OLOncology Letters1792-10741792-1082D.A. Spandidos10.3892/ol.2010.199ol-02-01-0021ArticlesClinical significance of GLUT-1 expression in patients with esophageal cancer treated with concurrent chemoradiotherapyCHIBAITARU1*OGAWAKAZUHIKO1*MORIOKATAKAMITSU2SHIMOJIHIDEAKI3SUNAGAWANAO2IRAHASHIRO1NISHIMAKITADASHI3YOSHIMINAOMI2MURAYAMASADAYUKI1
Department of Radiology, University of the Ryukyus, Okinawa, Japan
Department of Pathology, University of the Ryukyus, Okinawa, Japan
Department of Surgery, University of the Ryukyus, Okinawa, JapanCorrespondence to: Dr Kazuhiko Ogawa, Department of Radiology, University of the Ryukyus School of Medicine, 207 Uehara, Nishihara-cho, Okinawa 903-0215, Japan, E-mail: kogawa@med.u-ryukyu.ac.jp
This study aimed to investigate whether glucose transporter-1 (GLUT-1) expression in a pretreatment esophageal cancer biopsy was predictive of clinical outcomes in patients with esophageal cancer undergoing concurrent chemoradiotherapy (CRT). A total of 25 patients with esophageal cancer treated with concurrent CRT were reviewed. Radiotherapy was administered up to total doses of 40–66.6 Gy (median 66.6 Gy) with a single fraction of 1.8–2 Gy. Regarding chemotherapy, cisplatin (80 mg/m2 on day 1) and 5-fluorouracil (800 mg/m2 on days 2–6) were used concurrently with radiotherapy, every 3–4 weeks for a total of 1–2 courses. Tissue samples from esophageal carcinoma were obtained from the 25 patients by biopsy prior to concurrent CRT, and a semiquantitative analysis of GLUT-1 expression was performed using immunohistochemical staining. High GLUT-1 expression was observed in 7 of 25 (28%) patients, and GLUT-1 expression was significantly correlated with clinical T stage (p=0.0454), clinical N stage (p=0.0324) and initial response to CRT (p=0.0185). Patients with a high GLUT-1 expression had significantly poorer local control (LC) (5-year LC 28.6%) than those with a low expression (5-year LC 73.4%, p<005). Multivariate analysis revealed that GLUT-1 and the number of chemotherapy courses were independent prognostic factors for LC. Patients with a high GLUT-1 expression had significantly lower recurrence-free survival (RFS) compared to those with a low GLUT-1 expression (p=0.0405). Multivariate analysis revealed that GLUT-1, the number of chemotherapy courses and clinical M stage were independent prognostic factors for RFS. GLUT-1 expression was significantly correlated with clinical T stage, clinical N stage and initial response to concurrent CRT, and was predictive of LC and RFS for patients with esophageal cancer treated with concurrent CRT.
Esophageal cancer is one of the most difficult malignancies to cure, and the prognosis for these patients is poor (1–3). Although surgery is the main curative treatment for these tumors, chemoradiotherapy (CRT) was identified as a viable option for the treatment of esophageal carcinoma. The Radiation Therapy Oncology Group (RTOG) 8501 trial showed that CRT is superior to radiotherapy alone as primary treatment (4). However, a number of studies demonstrated that the patterns of failure observed following definitive CRT showed that locoregional failure is frequent, with approximately 50% of patients experiencing local failure (4,5). The identification of predictive markers for the response to CRT may improve patient selection and allow for response modifications such as more intensive treatments for poor responders.
Glucose-transporter-1 (GLUT-1) is a membrane receptor that mediates the passive export of glucose across plasma membranes and its expression increases in hypoxic conditions due to reduced oxidative phosphorylation and hypoxia inducible factor-1 (HIF-1) induction (6). GLUT-1 facilitates the metabolic adaptation of cells to hypoxia and is essential for survival and proliferation of glycolytic metabolism (7,8). Therefore, GLUT-1 expression may be a suitable marker of hypoxia and glucose metabolism, measured simply and cost-effectively as part of the routine histological assessment of tumors (9,10). GLUT-1 has been immunohistochemically detected in a variety of malignant tissues, including tumors of the breast, thyroid, head and neck, bladder and lung (11–15). In all cases, the tumor expression was increased as compared to that of the corresponding normal tissues. The over-expression of GLUT-1 in tumors was reported to be a marker for poor prognosis in colorectal, ovarian and non-small cell lung cancers (16–18). In esophageal cancer, a number of studies showed that GLUT-1 over-expression was associated with tumor aggressiveness and poor prognosis in patients with esophageal cancer treated with surgical resection (19,20). However, little information is available on the clinical significance of GLUT-1 expression in patients with esophageal cancer treated with concurrent CRT.
In the current study, GLUT-1 expression was retrospectively semiquantitated. Moreover, whether or not these levels were associated with clinicopathological characteristics and the clinical outcomes in patients with esophageal cancer treated with concurrent CRT was investigated.
Materials and methodsPatients and sample collection
Between 1997 and 2002, 37 patients with esophageal cancer were treated with concurrent CRT at the University of the Ryukyus Hospital, Japan. The study comprised primary esophageal carcinoma specimens from pretreatment biopsies obtained from 25 patients. The disease characteristics of the 25 patients, including tumor stage and tumor sites, were not significantly different compared to those of the 12 patients from which carcinoma specimens were not obtained. The histopathological diagnosis of the 25 patients was squamous cell carcinoma. No patients received chemotherapy or radiotherapy prior to the biopsy. The carcinoma specimens were obtained from the tumor edge, thereby avoiding the necrotic center. The specimens were immediately fixed in 10% buffered formalin.
The patient characteristics of the 25 patients are shown in Table I. Of the 25 patients, 1 was female and 24 were male, and the ages ranged from 45–78 years (median 62). The study was performed according to the guidelines approved by the institutional review board of our institution, and written informed consent was obtained from the 25 patients.
Concurrent chemoradiotherapy
External beam radiotherapy (EBRT) was administered with megavoltage equipment of photon energies ≥4 MeV. The total doses of EBRT ranged from 40–66.6 Gy with a single fraction of 1.8–2 Gy 5 days per week. The median total dose of the 25 patients was 66.6 Gy, and 22 of 25 patients (88.0%) were treated with a total dose of ≥60 Gy. The treatment field of EBRT consisted of a localized field in 4 of 25 patients (16%), and the primary tumor plus regional lymph nodes in the remaining 21 (84%). In the majority of patients, computed tomography (CT)-based treatment planning and conformal radiotherapy were used. Initially, anterior-posterior opposed fields were employed at doses of 32.4–40 Gy, and a booster dose of 14–34.2 Gy was administered, using bilateral oblique or multiple fields. The clinical target volume for the primary tumor was defined as the gross tumor volume plus 3 cm craniocaudally. The planning target volumes for the primary tumor and the metastatic lymph nodes were determined with 1 to 1.5 cm margins to compensate for set-up variations and internal organ motion. Lung heterogeneity corrections were not used.
Chemotherapy was administered concurrently with radiotherapy. One course of chemotherapy consisted of cisplatin (80 mg/m2 on day 1) and 5-fluorouracil (800 mg/m2 on days 2–6), with 3- to 4-week intervals for a total of 1–2 courses. The patients received antiemetics with granisetron and metoclopramide prior to chemotherapy administration.
Immunohistochemical staining for glucose-transporter-1 and evaluation of staining
Formalin-fixed, paraffin-embedded tumor sections were dewaxed in xylene and dehydrated using a series of ethanol solutions of increasing dilution. Staining for GLUT-1 was then perfromed using the Envision Dual link. This protocol uses a 3,3′-diaminobenzidine substrate system that enabled visualization of the GLUT-1 protein as a brown stain. For GLUT-1 staining, a 1/100 (10 mg/ml protein) concentration of affinity-pure rabbit antihuman GLUT-1 (Chemicon Europe) was utilized. An incubation time was performed overnight at 4°C for the primary antibody steps, whereas an incubation time of 30 min at room temperature was selected for each secondary antibody. The negative controls were prepared by omitting the primary antibodies. Following staining, sections were rinsed with water, counterstained with Gill’s hematoxylin and cover-slipped using an aqueous mountant.
Two independent pathologists blinded to the clinico-pathological data performed the scoring of the immunohistochemical staining. The percentage of positive tumor cells was semiquantitatively determined by assessing the whole biopsy specimen, and the mean percentage of positive tumor cells was calculated by the two pathologists. In the current study, each sample was characterized as either 1, low (0–30%); or 2, high (31–100%).
Statistical analysis
The median follow-up of 9 surviving patients was 57.8 months (range 2.8–107.7). In the current study, the initial response of the primary tumor was evaluated using the criteria of the Japanese Society for Esophageal Disease, which were based on findings from esophagograms and esophagoscopies (21). In brief, complete response (CR) was defined as the complete disappearance of tumor and no appearance of new lesions at least 4 weeks after treatment. Partial response (PR) was defined as a >50% reduction in the product of the perpendicular diameters of the tumor and no appearance of new lesions at least 4 weeks after treatment. Progressive disease (PD) was defined as a >25% increase in the product of the perpendicular diameters of the tumor or any new tumor. Any further conditions were defined as no change (NC). Disease recurrence was defined as recurrence or progression of the initial disease or the occurrence of new disease following CRT detected by a CT scan and/or esophagoscopy, which were performed every 3–4 months for 2 years and then twice a year. Overall survival (OS), recurrence-free survival (RFS) and local control (LC) rates were calculated actuarially according to the Kaplan-Meier method (22), and were measured from the first day of CRT. Differences between the groups were estimated using the Chi-square and generalized Wilcoxon tests (23). Multivariate analysis was performed using the Cox regression model (24). P=0.05 was considered to be statistically significant. Statistical analysis was performed with the SPSS software package (version 6.1; SPSS, Inc., Chicago, IL, USA).
Results
Representative examples of high or low GLUT-1 expression by immunohistochemical analysis are shown in Fig. 1. In the current study, a high GLUT-1 expression was observed in 7 of 25 (28%) patients, and the patients were divided into low and high GLUT-1 expression groups. Table I shows the clinical data and GLUT-1 expression in the tumor biopsies of the 25 patients. The proportion of patients with T4 tumors was significantly higher (p=0.0454) in the high GLUT-1 expression group than that of patients with low GLUT-1 expression. Moreover, the proportion of patients with N1 tumor was significantly higher (p=0.0324) in the high GLUT-1 expression group than that of patients with low GLUT-1 expression. Other characteristics, such as age and gender, did not correlate with the GLUT-1 expression.
Table II shows GLUT-1 expression and the initial response in 25 patients. A total of 12 of 13 patients (92.3%) exhibited a CR response in the low GLUT-1 expression group, while 6 of 12 patients (50.0%) exhibited a CR response in the high GLUT-1 expression group. Significant differences were noted between the low and high GLUT-1 expression groups regarding the initial response to concurrent CRT (p=0.0185).
At the time of this study, 16 patients (91.0%) had disease recurrences (local, 6 patients; regional lymph nodes, 2; distant metastasis, including bone or lung, 4; and multiple sites, 4 patients). Of the 16 patients with multiple recurrences, 2 patients had simultaneous local recurrence. Local recurrence occurred in 8 patients (32.0%) in total. The 5-year actuarial LC rate in the 25 patients was 61.9%. Fig. 2 shows the LC curves according to the GLUT-1 expression. Patients with high GLUT-1 expression had a significantly poorer LC (5-year LC; 28.6%) than those with low GLUT-1 expression (5-year LC; 73.4%; p<005). The univariate analysis showed that GLUT-1 expression, the number of chemotherapy courses, total radiation dose and clinical M stage had a significant impact on LC (Table III), while the multivariate analysis showed that GLUT-1 expression and the number of chemotherapy courses were independent prognostic factors for LC (Table IV).
Of the 25 patients, 16 (64.0%) succumbed to the disease during this study. Of the 16 patients, 13 succumbed to esophageal carcinoma and the remaining 3 patients succumbed without any sign of clinical recurrence (1, radiation pneumonitis; 1, pneumonia; and 1, unknown causes). The 5-year actuarial OS and RFS rate for the 25 patients was 27.3 and 31.3%, respectively. Fig. 3 shows the RFS curves according to GLUT-1 expression. Patients with a high GLUT-1 expression had a significantly lower RFS compared to those with a low GLUT-1 expression (p=0.0405). The univariate analysis showed that GLUT-1 expression, the number of chemotherapy courses and clinical M stage had a significant impact on OS, while the multivariate analysis, the three factors proved to be significant prognostic factors for RFS (Tables V and VI).
Late complications of NCI-CTC Grade 4–5 were observed in 2 patients (4.0%). One patient suffered grade 4 pericardical effusion requiring pericardial puncture 58 months after the completion of CRT. The remaining patient suffered grade 5 radiation pneumonitis and succumbed to radiation pneumonitis 4 months after CRT. The 2 patients were treated with a total dose of 66.6 Gy radiotherapy and 2 courses of chemotherapies.
Discussion
The current study showed that GLUT-1 expression is significantly correlated with clinical T and N stages in patients with esophageal carcinoma. The percentage of patients with T4 tumor was significantly higher in the high GLUT-1 expression group than that of patients with low GLUT-1 expression. Moreover, the percentage of patients with N1 tumor was significantly higher in the high GLUT-1 expression group than that of patients with a low GLUT-1 expression. A number of studies found an association between GLUT-1 expression and tumor stage (19,20). Tohma et al found that pathological T3–4 esophageal cancers showed higher percentages of GLUT-1 strong positive cells than T1–2 cancers, and lesions exhibiting lymph node metastasis showed higher percentages of GLUT-1 strong positive cells than lesions without lymph node metastasis (19). Kato et al showed that significant correlations between GLUT-1 expression and tumor stage were observed in patients with esophageal squamous cell carcinoma (20). The results of these authors, together with our results, proved that GLUT-1 expression is correlated with tumor aggressiveness in patients with esophageal carcinoma. GLUT-1 may be linked to invasiveness by supporting glycosis, which enhances tumor cell viability and provides energy for cell division and tumor growth (25).
The current study showed that GLUT-1 expression was significantly correlated with initial response to concurrent CRT, and patients with a high GLUT-1 expression had a significantly poorer LC (5-year LC, 28.6%) than those with a low expression (5-year LC, 73.4%; p<005). Multivariate analysis revealed that GLUT-1 and the number of chemotherapy courses were independent prognostic factors for LC. The relationship between GLUT-1 expression and the reduction in response to radiotherapy and chemotherapy is explained by the fact that GLUT-1 expression is a marker of cellular adaptive responses to hypoxia (26–28). The biological effect of radiotherapy was reported to have increased approximately 3-fold when irradiation was performed under well-oxygenated conditions compared to anoxic ones (29). Regarding rectal cancers, Brophy et al found that GLUT-1 expression was significantly associated with a reduced response to CRT (26). These authors showed that GLUT-1 expression appears to be a surrogate for tumor response to CRT in patients with esophageal carcinoma.
Regarding RFS, patients with a high GLUT-1 expression had significantly lower RFS compared to those with a low GLUT-1 expression (p=0.0405). The multivariate analysis showed that GLUT-1, the number of chemotherapy courses and clinical M stage were independent prognostic factors for RFS. Previous studies found that the GLUT-1 over-expression in esophageal carcinoma is a risk factor for mortality (19,20) The results of these authors, together with our results, suggest that GLUT-1 expression is predictive of clinical outcomes in patients with esophageal carcinoma treated with CRT.
It is well established that hypoxic conditions due to reduced oxidative phosphorylation, which may be a consequence of the increased proliferation observed in tumors, enhances GLUT-1 expression (6,30). GLUT-1 is considered to enhance glycolytic metabolism which has been correlated with tumor proliferative activity (8). Therefore, GLUT-1 expression appears to be a surrogate marker for not only hypoxia but also the metabolic activity of malignant tumors (31). Since the presence of hypoxia causes treatment resistance by radiotherapy and chemotherapy, and the high metabolic activity causes a higher proliferative activity in tumors, a high GLUT-1 expression may result in poor treatment outcome in patients with malignant tumors.
The increase in glucose transport noted in malignant tumors has also been detected using 18-fluorodeoxyglucose positron emission tomography (FDG-PET), which can quantify tumor glucose consumption (32,33). Regarding esophageal carcinoma, Taylor et al found that in patients undergoing surgical resection, increasing standardized uptake values (SUVmax) correlated with an increased GLUT-1 expression (34). GLUT-1 activity enhanced glycolytic metabolism which has been correlated with tumor proliferative activity (8). Westerterp et al showed that in patients with esophageal carcinoma, a significant correlation was found between FDG uptake and GLUT-1 expression (35). Kato et al found that GLUT-1 expression was related to FDG uptake and assessment of both FDG uptake and GLUT-1 expression may be useful for providing prognostic data in patients with esophageal carcinoma (36). However, GLUT-1 expression is obtained from superficial biopsy tissues and may not be representative of the tumor as a whole. Further studies are therefore required to investigate the correlations of GLUT-1 and FDG-PET in patients with esophageal carcinoma.
In conclusion, our results showed that GLUT-1 expression is significantly correlated with initial T and N stages, and response to concurrent CRT. Moreover, GLUT-1 is predictive of LC and DFS for patients with esophageal carcinoma treated with concurrent CRT. These findings suggest a role for GLUT-1 as a new prognostic biomarker for patients with esophageal cancer treated with CRT, and may allow for the selection of patients most likely to benefit from more intensive treatments. Furthermore, understanding the biological role of GLUT-1 may allow for response modification by targeting specific pathways. However, this study is a retrospective study with a relatively limited number of patients. Therefore further prospective studies are required to confirm our results.
ReferencesRothJAPutnumJBJrRichTAForastiereAACancer of the esophagusCancer: Principles And Practice Of Oncology5th editionDevitaVTJrHellmanSRosenbergSALippincott-RavenPA98010211997EarlamRCunha-MeloJROesophageal squamous cell carcinoma: I. A critical review of surgeryBr J Surg673813901980EarlamRCunha-MeloJROesophogeal squamous cell carcinoms: II. A critical view of radiotherapyBr J Surg674574611980CooperJSGuoMDHerskovicAChemoradiotherapy of locally advanced esophageal cancer: long-term follow-up of a prospective randomized trial (RTOG 85-01). Radiation Therapy Oncology GroupJAMA281162316271999MinskyBDPajakTFGinsbergRJINT 0123 (Radiation Therapy Oncology Group 94-05) phase III trial of combined-modality therapy for esophageal cancer: high-dose versus standard-dose radiation therapyJ Clin Oncol20116711742002BehroozAIsmail-BeigiFDual control of glut1 glucose transporter gene expression by hypoxia and by inhibition of oxidative phosphorylationJ Biol Chem272555555621997LinZWeinbergJMMalhotraRMerrittSEHolzmanLBBrosiusFCIIIGLUT-1 reduces hypoxia-induced apoptosis and JNK pathway activationAm J Physiol Endocrinol Metab2789589662000PessinJEBellGIMammalian facilitative glucose transporter family: structure and molecular regulationAnnu Rev Physiol549119301992AirleyRLoncasterJDavidsonSBromleyMRobertsSPattersonAHunterRStratfordIWestCGlucose transporter glut-1 expression correlates with tumor hypoxia and predicts metastasis-free survival in advanced carcinoma of the cervixClin Cancer Res79289342001AirleyRELoncasterJRaleighJAGLUT-1 and CAIX as intrinsic markers of hypoxia in carcinoma of the cervix: relationship to pimonidazole bindingInt J Cancer10485912003BrownRSWahlRLOverexpression of Glut-1 glucose transporter in human breast cancerCancer72297929851993HaberRSWeiserRLPritskerARederIBursteinDEGlut-1 glucose transporter in benign and malignant thyroid nodulesThyroid73633671997MellanenPMinnHGrenmanRHarkonenPExpression of glucose transporters in head and neck tumorsInt J Cancer566226291994ChangSLeeSLeeCKimJIKimYExpression of the human erythrocyte glucose transporter in transitional cell carcinoma of the bladderUrology554484522000KurataTOguriTIsobeTIshiokaSYamakidoMDifferential expression of facilitative glucose transporter (GLUT) genes in primary lung cancers and their liver metastasesJpn J Cancer Res90123812431999HaberRSRathanAWeiserKRGLUT-1 glucose transporter expression in colorectal carcinoma: a marker for poor prognosisCancer8334401998CartianaGFagottiGMegathaesAGlut-1 expression in ovarian carcinoma: association with survival and response to chemotherapyCancer92114411502001YounesMBrownRWStephensonMGondoMCaglePTOverexpression of Glut1 and Glut3 in stage 1 nonsmall cell lung carcinoma is associated with poor survivalCancer80104610511997TohmaTOkazumiSMakinoHOverexpression of glucose transporter 1 in esophageal squamous cell carcinomas: a marker for poor prognosisDis Esophagus181851892005KatoHTakitaJMiyazakiTGlut-1 glucose transporter expression in esophageal squamous cell carcinoma is associated with tumor aggressivenessAnticancer Res22263526392002Japanese Society for Esophageal DiseaseGuide Lines For The Clinical And Pathologic Studies On Carcinoma Of The Esophagus9th editionKanehara ShuppanTokyo59791999KaplanELMeierPNonparametric estimation from incomplete observationsJ Am Stat Assoc534574811958GehanEA generalized Wilcoxon test for comparing arbitrarily single-censored samplesBiometrica522032241965CoxDRRegression models and life tablesJ R Stat Soc341872201972KawamuraTKusakabeTSuginoTExpression of glucose transporter-1 in human gastric carcinoma: association with tumor aggressiveness, metastasis, and patient survivalCancer926346412001BrophySSheehanKMMcNamaraDADeasyJBouchier-HayesDJKayEWGLUT-1 expression and response to chemoradiotherapy in rectal cancerInt J Cancer125277827822009HockelMSchlengerKAralBMitzeMSchafferUVaupelPAssociation between tumor hypoxia and malignant progression in advanced cancer of the uterine cervixCancer Res56450945151996AirleyREPhillipsRMEvansAEHypoxia-regulated glucose transporter Glut-1 may influence chemosensitivity to some alkylating agents: Results of EORTC (First Translational Award) study of the relevance of tumour hypoxia to the outcome of chemotherapy in human tumour-derived xenograftsInt J Oncol26147714842005GrayLHCongerADEbertMHornseySScottOCThe concentration of oxygen dissolved in tissues at the time of irradiation as a factor in radiotherapyBr J Radiol266386481953ShettyMLoebJNVikstromKIsmail-BeigiFRapid activation of GLUT-1 glucose transporter following inhibition of oxidative phosphorylation in clone 9 cellsJ Biol Chem26817225172321993WarburgOOn the origin of cancer cellsScience1233093141956OgawaTInugamiAHatazawaJClinical positron emission tomography for brain tumors: comparison of fludeoxyglucose F 18 and L-methyl-(11)C-methionineAm J Neuroradiol173453531996AdamsSBaumRSchumm-DragerPUsadelKHorGLimited value of fluorine-18 fluorodeoxyglucose positron emission tomography for the imaging of neuroendocrine tumorsEur J Nucl Med2579831998TaylorMDSmithPWBrixWKCorrelations between selected tumor markers and fluorodeoxyglucose maximal standardized uptake values in esophageal cancerEur J Cardiothorac Surg356997052009WesterterpMSloofGWHoekstraOS18FDG uptake in oesophageal adenocarcinoma: linking biology and outcomeJ Cancer Res Clin Oncol1342272362008KatoHTakitaJMiyazakiTCorrelation of 18-F- fluorodeoxyglucose (FDG) accumulation with glucose transporter (Glut-1) expression in esophageal squamous cell carcinomaAnticancer Res23326332722003
Representative example of GLUT-1 expression in esophageal carcinoma. Immunohistochemical staining with anti-GLUT-1 antibody in esophageal carcinoma cells. (A) High and (B) low GLUT-1 expression.
Local control curves according to the GLUT-1 expression in esophageal carcinoma patients treated with concurrent chemoradiotherapy.
Disease-free survival curves according to the GLUT-1 expression in esophageal carcinoma patients treated with concurrent chemoradiotherapy.
GLUT-1 expression and clinicopathological characteristics in 25 patients with esophageal cancer treated with concurrent chemoradiotherapy.
GLUT-1 expression
Variable
No. of patients
Negative
Positive
P-value
Gender
Male
24
18
6
0.1017
Female
1
0
1
Age (years)
<60
8
4
4
0.1663
≥60
14
11
3
Clinical T stage (UICC 2002)
T1–3
15
13
2
0.0454
T4
10
5
5
Clinical N stage (UICC 2002)
N0
8
8
0
0.0324
N1
17
10
7
Clinical M stage (UICC 2002)
M0
20
16
4
0.0747
M1
5
2
3
KPS (%)
100–70
23
17
6
0.4701
≤60
2
1
1
Tumor site
Ce or Ut
12
8
4
0.5682
Mt or Lt
13
10
3
Total radiation dose
<60 Gy
3
2
1
0.8264
≥60 Gy
22
16
6
No. of chemotherapy courses
1
7
4
3
0.3021
2
18
14
4
UICC, International Union Against Cancer; KPS, Karnofsky performance status; Ce, cervical esophagus; Ut, upper thoracic; Mt, middle thoracic; Lt, lower thoracic.
GLUT-1 expression and initial response in 25 patients with esophageal cancer treated with concurrent chemoradiotherapy.