The majority of patients with operable esophageal cancers present with locally advanced disease, for which surgical resection as a sole treatment modality has been historically associated with poor survival. Local and systemic recurrences develop in over 80% of surgically treated patients, typically within 6–12 months postoperatively, and are often rapidly fatal. This pattern of local and systemic failure highlights the shortcomings of surgical resection alone as a modality of local tumor control, as well as the high propensity of the disease for early occult systemic dissemination. These observations have driven interest in multimodality treatment approaches dating back to the early 1980s with the objective of improving survival by enhancing loco-regional disease control and eliminating micrometastatic disease. Three major induction modalities have been employed, including preoperative chemotherapy, preoperative radiotherapy, or a combination of the two. Despite the large number of randomized trials conducted to date, controversy persists regarding the treatment of choice for patients with locally advanced esophageal cancer. In this communication, we discuss the pertinent level 1 evidence as it relates to the following questions: is neoadjuvant treatment warranted? If so, what is the optimal neoadjuvant regimen? What is the role of surgery in the setting of modern chemotherapy and radiation therapy, where definitive chemoradiotherapy is increasingly utilized? Is there a role for adjuvant therapy? With these questions in mind, we have reviewed what we consider to be some of the most important recent studies highlighting the management of esophageal cancer— particularly in the neoadjuvant setting—and offer our perspective on managing such a complex and deadly disease.
Is neoadjuvant therapy warranted?
At least 14 randomized trials (1-6) have compared preoperative chemotherapy followed by surgery (CS) with surgery alone (S). The majority of these trials are vastly statistically underpowered to permit meaningful conclusions from their results. The four appropriately powered trials that are frequently cited in the esophageal literature are summarized in Table 1. Two of these trials, reported around the turn of the millennium, compared perioperative cisplatin (Cis) and fluorouracil (FU) followed by surgery with surgery alone. The North American trial (USA Intergroup 113) (1) randomized 443 patients (50% adenocarcinoma). The rate of R0 resection was essentially equivalent between the two arms (CS: 63%; S: 59%), and the overall 5-year survival was identical at 5 and 7 years (20%). The larger European trial (OEO2) (2) randomized 400 patients to CS and 402 patients to S only. The rate of adenocarcinoma was over 66% in both arms. Both R0 resection rates and number of nodal metastases favored the CS arm (CS: 60% vs. S: 54% and CS: 48% vs. S: 58%, respectively). Overall survival at 5 years also favored the CS arm (CS: 23% vs. S: 17%) and was consistent for both squamous cell carcinoma and adenocarcinoma. Unfortunately, these conflicting results did not bring the desired clarity to the utility of chemotherapy in the preoperative setting.
In the ensuing decade two additional trials investigated the role of preoperative chemotherapy specifically in patients with adenocarcinoma of the esophagus and gastroesophageal junction (GEJ). The larger of these trials by Cunningham, et al. (MAGIC Trial) (3) randomized 503 patients with carcinoma of the stomach, GEJ, and distal esophagus to either 3 preoperative cycles of epirubicin, cisplatin, and fluorouracil (ECF) followed by surgery and 3 additional cycles of ECF or to surgery alone. Patients with cancers of the GEJ and lower esophagus accounted for roughly 25% of patients in each arm. Overall 5-year survival was 36.3% in the perioperative chemotherapy arm and 23% in the surgery alone arm without evidence of heterogeneity of treatment effect based on tumor location.
Based on the size and rigorous design of the MAGIC trial, preoperative chemotherapy with ECF is now considered one standard of care for the treatment of operable adenocarcinoma of the esophagus and GEJ in Europe and to some extent in the United States.
Further support for preoperative chemotherapy for esophageal adenocarcinoma comes from a phase III trial conducted in France by the Fédération Nationale dex Centres de Lutte contre le Cancer (FNCLCC) and the Fédération Francophone de Cancérologie Digestive (FFCD), comparing perioperative chemotherapy (Cis + FU) and surgery to surgery alone (4). In contrast to MAGIC, the French trial had a much higher percentage of patients with lower esophageal or GEJ adenocarcinoma (75% vs. 26%). The investigators reported a significant improvement in 5-year overall survival in the chemotherapy and surgery group compared to surgery alone (38% vs. 24%, respectively). There were some obvious limitations to these large perioperative chemotherapy trials, including the lack of modern staging modalities such as endoscopic ultrasound /positron emission tomography. Additionally, fewer than 50% of eligible patients received their assigned post-operative chemotherapy. Nevertheless, the available evidence supports the superiority of preoperative chemotherapy over surgery alone as an acceptable multimodality standard of care for patients with adenocarcinoma of the esophagus and GEJ.
At least 13 randomized trials (7-13) have investigated the role of preoperative chemoradiation (CRS) versus surgery alone (S). Seven trials investigated CRS exclusively in patients with squamous cell carcinoma, two in patients with adenocarcinoma, and 5 included patients with both cell types. All utilized platinum/FU chemotherapy with 20–50 Gy of radiation delivered concurrently. As in the preoperative chemotherapy trials, the majority of these trials were underpowered to satisfactorily answer the question. The largest of these trials were reported by Burmeister, Bosset, and Van Hagen, but only the latter trial (CROSS) met its primary endpoint of improved overall survival (7). CROSS was a multi-institutional phase III trial that randomized 366 patients with either squamous cell or adenocarcinoma of the esophagus/GEJ to preoperative chemoradiation followed by surgery (CRS) or surgery alone (S) (Table 2). Nearly 23% of patients had squamous cell cancer. Preoperative chemoradiotherapy consisted of weekly carboplatin and paclitaxel for 5 weeks with concurrent radiotherapy of 41.4 Gy delivered in 23 fractions. Ninety-five percent of patients in the CRS arm completed their assigned preoperative treatment. The R0 resection rate was significantly higher in the CRS group versus surgery alone (92% vs. 69%). The pathologic complete response was 29% (23% for adenocarcinoma versus 49% for squamous cell carcinoma). Five-year survival was significantly higher in the CRS arm (47% vs. 33%). The difference in overall survival was far more prominent in patients with squamous cell carcinoma (median survival: CRS: 81 months, S: 21 months) than adenocarcinoma (CRS: 43 months, S: 27 months), likely reflecting the higher pathological response rate in patients with squamous cell cancers. Patients in the CRS arm had lower rates of locoregional (22% vs. 38%) and distant failures (39% vs. 48%).
The CROSS trial established the superiority of preoperative chemoradiation to surgery alone in patients with locally advanced esophageal cancer and confirmed CRS as a standard of care for squamous cell and adenocarcinoma of the esophagus and GEJ. However, there are potentially important limitations to the CROSS trial, including its wider applicability to patients with esophageal cancer. For example, fewer than 45% of the 837 patients screened for this trial were eventually eligible for randomization. Another factor to consider is that the adjusted hazard ratio for patients with adenocarcinoma was not statistically significant (P value: 0.059). These considerations will probably generate more interest in defining the optimal induction strategy for patients with adenocarcinoma of the esophagus.
What is the optimal preoperative strategy?
Meta-analysis has been performed to determine the best preoperative strategy (14,15). A recent meta-analysis (14) identified 5 randomized trials that compared preoperative chemotherapy with preoperative chemoradiation (Table 3). Two trials were done exclusively in patients with adenocarcinoma, two in patients with squamous cell carcinoma and one trial that included both cell types. The chemotherapy regimen in all trials was Cis/FU and the radiotherapy dose varied between 30 and 40 Gy. Notably, all of these trials were either not adequately powered or were closed prematurely and therefore were inadequately powered to detect a survival advantage. The meta-analysis showed that preoperative chemoradiation significantly increased the rates of R0 resection (89% vs. 77%) and complete pathological response (22% vs. 3.7%). Nonetheless, a survival advantage was only observed in patients with squamous cell carcinoma (57% vs. 42.8%). In patients with adenocarcinoma, 3-year survival did not differ significantly between preoperative chemoradiation and preoperative chemotherapy (46% vs. 41%). As previously stated, since these trials were grossly underpowered, the level of evidence provided is insufficient to make a robust recommendation in favor of a specific induction strategy.
Does esophagectomy have a role after chemoradiation?
The high pathological complete response rate reported after chemoradiotherapy has prompted some to question the role of esophagectomy after such therapy. This view has been gaining traction in the United States, especially in patients with squamous cell carcinoma. The evidence supporting omission of esophagectomy after chemoradiation is derived mainly from FFCD 9102 (10,11), a French randomized trial, in which 259 patients with locally advanced esophageal cancer (cT3N0-1M0) were randomly allocated to either chemoradiation followed by surgery or definitive chemoradiation. Nearly 90% of patients had squamous cell carcinoma. Chemotherapy consisted of two cycles of FU and Cis and either conventional (46 Gy in 4.5 weeks) or “split-course” (15 Gy, days 1 to 5 and 22 to 26) concurrent radiotherapy. Patients who responded were then randomized to either surgery or continuation of chemoradiotherapy (three cycles of FU and Cis and either conventional 20 Gy or split-course 15 Gy radiotherapy). Two-year survival and median survival were both higher in the chemoradiotherapy alone arm (40% vs. 34% and 19.3 vs. 17.7 months, respectively). However, two-year local control rate was significantly better in the surgery arm (66% vs. 57%) and fewer patients required stent placement after esophagectomy (5% vs. 32%). Three-month mortality was much higher in the surgery group (9.3% vs. 0.8%). The authors thus concluded that in patients with squamous cell carcinoma who respond to chemoradiotherapy, there is no benefit from the addition of surgery after chemoradiation compared with the continuation of additional chemoradiation. However, the trial has been criticized for only randomizing responders to chemoradiation, since it can be argued that non-responders would be as or even more likely to benefit from surgical resection. Furthermore, the bulk of the available level I evidence on chemoradiation and squamous cell cancer of the esophagus is derived from trials of trimodality therapy versus surgery alone. Therefore, we prefer to treat patients with locally advanced squamous cell cancer with induction chemoradiation with preoperative intent. Esophagectomy may be omitted in patients with poor performance status or those with prohibitive co-morbidities. Patients with a complete clinical response, defined as physiological uptake on PET scanning and absence of endoscopic evidence of disease, may also elect to defer surgical resection. The data supporting non-operative therapy in patients with adenocarcinoma are even less compelling. Pathological complete responses after chemoradiation in this subset of patients ranges between 15% and 25%. Notably, we and others have shown that even in patients with adenocarcinoma who achieve complete clinical response, as previously defined after chemoradiation, approximately 30–40% have residual disease (16,17). Therefore, absent compelling contraindications, surgical resection remains an essential component of the treatment plan.
Few trials have evaluated postoperative therapy for esophageal cancer (18-20), and much of the data emanates from trials designed using a perioperative regimen, mostly for gastric cancers. An important early trial, the SWOG-directed Intergroup 0116, compared adjuvant chemoradiotherapy following curative resection of gastric cancer versus observation (18,19). Twenty percent of these patients had primary GE junction tumors, and therefore the results have often been used to justify similar adjuvant treatments for esophageal cancer. Following R0 resection of gastric or GE adenocarcinomas, patients were randomly assigned to either observation or chemoradiotherapy. Chemoradiotherapy consisted of bolus FU and leucovorin (LV) before, during, and after radiotherapy. The total radiation dosage was 45 Gy. Treatment toxicity was significant, and the trial regimen is no longer used. Only 64% of patients in the adjuvant chemoradiotherapy group completed the full course. Nearly 70% of patients had T3 or T4 tumors, and over 80% had nodal metastasis. Median overall survival in the surgery alone group was 27 months compared to 36 months in the chemoradiotherapy group. Local recurrence was higher in the surgery alone group compared to the chemoradiotherapy group (29% vs. 19%). While the Intergroup trial offers some support to the use of adjuvant therapy, particularly in node-positive patients, the fact that the trial was designed to evaluate advanced gastric cancers, together with the significant toxicity of its regimen, make its relevance to the treatment of esophageal cancer less clear. Furthermore, the majority of patients in the trial did not have what most would consider oncologically adequate lymph node dissection.
At the 2016 American Society of Clinical Oncology annual meeting, the results of a large phase III trial, the CRITICS study, were presented (21). Although this trial was designed to evaluate adjuvant therapy in gastric cancers, 17% of patients had GE junction adenocarcinomas. Patients with Ib-Iva resectable gastric adenocarcinoma were randomized to either preoperative chemotherapy followed by surgery and adjuvant chemotherapy versus preoperative chemotherapy followed by surgery and adjuvant chemoradiotherapy. Neoadjuvant chemotherapy in both arms consisted of 3 cycles of epirubicin, cisplatin/oxaliplatin, and capecitabine (ECC/EOC). Surgery was either total or partial gastrectomy with en bloc lymphadenectomy and a minimum of 15 lymph nodes removed. Adjuvant chemotherapy consisted of an additional 3 courses of ECC/EOC and adjuvant chemoradiotherapy consisted of 45 Gy total dose radiation with concurrent weekly Cis and daily capecitabine. The primary endpoint was overall survival. Five-year survival was 41.3% in the chemotherapy group versus 40.9% in the chemoradiotherapy group. These results suggest that performing an adequate node dissection might eliminate the need for radiation as an added modality of local control.
The data supporting adjuvant therapy are soft, and therefore we place priority on neoadjuvant treatment. We believe patients better tolerate treatment in this setting, particularly in light of the high rate of treatment drop out in the adjuvant trials as noted above. We reserve adjuvant chemotherapy for those rare, highly selected patients—patients with T1 tumors, for example—who do not receive neoadjuvant treatment and are found to have occult nodal disease at the time of surgery.
There no longer remains any question as to whether preoperative treatment should be given in some manner for patients with resectable locoregionally advanced esophageal cancer. However, the best preoperative treatment is still not clearly established. Several ongoing randomized trials are investigating the optimal preoperative regimen. For example, the FLOT-4 trial (22), a phase II/III trial from Germany, has randomly allocated 714 patients with cancer of the stomach and GEJ to the MAGIC regimen (ECF/ECX) or to perioperative fluorouracil, leucovorin, oxaliplatin, and docetaxel (FLOT). Preliminary analysis of the phase II portion of the trial shows that patients receiving the FLOT regimen have a higher rate of pathological complete response and minimal residual disease compared with patients receiving the MAGIC regimen (29% vs. 15%). Three additional phase III trials are directly comparing preoperative chemotherapy with preoperative chemoradiation. The Neo-AEGIS trial (23) will randomize 366 patients with adenocarcinoma of the GEJ and esophagus to the MAGIC regimen followed by surgery or the CROSS protocol. The ESOPEC trial (24) will randomize 438 patients with adenocarcinoma of the esophagus to either the previously mentioned FLOT regimen followed by surgery or the CROSS protocol. Finally the NExT trial (JCOG 1109), a 3-arm phase II trial (25), will randomize over 500 patients with squamous cell cancer to either of two chemotherapy regimens (Cis/FU or DCF) followed by surgery or chemoradiation followed by surgery. It is hoped that these trials will provide clarity regarding the optimal induction strategy. Finally, the introduction of immune checkpoint inhibitors has literally transformed the care of patients with melanoma, non-small cell lung cancer, kidney, and bladder cancer. Several phase III trials are currently ongoing using immune checkpoint inhibitors in patients with advanced gastric and esophageal cancers based on promising results from early phase trials. Our group has recently initiated a phase II trial combining the immune checkpoint inhibitor pembrolizumab (anti-PD1) with preoperative chemoradiation followed by esophagectomy and maintenance immunotherapy in patients with esophageal adenocarcinoma. The promise that immunotherapy will prove as transformative for esophageal cancer patients as it has been for patients with other solid tumors is tantalizing indeed.
Our group was an early advocate of neoadjuvant chemotherapy alone followed by surgical resection, and we did not routinely use radiation therapy in the preoperative setting. Given that most patients who succumb to esophageal cancer do so because of distant disease, we believe that chemotherapy is an important component of treatment, and we have typically administered such treatment in the neoadjuvant setting. However, we also believe that by performing a more radical en bloc resection, we can achieve higher rates of R0 resection and superior local control, which is in our view the primary benefit of radiation therapy, yet without subjecting patients to the added potential toxicity and post-operative adverse events that may result from trimodality therapy (26-29). Spicer recently reported (30) on the experience of three large institutions, including our own, with en bloc resection for patients with cT3N1 esophageal cancer treated with either preoperative chemoradiation (100 patients) or preoperative chemotherapy (114 patients). He found no difference between the two groups of patients in either overall or disease-free survival. Notably, there was no difference between the groups in locoregional recurrence rates suggesting that an en bloc esophagectomy after chemotherapy alone achieves local control rates comparable to those reported after trimodality therapy, thus emphasizing the role of surgery as a sufficient modality for local control. A more streamlined bimodality approach serves a suitable platform for the addition of novel additional therapies such as targeted or immunotherapy.
Conflicts of Interest: The authors have no conflicts of interest to declare.
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