- Open Access
Prospective phase II study of preoperative short-course radiotherapy for rectal cancer with twice daily fractions of 2.9 Gy to a total dose of 29 Gy - Long-term results
© Guckenberger et al; licensee BioMed Central Ltd. 2009
- Received: 24 August 2009
- Accepted: 21 December 2009
- Published: 21 December 2009
To evaluate clinical outcome after preoperative short-course radiotherapy for rectal cancer with twice daily fractions of 2.9 Gy to a total dose of 29 Gy and adjuvant chemotherapy for pathological stage UICC ≥ II.
118 patients (median age 64 years; male : female ratio 2.5 : 1) with pathological proven rectal cancer (clinical stage II 50%, III 41.5%, IV 8.5%) were treated preoperatively with twice daily radiotherapy of 2.9 Gy single fraction dose to a total dose of 29 Gy; surgery was performed immediately in the following week with total mesorectal excision (TME). Adjuvant 5-FU based chemotherapy was planned for pathological stage UICC ≥ II.
After low anterior resection (70%) and abdominoperineal resection (30%), pathology showed stage UICC I (27.1%), II (25.4%), III (37.3%) and IV (9.3%). Perioperative mortality was 3.4% and perioperative complications were observed in 22.8% of the patients. Adjuvant chemotherapy was given in 75.3% of patients with pathological stage UICC ≥ II. After median follow-up of 46 months, five-year overall survival was 67%, cancer-specific survival 76%, local control 92% and freedom from systemic progression 75%. Late toxicity > grade II was observed in 11% of the patients.
Preoperative short-course radiotherapy, total mesorectal excision and adjuvant chemotherapy for pathological stage UICC ≥ II achieved excellent local control and favorable survival.
- Rectal Cancer
- Planning Target Volume
- Total Mesorectal Excision
- Late Toxicity
- Biological Effective Dose
Multimodality treatment for rectal cancer is well established for more than 20 years after adjuvant radiochemotherapy has shown to improve overall survival . Significant progress has been made in surgical, radiation and medical therapy: total mesorectal excision (TME) has become a surgical standard  and neoadjuvant radiotherapy (± chemotherapy) improved outcome compared to postoperative treatment.
However, there is considerable debate regarding the best approach to preoperative therapy. The CAO/ARO/AIO-94 trial reported improved local control with decreased toxicity after preoperative compared to postoperative radiochemotherapy : this so-called long-course treatment delivers conventionally fractionated radiotherapy of 45 Gy to 50 Gy and delayed surgery is performed to allow for tumor regression. So-called short-course preoperative radiotherapy with 5 fractions of 5 Gy and immediate surgery has shown to improve survival compared to surgery alone in the pre-TME era . Combined with documented quality controlled TME-surgery, short-course preoperative radiotherapy decreased rates of local recurrence, however, no survival benefit was observed . A recent update of this Dutch TME trial confirmed the benefit regarding local control; however, systemic disease progression limited survival. One Polish study compared preoperative short-course radiotherapy with preoperative long-course radiochemotherapy and no differences in survival, local control, late toxicity and quality of life were observed [6, 7].
We report on a phase II study for rectal cancer clinical stage UICC ≥ II with neoadjuvant short-course radiotherapy followed by immediate TME surgery. The protocol differs in two important aspects form the original Swedish and Dutch protocol. Because the high single fraction dose of 5 Gy remains an issue of concern in short-course preoperative radiotherapy, a modification of the 5 × 5 Gy fractionation was introduced: a total dose of 29 Gy was delivered with twice daily fractions of 2.9 Gy; an interval of at least 6 hours between the daily fractions was mandatory to allow recovery of normal tissue and the total treatment time of one week was maintained. Additionally, adjuvant chemotherapy was indicated in cases of pathological stage UICC ≥ II aiming at decreasing rates of systemic progression. This article reports the long-term clinical results of the 118 patients treated between 2000 and 2007.
It was the aim of this trial, to evaluate the clinical outcome of short-course preoperative radiotherapy with adjuvant chemotherapy for rectal cancer with UICC ≥ II in a prospective fashion. Patients with surgery planned at the University Hospital Würzburg or one affiliated academic teaching hospital were eligible for this prospective phase II study. Patients needed to have pathological proven rectal cancer UICC stage II to IV at any age and Karnofsky index > 70. The upper limit of the lower tumor border was 15 cm from the anal verge. Inclusion of stage IV was limited to patients who presented with potentially resectable hepatic metastases.
Neoadjuvant radiochemotherapy was chosen instead of participation in this trial if the surgeon and radiation oncologist expected that downstaging could 1) achieve sphincter preservation in patients with very low tumor location or 2) improve complete resectability in patients with cT4 tumors. Patients with invasion of the sphincter or very low tumor location, where no sufficient downstaging for sphincter preservation after neoadjuvant radiochemotherapy was assumed, were eligible for this trial.
Prior irradiation of the pelvic region and severe comorbidities, which contraindicate adjuvant chemotherapy, were exclusion criteria. All Patients provided written informed consent upon participation and the protocol was approved by the institutional review board of the University Hospital Würzburg.
Study Design and Treatment
Staging of the patients required colonoscopy of the rectum and entire large bowel and computed tomography of the pelvis, abdomen and chest. Endorectal ultrasound was performed for staging of T and N status; pelvic MRI was not routine practice at the time, when this protocol was developed.
A belly board was used for patient set-up in prone position at radiotherapy treatment planning and delivery. Treatment planning was based on computed tomography. The superior border of the planning target volume (PTV) was the top of the fifth lumbar vertebra in patients with cN+ and/or tumor location in the proximal third of the rectum and the top of the first sacral vertebra in patients with cN- and tumor location in the middle and lower third of the rectum. The inferior border of the PTV was 1 cm below the pelvic floor and the perineum was included if abdominoperineal resection (APR) was planned. In axial directions, the PTV encompassed the rectum, presacral space and the pelvic lymphatics. Radiotherapy was based on three dimensional conformal treatment planning; a three field technique with one posterior field and two wedged lateral fields was applied using 18 MV photon energy for the lateral fields and 6 MV photon energy for the posterior field. A total dose of 29 Gy was prescribed with twice daily fraction doses of 2.9 Gy; interval between the daily fractions was at least 6 hours. Radiotherapy treatment was always delivered within one week starting on Monday to Friday. This total dose of 29 Gy equates the standard protocol of 5 × 5 Gy according the LQ-model with an α/β-ratio of 10 Gy for the tumor to compensate for the lower single fraction dose.
Surgery was planned in the week immediately after radiotherapy. Patients underwent radical resection of the rectal cancer with total mesorectal excision (TME). Surgery was performed at the Department of Surgery of the University Hospital Würzburg (n = 95) or an affiliated academic teaching hospital (n = 22).
Adjuvant chemotherapy was planned for patients with pathological stage UICC ≥ II. 5-Fluorouracil (5-FU) (425 mg/m2) as bolus infusion and folinic acid (25 mg/m2) was given for five days/cycle and six cycles were planned every 28 days.
Patients were routinely followed up at 6 weeks, every three months for the first two years, every six months for another three years and once annually thereafter. Acute toxicity during treatment and within the first 6 months was scored using the CTC 2.0 and later the CTCAE v3.0; chronic toxicity more than 6 months after treatment was scored with CTCAE v3.0.
Calculation of biological effective doses
where n is the number of fractions and d the single fraction dose (Gy).
with a daily repair rate γ/α of 0.6 Gy, which is a measure for how much dose is lost per day due to tumor tissue repair. A proliferation delay Tk of 7 days was used (Colorectal Cancer Collaborative Group, 2001), which was subtracted from the overall treatment time T. No tumor tissue repair was assumed for a total treatment time of 5 days and both T and Tk were set to 0 days.
Survival and recurrence data were calculated by the Kaplan-Meier method using Statistica v7 software (Statsoft, Tulsa, OK, USA). Overall survival (OS), cancer-specific survival (CSS), disease-free survival (DFS), local control (LC) and freedom from systemic progression (FSP) were calculated. Results for different subgroups were compared using the log-rank statistic. Results with p < 0.05 were considered as statistically significant.
Treatment and toxicity
Baseline characteristics of all 118 patients
Age median/range (years)
64/30 - 84
Clinical tumor stage no. (%)
Clinical nodal stage no. (%)
Clinical UICC stage no. (%)
Tumor location no. (%)
Upper third of rectum
Middle third of rectum
Lower third of rectum
RT according to protocol no. (%)
Interval between end of RT and surgery median/range (days)
3/3 - 10
Type of surgery no. (%)
Protective stoma after LAR
Pathological tumor stage no. (%)
Pathological nodal stage no. (%)
Pathological UICC stage no. (%)
Resection status no. (%)
R1 (all local)
R2 (all systemic)
Number of removed lymph nodes Median/range
Indication for chemotherapy no. (%)
Actually performed chemotherapy no. (%)
5-FU & LV chemotherapy
Number of patients (%)
Administration of adjuvant chemotherapy was indicated in 81 patients with pathological stage UICC II - IV. However, chemotherapy was delivered in only 61/81 (75.3%) of these patients. 35 patients were treated with 5-FU and folinic acid, 15 patients with FOLFOX4 and 11 patients with other protocols. Pre-treatment performance status was significantly better in the subgroup treated with adjuvant chemotherapy compared to the subgroup not receiving adjuvant chemotherapy (p = 0.002). Additionally, postoperative complications were observed more frequently in the subgroup, which was not treated with adjuvant chemotherapy (41% versus 18%).
Severe late toxicity grade > II CTCAE v3.0
Number of patients (%)
Late anastomotic leakage
Small bowel ileus
Survival and recurrence
Five-year CSS was 76% for all patients (Fig. 1). Thirty-six patients died during follow-up and cause of death was progression of rectal cancer (n = 19), intercurrent disease (n = 14), and unknown (n = 3). Time to death was median 15 months and 31 months for patients dying from rectal cancer or from intercurrent disease, respectively; all patients, who died from intercurrent disease, had no evidence of recurrent tumor. Five-year DFS for all patients excluding UICC stage IV was 65% (Fig. 1). Five-year DFS was 78%, 71% and 52% for UICC stage I, II and III, respectively.
Five-year FSP was 75% for all patients and 80% for patients after exclusion of stage UICC IV (Fig. 2); median time to systemic progression was 23 months.
Preoperative short-course radiotherapy with five fractions of 5 Gy is well established to increase survival after conventional surgery  and to increase local control after TME surgery [5, 8]]. This study modified the short course regime in two aspects: radiotherapy was delivered with twice daily fractions of 2.9 Gy to a total dose of 29 Gy in one week immediately prior to surgery and adjuvant chemotherapy was planned for UICC stage ≥ II.
After a sufficiently long follow-up of median 46 months, five-year OS was 67% in our patient cohort. This compares well to data from the literature. The Swedish Rectal Cancer Trial reported a five-year OS of 58% for the group treated with preoperative radiotherapy despite a more favourable distribution with regard to tumor stages . The distribution of the UICC stage in the Dutch TME trial was similar to our study and five-year OS was 64% after preoperative radiotherapy and quality controlled TME surgery ; that study had a higher proportion of patients with low tumor location. The recently published MRC CR07 trial reported a five-year OS of 70% ; adjuvant chemotherapy with 5-FU and leucovorin was allowed and given to 40% of the patients after preoperative radiotherapy and TME surgery. After preoperative long-course radiochemotherapy in the German Rectal Cancer Trial, five-year OS was 76% .
Similar to the two randomized trials using short-course preoperative radiotherapy followed by TME surgery [4, 5], local control was high in the present study with a five-year local control rate of 92%. Six local recurrences were observed and R1 resection had been performed in two of these six patients. Interestingly, two local recurrences developed late: 4 and 5 years after treatment. This observation of late local recurrences after more than 3 years is in agreement with Peeters et al. , whereas late local recurrences were rare in the Swedish Rectal Cancer Trial  and the MRC CR07 trial . Despite high rates of local control, about 25% of the patients suffered from systemic progression of disease resulting in DFS of 65% after five years. This contrast of low rates of systemic control on the one hand and excellent local control on the other hand, implicates the need for more effective systemic chemotherapy.
Adjuvant 5-FU based chemotherapy was planned for UICC stage ≥ II in our study; however, only 74% of these patients actually received chemotherapy. Lower performance status and more frequent postoperative complications prevented administration of chemotherapy in a quarter of the patients. Despite the planned use of bolus 5-FU and LV chemotherapy, 40% of the patients were treated with different regimes, most frequently FOLFOX, after the MOSAIC trial had been published . The difficulty of postsurgical (radio-) chemotherapy has been described by Sauer et al.: 89% and 50% of the patients in the preoperative and postoperative radiochemotherapy group received full dose chemotherapy, respectively . Whether the difference in the proportion of patients with adjuvant chemotherapy between our study and long-course preoperative radiochemotherapy in the CAO/ARO/AIO-94 trial is related to the short-course radiotherapy remains speculative. However, acute toxicity during short-course radiotherapy was very mild and perioperative morbidity was similar to the preoperative arm in the German study, which does not support the hypothesis of a detrimental effect of short-course radiotherapy. Differences in patient characteristics and differences in the aggressiveness to perform adjuvant chemotherapy are most likely to explain this difference.
Our own data do not allow the conclusion that adjuvant chemotherapy improves clinical outcome but clearly prove its feasibility with favourable results. Five-year OS was 70% and 50% when adjuvant chemotherapy was given or withheld, respectively, but this difference did not reach statistical significance. The patient number in our study is certainly too small for such subgroup analysis. Assuming a difference between the two groups, this difference could result from improved outcome after adjuvant chemotherapy or from differences in patients' performance status and postoperative morbidity.
Although patients with rectal cancer clinical UICC stage I were excluded from this study, pathological UICC stage I was observed in 27% of the patients. Staging of the T and N status was based on endosonography, which was considered as best practice at the time this study protocol was developed [12–14]. Endorectal ultrasound was performed in 95% of our patients. However, the inaccuracy of endosonography in daily clinical routine is well known and the overstaging rate of about 25% compares well to data from other studies. The German Rectal Cancer Trial comparing preoperative with postoperative radiochemotherapy found a 18% rate of UICC stage I patients in the group treated with postoperative radiochemotherapy . Widder et al reported 33% of the patients with UICC stage I disease after short-course preoperative radiotherapy . This suboptimal performance of endosonography may be caused by inconsistent operator experience  or prior biopsy of the cancer, which was shown to result in decreased accuracy of endosonography staging . Recently, pelvic magnetic resonance imaging (MRI) showed excellent accuracy for evaluation of the extramural depth of tumor invasion ; however, staging of the N status and differentiation between clinical stage UICC I and II is difficult even with MRI imaging [19, 20]. These uncertainties of preoperative staging, where overstaging of the T stage was the most frequent finding in pathological analysis, are considered strong arguments for preoperative short course radiotherapy, where downstaging is usually not observed and pathological staging can then be used for selection of patients, which might benefit from adjuvant chemotherapy.
Perioperative mortality was 3.4% and anastomotic leakage was the most frequent complication with an incidence rate of 8.5% in our study. This compares well with published data in literature, which shows that preoperative short course radiotherapy with multi-field radiation techniques is not associated with an increased risk of acute perioperative complications [21, 22]. However, patients need to be informed about the increased risk of late toxicity and complications. Increased bowel frequency, incontinence, urgency, and emptying difficulties have been described by Dahlberg et al. after radiotherapy in the Swedish Rectal Cancer Trial . Peeters et al. reported similar findings with increased rates of fecal incontinence, anal blood loss and lower satisfaction with bowel function in irradiated patients compared with patients who underwent TME alone . The most frequent severe late toxicity was late anastomotic leakage with abscess formation, which was observed in 4 patients (3.4%). This rather high rate of late anastomotic leakage has not been described in the literature. In contrast, the overall rate of late toxicity > grade II toxicity was 10%, which is comparable to other studies on preoperative short-course radiotherapy and long-course radiochemotherapy: small bowel ileus was observed in 3.4%, chronic diarrhoea in 2.5% and anal incontinence in only 1% of the patients. Similar to experiences from other malignancies in the pelvic region [25–28], the use of more conformal radiotherapy treatment planning techniques could reduce toxicity in future protocols.
Calculation of biological effective doses (BED) for the rectal tumor (α/β = 10 Gy) and late normal tissue toxicity (α/β = 3 Gy)
29 Gy (10 × 2.9 Gy)
25 Gy (5 × 5 Gy)
45 Gy (25 × 1.8 Gy)
50.4 Gy (28 × 1.8 Gy)
Tumor OTT (α/β = 10 Gy)
Tumor (α/β = 10 Gy)
Normal tissue (α/β = 3 Gy)
Preoperative short-course radiotherapy is certainly not the optimal approach for all patients with rectal cancer, and this was considered in the inclusion criteria of this study. Neoadjuvant radiochemotherapy outside this trial was chosen instead of preoperative short-course radiotherapy if the surgeon and radiation oncologist expected that downstaging could 1) improve complete resectability in patients with cT4 tumors or 2) achieve sphincter preservation in patients with low tumor location. Patients with invasion of the sphincter or very low tumor location, where no sufficient downstaging for sphincter preservation after neoadjuvant radiochemotherapy was assumed, were eligible. Despite this trial was limited to potentially resectable patients and only one patient with cT4 disease was included, a 5.1% incomplete resection rate was observed. It is speculative, but MRI could be used for selection of patients with a small predicted circumferential margin : these patients could benefit from long-course radiochemotherapy instead of short-course radiotherapy.
Preoperative short course radiotherapy with twice daily fractions of 2.9 Gy to a total dose of 29 Gy combined with adjuvant 5-FU based chemotherapy for rectal cancer UICC stage ≥ II was well tolerated with low rates of acute and late toxicity. Treatment resulted in favourable local control and survival. High rates of systemic progression require intensification of systemic chemotherapy.
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