by 7 patients and with 11 patients suffering from grade 2 pneumonitis the latter was the most frequent toxicity in this analysis. Three patients developed grade 3 esophagitis, two grade 3 chest wall ulcers, and two patients developed grade 3 cough. Overall no grade 4 or 5 toxicity occurred.

In conclusion, few studies with small patient numbers are available about SBRT for re-irradiation of NSCLC. Definition of re-irradiation differs among the studies as well as total doses and fractionation schemes. Overall survival seems to depend particularly on patient selection and is limited by systemic progression. All investigations do show promising local control rates that seem to exceed RT with conventional techniques. Furthermore small field SBRT for re-irradiation to the chest seems to be safe.

SBRT for reirradiation after prior SBRT has been evaluated in a retrospective analysis of 32 patients by Peulen et al. [44]. 29 patients received two SBRT courses, two received three and one patient even four SBRT courses. Re-irradiation was defined as an overlap of more than 50% of the PTV. The median interval between the two SBRT courses was 14 months and the median follow-up time from the beginning of re-irradiation 12 months, respectively. Most patients (n = 23) were treated for pulmonary metastases. The results showed eight patients with grade 3–4 toxicity and three patients suffered from grade 5 toxicity and died of massive haemorrhage. All patients with grade 4–5 toxicity were treated for centrally located tumors. Additionally, larger clinical target volumes (CTV) were associated with severe toxicity and poorer local control. LC 5 months after re-treatment was 52% with actuarial 1-year and 2-year survival rates of 59% and 43%, respectively.

Consequently, a second course of SBRT with overlapping target volumes should only be considered in cases of small recurrent tumors and peripheral location.

SBRT re-irradiation for head & neck cancer

Therapy options for locoregional recurrences in previously irradiated head and neck patients are limited. Salvage surgery is the standard treatment for small relapses [45, 46]. But with further locoregional spread, surgery alone is not sufficient. In the past patients considered inoperable often received palliative chemotherapy with low response rates ranging from 10% to 40% [47, 48]. Salama et al. reported the long-term outcome of concurrent treatment with chemotherapy and re-irradiation of patients suffering from recurrent or second primary squamous cell carcinoma of the head and neck (SCCHN) [17]. Full-dose re-irradiation in this multimodal therapy setting showed promising results for long-term survival. 115 patients had been treated with conventional RT techniques for the initial and the second course. Locoregional control and freedom from distant metastasis rate at three years was 51% and 61%, respectively. Re-treatment was highly toxic with 19 treatment related toxic events, five of them due to carotid haemorrhages. The authors came to the conclusion that re-irradiation of recurrent head and neck cancer should be limited to clinical trials.

As normal tissue toxicity was significant after conventional RT, the introduction of SBRT in the re-irradiation of head and neck cancer patients has been pursued in the last years. Several approaches for SBRT have been published recently.

Voynov et al. reviewed 22 patients re-treated with SBRT in recurrent previously irradiated SCCHN [49]. Using the Cyberknife patients were irradiated with a median single fraction dose of 5 Gy for a median of 5 fractions (details see Table 3). Re-treatment with SBRT was considered to be safe as no grade 4 or 5 toxicities or late toxicities occurred. In 2009 Roh et al. published an analysis of 36 patients with recurrent head and neck cancer re-irradiated with Cyberknife radiosurgery (RS) with three fractions of 10 or 13 Gy (34 sites of 44). The authors changed to a fractionation schedule of five fractions of 5 Gy or 8 Gy [50]. 15 patients (42.9%) showed complete tumor regression and 13 (37.1%) partial regression with median local control rates and overall survival rates after one year of 61% and 52.1%, respectively. Late adverse events were observed in three patients: two grade 4 and one grade 5 toxicity: one patient suffered from mandible bone necrosis five months after RS; the treated submandibular tumor mass abutted the mandible in that case. Two patients developed a chronic mucosal ulcer, trismus and skull-base necrosis 4–6 months after treatment. All of these patients had received a full dose radiation of 66 to 70.2 Gy in the first RT-course and a RS dose of 30 to 39 Gy in 3 fractions. The authors mentioned that these RS doses might be too high: 30 to 39 Gy in 3 fractions are equivalent to 80-130 Gy in conventionally 2 Gy-fractionated radiotherapy based on an α/β of 3 Gy. After adapting the dose and fractionation protocol to 25–40 Gy in 5 fractions (biologically equivalent dose 40–90 Gy2) no late complications have been observed so far. Besides dose and fractionation the inter-/intratreatment mucosal movement due to swallowing and respiration was mentioned as a risk for chronic mucosal ulceration.

Table 3 SBRT reirradiation for head and neck cancer
Full size table

Unger et al. reported on stereotactic RS reirradiation in 65 head and neck cancer patients [51]. Treatment sites were oropharynx (n = 13), hypopharynx (n = 8), naso-pharynx (n = 7), paranasal sinus (n = 7), neck (n = 7), and others (n = 23). Patients were treated with SBRT reirradiation definitively (n = 38) or in palliative intention due to metastatic or untreated local disease (n = 27). Nine patients had complete macroscopic resection before SBRT and 33 patients were treated with simultaneous chemoradiotherapy. Initial RT dose was median 67 Gy (32–120 Gy) and median treatment interval between initial course and SBRT 26 months. Most patients were treated with 5 x 6 Gy (2–5 × 4–12Gy) but dose and fractionation was individualized by the treating physician and total dose was commonly reduced after complete macroscopic resection. For 56 patients evaluable for response, complete, partial and no response was observed in 30 patients (54%), 15 patients (27%) and 11 patients (20%), respectively. Median overall survival was 12 months. The OS rate was 41% for definitively treated patients and the locoregional control rate 30% in these patients. The authors reported that nasopharynx site, surgical resection and higher total dose were significantly correlated with improved locoregional control and nonsquamous histology and surgical resection with improved OS. One patient died of unspecified causes 2 weeks after reirradiation, considered treatment related. Grade 4 late toxicities were observed in six patients (9%) including soft tissue necrosis, arterial bleeding, fistula formation and severe dysphagia. No association of higher RS dose or higher cumulative dose with severe late complications was seen, though quantitative analysis were limited due to the small number of events.

Heron et al. conducted a phase I dose escalation trial of re-irradiation with SBRT for recurrent SCCHN in 2009 [52]. 25 SCCHN patients were reirradiated either with 5 × 5 Gy (n = 3), 5 × 6.4 Gy (n = 3), 5 × 7.2 Gy (n = 3), 5 × 8 Gy (n = 6) or 5 × 8.8 Gy (n = 10). The authors observed treatment response in 76% of the patients. However, they could not correlate dose and tumor size to the probability of local control. The authors could not find an association between dose and toxicity due to the small number of adverse events. The highest dose applied (44 Gy) was considered to be adequate for a phase II trial. To increase efficacy of SBRT reirradiation, later on Heron et al. investigated combinations of SBRT with cetuximab [53]. Therefore they compared two patient groups in a retrospective-matched cohort study: 35 patients were treated with SBRT reirradiation alone or with additional weekly cetuximab during SBRT, respectively. Toxicities were comparable in both patient cohorts and an overall survival benefit was seen for the cetuximab arm. Feasibility and efficacy of SBRT reirradiation with or without cetuximab also was shown recently by Comet et al. [54].

In a retrospective analysis of 51 patients re-irradiated for locally recurrent nasopharyngeal carcinoma (LRNPC) Ozyigit et al. compared 24 patients treated with SBRT to 27 patients treated with 3D-CRT [55]. Median total dose in the first treatment course was 67.4 Gy (range, 59.4–70 Gy) for the 3D-CRT group and 70 Gy (range, 48–70 Gy) for the SBRT group (p = 0.1). Median total reirradiation dose was 57 Gy with a single fraction dose of 2 Gy per day using 3D-CRT. Patients in the SBRT arm were retreated with a total dose of 30 Gy delivered over 5 consecutive days. There was no significant difference in the 2-year actuarial local control rate (82% and 80% for the SBRT and 3D-CRT group, respectively, p=0.6) and the 2-year actuarial cancer-specific survival (64% and 47% for the SBRT and 3D-CRT group, respectively, p=0.4). In contrast the authors observed a significant difference in the rate of late side effects. Serious late toxicities occurred in 21% of the patients treated with SBRT compared to 48% of the patients treated with 3D-CRT. The follow-up was similar for SBRT and 3D-CRT with median 23 months and 24 months, respectively, and patient characteristics were comparable as well. Taken into account that serious late toxicities after reirradiation of LRNPC had been reported before to be as high as 15-45% [56–59] SBRT therefore seems to be an attractive treatment modality with less late side effects and shorter treatment times for the re-irradiation of LRNPC.

Vargo et al. recently reported on SBRT in recurrent, nonsquamous cell cancers of the head and neck [60]. 34 patients were re-irradiated with a median SBRT dose of 40 Gy in 5 fractions. The toxicity and quality of life were followed prospectively with a median follow-up of 10 months. The authors found promising local control rates of 77% and 59% after 6 months and 12 months, respectively. For tumors < 25 ml they reported a significant improvement of local control compared to larger tumors (> 25 ml). Acute and late grade 3 toxicities occurred in 15% and 6% of the patients respectively and no grade 4 or 5 toxicities were observed.

In conclusion, SBRT in the re-irradiation situation for head and neck tumors is a promising salvage therapy modality with encouraging local control rates and justifiable toxicities. Severe late adverse events (grade 4–5 toxicities) have been reported in some studies but are less frequent than in patients re-treated with conventional techniques. Very high single fraction doses of 10–13 Gy or higher should be avoided. Up to now, no investigations have been performed for comparison of SBRT and IMRT reirradiation. The latter has been analyzed for reirradiation of head and neck cancers over the last years showing encouraging results as well.

SBRT re-irradiation for pelvic tumors

Primary treatment of pelvic cancers such as adenocarcinoma of the rectum, prostate cancer or gynaecological tumors often includes radiotherapy. The locoregional recurrence rate in women treated with radiochemotherapy for cervical cancer is 35% over all stages [8] and 3% to 15% in patients treated for rectal adenocarcinoma [61]. Patients are frequently not considered eligible for salvage surgery especially in the case of lateral pelvic wall involvement or tumor abutment to the iliac vessels [62].

Dewas et al. presented a retrospective study of 16 patients reirradiated with Cyberknife for lateral pelvic recurrences [63]. Patients were treated for recurrences of primary anal canal cancer (6 patients), rectal cancer (4 patients), uterine cervix cancer (4 patients), endometrial cancer (1 patient) and bladder carcinoma (1 patient). Patients had been treated before with a median RT dose of 45 Gy (range, 20 Gy – 96 Gy), median interval between first RT course and retreatment was 5.1 months. In the second course using SBRT, 36 Gy in 6 fractions were delivered over three weeks. The median follow-up was 10.6 months (1.9 to 20.5 months). The authors reported a 1-year local control rate of 51.4%, median disease-free survival of 8.3 months and actuarial one-year survival of 46%. Adenocarcinoma showed a tendency for better local control compared to sqamous cell carcinoma (p = 0.09). Acute and late toxicities were limited to grade ≤ 2.

Guckenberger et al. [64] reported a series of 19 patients using SBRT for treatment of locally recurrent cervical (n=12) or endometrial (n=7) cancer; three patients were re-irradiated after adjuvant external beam radiotherapy (n=1; conventionally fractionated 50 Gy) or definitive external beam radiotherapy and brachytherapy (n=2; conventionally fractionated 50–56 Gy; brachytherapy 3 × 8 Gy and 5 × 8.5 Gy) in the primary situation. Patients were treated with 3 × 10 Gy (n=2) or 4 × 7 Gy (n=1) with dose prescription to the 65% isodose. No acute toxicity was observed but one patient developed an ileus 6 months after SBRT. All patients were locally controlled but follow-up was short ranging between 8 and 18 months. Two patients died 8 and 23 months after SBRT.

In 2009 Deodato et al. published preliminary results of SBRT in local and distant recurrences of gynaecological tumors (RGT) [65]. The analyses included 11 patients treated with SBRT of whom 6 received SBRT as a reirradiation. Previous RT doses ranged from 37.5 to 65 Gy (median 50.2 Gy). 8 patients had been pretreated with chemotherapy, and 5 patients with surgery. Re-irradiation was performed with 5 × 4 Gy, 5 × 5 y or 5 × 6 Gy on five consecutive days on base of an institutional dose-escalation protocol. PTV ranged from 4.0 cc to 273.0 cc (median, 42.0 cc). No patient showed acute toxicity or late toxicity grade > 2. With a median follow-up of 19 months (range, 2–37 months) the authors reported a 2-year local progression-free survival (LPFS) of 81.8% and a 2-year metastases-free survival of 54.5%. In a subgroup analysis the 2-year LPFS of patients treated with the highest dose of 30 Gy was 87.5% and 66.7% for the remaining population indicating better local control for the higher treatment dose.

Recently, Jereczek-Fossa et al. reported on SBRT for solitary recurrent primary, lymph node, or metastatic prostate cancer [66]. 34 patients (38 lesions) were treated with SBRT using the robotic Cyberknife system: 15 patients were reirradiated for local recurrence, 4 patients were reirradiated for anastomosis recurrence, 16 patients were treated for single lymph node recurrence and 3 patients were treated for single metastasis. Median SBRT dose was 30 Gy in 4.5 fractions and was performed as a reirradiation in 27 of the 38 treated lesions, that is the recurrent lesion was located in the previously irradiated volume. 18 patients received androgen deprivation (median duration, 16.6 months) in addition to SBRT. The median follow up was 16.9 months (range, 3 – 35.2 months). The mean interval between primary diagnosis of prostate cancer and time of SBRT was 66 months (24 – 180 months). 7 acute urinary events (18% of all treatments) were reported (3 cases of grade 1, 2 cases of grade 2, and 2 cases of grade 3 events). Grade 3 acute urinary events included macroscopic hematuria and a worsening of urinary incontinence already existing before SBRT due to prostatectomy. All but one acute urinary event developed in patients with local/anastomosis recurrence. Only one acute rectal grade 1 event occurred (3% of all patients). The authors observed 7 late urinary events (3 cases of grade 1, 2 cases of grade 2 and 2 cases of grade 3 events). Grade 3 late urinary events included transient macroscopic hematuria and a persistent worsening of urinary incontinence, that occurred in the same patient who had an acute grade 3 event. These late urinary toxicities were observed in patients treated for local recurrence to the prostate region and patients treated for lymph node recurrences. Two late rectal events were reported (1 grade 1 and 1 grade 2, not otherwise specified). Biochemical response was reported in 32 of 38 lesions. Considering lesions treated with SBRT alone (no concomitant systemic therapy), a complete PSA response was observed in 9 lesions (56.25%) and a partial PSA response in 4 lesions (25%). Disease progression was reported in 14 lesions after a median of 10 months (range, 2 – 17 months) but in-field progression occurred in only 3 lesions. Time to progression was 11 months when androgen deprivation was added to SBRT and 10 months without. Progression-free survival rate was 42.6% at 30 months. With regard to these data SBRT as retreatment for locally or regionally recurrent prostate cancer seems to be practicable with good in-field tumor control and a low toxicity rate. Further analyses are needed to validate these findings and to identify patients with best benefit of SBRT treatment.

Defoe et al. analyzed 14 patients treated with SBRT for presacral recurrent adenocarcinoma of the rectum [67]. All patients had been previously irradiated with a median of 50.4 Gy (range, 20 – 81 Gy). The treatment dose for reirradiation was 36 Gy in 3 fractions for 11 patients and 3 patients were treated with a single fraction of 12, 16 or 18 Gy. Median tumor volume was 52.5 cc (range, 19 – 110 cc). Time of median follow-up was 16.5 months (range, 6 – 69 months). The one- and two-year LC rates were 90.9% and 68.2%, respectively. Overall survival was 90% after one year and 78.8% after two years. Neither dose and fractionation nor tumor volume were significantly correlated with LC and OS. No grade 3 or 4 genitourinary, gastrointestinal, or neurologic toxicities occurred. One patient suffered from a recurrent pelvic abscess after SBRT, with need for drainage. Seven patients (50%) reported pain with recurrence before retreatment with SBRT and four of these patients (57.1%) had no pain after SBRT without any need for analgetic medication. SBRT in this small patient cohort has been an efficient and well-tolerated treatment for presacral recurrent rectal cancer.

In summary the role of SBRT in the reirradiation of pelvic recurrences is currently poorly investigated. Recurrences from gynaecological tumors are most frequently treated in palliative intention with chemotherapy [68]. In case of lateral pelvic tumor recurrence, retreatment with surgery is rarely possible due to pelvic wall or iliac vessel involvement. Similarly, patients suffering from presacral recurrence of rectal cancer often are not amendable for curative resection, but even without treatment do have a median survival of up to 8 months [69]. If no treatment is offered or even if chemotherapy alone without any local treatment is given, these patients develop local complications particularly pain with dramatic decrease of their quality of life [70]. SBRT therefore might be a well-tolerated and short treatment to palliate local symptoms and achieve improved local control. In recurrent prostate cancer after primary treatment, androgen deprivation is indicated for most patients. As surgery is rarely performed in these patients due to advanced age and tendency for systemic dissemination, SBRT might be a feasible and safe treatment supplement to systemic hormonal therapy.

Conclusion

Locoregional recurrences are a frequent challenge in oncology. Nevertheless, conventional radiotherapy for re-irradiation has been performed in only few patients due to the risk of normal tissue toxicity. SBRT may allow a paradigm shift in this important clinical setting, where alternative treatment options are limited.

The recurrent macroscopic tumor is precisely visualized using modern multimodal imaging technologies and the target volume is confined to gross tumor volume without inclusion of elective nodal regions or volumes of potential microscopic tumor extension. Safety margins are minimized by accurate, image-guided treatment delivery and highly conformal treatment planning further reduces exposure of normal tissue. SBRT combines these technologies and allows hypo-fractionated dose escalation in these small target volumes. Shorter treatment times of SBRT are a considerable advantage in this clinical setting as re-treatment often takes place in a palliative intention.

This small volume but intensified SBRT re-irradiation has shown promising results with high rates of local tumor and symptom control and simultaneously low rates of severe normal tissue toxicity. Most mature results have been described for SBRT re-irradiation of vertebral metastases with high rates of pain and local control; toxicity, especially radiation induced myelopathy, was low in all series. Re-irradiation in the head-and-neck, thoracic and pelvic region has gained interest with availability of SBRT and preliminary clinical results are promising.

However, most if not all data available about SBRT re-irradiation are based on small single institution studies with limited follow-up. The details of SBRT practice in terms of patient selection criteria, total irradiation dose, fractionation, normal tissue dose constraints and target volume concept varied substantially between studies. Patient selection bias and publication bias are additional potential confounding factors. Consequently, prospective studies are required for standardization of the promising concept SBRT in the re-irradiation setting.

Acknowledgements

This publication was funded by the German Research Foundation (DFG) and the University of Wuerzburg in the funding programme Open Access Publishing.