Preoperative chemoradiotherapy for locally advanced gastric cancer
© Pepek et al.; licensee BioMed Central Ltd. 2013
Received: 10 September 2012
Accepted: 28 December 2012
Published: 4 January 2013
To examine toxicity and outcomes for patients treated with preoperative chemoradiotherapy (CRT) for gastric cancer.
Patients with gastroesophageal (GE) junction (Siewert type II and III) or gastric adenocarcinoma who underwent neoadjuvant CRT followed by planned surgical resection at Duke University between 1987 and 2009 were reviewed. Overall survival (OS), local control (LC) and disease-free survival (DFS) were estimated using the Kaplan-Meier method. Toxicity was graded according to the Common Toxicity Criteria for Adverse Events version 4.0.
Forty-eight patients were included. Most (73%) had proximal (GE junction, cardia and fundus) tumors. Median radiation therapy dose was 45 Gy. All patients received concurrent chemotherapy. Thirty-six patients (75%) underwent surgery. Pathologic complete response and R0 resection rates were 19% and 86%, respectively. Thirty-day surgical mortality was 6%. At 42 months median follow-up, 3-year actuarial OS was 40%. For patients undergoing surgery, 3-year OS, LC and DFS were 50%, 73% and 41%, respectively.
Preoperative CRT for gastric cancer is well tolerated with acceptable rates of perioperative morbidity and mortality. In this patient cohort with primarily advanced disease, OS, LC and DFS rates in resected patients are comparable to similarly staged, adjuvantly treated patients in randomized trials. Further study comparing neoadjuvant CRT to standard treatment approaches for gastric cancer is indicated.
Postoperative chemoradiotherapy (CRT), perioperative chemotherapy (ChT) or postoperative ChT are the current standards of care for resectable gastric cancer based on the outcomes of phase III randomized trials[1–4]. While these strategies have been shown to improve disease-related outcomes compared to surgery alone, they are associated with higher rates of treatment-related morbidity. Illustrating this fact, only 64% of patients in the Intergroup-0116 trial and 42% in the Medical Research Council Adjuvant Gastric Infusional Chemotherapy (MAGIC) trial were able to complete their prescribed treatment courses[1, 2].
Preoperative CRT has been established as the primary treatment modality in other gastrointestinal malignancies, including esophageal[5–8] and rectal cancer. Preoperative CRT has several potential biological and technical advantages. The presence of intact tumor vasculature and oxygenation may enhance responsiveness to radiotherapy (RT) and systemic therapy. This treatment approach may also sterilize the surgical field, potentially reducing the risk of local tumor dissemination at resection. Preoperative CRT may also allow design of smaller and more accurate radiation treatment fields which could improve treatment tolerance, as well as identify patients with biologically aggressive disease in whom surgery should be avoided. In addition, postoperative morbidity following upfront gastrectomy can be significant, resulting in the delay or omittance of adjuvant therapy administration[1, 2, 10]. Lastly, preoperative CRT may result in tumor downstaging, facilitating curative (R0) resection rates while decreasing the risk of local tumor recurrence.
There are scant prospective data on clinical outcomes utilizing preoperative RT for gastric cancer. Trials of neoadjuvant RT or CRT compared to surgery alone have shown an overall survival (OS) advantage with preoperative treatment in patients with esophageal and gastric cardia adenocarcinomas[5, 11]. Additionally, several small phase II trials examining the role of induction ChT followed by preoperative CRT for gastric cancer showed encouraging rates of pathologic complete response (pCR) and R0 resections, with acceptable rates of acute and late toxicity[12–14]. Single institution experiences examining a neoadjuvant approach for gastric cancer have also been published[15–17], but data looking at preoperative CRT without induction ChT are limited. The intent of this study is to examine our institutional experience with neoadjuvant CRT for potentially resectable gastric adenocarcinoma, evaluating treatment-related toxicity, R0 resection rates, pCR rates, and disease-related endpoints.
This Institutional Review Board-approved study included patients who underwent preoperative CRT for non-metastatic gastroesophageal (GE) junction and gastric adenocarcinoma at Duke University Medical Center between 1987 and 2009. Medical records, pertinent radiographs and RT fields were reviewed to obtain patient demographics, operative findings, pathology, toxicity, and to determine local-regional and distant recurrence patterns. Tumor epicenter, GE junction involvement and tumor (T) and nodal (N) staging were determined using upper endoscopy, radiographic imaging and/or endoscopic ultrasound (EUS).
The institutional policy has been to proceed directly to resection for early stage gastric cancer in most patients. In general, patients with locally advanced disease, which includes those with large primary tumors (≥ T3 tumors), extensive local-regional nodal involvement or where a R0 surgical resection may not be feasible initially, are usually referred for preoperative CRT following evaluation by a multidisciplinary team.
Only Siewert type II/III GE junction and gastric adenocarcinomas were included in this analysis. Patients with direct tumor extension into adjacent organs who were still thought to be candidates for resection were included. Patients were excluded if the initial treatment plan was for definitive or palliative CRT, or if they were found to have metastatic disease during pre-treatment workup.
Guidelines for preoperative RT planning for gastric cancer have been previously published and can serve as a framework for our general approach to treatment field design. External beam RT was delivered via high energy linear accelerators using 6 MV or 15 MV photons. Multi-field external beam RT plans were typically designed to cover the primary tumor and local-regional lymph node basins. In recent years, a deep inspiratory breath-hold technique during RT was utilized for patients with significant tumor motion. Induction, concurrent and adjuvant ChT selection was at the discretion of the treating Medical Oncologist. Surgical resection typically occurred 4–6 weeks after CRT completion. The type of surgery depended upon the treating surgeon’s preference, primary tumor location and disease extent.
Each patient was staged using the American Joint Committee on Cancer gastric cancer staging guidelines, 6th edition. Tumor downstaging was defined as a decrease in either T stage and/or N stage at the time of resection. Patterns of failure were determined by imaging studies and/or by findings obtained from diagnostic procedures such as laparoscopy, laparotomy or computed tomography (CT)-guided biopsies. Local recurrence was defined as disease recurrence within the remaining stomach, the operative bed or local-regional (lower paraesophageal, gastrohepatic, celiac, superior mesenteric, porta hepatis, and splenic) lymph nodes basins. Radiographic lymph node recurrences were defined as lymph nodes ≥ 1 cm on CT which had increased in size on serial imaging and/or were hypermetabolic on positron emission tomography (PET). Distant recurrence was defined as any recurrence outside the aforementioned sites. A consensus opinion was reached by two authors (J.P. and B.C.) on all suspected cases of local and distant recurrences as a means to improve accuracy.
The Kaplan-Meier method was used to estimate 3-year OS, disease-free survival (DFS) and local control (LC) probabilities with 95% confidence intervals (95% CI). All disease-related endpoints were calculated from the preoperative therapy start date. Testing for time to event differences between groups was performed using the log-rank (Mantel-Cox) test. Analysis was performed using SPSS 19.0.0 (IBM Corporation, Somers, NY).
Toxicity was assigned using the National Cancer Institute Common Toxicity Criteria for Adverse Events version 4.0 (CTCAE v4.0). Acute toxicity was defined as any toxicity from the start of preoperative therapy until surgery. Late toxicity was defined as any toxicity greater than 90 days after surgery.
Forty-eight patients were included in the present analysis. Thirty-three were treated from the year 2000 onward. Median follow-up was 42 months (range 17–144). Twenty-nine patients (61%) were clinical stage III, and five patients (10%) were clinical T4 at presentation. Thirty-one (65%) were clinically node positive. Staging PET scan was used for 19 patients (40%) and CT scan was used for 28 (59%). One patient with stage IB disease did not receive radiographic staging due to pregnancy at the time of diagnosis. Thirty-six patients (75%) underwent baseline EUS prior to CRT. Fourteen patients underwent pre-treatment laparoscopy or laparotomy.
Patient and tumor characteristics for patients undergoing preoperative chemoradiotherapy for gastric adenocarcinoma (n = 48)
Primary site location*
Stage at presentation (AJCC 6)
Treatment characteristics for patients undergoing preoperative chemoradiotherapy for gastric adenocarcinoma (n = 48)
5-FU or Capecitabine
No surgical resection
Thirty-six patients (75%) underwent surgery. Total gastrectomy was performed in 13 patients, partial gastrectomy in 9 patients and esophagogastrectomy in 14 patients (Table 2). The median number of lymph nodes sampled was 6 (range 0–34). The R0 resection rate was 86% (n = 31). Overall tumor downstaging was seen in 18 of 28 patients (64%) who had EUS prior to starting preoperative therapy. T stage downstaging was seen in 19 patients (68%). Of the 36 patients who underwent surgery, 13 of 22 (59%) who were clinically node positive on initial evaluation were pathologically node negative. A pCR was seen in 7 of 36 patients (19%). Nine (25%) received adjuvant ChT after a R0 resection. Of those, seven patients received postoperative fluoropyrimidine-based ChT. Patients did not undergo definitive surgical resection due to distant metastases found on restaging scans or exploratory laparotomy (n = 9), patient refusal (n = 2) or poor performance status following preoperative CRT (n = 1). One patient who underwent gastrectomy was found to have peritoneal carcinomatosis on final pathology despite negative intraoperative frozen sections.
Grade 3–4 chemoradiotherapy-associated acute toxicity (n = 48)
Worst Hematologic Toxicity
Worst Non-Hematologic Toxicity
Long-term (≥ 3 month) toxicity for patients undergoing surgery (n = 36)
The primary treatment modality for patients with localized gastric cancer is surgery. However, rates of both local and distant recurrence remain high following curative intent resection alone[20–23]. Several small prospective studies have examined the use of induction ChT prior to preoperative CRT for potentially resectable gastric cancer[12–14]. Single institution experiences using either preoperative ChT and/or CRT have also been described[15–17], although the data examining a neoadjuvant approach in gastric cancer remains limited. Our institution has favored an approach of neoadjuvant CRT without induction ChT for patients primarily with locally advanced disease, prompting the present analysis of treatment-related toxicities and outcomes for this group of patients.
Preoperative CRT was well tolerated in our series, with 96% of patients able to complete the prescribed treatment course and only six patients requiring treatment break. Similarly, in a pilot study from Lowy et al., 96% (23 of 24 patients) were able to complete neoadjuvant fluoropyrimidine-based CRT without treatment break. These studies are in contrast to results from the Intergroup-0116 trial where only 64% of 281 patients were able to complete the prescribed postoperative protocol. Improved compliance and acceptable acute toxicity rates with neoadjuvant CRT seen in our series may be due in part to smaller RT treatment fields and/or improved performance status at the time of CRT compared to the post-gastrectomy setting.
Acute and late toxicity data assessing neoadjuvant CRT for gastric cancer are limited[12, 13, 24]. In our series, four surgical patients (11%) experienced symptomatic anastomotic leak requiring intervention, which is similar to rates seen in a pilot study of preoperative CRT and a Dutch Gastric Cancer Group trial evaluating extended lymphadenectomy for gastric cancer. With respect to late toxicity, 5% of patients in RTOG 9904 evaluating preoperative CRT experienced late grade 3 toxicity, which is lower than in our series. Most occurrences of late grade 3 toxicities in our cohort were dysphagia, with an estimated 21% actuarial risk of requiring esophageal dilation at one year. It is possible that these comparative differences may be attributable to variations in scoring toxicity between studies.
Thirty-day postoperative mortality was 6% in our analysis, which is consistent with previously reported mortality rates examining neoadjuvant CRT for gastric[14, 24] and esophageal malignancies[5, 8, 26]. The influence of preoperative CRT on perioperative mortality remains debatable when compared to upfront surgical resection. In the POET trial by Stahl et al., preoperative CRT was associated with a non-significant increase in postoperative mortality compared to a ChT alone approach. However, the CROSS trial showed no difference in operative mortality for patients who received preoperative CRT versus those undergoing surgery alone for esophageal cancer. Similarly, previously published data from our institution suggested that induction therapy for esophagogastrectomy patients was not associated with an increased risk of surgical mortality on multivariable analysis.
Historically, the inability to achieve a curative resection with surgery alone for gastric cancer is high and portends a poor prognosis. One randomized trial demonstrated an improvement in OS for gastric cancer patients achieving R0 resection. Additionally, the MAGIC trial showed a statistically significant improvement in R0 resections among surgical patients who received preoperative ChT. Using these trials as guides, it can be inferred that a preoperative approach may improve disease-related outcomes. The R0 resection rate for those undergoing surgery in our series (86%) is comparable to prospective studies utilizing neoadjuvant CRT for gastric cancer[12–14, 24]. This is particularly encouraging as many patients had locally advanced, potentially unresectable disease at presentation with accompanying adverse histologic features, including signet ring cell histology and linitis plastica. Our data underscore the importance of achieving a R0 resection, with 3-year OS of 54% compared to 0% for those undergoing R1 resection.
Several series have demonstrated that pathologic response to CRT is predictive of patient outcomes[12, 13, 15–17]. Three phase II trials from Ajani et al. showed pCR rates ranging from 20% to 30% with the use of induction CT followed by concurrent CRT,[12–14] with associated improvements in OS and DFS in these patients. A series from M.D. Anderson reported a 23% pCR rate with either induction ChT followed by concurrent CRT or concurrent CRT for both GE junction and gastric malignancies. In this study, pCR was the only statistically significant predictor of LC based on multivariable analysis. Similarly, another recent report showed lower recurrence rates and greater OS, DFS and relapse-free survival in the pCR group versus the non-pCR group. The pCR rate in the present analysis appears consistent with other series, but did not translate into improved OS in our cohort. Although LC was 100% in the pCR group, the low absolute numbers of patients and high distant failure rates potentially diluted any impact of pCR within our study. Nevertheless, most data suggest that gastric cancer patients who have a pCR have more favorable outcomes. Data examining preoperative ChT alone for resectable gastric cancer show pCR rates of only 0-7%[2, 32, 33], suggesting that the addition of RT with concurrent ChT may improve tumor response and disease-related endpoints compared to a ChT alone approach. This was demonstrated in a recent randomized trial evaluating preoperative ChT versus CRT in GE junction cancer patients.
While the number of events are small, our data suggest that both local and distant recurrences are still problematic despite aggressive combined modality therapy. Most patients recurred distantly as their first site of recurrence, which is concordant with other published series[12, 16]. The actuarial local recurrence rate in our cohort was 28% for all patients and 27% in the subset of patients who underwent gastrectomy. While these rates are slightly higher than expected, even for those with a R0 resection, this may be attributable to the aggressive and locally advanced nature of disease seen in our cohort as well as variability in RT treatment field design over the study period. Optimizing ChT regimens, including the use of novel conventional and targeted biologic therapies, may be a potential way to improve pathologic response and R0 resection rates, reduce distant recurrences, and improve survival rates in future trials examining preoperative CRT. Advancements in pre-treatment staging are also critical to better select appropriate surgical candidates. Two such examples include PET/CT, which may improve accuracy for preoperative staging, and staging laparoscopy, which may identify the approximately 20-40% of patients with localized disease based on preoperative CT but who demonstrate peritoneal metastases at laparoscopy[35, 36].
The present study has a number of limitations inherent to retrospective series. First, our cohort is limited by small patient numbers, resulting in few total events and wide confidence intervals for actuarial data. Second, clinical and pathological data were not collected prospectively which allows for selection bias to be introduced. Furthermore, local and distant recurrences were not always pathologically confirmed, with most diagnosed by CT imaging, potentially underestimating local and distant recurrences within the study. During surgery, a median of 6 lymph nodes were sampled which may be insufficient for adequate dissection of regional lymph nodes. However, the limited extent of lymph node dissection appears consistent with national data from the Surveillance, Epidemiology, and End Results (SEER) cancer registry which showed that a median of 8 lymph nodes were sampled during gastric cancer resection, with only 25% of patients having 15 or more lymph nodes examined. Additionally, the impact of preoperative CRT on lymph node harvest in gastric cancer is not well defined. Nevertheless, a more extensive dissection may have improved disease-specific outcomes in our cohort given the potential for understaging with a limited lymph node sampling[37, 38].
Comparison of present series to prospective preoperative chemoradiotherapy trials in gastric cancer
R0 resection (%)*
pCR rate (%)*
Overall survival (%)**
M.D. Anderson (Lowy et al.)
Multi-institutional (Ajani et al.)
M.D. Anderson(Ajani et al.)
RTOG 9904 (Ajani et al.)
Current series (Pepek et al.)
In conclusion, preoperative CRT for gastric cancer is reasonably well tolerated with acceptable rates of perioperative morbidity and mortality. R0 resection rates and pCR are encouraging with this treatment strategy. Despite evaluating a cohort with primarily advanced disease and adverse histologic features, LC, DFS and OS rates in resected patients are comparable to similarly staged, adjuvantly treated patients in randomized trials. Further study comparing neoadjuvant CRT to standard treatment approaches for gastric cancer is warranted.
Presented at the 52th Annual Meeting of the American Society of Radiation Oncology, San Diego, California, October 31-November 4, 2010.
This single-institutional series evaluates the role of preoperative chemoradiotherapy in patients with locally advanced gastric cancer. Disease-related outcomes for resected patients appear comparable to similarly staged, adjuvantly treated patients in randomized trials with acceptable rates of perioperative morbidity and mortality.
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