Pathologic response to neoadjuvant treatment in locally advanced rectal cancer and impact on outcome
Original Article

Pathologic response to neoadjuvant treatment in locally advanced rectal cancer and impact on outcome

Mahshid Jalilian1, Sidney Davis1, Mohammadreza Mohebbi2, Bhuvana Sugamaran1, Ian W. Porter1, Stephen Bell3, Satish K. Warrier3, Roger Wale3

1William Buckland Radiotherapy Centre, Alfred Hospital, 55 Commercial Road, Melbourne, Victoria 3004, Australia;2Biostatistics Unit, Faculty of Health, Deakin University, Burwood Highway, Burwood, Victoria 3125, Australia;3Department of Colorectal Surgery, Alfred hospital, 55 Commercial Road, Melbourne, Victoria 3004, Australia

Contributions: (I) Conception and design: M Jalilian, M Mohebbi, S Davis; (II) Administrative support: M Jalilian, S Davis, B Sugamaran; (III) Provision of study material or patients: M Jalilian, IW Porter, S Bell, SK Warrier, R Wale; (IV) Collection and assembly of data: M Jalilian, B Sugamaran; (V) Data analysis and interpretation: M Jalilian, M Mohebbi; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

Correspondence to: Mahshid Jalilian. 55 Commercial Road, Melbourne, Victoria, 3004, Australia. Email: jalilian.m@gmail.com.

Background: Downstaging and pathologic complete response (pCR) after chemoradiotherapy (CRT) may improve progression-free survival and overall survival (OS) after curative therapy of locally advanced adenocarcinoma of rectum. The purpose of this study is to evaluate the pathologic response subsequent to neoadjuvant chemoradiation in locally advanced rectal adenocarcinoma and any impact of response on oncological outcome [disease-free survival (DFS), OS].

Methods: A total of 127 patients with histologically-proven rectal adenocarcinoma, locally advanced, were treated with preoperative radiotherapy and concurrent 5-fluorouracil (5 FU), and followed by curative surgery. Pathologic response to neoadjuvant treatment was evaluated by comparing pathologic TN (tumour and nodal) staging (yp) with pre-treatment clinical staging. DFS and OS were compared in patients with: pCR, partial pathologic response and no response to neoadjuvant therapy.

Results: 14.96% (19 patients) had a pCR, 58.27% [74] showed downstaging and 26.77% [34] had no change in staging. At follow-up (range, 4–9 years, median 6 years 2 months or 74 months), 17.32% [22] showed recurrence: 15.74% [20] distant metastasis, 1.57% [2] pelvic failure. 10.5% [2] of the patients with pCR showed distant metastasis, none showed local recurrence. In the downstaged group, nine developed distant failure and two had local recurrence (14.86%). Distant failure was seen in 26.47% [9] of those with no response to neoadjuvant treatment. DFS and OS rates for all groups were 82.67% and 88.97% respectively. Patients with pCR showed 89.47% DFS and 94.7% OS. In partial responders, DFS was 85.1% and OS was 90.5%. In non-responders, DFS and OS were 73.5% and 82.3% respectively. Patients with pCR had a significantly greater probability of DFS and OS than non-responders. Rectal cancer-related death was 11.02% [14]: one patient (5.26%) with pCR, 9.47% [7] in the downstaged group and 17.64% [6] of non-responders.

Conclusions: The majority of patients showed some response to neoadjuvant treatment. Findings of this study indicate tumour response to neoadjuvant CRT improves the long-term outcome, with a better result in patients with pCR.

Keywords: Rectal cancer; chemoradiotherapy (CRT); histopathology response; outcome

Submitted Mar 08, 2016. Accepted for publication Apr 11, 2016.

doi: 10.21037/jgo.2016.05.03

Introduction

Preoperative chemoradiotherapy (CRT) results in local control improvement and downstaging with, subsequently, the increased possibility of sphincter sparing in low rectal tumour and less toxicity in comparison with postoperative chemoradiation (1,2). Pathologic downstaging of a rectal cancer occurs when the final pathologic stage response is less than the preoperative stage of the tumour. A pathologic complete response (pCR) (absence of cancer cells in the resected surgical specimen) can occur after neoadjuvant treatment and this result may confer a survival advantage [overall survival (OS) and disease-free survival (DFS)] (3-12).

The aim of the current study is to assess the pathologic response rates following neoadjuvant CRT and evaluate the influence of response to neoadjuvant treatment on the long-term outcome in patients with locally advanced rectal cancer.

Methods

Patients

A total of 127 patients with locally advanced (clinical T3, T4 or node positive), biopsy proven adenocarcinoma of the rectum were involved in this retrospective review, with the mean age of 62.1 years (SD: 11.1 years) (ages ranged from 27–83 years). 33.85% (43 patients) were female and 66.15% (84 patients) male.

Pre-treatment staging was performed by endorectal ultrasound (ERUS) or magnetic resonance imaging (MRI), in addition to a range of other investigations including computed tomography (CT) of chest and abdomen, colonoscopy, complete blood count, blood chemistry and carcinoembriogenic antigen (CEA). All patients were treated at The Alfred Hospital, Melbourne, Australia, between 2005 and 2010.

Institutional review board approval was granted for this study.

Treatment

After signing informed consent forms, all patients received neoadjuvant radiotherapy, concurrent with 5-fluorouracil (5 FU), at the William Buckland Radiotherapy Centre (WBRC) at The Alfred Hospital. Patients received either 45 or 50.4 Gray (Gy) radiotherapy, 1.8 Gy per fraction, one fraction per day, and were treated 5 days per week. Treatment was delivered using a 3-field 18/6 MV photon technique on a lineal accelerator. The clinical target volume included the primary tumour and regional lymph nodes (mesorectal, presacral, internal iliac, obturator). All patients received either bolus or continue infusion 5 FU.

After radical surgery, all patients received adjuvant chemotherapy with weekly 379 mg per square meter 5 FU for 20 weeks.

Follow-up

Pathologic response was assessed by comparing postoperative pathologic staging (yp) with preoperative clinical staging and grouped as pathologic complete responders (pCR), partial responders (decrease in tumour or nodal staging) and non-responders.

During a median follow-up of 74 months, patients were clinically evaluated (history and examination) and were referred for radiological assessment (chest X-ray, abdominal-pelvic CT scan, colonoscopy and other investigations) as per clinical indications.

DFS was defined as the time between surgery and first recurrence (local or distant). Cancer specific survival was defined as the time between surgery and the time that cancer-related death occurred.

Statistical methods

Continuous data were expressed as mean (SD), median and the range between parentheses.

Qualitative data are presented as absolute numbers or percentages. Comparative analysis of the quantitative data was performed using the Student’s t-test. The chi-square or Fisher’s exact tests were used for comparing proportions as appropriate. Odds ratio (OR) and 95% confidence interval (CI) were reported for significant associations. Estimates of DFS and OS were calculated using the Kaplan-Meier method. Patient and disease factors were evaluated using log-ranked test, with result reported as median and 95% CI. Statistical significance was defined as P≤0.05.

Results

Patients and tumour characteristics

A total of 127 patients were involved in this study with the mean age of 62.1 years (SD: 11.1 years) (range, 27–83 years), 33.85% (43 patients) were female and 66.15% (84 patients) were male.

Fifty percent of the patients were staged by ERUS, 48.4% by MRI and 1.6% had both modalities for staging.

Patients and tumour characteristics are listed in Table 1.

Table 1
Table 1 Patients and tumour characteristics
Full table

Pathologic response

pCR was seen in 14.96% (19 patients) of participants. 58.26% (74 patients) of patients displayed partial response and TN staging did not change in 26.77% (34 patients). There was no significant association between patients and tumour characteristics and response to treatment (Table 2).

Table 2
Table 2 Patients and tumour characteristics and response to treatment
Full table

Treatment outcome

After a median follow-up of 74 months, 22 patients (17.32%) showed recurrence, including local and distant failure. Twenty patients developed distant metastases: six cases with liver metastases, six patients developed pulmonary metastases, one recurred in bone, two had pelvic recurrence and seven patients had metastases in more than one site (Table 3).

Table 3
Table 3 Site and number of recurrence
Full table

DFS and cancer-related survival were 82.67% and 88.97% respectively. DFS curve according to pathologic response is shown in Figure 1. OS curve according to pathologic response is shown in Figure 2.

Figure 1 Kaplan-Meier curves for disease-free survival (DFS).
Figure 2 Kaplan-Meier curves for overall survival (OS).

Discussion

Neoadjuvant CRT before curative surgery is a widely adopted treatment method in locally advanced adenocarcinoma of rectum, especially in low and fixed rectal tumour, to improve resectability, tumour control and preserve anal sphincter.

Pathologic response to neoadjuvant treatment in locally advanced rectal adenocarcinoma may predict a survival advantage (DFS and OS) (2,3,5-7,13,14). pCR rates following preoperative CRT are shown in a body of research literature to range from 9% to 30% (1,2,7,8,10,11,15,16) while some studies report a partial response to neoadjuvant treatment of 51% (6,11). The correlation between response to neoadjuvant treatment and oncologic outcome has been reported in other studies (3,4,6-12,17-23).

To our knowledge, the data presented in this study is one of the largest single-institution reports in the Australian literature looking at response rates and long-term outcomes of patients with locally advanced, rectal adenocarcinoma.

In our study, 58.26% of the patients showed some response to preoperative treatment. pCR was found in 14.96% of patients, which is comparable to European studies which reported rates of 11–16% (1,2,16). None of our patients with complete response to neoadjuvant treatment showed local recurrence. A lower rate of distant failure was observed in the pCR group compared with the other two groups and partial responders had less recurrence than non-responders.

DFS and OS in the pCR group were 89.47% and 94.7% respectively.

In partial responders, DFS and OS were 85.1% and 90.5% and in non-responders were 73.5% and 82.3% respectively. Table 4 demonstrates recurrence and cancer-related death of the three groups of responders.

Table 4
Table 4 Recurrence and cancer-related deaths by responder groups
Full table

Conclusions

This study revealed that preoperative chemoradiation for locally advanced adenocarcinoma of the rectum resulted in a pathologic response of the primary tumour and lymph nodes in the majority of patients studied. Our results indicate pCR is achievable in a proportion of patients and that response to pre-operative CRT can be used as a predictor of tumour recurrence rate and long-term outcome.

Acknowledgements

None.

Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.

Ethical Statement: The study was approved by institutional ethics board (No. 218/12).

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Cite this article as: Jalilian M, Davis S, Mohebbi M, Sugamaran B, Porter IW, Bell S, Warrier SK, Wale R. Pathologic response to neoadjuvant treatment in locally advanced rectal cancer and impact on outcome. J Gastrointest Oncol 2016;7(4):603-608. doi: 10.21037/jgo.2016.05.03

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