- Research article
- Open Access
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Results of radiation therapy combined with nedaplatin (cis-diammine-glycoplatinum) and 5-Fluorouracil for postoperative locoregional recurrent esophageal cancer
- Keiichi Jingu†1Email author,
- Kenji Nemoto†1,
- Haruo Matsushita1,
- Chiaki Takahashi1,
- Yoshihiro Ogawa1,
- Toshiyuki Sugawara1,
- Eiko Nakata1,
- Yoshihiro Takai1 and
- Shogo Yamada1
© Jingu et al; licensee BioMed Central Ltd. 2006
- Received: 01 November 2005
- Accepted: 04 March 2006
- Published: 04 March 2006
Although the effectiveness of radiotherapy with concurrent administration of several anti-tumor drugs for postoperative recurrent esophageal cancer has been demonstrated, the results are not satisfactory. The purpose of the present study was to evaluate the effectiveness and safety of radiotherapy combined with nedaplatin and 5-FU for postoperative locoregional (excluding hematogenous metastasis) recurrent esophageal cancer.
In June 2000, we started a phase II study on treatment of postoperative locoregional recurrent esophageal cancer with radiotherapy (60 Gy/30 fr/6 weeks) combined with chemotherapy consisting of two cycles of nedaplatin (70 mg/m2/2 h) and 5-FU (500 mg/m2/24 h for 5 days).
The primary endpoint of the present study was overall survival rate, and the second endpoints were irradiated-field control rate, tumor response and toxicity.
A total of 30 patients were included in this study. The 1-year and 3-year overall survival rates were 60.6% and 56.3%, respectively, with a median survival period of 39.0 months, and the 1-year and 3-year irradiated-field control rates were 86.4% and 72%, respectively. Complete response and partial response were observed in 13.3% and 60.0% of the patients, respectively. Grade 3 or higher leukocytopenia and thrombocytopenia were observed in 30% and 3.3% of the patients, respectively, but renal toxicity of grade 3 or higher was not observed. The regimen was completed in 76.7% of the patients.
In univariate analysis, the difference between survival rate in preradiotherapy performance status, recurrent pattern (worse for patients with anastomotic recurrence) and age (worse for younger patients) were statistically significant.
Radiotherapy combined with nedaplatin and 5-FU is a safe and effective salvage treatment for postoperative locoregional recurrent esophageal cancer.
- Esophageal Cancer
- Radiation Therapy Oncology Group
- Normal Tissue Complication Probability
- Anastomotic Recurrence
Since the mid-1980's, extended radical esophagectomy with three-field (neck, mediastinum, and abdomen) lymph node dissection has been performed, and it seems to have improved survival of patients with esophageal cancer [1–3]. However, there is recurrence in 27~52% of operated patients and locoregional recurrence in 41.5~55% of patients with postoperative recurrence [3–9]. Although the effectiveness of radiotherapy and concurrent chemoradiotherapy using cisplatin (CDDP) + 5-fluorouracil (5-FU) or a combination of several anti-tumor drugs for postoperative recurrent esophageal cancer has been demonstrated, median survival periods have been only 7.0~11.0 months [9–19]. These results are not satisfactory.
Based on these facts, we started a phase study II on the effectiveness of radiotherapy combined with CDGP and 5-FU for postoperative locoregional recurrence of esophageal cancer.
In June 2000, we started the present study in three institutes, Tohoku University Hospital and two affiliated hospitals, according to the following protocol.
All patients had histologically proven squamous cell carcinoma of the esophagus. Patient selection criteria included 1) 30 to 80 years of age, 2) Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 3, 3) no other active cancer, 4) no serious cardiac, liver, or pulmonary disease, 5) creatinine clearance of more than 50 ml/min, 6) adequate bone marrow function (leukocyte count of 4000/μl, platelet count of 100,000/μl, 7) locoregional recurrence (including para-aortic lymph node metastasis) without distant metastasis after no residual tumor (R0) resection; extended radical esophagectomy with three-field (neck, mediastinum, and abdomen) lymph node dissection, and 8) no previous therapy other than R0 resection.
Recurrence was diagnosed comprehensively by upper gastrointestinal endoscopy, ultrasonography, computed tomography (CT), physical findings and/or cytology.
A linear accelerator (4 MV or 10 MV) was used as the X-ray source. The target volume was localized for radiotherapy in all patients by CT planning. The daily fractional dose of radiotherapy was 2.0 Gy, administered 5 days a week, and the total dose was 60.0 Gy. For 11 patients who had metastasis of lymph nodes in some regions or metastasis of many lymph nodes in one region, a T-shaped field (including the bilateral supraclavicular, mediastinal and abdominal regions) was used. For the remaining 19 patients, local fields with a margin of 1 to 2 cm from the macroscopic tumor were used. After a total dose of 40 Gy, the field was changed for all patients to avoid the spinal cord, and only macroscopic lesions were irradiated with a margin of 1 to 1.5 cm. To decrease the incidence of radiation pneumonitis, we avoided as much as possible irradiating more than 30% of V20, which is the percentage of the total lung volume that received > 20 Gy.
Completion of the regimen in this study was defined as completion of two cycles of full-dose CDGP + 5-FU for a total radiotherapy dose of 60 Gy without suspension of treatment.
The overall survival, relapse-free survival and irradiated-field control rates were calculated from the first date of radiotherapy.
The primary endpoint of the current study was overall survival rate, and the second endpoints were tumor response, relapse-free survival rate, irradiated-field control rate and toxicity.
RECIST (Response Evaluation Criteria in Solid Tumors) was used to determine the tumor response. Tumor response was evaluated by CT 1~2 months after chemoradiotherapy. The number of mean measurable lesions was 1.8 per patient, and the response was evaluated according to agreement of more than two radiation-oncologists. In the present study, metastasis of para-aortic lymph nodes was defined as regional recurrence.
Follow-up evaluations were performed every 3~6 months for the first 2 years and every 12 months thereafter by endoscopy and CT.
We defined what only progression disease (PD) according was the failure of the present regimen (relapse again).
Survival estimates were calculated using the Kaplan-Meier method, and differences were evaluated by the log-rank test. Cox's proportional hazards regression model was used for univariate survival analysis. Age, preoperative stage (I – II vs. III – IV: Union International Contre le Cancer 1997 (UICC1997)), time interval between surgery and recurrence, pre-radiotherapy performance status (0–1 vs. 2–3), radiation field (local alone vs. T-shaped), acute tumor response (complete regression (CR) ~ partial regression (PR) vs. stable disease (SD) ~ PD), relapse again inside the irradiated field (yes vs. not), number of cycles of chemotherapy (one vs. two), recurrent pattern (anastomotic vs. non-anastomotic) and number of recurrent regions (one region vs. multiple regions) were entered into univariate analysis. In univariate analysis, age and time interval between surgery and recurrence were not classified in categories. A p value of less than 0.05 was considered significant. All analyses were performed using SPSS 11.0.
Toxicity was graded according to the Common Terminology Criteria for Adverse Events (CTCAE v3.0).
The present study protocol was reviewed and approved by the Tohoku University Hospital Institutional review board, and informed consent was obtained from each patient before conducting the treatment.
Number of patients
Preoperative Stage (UICC* 1997)
Number of patients
Site of recurence
Number of patients
supraclavicular lymph node
mediastinal lymph node
abdominal lymph node
Performance Status (ECOG†)
Number of patients
State at last observation date (August 31, 2005)
Number of patients
The last observation date was August 31, 2005. The median follow-up period was 12.5 months (range, 4.0 to 62.0 months) for all patients and 18.0 months (range, 4.5 to 62.0 months) for patients still alive. Sixteen of the 30 patients had relapse again. Thirteen patients out of a total of 30 died; 10 patients due to progression disease, 2 patients due to intercurrent diseases and one patient due to iatrogenic cause. At the last observation date, 15 patients remained alive, and 2 patients were lost to follow up.
Treatment response (RECIST: Response Evaluation Criteria in Solid Tumors)
Contents and results of radiotherapy (with or without chemotherapy) for postoperative recurrent esophageal cancer. in previous studies. The numbers in parenthesis are a numbers of patients.
median survival time
1-year survuval rate
JL Raoul 
radiotherapy + chemotherapy
H Yamanaka 
radiotherapy + CDGP§ + 5-FU#
K Nemoto 
radiotherapy alone(21) or radiotherapy + CDDP* + 5-FU (12)
Y Nishimura 
radiotherapy + CDDP + 5-FU
H Shimada 
chemoradiotheray(47), chemotherapy alone(17), radiotherapy alone(12)
K Nemoto 
radiotherapy + CDGP + 5-FU
Major toxicities related to this regimen (the Common Terminology Criteria for Adverse Events: CTCAE v3.0)
heartburn or mucositis
Prognostic factors. Cox's proportional hazards regression model was used for univariate survival analysis.
median survival time
preoperative stage (UICC§ 1997)
I – II
III – IV
number of cycles of chemotherapy
time interval between surgery and recurrence
tumor response (RECIST*)
relapse again inside irradiated field
number of recurrent regions
There have been some studies on the effectiveness of radiotherapy (with or without chemotherapy) for treatment of postoperative recurrent esophageal cancer. In those studies, the median survival periods were 7.0~9.5 months and the 1-year survival rates were 28~69% (Table 3) [12–16, 25]. The median survival periods in previous studies on the effectiveness of chemotherapy alone for treatment of recurrent esophageal cancer were similar, 5.0~10.5 months [10, 17–19]. None of the results were good. In 2001, we also reported the results of a study on the effectiveness of radiotherapy (with or without concurrent chemotherapy) for treatment of postoperative locoregional recurrent esophageal cancer: the median survival period of patients who did not undergo chemotherapy was 7.0 months, the median survival period of patients who underwent chemotherapy (CDDP and 5-FU) was 9.0 months, and the overall 1-year and 3-year survival rates were 33 and 15%, respectively . In 2003, we reported the results of a study on the effectiveness of radiotherapy combined with CDGP + 5-FU in our institution for treatment of 7 patients with postoperative locoregional recurrent esophageal cancer: the 1-year survival rate was 69% (The median survival period could not be calculated.) . Compared with these results, the results of the present study showing overall median survival period of 39.0 months and 1-year survival rate of 60.6% were excellent. Although it seems natural that chemoradiotherapy is more effective than radiotherapy or chemotherapy alone because of their synergistic and/or additive effects, the high rate of completion of the regimen because of less toxicities of CDGP and the high local control rate might have contributed to the better results in our study than those in previous studies on chemoradiotherapy. Although we have no evidence, CDGP or CDGP + 5-FU might have a greater synergy with radiation than CDDP or CDDP + 5-FU. However, we also should consider some biases: for example, the observation period was too short to determine long-term results, patients with performance status of 4 were excluded, patients who had hematogenous metastasis were excluded, all patients had squamous cell carcinoma by pure chance, high dose radiotherapy could be performed easily because of the unused adjuvant nor neoadjuvant therapy in association with initial surgery, and some of the 16 patients who had relapse again were treated with second-line salvage chemotherapy (docetaxel alone, TS-1 alone, or combined with CDDP or CDGP and docetaxel) after relapse again. The median survival period of the 16 patients after relapse again was 9.5 months (95%CI = 2.4–15.6).
However, only 5 of the 30 patients in the present study had relapse again inside the irradiation field. Irradiated-field control rates were 86.4% at 1-year and 72% at 3-year. Eleven of the 30 patients had relapse again in lymph nodes outside the irradiation field or in distant organs. There was no significant difference between survival periods of patients who had relapse again inside the irradiated-field and patients who had no relapse again inside irradiated-field. However, we believe that the high irradiated-field control rate of this protocol contributed to prolongation of survival. Although there was also no significant difference (median survival time; one region vs. multiple regions: 39.0 vs. 6.5 months, p = 0.19), number of recurrent regions also might have no small effect on survival.
Regarding the optimal irradiation field, we have experienced whether we need to irradiate to three-field including the bilateral supraclavicular, mediastinal and celiac regions or just the recurrent region of recurrence. In the present study, a T-shaped field was used in 11 patients. Although there was no significant difference, the median survival period of patients who received irradiation to the recurrent region alone was longer than that of patients who received T-shaped field irradiation (local vs. T-shaped: 39.0 vs. 14.0 months, p = 0.17; log-rank test). It was thought that this difference in the median survival period was due to the fact that a T-shaped field was often used for patients having multiple regional recurrences, although there was no significant correlation. Moreover, the problem of the significantly high rate of adverse events in patients who were treated with a T-shaped field remains, although most of these adverse events were controllable. To our knowledge, there is no report about irradiation fields for postoperative recurrent esophageal cancer. Prospective randomized studies on irradiation fields are needed.
The optimal radiation dose for recurrent esophageal cancer had also not been determined. About 60 Gy of radiotherapy combined with chemotherapy is preferred in Japan. Since TD5/5 (prediction radiation-dose of normal tissue complication probability at 5% within 5 years after radiotherapy) of the stomach is 60 Gy  and since one of our patients died of necrosis of the stomach, which had been used for thoracic esophageal substitution, 6 months after the end of 66 Gy radiotherapy, we avoid irradiation to the gastric tube with a total dose of more than 60 Gy. We have no major matter of stomach using 60 Gy/30 fractions/6 weeks radiotherapy. But the tolerance radiation-dose of gastric tube with chemotherapy has not been known. Although patients with primary esophageal cancer in the Intergroup Trial (INT) 0123 (Radiation Therapy Oncology Group (RTOG) 94-05) study were assigned randomly to receive combined-modality therapy consisting of CDDP (75 mg/m2 bolus day 1) + 5-FU (1000 mg/m2/24 hours for 4 days) with concurrent 64.8 Gy of radiotherapy or the same chemotherapy schedule but with concurrent 50.4 Gy of radiotherapy, there was no significant difference in median survival, 2-year survival, or local/regional failure and local/regional persistence of disease . Therefore, at present, four cycles of CDDP + 5-FU combined with 50 Gy of radiotherapy is a standard chemoradiotherapy regimen for advanced esophageal cancer in U.S.A.. As for primary esophageal cancer, a total dose 50 Gy radiotherapy with concurrent chemotherapy may be sufficient for recurrent esophageal cancer. It is necessary to investigate prospectively the optimal radiation dose for postoperative locoregional recurrent esophageal cancer.
CDGP has shown less renal toxicity but an anti-tumor effect similar or superior to that of CDDP in some preclinical and clinical studies [20–23]. Although the optimal doses of CDGP and 5-FU with radiotherapy have not been determined, we used doses of the anti-tumor drugs in the present study based the report by Yoshioka et al. . They administered CDGP at a dose of 80 or 100 mg/m2/2 hours and 5-FU at a dose of 350 or 500 mg/m2/24 hours for 5 days and recommended 100 mg CDGP/m2 and 500 mg 5-FU/m2. In the present study, we decided to administer CDGP at a 70% dose of their recommendation with consideration of concurrent radiotherapy.
The major toxicities are listed in Table 4. About major toxicities of this protocol in the acute phase, grade 4 toxicity was observed in only two patients. Grade 3 or higher toxicities of neutropenia, thrombocytopenia and esophagitis occurred in 30%, 3.3% and 3.3% of the patients, respectively. However, these grade 3 toxicities were temporary or controllable, and the protocol was performed in 23 patients without suspension or discontinuation and without reduction in the dose of chemotherapy. Therefore, the rate of completion of this regimen was high (76.7%). Compared to results of some clinical studies on chemoradiotherapy, for example, a phase II study by Ohtsu et al. , Japan Clinical Oncology Group Trial (JCOG) 9516 , a report by Burmeister et al. , RTOG 85-01  and INT 0123 , which cause a standard regimen for primary esophageal cancer in U.S.A., the rate of grade 4–5 toxicity in this study was low. The chemoradiotherapy protocol used in this study is therefore feasible and safe. The results of several studies, including the present study, indicate that CDGP + 5-FU is no less safe and effective than CDDP + 5-FU [16, 17, 24, 25]. Extensive prospective randomized studies are needed to compare the effectiveness and safety of radiotherapy combined with CDGP + 5-FU and those of radiotherapy combined with CDDP + 5-FU.
As prognostic factors of postoperative recurrent esophageal cancer, PS, age (worse for younger patients) and recurrent pattern (worse for patients with anastomotic recurrence), which had no correlation with others, were significantly associated with survival in univariate analysis in the present study (Table 5). The reason for the poor prognosis of young patients is not known. Tumors in younger patients may be aggressive, although there was no significant correlation between age and the time interval between surgery and relapse in the present study. The reason for the poor prognosis of patients with anastomic recurrence might be because of the significant correlation with PS and pattern of recurrence (p = 0.002, Pearson's product moment correlation coefficient = -0.539; the patients with anastomic recurrence were worse PS). We previously reported that the interval between surgery and relapse was a prognostic factor of recurrent esophageal cancer , but this was not selected as a prognostic factor in univariate analysis in the present study.
The present protocol of radiotherapy combined with nedaplatin and 5-fluorouracil is a safe and effective salvage treatment for postoperative locoregional recurrent esophageal cancer.
- Akiyama H, Tsurumaru M, Udagawa H, Kajiyama Y: Radical lymph node dissection for cancer of the thoracic esophagus. Ann Surg. 1994, 220: 364-373.View ArticlePubMedPubMed CentralGoogle Scholar
- Fujita H, Kakegawa T, Yamana H, Shima I, Toh Y, Tomita Y, Fujii T, Yamasaki K, Higaki K, Noake T, Ishibashi N, Mizutani K: Mortality and morbidity rates, postoperative course, quality of life, and prognosis after extended radical lymphadenectomy for esophageal cancer. Ann Surg. 1995, 222: 654-662.View ArticlePubMedPubMed CentralGoogle Scholar
- Nakagawa S, Kanda T, Kosugi S, Ohashi M, Suzuki T, Hatakeyama K: Recurrence pattern of squamous cell carcinoma of the thoracic esophagus after extended radical esophagectomy with three-field lymphadenectomy. J Am Coll Surg. 2004, 198: 205-211. 10.1016/j.jamcollsurg.2003.10.005.View ArticlePubMedGoogle Scholar
- Law SY, Fok M, Wong J: Pattern of recurrence after oesophageal resection for cancer: clinical implications. Br J Surg. 1996, 83: 107-111.View ArticlePubMedGoogle Scholar
- Bhansali MS, Fujita H, Kakegawa T, Yamana H, Ono T, Hikita S, Toh Y, Fujii T, Tou U, Shirouzu K: Pattern of recurrence after extended radical esophagectomy with three-field lymph node dissection for squamous cell carcinoma in the thoracic esophagus. World J Surg. 1997, 21: 275-281. 10.1007/s002689900228.View ArticlePubMedGoogle Scholar
- Kato H, Miyazaki T, Nakajima M, Sohda M, Fukai Y, Masuda N, Fukuchi M, Manda R, Tsukada K, Kuwano H: Prediction of hematogenous recurrence in patients with esophageal carcinoma. Jpn J Thorac Cardiovasc Surg. 2003, 51: 599-608.View ArticlePubMedGoogle Scholar
- Hulscher JB, van Sandick JW, Tijssen JG, Obertop H, van Lanschot JJ: The recurrence pattern of esophageal carcinoma after transhiatal resection. J Am Coll Surg. 2000, 191: 143-148. 10.1016/S1072-7515(00)00349-5.View ArticlePubMedGoogle Scholar
- Kyriazanos ID, Tachibana M, Shibakita M, Yoshimaru H, Kinugasa S, Dhar DK, Nakamoto T, Fujii T, Nagasue N: Pattern of recurrence after extended esophagectomy for squamous cell carcinoma of the esophagus. Hepatogastroenterology. 2003, 50: 115-120.PubMedGoogle Scholar
- Fahn HJ, Wang LS, Huang BS, Huang MH, Chien KY: Tumor recurrence in long-term survivors after treatment of carcinoma of the esophagus. Ann Thorac Surg. 1994, 57: 677-681.View ArticlePubMedGoogle Scholar
- Airoldi M, Cortesina G, Giordano C, Pedani F, Bumma C, Gabriele P: Docetaxel and vinorelbine: an effective regimen in recurrent squamous cell esophageal carcinoma. Med Oncol. 2003, 20: 19-24. 10.1385/MO:20:1:19.View ArticlePubMedGoogle Scholar
- Sato N, Ishida K, Ikeda K, Koeda K, Ohtsuka K, Kimura Y, Aoki K, Ogasawara S, Iwaya T, Saito K: Treatment of patients with recurrent esophageal carcinoma. Gan To Kagaku Ryoho. 1998, 25: 314-320.PubMedGoogle Scholar
- Nishimura Y, Koike R, Nakamatsu K, Kanamori S, Suzuki M, Shigeoka H, Shiozaki H: Concurrent chemoradiotherapy with protracted infusion of 5-FU and Cisplatin for postoperative recurrent or residual esophageal cancer. Jpn J Clin Oncol. 2003, 33: 341-345. 10.1093/jjco/hyg065.View ArticlePubMedGoogle Scholar
- Raoul JL, Le Prise E, Meunier B, Julienne V, Etienne PL, Gosselin M, Launois B: Combined radiochemotherapy for postoperative recurrence of oesophageal cancer. Gut. 1995, 37: 174-176.View ArticlePubMedPubMed CentralGoogle Scholar
- Shimada H, Kitabayashi H, Nabeya Y, Okazumi S, Matsubara H, Funami Y, Miyazawa Y, Shiratori T, Uno T, Itoh H, Ochiai T: Treatment response and prognosis of patients after recurrence of esophageal cancer. Surgery. 2003, 133: 24-31. 10.1067/msy.2003.31.View ArticlePubMedGoogle Scholar
- Nemoto K, Ariga H, Kakuto Y, Matsushita H, Takeda K, Takahashi C, Takai Y, Yamada S, Hosoi Y: Radiation therapy for loco-regionally recurrent esophageal cancer after surgery. Radiotherapy and Oncology. 2001, 61: 165-168. 10.1016/S0167-8140(01)00392-9.View ArticlePubMedGoogle Scholar
- Nemoto K, Matsushita H, Ogawa Y, Takeda K, Takahashi C, Britton KR, Takai Y, Miyazaki S, Miyata T, Yamada S: Radiation therapy combined with cis-diammine-glycolatoplatinum (Nedaplatin) and 5-fluorouracil for untreated and recurrent esophageal cancer. Am J Clin Oncol. 2003, 26: 46-49. 10.1097/00000421-200302000-00010.View ArticlePubMedGoogle Scholar
- Muro K, Ando N, Nishimaki T, Ohtsu A, Aogi K, Aoyama N, Nagai K, Kato H: A phase II study of nedaplatin and 5-fluorouracil in metastatic squamous cell carcinoma of the esophagus: Japan Clinical Oncology Group study (JCOG 9905). Proc ASCO. 2003, 22: 277-Google Scholar
- Urba SG, Chansky K, Van Veldhuizen PJ, Pluenneke RE, Benedetti JK, Macdonald JS, Abbruzzese JL: Gemcitabine and Cisplatin for patients with metastatic or recurrent esophageal carcinoma: A Southwest Oncolgy Group study. Investigational New Drugs. 2004, 22: 91-97. 10.1023/B:DRUG.0000006179.20974.af.View ArticlePubMedGoogle Scholar
- Hsu CH, Cheng AL, Hsu C, Yang CH, Lu YS, Lin CC, Bu CF, Yeh KH: A phase II study of weekly methotrexate, cisplatin, and 24-hour infusion of high-dose 5-fluorouracil and leucovorin (MP-HDFL) in patients with metastatic and recurrent esophageal cancer improving toxicity profile by infusional schedule and double biochemical modulation of 5-fluorouracil. Anticancer Res. 2002, 22: 3621-3627.PubMedGoogle Scholar
- Sasaki Y, Amano T, Morita M, Shinkai T, Eguchi K, Tamura T, Ohe Y, Kojima A, Saijo N: Phase I study and pharmacological analysis of cis-diammine (glycolate)platinum(254-S; NSC 375101D) administered by 5-day continuous intravenous infusion. Cancer Res. 1991, 51: 1472-1477.PubMedGoogle Scholar
- Taguchi T, Wakui A, Nabeya K, Kurihara M, Isono K, Kakegawa T, Ota K: A phase II clinical study of cis-diammine glycolato platinum, 254-S, for gastrointestinal cancers. 254-S Gastrointestinal Cancer Study Group Gan To Kagaku Ryoho. 1992, 19: 483-488.Google Scholar
- Uchida N, Takeda Y, Hojo K, Maekawa R, Sugita K, Yoshioka T: Sequence-dependent antitumour efficacy of combination chemotherapy of nedaplatin, a novel platinum complex, with 5-fluorouracil in an in vivo murine tumour model. Eur J Cancer. 1998, 34: 1796-1801. 10.1016/S0959-8049(98)00194-4.View ArticlePubMedGoogle Scholar
- Kameyama Y, Okazaki N, Nakagawa M, Koshida H, Nakamura M, Gemba M: Nephrotoxicity of a new platinum compound, 254-S, evaluated with rat kidney cortical slices. Toxicol Lett. 1990, 52: 15-24. 10.1016/0378-4274(90)90161-E.View ArticlePubMedGoogle Scholar
- Yoshioka T, Gamoh M, Shineha R, Ishibashi S, Shibata H, Suzuki T, Murakawa Y, Kato S, Shimodaira H, Kato S, Ishioka C, Kanamaru R: A new combination chemotherapy with cis-diammine-glycolatoplatinum (Nedaplatin) and 5-fluorouracil for advanced esophageal cancers. Inter Med. 1999, 38: 844-848.View ArticleGoogle Scholar
- Yamanaka H, Motohiro T, Michiura T, Asai A, Mori T, Hioki K: Nedaplatin and 5-FU combined with radiation in treatment for esophageal cancer. Jpn J Thorac Cardiovasc Surg. 1998, 10: 943-948.View ArticleGoogle Scholar
- Minsky BD, Pajak TF, Ginsberg RJ, Pisansky TM, Martenson J, Komaki R, Okawara G, Rosenthal SA, Kelsen DP: INT 0123 (Radiation Therapy Oncology Group 94-05): phase III trial of combined-modality therapy for esophageal cancer: high-dose versus Standard-dose radiation therapy. J Clin Oncol. 2002, 20: 1167-1174. 10.1200/JCO.20.5.1167.View ArticlePubMedGoogle Scholar
- Emami B, Lyman J, Brown A, Coia L, Goitein M, Munzenrider JE, Shank B, Solin LJ, Wesson M: Tolerance of normal tissue to therapeutic irradiation. Int J Radiat Oncol Biol Phys. 1991, 21: 109-122.View ArticlePubMedGoogle Scholar
- Ohtsu A, Boku N, Muro K, Chin K, Muto M, Yoshida S, Satake M, Ishikura S, Ogino T, Miyata Y, Seki S, Kaneko K, Nakamura A: Definitive chemoradiotherapy for T4 and/or M1 lymph node squamous cell carcinoma of the esophagus. J Clin Oncol. 1999, 17: 2915-2921.PubMedGoogle Scholar
- Ishida K, Ando N, Yamamoto S, Ide H, Shinoda M: Phase II study of cisplatin and 5-fluorouracil with concurrent radiotherapy in advanced squamous cell carcinoma of the esophagus: a Japan Esophageal Oncology Group (JEOG)/Japan Clinical Oncology Group Trial (JCOG9516). Jpn J Cli oncol. 2004, 34: 615-619. 10.1093/jjco/hyh107.View ArticleGoogle Scholar
- Burmeister BH, Denham JW, O'Brien M, Jamieson GG, Gill PG, Devitt P, Yeoh E, Hamilton CS, Ackland SP, Lamb DS, Spry NA, Joseph DJ, Atkinson C, Walker QJ: Combined modality therapy for esophageal carcinoma: preliminary results from a large Australasian multicenter study. Int J Radiat Oncol Biol Phys. 1995, 32: 997-1006. 10.1016/0360-3016(94)00449-U.View ArticlePubMedGoogle Scholar
- Cooper JS, Guo MD, Herskovic A, Macdonald JS, Martenson JA, Al-Sarraf M, Byhardt R, Russell AH, Beitler JJ, Spencer S, Asbell SO, Graham MV, Leichman LL: Chemoradiotherapy of locally advanced esophageal cancer: long-term follow-up of a prospective randomized trial (RTOG 85-01). Radiation Therapy Oncology Group. J Am Med Assoc. 1999, 281: 1623-1627. 10.1001/jama.281.17.1623.View ArticleGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/6/50/prepub
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