Tumor regression and survival after perioperative MAGIC-style chemotherapy in carcinoma of the stomach and gastroesophageal junction
BMC Surgery volume 15, Article number: 66 (2015)
We assessed the effectiveness of perioperative MAGIC-style chemotherapy in our series focused on the tumor regression grade and survival rate.
We conducted a retrospective study of 53 patients following a perioperative regimen of epirubicin, cisplatin, and fluorouracil or capecitabine (ECF/X). Forty-four (83 %) neoplasias were located in the stomach and 9 (17 %) were located at the esophagogastric junction. Perioperative chemotherapy completion, resection, TNM staging, the tumor regression grade (Becker’s classification) and survival were analyzed.
Forty-five patients (85 %) completed the 3 preoperative cycles. R0 resection was achieved in 42 (79 %) patients. Thirty-five (66 %) patients completed the 3 postoperative cycles. Nine carcinomas (17 %) were considered major responders after preoperative chemotherapy. With multivariate analysis, only completion of perioperative chemotherapy (HR: 0.25; 95%CI: 0.08 – 0.79; p = 0.019) was identified as an independent prognostic factor for disease-specific survival. However, the protective effect of perioperative therapy was lost in patients with ypT3-4 and more than 4 positive lymph nodes (HR: 1.16; 95%CI: 1.02 – 1.32; p = 0.029). The tumor regression grade (major vs minor responders) was at the limit of significance only with univariate analysis. The 5-year overall and disease-specific survival rates were 18 % and 22 % respectively.
The percentage of major responder tumors after preoperative chemotherapy was low.
Completion of perioperative ECF/X chemotherapy may benefit patients with gastric carcinomas that do not invade the subserosa with few positive lymph nodes.
In Europe, gastric carcinoma patients have an average 5-year survival rate of approximately 30 %, although there is wide variation among and within countries . The prognosis in the absence of peritoneal or distant dissemination continues to be poor when lymph node (LN) invasion exists, even when an R0 surgical resection with extended lymphadenectomy is achieved [2, 3]. The effects of extended D2 lymphadenectomy on disease-free survival have not been well established in Western countries [4, 5]. However, some current clinical guidelines recommend a spleen and pancreas preserving D2 lymphadenectomy [6, 7].
Different strategies have been developed to improve the poor prognosis associated with radical surgical resection of localized gastric cancer. Adjuvant radiochemotherapy, which improved the median overall survival rates in the INT 0116 prospective randomized clinical trial  has been questioned in patients with lymph node negative disease and after D2 lymphadenectomies [9, 10]. Adjuvant chemotherapy has been consistently effective after D2 lymphadenectomies in prospective, randomized clinical trials involving only Eastern populations [11, 12]. Thus, perioperative treatment including neoadjuvant chemotherapy (NAC) has emerged as the most attractive approach. In fact, the MAGIC  and FNCLCC-FFCD  prospective randomized clinical trials have found positive effects of the use of NAC on the curative resection rates, disease-free survival and overall survival.
Nevertheless, little is known about tumor regression after neoadjuvant chemotherapy regimen of epirubicin, cisplatin, and fluorouracil or capecitabine (ECF/X), although partial or minimal regression has been reported in 54 % of gastric carcinomas . Assessment of the histopathological changes after NAC is the best method for evaluating tumor response to chemotherapy [16–18] and recent data have shown that complete or subtotal tumor regressions are the only independent prognostic factors for survival .
In this study, we assessed the effectiveness of the MAGIC perioperative chemotherapy regimen by analyzing the tumor regression grade, and survival rate.
Patients and methods
From March 2006 to December 2012 patients with stages II and III gastric and esophagogastric junction (EGJ) carcinomas underwent a perioperative MAGIC regimen chemotherapy at the Elche University Hospital and the Vega Baja Hospital. Patients showing symptoms of outlet obstruction or morbidity that precluded chemotherapy were excluded. The diagnostic and staging workup included an upper endoscopy with biopsy and a CT scan for all patients. After 2008, EUS was usually performed unless carcinomatosis or distant metastases were suspected based on CT scan. Staging laparoscopy was mostly indicated when CT or EUS showed signs of linitis, tumor invasión of adjacent structures or ascitis. Written informed consent was obtained from all patients.
This study was approved by the ethics committee of the University Hospital of Elche.
The following clinical variables were analyzed in this study: age, gender, location, completion and morbidity after preoperative chemotherapy, type of gastrectomy or esophagectomy, extent of LN dissection as stated by the surgeon, surgical morbidity and mortality, completion and morbidity of postoperative chemotherapy, recurrence, and overall and specific survival. The histopathological variables analyzed were the depth of invasion (ypT), total and positive LNs retrieved, LN staging (ypN), carcinomatosis, peritoneal lavage cytology, liver metastasis (ypM), histological type, grade, and tumor regression grade according to Becker’s classification . Tumors with complete regression (grade 1a) or subtotal (<10 % of residual tumor) regression (grade 1b) were considered major responders. Tumors with partial (10–50 % residual tumor) regression (grade 2), or with minimal or no regression (>50 % residual tumor) (grade 3) were classified as minor responders. Gastric and EGJ tumors were staged according to the 7th edition International Union Against Cancer (UICC) TNM pathological classification.
Treatment and follow-up
ECF/X regimen chemotherapy was administered for 3 cycles preoperatively and three cycles postoperatively. Each 3-week cycle consisted of epirubicin (E) (50 mg per square meter of body-surface area) by intravenous bolus on day 1, cisplatin (C) (60 mg per square meter) intravenously with hydration on day 1, and fluorouracil (F) (200 mg per square meter) daily for 21 days by continuous intravenous infusion or capecitabine (X) twice a day (625 mg per square meter) for 21 days .
After preoperative chemotherapy subtotal or total gastrectomy was undertaken in gastric or type III esophagogastric junction (EGJ) carcinomas. In patients with type I or II EGJ carcinomas, an Ivor Lewis partial esophagectomy was performed. Perigastric lymph node stations (1 to 6) were removed in D1 lymphadenectomies. Additionally, lymph node stations 7, 8a, 9, and 11p were removed in modified D2 lymphadenectomies. Inferior periesophageal and subcarinal lymph nodes were also removed in EGJ type I or II carcinomas. D1 or modified D2 lymphadenectomies were chosen according to the surgeon’s criteria.
Routine follow-up examinations consisted of a clinical interview and blood analyses including tumor markers CEA, CA 19.9 and CA125 every 3 months for the first 2 years after surgery and every 6 months thereafter. CT scans were performed every 6 months the first 2 years after surgery and yearly thereafter.
A Kaplan Meier survival analysis was performed using a log-rank test to estimate differences in the 5-year disease-specific survival rates. Multivariate survival analysis was performed using a Cox regression model. Prognostic factors were compared using hazard ratios with a 95 % confidence interval. To identify independent risk factors and to control for possible bias from patients diagnosed as M1 over the course of perioperative treatment, a Cox regression analysis (stratified by ypM) was performed. The model included variables identified by univariate survival analysis as more influential. SPSS for Windows version 20 was used for the statistical analysis.
Fifty-three patients were included in the study. The clinical characteristics of the patients are summarized in Table 1. Sixteen patients (30.2 %) were older than 70 years of age. EUS was performed in 32 (60.4 %) patients and staging laparoscopy in 8 (15.1 %) patients, with 6 laparoscopies occurring after EUS. Neoplasias were located in the stomach in 44 (83 %) cases and at the esophagogastric junction in 9 (17 %) cases.
Forty-five (84.9 %) patients completed the 3 preoperative cycles. Ten (18.9 %) patients developed grade 3 or 4 hematologic toxicity, which delayed the administration of the next chemotherapy cycle in 6 cases and caused early termination of chemotherapy in 2 (3.8 %) patients. One patient died from a pulmonary embolism. Ten (18.9 %) patients developed grade 3 or 4 non-hematologic toxicity, which forced an end to chemotherapy in 7 (13.2 %) cases and delayed administration of the next chemotherapy cycle in 2 patients.
Thirty-five (66 %) patients received the 3 postoperative cycles, and thus, they completed all the perioperative treatment. Eleven of those patients developed hematologic toxicity that caused only a delay in the administration of the next cycle. One patient developed grade 3 or 4 non-hematologic toxicity that caused a delay of the next cycle. Nine (17 %) patients were shifted to another chemotherapy regimen, and 2 (3.8 %) patients started a radiochemotherapy Macdonalds’s schema. Reasons for changing the chemotherapy regimen were evidence of residual or advanced disease after surgery in 6 patients, toxicity in 2 patients, and patient’s preference in one case. In case of advanced or residual disease, all patients were shifted to docetaxel, cisplatin and fluorouracil (DCF regimen). Seven (13.2 %) patients did not undergo postoperative treatment.
Peritoneal carcinomatosis, pancreatic infiltration or liver metastasis at the time of surgery precluded resection in 4 (7.5 %) patients. Resection was accomplished in 48 patients (90.6 %). Six partial esophagectomies, 9 subtotal gastrectomies and 33 total gastrectomies were performed. An R0 resection was initially obtained in 44 patients, but positive peritoneal lavage cytology was identified postoperatively in 2 of these patients (ypM1); therefore R0 resection was ultimately achieved in 42 (79.2 %) patients. R1 resection was obtained in 1 patient, with a positive proximal margin and several localized peritoneal nodules on the pancreatic surface. R2 resection was performed in 3 patients; one received only a single cycle of preoperative chemotherapy and also showed several localized peritoneal nodules on the pancreatic surface. The laparotomy findings of ypM1 patients are detailed in Table 2.
No significant correlation was found between extent of the lymph node dissection stated by the surgeon and the number of lymph nodes retrieved by the pathologist. Modified D2 lymphadenectomy was more frequently performed than D1 (38 vs 10 patients), but 16 or more lymph nodes were harvested in only 18 of the 38 (47.4 %). Conversely, at least 16 lymph nodes were harvested in 5 of the 10 (50 %) D1 lymphadenectomies performed. Ten or more lymph nodes were analyzed in 37 (77.1 %) patients.
The morbidity after resection was 20.8 %. The surgical mortality was 0 %.
The pathological characteristics of the tumors are detailed in Table 1. Twenty-four (50 %) carcinomas were staged as pT4. The median number and range of the retrieved lymph nodes was 14.5 (5-43). Thirty-one (64.6 %) of the resected specimens had positive lymph nodes.
Nine cases (17 %) were considered major responders after preoperative chemotherapy (2 with complete and 7 with subtotal tumor regression) (Table 3). In addition, 2 patients showed complete or subtotal tumor regression but also had positive lymph nodes and they were classified as minor responders. In 31 (64.6 %) patients minimal or no tumor regression was observed (Tables 2 and 4). Peritoneal lavage cytology was performed in 36 (69 %) patients and was positive in 4 (11.1 %).
The major and minor tumor responders are detailed in Tables 3 and 4. Among patients with R0 resection who were classified as minor responders to chemotherapy, 4 tumors were classified as stage IA (1 patient) and stage IB (3 patients) after the pathological study but 2 of them were classified as stage IIA and IIIB by EUS before the treatment’s onset. Five of the 23 (21.7 %) patients staged as uT4 presented with M1 disease at surgery.
The median follow-up of the series was 19 (3–68) months and the median follow-up of the patients alive was 43 (9–68) months. Seventy-nine percent of patients died or were followed for more than 2 years. The 5-year overall and disease-specific survival rates were 18 % and 22 % respectively (Fig. 1a and b).
After univariate analysis of the 5-year disease-specific survival, the completion of perioperative chemotherapy (p < 0.001), completion of NAC (p < 0.007), depth of invasion (ypT0-2 vs ypT3-4) (p < 0.01), LN staging (ypN0 vs. ypN2-3) (p < 0.001), number of positive LNs (p < 0.001), and metastasis (ypM0 vs. ypM1) (p < 0.001) were shown to be significant (Fig. 2a–c). LN staging (ypN1 vs. ypN2-3) (p < 0.051) and tumor regression grade (major vs. minor responders) (p < 0.051) were at the limit of significance (Fig. 2c, 2d).
Of the 9 patients with complete or subtotal tumor regression (Becker’s grade 1a and 1b), 3 patients died due to recurrence (33.3 %), 4 patients were disease-free after 3 or more years of follow-up (44.4 %), and 2 patients died during early follow-up due to pulmonary thromboembolism (5th month) and cardiomyopathy (9th month). Of the 33 patients in which R0 resection was achieved but partial, minimal or no tumor regression (Becker’s grade 2 and 3) was observed, 23 (69.7 %) had recurrence, 10 (30.3 %) were disease-free, and 1 patient died due renal cancer progression. The 5-year disease-specific survival rate of patients with regressions grades 1a and 1b was 47.6 %, and was 16.8 % for patients with grades 2 and 3 (Fig. 2d).
A multivariate survival analysis stratified by ypM was performed including the following variables: completed vs. incompleted perioperative chemotherapy, number of positive LNs, ypT3-4 vs. ypT < 3, major vs. minor tumor regression grade, and an interaction factor composed of the completion of perioperative chemotherapy, ypT, and the number of positive LNs (Table 5). Only completion of perioperative chemotherapy (HR: 0.25; 95 % CI: 0.08–0.79; p = 0.019) was identified as an independent prognostic factor for the 5-year disease-specific survival. However, the completion of perioperative chemotherapy, depth of invasion and number of positive LNs were related, and patients with ypT3-4 and more than 4 positive LNs did not show increased survival rates even if they completed perioperative chemotherapy (HR: 1.16; 95 % CI: 1.02–1.32; p = 0.029). The 5-year disease-specific survival rate of the patients who completed perioperative chemotherapy was 29.6 % (Fig. 2a).
In this study, a high percentage of patients completed preoperative chemotherapy (85 %), and a high percentage of R0 resection was achieved (79 %). Completion of preoperative chemotherapy was higher in the perioperative-chemotherapy arm of the MAGIC trial (91 %), but R0 resection was achieved in only 69 % of the cases. Additionally, a higher percentage of our patients completed all 3 postoperative cycles (66 %) compared to those in the MAGIC trial (42 %) . In our study, one patient died during the neoadjuvant period due to pulmonary embolism. It has been reported that up to 3 % of lethal thrombo-embolic episodes occur during the preoperative period .
Completion of perioperative chemotherapy was the only independent prognostic factor in our study, and it was associated with a significant improvement of the 5-year specific-survival rate of these patients. However, the beneficial effects of perioperative chemotherapy were not observed in patients that had both tumors infiltrating subserosa or beyond and who had more than 4 positive lymph nodes. These data suggest that the impact of the ECF/X regimen on survival is mild. The overall and 5-year disease-specific survival rate of the series was quite poor compared to the 36 % obtained in the perioperative-chemotherapy group of the MAGIC trial, despite the higher percentage of R0 resection achieved in our study. This difference cannot be easily explained by different pathological findings, because the number of patients with tumors reaching the serosa or beyond (50 %), and tumors without lymph node metastasis (35 %) were very similar in this study and the MAGIC trial (48 % and 31 % respectively). Nevertheless, the higher percentage of pN3 tumors found in our study (27 % vs. 16 %) may lead to poorer 5-year survival rates. Finally, a recent study  reported a similar overall survival to that achieved in the MAGIC trial but also the percentage of pN2-pN3 was significant lower (29 %) than the shown in our study (48 %).
Little information is available on the tumor regression grade produced by the preoperative ECF/X regimen in gastric cancer [15, 22]. These reported studies used different classification systems to assess tumor regression, which prevents direct comparisons with our findings. In our study, complete or subtotal regression was only observed in 17 % of carcinomas, but these patients had better 5-year survival rates compared to those with partial or minor tumor regression. This relatively low percentage of major responders has been observed in other gastric cancer studies in which different chemotherapy regimens or radiochemotherapy schemas were preoperatively administered [19, 23, 24]. Notably, patients with subtotal or even complete tumor regression of the primary tumor may also have LN metastasis which occurred in 2 of the patients in this study, a finding that has previously been reported by others . Major tumor regression was consistently supported comparing the uTN to ypTN classifications in this group of carcinomas. Several studies agree that complete or subtotal regression, but not partial regression, is associated with higher disease-free survival rates [19, 24, 25]. In a large series analyzing tumor regression after different neoadjuvant cisplatin-based regimens , multivariate analysis identified only complete or subtotal tumor regression and ypN status as independent prognostic factors for survival. Additionally, no difference in the mean survival was identified between patients with partial and minor tumor regression, which is why we combined these patients into one cohort. It must be highlighted that tumor regression was minimal or absent in a large percentage of our patients (67 %). In a similar way, another study of perioperative ECF/X chemotherapy reported less than 50 % tumor regression in 54 % of the cases . This fact suggests that patients with minor or no regression tumors may be at a risk of developing micrometastasis or peritoneal seeding during the neoadjuvant period. In a study of locally advanced gastric carcinomas in which a second laparoscopy was performed after neoadjuvant chemotherapy, free peritoneal tumor cells were detected in 24 % of patients with a previous negative staging laparoscopy, which confirms that the risk is real .
It is crucial to identify new biomarkers that predict tumor response or resistance to chemotherapy regimens to avoid the delay of potentially curative surgery in patients with non-responsive tumors [27, 28]. HER2 overexpression showed to be a useful biomarker in inoperable or metastatic gastric and esophagogastric carcinomas for selective treatment with trastuzumab in combination with chemotherapy . On the other hand, ERCC1 nuclear protein expression in clinicopathological studies  and leptin expression in in vitro studies  have been associated with poor pathologic response to platinum-based chemotherapy regimens. Therefore, biomarkers of drugs resistance should be included in future clinical trials.
EUS was useful in selecting the patients included in the perioperative MAGIC regimen except in 2 cases. EUS is recommended for workup staging in some clinical guidelines [6, 7], and it is reportedly more accurate in staging T3 and T4 tumors but less reliable for N staging . However, EUS was not useful in appropriately selecting the uT4a tumors that should undergo a staging laparoscopy for detection of carcinomatosis. Thus, 22 % of the uT4a tumors were staged as upM1 after surgery, a result that is similar to the findings reported by other authors .
The most important limitation of this study was the relative small sample size. Other studies confirm how difficult it can be to recruit gastric cancer patients for perioperative chemotherapy, which was evident in the two largest studies with patients from 50 and 28 participant centers that required 8 years to close [13, 14]. Another study carried out in one institution assessed the perioperative MAGIC regimen in one hundred gastro-esophageal carcinomas, but only 32 gastric tumors were included .
Completion of perioperative ECF/X chemotherapy was an independent prognostic factor for the 5-year disease-specific survival, although higher survival rates were impaired in patients with tumors that were invading the subserosa or beyond and more than 4 positive lymph nodes. A small proportion of patients with gastric carcinomas showed complete or subtotal tumor regression after perioperative ECF/X chemotherapy.
Lepage C, Sant M, Verdecchia A, Forman D, Esteve J, Faivre J. Operative mortality after gastric cancer resection and long-term survival differences across Europe. Br J Surg. 2010;97:235–9.
Maruyama K, Gunven P, Okabayashi K, Sasako M, Kinoshita T. Lymph node metastases of gastric cancer. General pattern in 1931 patients. Ann Surg. 1989;210(5):596–602.
Siewert JR, Bottcher K, Stein HJ, Roder JR. Relevant prognostic factors in gastric cancer. Ten-year results of the german gastric cancer study. Ann Surg. 1998;228(4):449–61.
Cuschieri A, Weeden S, Fielding J, Bancewicz J, Craven J, Joypaul V, et al. Patient survival after D1 and D2 resections for gastric cancer: long-term results of the MCR randomized surgical trial. Br J Cancer. 1999;79:1522–30.
Songun I, Putter H, Kranenbarg EMK, Sasako M, van de Velde CJH. Surgical treatment of gastric cancer: 15-year follow-up results of the randomised nationwide Dutch D1D2 trial. Lancet Oncol. 2010;11:439–49.
Waddell T, Verheij M, Allum W, Cunningham D, Cervantes A, Arnold D. Gastric cancer: ESMO-ESSO-ESTRO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2013;24 Suppl 6:vi57–63.
Gastric Cancer. NCCN Clinical Practice Guidelines in Oncology. V1.2013. www.nccn.org.
Smalley SR, Benedetti JK, Haller DG, Hundahl SA, Estes NC, Ajani JA, et al. Updated analysis of SWOG-Directed Intergroup Study 0116: A phase III trial of adjuvant radiochemotherapy versus observation after curative gastric cancer resection. J Clin Oncol. 2012;30(19):2327–33.
Shridhar R, Dombi GW, Weber J, Hoffe SE, Meredith K, Konski A. Adjuvant radiation therapy increases overall survival in node-positive gastric cancer patients with aggressive surgical resection and lymph node dissection. A SEER Database Analysis. Am J Clin Oncol. 2012;35(3):216–21.
Lee J, Lim DH, Kim S, Park SH, Park JO, Park YS, et al. Phase III trial comparing capecitabine plus cisplatin versus capecitabine plus cisplatin with concurrent capecitabine radiotherapy in completely resected gastric cancer with D2 lymph node dissection: The ARTIST Trial. J Clin Oncol. 2012;30(3):268–73.
Sasako M, Sakuramoto S, Katai H, Kinoshita T, Furukawa H, Yamaguchi T, et al. Five-Year Outcomes of a randomized phase III trial comparing adjuvant chemotherapy with S-1 versus surgery alone in stage II or III gastric cancer. J Clin Oncol. 2011;29(33):4387–93.
Bang YJ, Kim YW, Yang HK, Chung HC, Park YK, Lee KH, et al. Adjuvant capecitabine and oxaliplatin for gastric cancer after D2 gastrectomy (CLASSIC): a phase 3 open-label, randomised controlled trial. Lancet. 2012;379:315–21.
Cunningham D, Allum WH, Stenning SP, Thompson JN, Van de Velde CJH, Nicolson M, et al. Perioperative chemotherapy versus surgery alone for resectable gastroesophageal cancer. N Engl J Med. 2006;355(1):11–20.
Ychou M, Boige V, Pignon JP, Conroy T, Bouché O, Lebreton G, et al. Perioperative chemotherapy compared with surgery alone for resectable gastroesophageal adenocarcinoma: An FNCLCC and FFCD multicenter phase III trial. J Clin Oncol. 2011;29(13):1715–21.
Reece-Smith AM, Saha S, Cunnell ML, Hameed K, Bessell EM, Duffy JP, et al. MAGIC in practice: experience of peri-operative ECF/X chemotherapy in gastro-esophageal adenocarcinomas. J Surg Oncol. 2012;106(6):748–52.
Mandard AM, Dalibard F, Mandard JC, Marnay J, Henry-Amar M, Petiot JF, et al. Pathologic assessment of tumor regression after preoperative chemoradiotherapy of esophageal carcinoma. Clinicopathologic correlations. Cancer. 1994;73:2680–6.
Becker K, Mueller JD, Schulmacher C, Ott K, Fink U, Busch R, et al. Histomorphology and grading of regression in gastric carcinoma treated with neoadjuvant chemotherapy. Cancer. 2003;98(7):1521–30.
Rödel C, Martus P, Papadoupoulos T, Füzesi L, Klimpfinger M, Fietkau R, et al. Prognostic significance of tumor regression after preoperative chemoradiotherapy for rectal cancer. J Clin Oncol. 2005;23(34):8688–96.
Becker K, Langer R, Reim D, Novotny A. Meyer zum Buschenfelde C, Engel J. et al. Significance of histopathological tumor regression after neoadjuvant chemotherapy in gastric adenocarcinomas: a summary of 480 cases. Ann Surg. 2011;253(5):934–9.
Cunningham D, Starling N, Rao S, Iveson T, Nicolson M, Coxon F, et al. Capecitabine and oxaliplatin for advanced esophagogastric cancer. N Engl J Med. 2008;358(1):36–46.
Bringeland EA, Wasmuth HH, Fougner R, Mjones P, Gronbech JE. Impact of perioperative chemotherapy on oncological outcomes after gastric cancer surgery. Br J Surg. 2014;101:1712–20.
Fareed KR, Ilyas M, Kaye PV, Soomro IN, Lobo DN, Parsons SL, et al. Tumour regression grade (TRG) analyses in patients with resectable gastro-oesophageal adenocarcinomas treated with platinum-based neoadjuvant chemotherapy. Histopathology. 2009;55:399–406.
Wang LB, Teng RY, Jiang ZN, Hu WX, Dong MJ, Yuan XM, et al. Clinicopathologic variables predicting tumor response to neoadjuvant chemotherapy in patients with locally advanced gastric cancer. J Surg Oncol. 2012;105:293–6.
Ajani JA, Winter K, Okawara GS, Donohue JH, Pisters PW, Crane CH, et al. Phase II trial of preoperative chemoradiation in patients with localized gastric adenocarcinoma (RTOG 9904): quality of combined modality therapy and pathologic response. J Clin Oncol. 2006;20(24(24)):3953–8.
Ott K, Blank S, Becker K, Langer R, Weichert W, Roth W, et al. Factors predicting prognosis and recurrence in patients with esophago-gastric adenocarcinoma and histopathological response with less than 10 % residual tumor. Langenbecks Arch Surg. 2013;398(2):239–49.
Lorenzen S, Panzram B, Rosenberg R, Nekarda H, Becker K, Schenk U, et al. Prognostic significance of free peritoneal tumor cells in the peritoneal cavity before and after neoadjuvant chemotherapy in patients with gastric carcinoma undergoing potentially curative resection. Ann Surg Oncol. 2010;17:2733–9.
Lacueva FJ, Perez-Ramos M, Soto JL, Oliver I, Andrada E, Medrano J, et al. Multidrug resistance-associated protein (MRP1) gene is strongly expressed in gastric carcinomas. Analysis by immunohistochemistry and real-time quantitative RT-PCR. Histopathology. 2005;46(4):389–95.
Okines AFC. Gonzalez de Castro D, Cunningham D, Chau I, Langley RE, Thompson LC, et al. Biomarker analysis in oesophagogastric cancer: Results from the REAL3 and TransMAGIC trials. Eur J Cancer. 2013;49:2116–25.
Bang YJ, Van Cutsem E, Feyereislova A, Chung HC, Shen L, Sawaki A, et al. Trastuzumab in combination with chemotherapy versus chemotherapy alone for treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer (ToGA): a phse 3, open-label, randomised controlled trial. Lancet. 2010;376:687–97.
Fareed KR, Al-Attar A, Soomro IN, Kaye PV, Patel J, Lobo DN, et al. Tumour regression and ERCC1 nuclear protein expression predict clinical outcome in patients with gastro-oesophageal cancer treated with neoadjuvant chemotherapy. Br J Cancer. 2010;102:1600–7.
Bain GH, Collie-Duguid E, Murray GI, Gilbert FJ, Denison A, MCkiddie F, et al. Tumour expression of leptin is associated with chemotherapy resistance and therapy-independent prognosis in gastro-oesophageal adenocarcinomas. Br J Cancer. 2014;110:1525–34.
Puli SR, Reddy JBK, Bechtold ML, Antillon MR, Ibdah JA. How good is endoscopic ultrasound for TNM staging of gastric cancers? A meta-analysis and systematic review. World J Gastroenterol. 2008;14(25):4011–9.
Power DG, Schattner MA, Gerdes H, Brenner B, Markowitz AJ, Capanu M, et al. Endoscopic ultrasound can improve the selection for laparoscopy in patients with localized gastric cancer. J Am Coll Surg. 2009;208(2):173–8.
We thank Dr. Javier Escrig-Sos from Castellon University Hospital (Spain) for his statistical advice.
The authors declare that they have no competing interests.
MF: participated in the design of the study and its coordination, carried out the surgical treatment, and helped to draft the manuscript. GJ: conceived the study, participated in the design of the study and its coordination, carried out the chemotherapy treatment, and helped to draft the manuscript. OA: participated in the design of the study and carried out the pathological study. M-BA: participated in the design of the study and carried out the surgical treatment. S-VJ: participated in the design of the study and carried out endoscopic ultrasound. MP: participated in the design of the study and its coordination. MMA: participated in the design of the study and its coordination, carried out the surgical treatment. RJA: carried out the pathological study. CR: participated in the design of the study and helped to draft the manuscript. LFJ: conceived the study, carried out the surgical treatment, participated in the design of the study and its coordination, and helped to draft the manuscript. All authors have read and approved the final manuscript
About this article
Cite this article
Mingol, F., Gallego, J., Orduña, A. et al. Tumor regression and survival after perioperative MAGIC-style chemotherapy in carcinoma of the stomach and gastroesophageal junction. BMC Surg 15, 66 (2015). https://doi.org/10.1186/s12893-015-0054-9