Adjuvant concurrent chemoradiation using intensity-modulated radiotherapy and simultaneous integrated boost for resected high-risk adenocarcinoma of the distal esophagus and gastro-esophageal junction
© Yaremko et al.; licensee BioMed Central Ltd. 2013
Received: 7 September 2012
Accepted: 28 December 2012
Published: 11 February 2013
Multimodality therapy leads to improved outcomes for adenocarcinoma of the distal esophagus and gastroesophageal junction (GEJ) over surgery alone. At our institution, adjuvant chemoradiation (chemoRT) using IMRT and SIB is standard of care for resected high-risk disease. In this study, we review our experience with a recent cohort of patients treated in this manner.
Methods and materials
We identified 18 patients with resected T3 and/or N1 adenocarcinoma of the distal esophagus and GEJ who received adjuvant chemoRT. A large elective volume (PTV1) and a smaller high-risk volume (PTV2) were irradiated simultaneously using IMRT and an SIB technique. All patients received concurrent chemotherapy. Relevant clinical outcomes are reported.
The median dose to 95% of PTV1 was 3747cGy and to 95% of PTV2 was 4876cGy. All RT was given in a median of 28 daily fractions. Four patients did not complete chemotherapy. At a median follow up of 952 days from the start of RT, 7 of 18 patients were dead; of these, 3 had developed local recurrence only; 3 had developed both local and distant recurrence; 1 died of a late toxicity, without recurrence. OS was 88% at 1year, 76% at 2 years and 58% at 3 years. Freedom from local recurrence was 88% at 1 year, 82% at 2 years and 82% at 3 years. Freedom from distant recurrence was 72% at 1 year, 67% at 2 years and 56% at 3 years. Toxicity was acceptable.
Adjuvant concurrent chemoRT with IMRT and SIB is feasible for resected high-risk adenocarcinoma of the distal esophagus and GEJ. Our results describe how modern treatment techniques can be employed as part of a treatment paradigm that is neither commonly used nor commonly described in the literature.
The incidence of adenocarcinoma of the distal esophagus, gastro-esophageal junction (GEJ) and proximal stomach is increasing . These cancers can grow to an advanced size before becoming apparent, and they can access an extensive lymphatic network , increasing the risk of metastasis and compromising outcome. For such reasons, the prognosis for this disease remains dismal. The mainstay of curative-intent treatment is surgery, where outcome correlates with the completeness of surgical resection . Unfortunately, surgery alone is rarely curative if there is nodal involvement , and thus there is a clear need to establish improved mechanisms for delivering adjuvant therapy.
Individually, the benefits of radiotherapy (RT) and chemotherapy beyond surgery are modest . The best outcomes have been achieved with trimodality therapy, where meta-analysis has identified significantly improved overall survival (OS) over surgery alone with the use of induction chemoRT [6–8]. Based upon such results, neoadjuvant chemoRT has become the standard of care for resectable carcinoma of the esophagus and GEJ.
Despite this, adjuvant concurrent chemoRT remains our institutional standard of care for patients with respectable carcinoma of the distal esophagus and/or GEJ. Such patients are taken immediately to surgery, after which those with pathologically proven T3 or N1 disease are offered adjuvant chemoRT. Historically, we delivered such treatment using multiphase 3-dimensional conformal radiotherapy (3DCRT) techniques [9, 10]. We have now established intensity-modulated radiotherapy (IMRT) with simultaneous integrated boost (SIB) as our new standard. We review herein our recent clinical experience with this novel technique in a cohort of patients.
This retrospective review was performed with the approval of our Institutional Health Sciences Research Ethics board.
Fifteen patients had video-assisted transhiatal esophagectomy with cervical anastomosis. One patient had transhiatal esophagectomy with right video-assisted mobilization of the esophagus. One patient required trans-thoracic esophagectomy with thoracotomy (three-hole esophagectomy). One patient required open transhiatal esophagectomy with laparotomy. All technically accessible lymph nodes were removed from the lower thoracic and upper abdominal nodal basins. Marking clips were placed to guide adjuvant radiotherapy treatment planning.
Prior to the start of RT, patients received two cycles of epirubicin-cisplatin-5-fluorouracil (ECF) alone (epirubicin: 50 mg/m2; cisplatin: 60 mg/m2; 5FU infusion: 200 mg/m2•d). This was followed by a further two cycles of CF given concurrently with RT (cisplatin: 60 mg/m2; 5FU infusion: 200 mg/m2•d). Each cycle was 3 weeks in duration, with the understanding that any cycle(s) could be given at reduced dose (or withheld altogether) at the discretion of the treating Medical Oncologist.
Radiotherapy treatment planning
All patients went for CT simulation during cycle 2 of chemotherapy. Prior to 2008, free-breathing CT simulation scans were standard. From 2008 onward, we used 4-dimensional CT (4DCT) to incorporate respiratory motion. Motion management was established using the Real-Time Position Management™ (RPM™) system (Varian Incorporated, Palo Alto, CA). All patients were immobilized with arms up, in a vacuum fixation device. Intravenous and oral contrast agents were not used.
Delineation of ICRU target volumes
We defined two clinical target volumes (CTV). Lower-dose volume CTV1 covered nodal basins at risk of harboring metastatic disease: the celiac axis, porta hepatis and splenic hilar nodes in the abdomen, and levels 1 through 8 in the mediastinum. In all cases, the superior border of CTV1 was set 3 cm superior to the anastomosis. Boost volume CTV2 covered the pre-surgical location of the primary disease, any bulky adenopathy and sites of close or positive margins. In general, CTV2 included the lower mediastinum and upper abdomen. For a single patient, CTV2 also included the anastomosis because of a close longitudinal surgical margin.
Prior to 2008, we applied margins of 1 cm superiorly-inferiorly and 5 mm radially to CTV 1 and CTV2 to account for tumor motion. From 2008 onwards, once 4DCT became standard, we delineated CTV1 and CTV2 on both the full-expiration and full-inspiration images to account for respiratory motion. We then added an isotropic margin of 3 mm to account for residual motion, defining internal target volumes (ITV) ITV1 and ITV2. Finally, we added a 5 mm isotropic margin around ITV1 and ITV2 for setup, defining planning target volumes (PTV) PTV1 and PTV2.
Historically, we treated these patients in two phases using 3DCRT: in phase 1, a large elective volume, including the anastomosis, was treated to 3600 cGy in 20 daily fractions. Our decision to include the anastomosis was rooted in RTOG 8501, where essentially the entire mediastinum was treated to 3600 cGy in 20 fractions . In phase 2, the high-risk boost volume was treated to 1440 cGy in 8 daily fractions (5040 cGy in 28 fractions total). Radiation portals for the phase 2 boost were defined according to pre-operative imaging and pathology .
PTV1 and PTV2 represent the modern cognates of our previous technique . PTV1 and PTV2 were treated using a simultaneous integrated boost (SIB) technique. All treatment was delivered using IMRT. PTV1 was prescribed a nominal dose of 3900 cGy in 28 daily fractions, representing a biologically equivalent dose to our historical standard of 3600 cGy in 20 fractions. PTV2 was, for most patients, prescribed a nominal dose of 5040 cGy in 28 daily fractions; two patients were prescribed 5400 cGy in 30 daily fractions, with the higher dose selected because of close surgical margins at the original tumor location.
Organs at risk
Dose to normal tissues was limited according to published standards [12, 13]. For the lung, we defined an evaluable lung volume as the total lung less any overlap with CTV1 (TL-CTV1). This volume was typically limited to 20 Gy to ≤30%, and a mean dose of 18 Gy or less.
Because our new technique represents a revision of our previous technique, a dosimetric comparison of our historical cohort and our current cohort would be instructive. Unfortunately, our historical cohort was planned using either an outdated treatment planning system (now decommissioned), or using plain-film radiography. Either way, a detailed dosimetric analysis of our original cohort is no longer possible. However, it is possible to re-plan our modern cohort using our previous technique . We performed this comparison for all 18 cases. The 3DCRT plan was prescribed to 3600 cGy in 20 fractions to PTV1, followed by a sequential boost of 1440 cGy in 8 fractions to PTV2; the IMRT-SIB plan was planned to 3900 cGy to PTV1 and 5040 cGy to PTV2, given concurrently in 28 fractions via an SIB technique. For the purpose of this comparison, the prescription isodose for the 3DCRT plan was adjusted until the dose covering 95% of PTV2 (the D95) was the same as that for the IMRT-SIB plan. Corresponding dosimetric data were generated, and a statistical comparison was performed via a 2-sided, paired t-test.
Resultant dosimetry of clinically treated cohort
volume PTV1 (cm3)
volume PTV2 (cm3)
PTV2 / PTV1
PTV1: mean dose (cGy)
PTV1: D95* (cGy)
PTV2: mean dose (cGy)
PTV2: D95* (cGy)
Toxicity was graded retrospectively using the Common Toxicity Criteria for Adverse Events (CTCAE) version 4.03 .
For the purposes of this review, “acute” was defined as ≤ 180 days from the start of RT.
Nine of 18 patients experienced acute esophageal toxicity. There were five cases of acute esophagitis (grade 1: n = 4; grade 2: n = 1), occurring at a median of 26 days after starting RT. There were 4 cases of acute stricture requiring dilatation (grade 3), occurring at a median of 37 days after starting RT. For 3 of these, dilatation occurred 36, 37 and 41 days after starting RT; for the fourth, dilatation occurred 86 days prior to the start of RT (or 121 days after surgery). One of these patients subsequently developed acute tracheo-esophageal fistula (TEF) 54 days after starting RT, requiring early discontinuation of RT (26 of 28 fractions completed) and urgent surgical repair. The affected patient was free of recurrence at the time of this analysis (238 days after start of RT).
Six of 18 patients experienced acute pulmonary toxicity. There were 2 cases of acute aspiration pneumonitis, occurring 36 days (grade 2) and 97 days (grade 1) after the start of RT (or 167 and 218 days after surgery). Four patients experienced acute grade 1 non-aspiration pneumonitis, without evidence of aspiration on imaging, occurring at a median of 35 days after starting RT.
There were 3 cases of acute grade 1 nausea, 2 cases of acute grade 2 nausea, and 2 cases of acute grade 3 nausea, occurring at a median of 0 days prior to the start of RT. In other words, 4 patients already had established nausea prior to initiation of RT.
Fourteen of 18 patients completed all 4 cycles of chemotherapy. Of the 4 patients who did not, 3 completed 3 cycles, while 1 patient (age 86) completed 1 only cycle before stopping voluntarily (this same patient also voluntarily discontinued RT after only 21 of 28 prescribed fractions). Thirteen of 18 patients experienced acute neutropenia, occurring at a median of 20 days prior to the start of RT (grade 1: n = 2; grade 2: n = 7; grade 3: n = 3; grade 4: n = 1). All 18 patients experienced acute lymphopenia (grade 1: n = 0; grade 2: n = 1; grade 3: n = 6; grade 4: n = 11), occurring at a median of 32 days prior to the start of RT. Fifteen of 18 patients experienced acute thrombocytopenia (grade 1: n = 8; grade 2: n = 6; grade 3: n = 1; grade 4: n = 0), occurring at a median of 13 days after the start of RT. In total, 14 patients required either a 1-week delay in at least 1 chemotherapy cycle or a dose-reduction of at least 1 chemotherapy agent.
Three patients experienced clinically significant late toxicity. One patient developed grade 5 (fatal) aspiration pneumonitis 357 days after the start of RT. This occurred several months after the patient developed both LR and widespread DR. The patient was debilitated and frail and died only 1 day after aspirating. A second patient experienced esophageal stricture 528 days after starting RT. This patient did not experience acute stricture and responded very well to dilatation. At the most recent follow up assessment, the patient was alive and free of recurrence (966 days after the start of RT). A third patient experienced TEF and grade 5 aspiration pneumonitis 761 days after the start of RT. This patient required multiple dilatations, before, during and after chemoRT and eventually required stricturoplasty, 18 months after the start of RT. Approximately 7 months after stricturoplasty, this patient experienced an acute breakdown of both the transposed esophagus and trachea, leading directly to aspiration and death. At the time of death, the patient‘s disease was under control, with no clinical evidence of LR or DR.
We identified 11 cases of late lymphopenia, with mildly decreased lymphocyte count persisting at a median of 319 days after start of RT. For 3 of these patients, lymphocyte counts eventually returned to normal levels. For the remaining 8 patients, lymphocyte counts remained persistently yet mildly decreased on all subsequent follow-up. We did not identify any late neutropenia or late thrombocytopenia. We did not identify any late nausea.
Dosimetric comparison within the same cohort: IMRT-SIB technique versus classic 3DCRT technique
p (2-sided t-test)
V20 (TL-CTV1) (−)
V10 (TL-CTV1) (−)
mean dose (TL-CTV1) (cGy)
liver mean dose (cGy)
heart mean dose (cGy)
cord maximum (absolute) (cGy)
cord maximum (2 cm3 volume) (cGy)
right kidney mean dose (cGy)
left kidney mean dose (cGy)
mean value of (D95*/prescription dose) for PTV1 (−)
mean value of (D95*/prescription dose) for PTV2 (−)
In this retrospective review of patients with resected high-risk adenocarcinoma of the distal esophagus and GEJ, we describe a novel technique for the delivery of adjuvant chemoRT.
In North America, neoadjuvant chemoRT is the established standard of care for resectable carcinoma of the distal esophagus and GEJ [6–8]. By comparison, the routine use of adjuvant chemoRT is far less common. The published literature regarding adjuvant chemoRT for resected carcinoma of the distal esophagus is characterized mostly by single-institution studies and retrospective reviews, representing a variety of approaches. Our original retrospective study suggested an OS benefit to adjuvant chemoRT over surgery alone, with median overall survival (OS) being extended to 47.5 months with adjuvant chemoRT versus 14.1 months without (p = 0.001) . Irradiation of the anastomosis was associated with a significant improvement in local and regional relapse  and reduced recurrence at the anastomotic site , implying the importance of local control as a determinant of outcome . Similar benefits of adjuvant chemoRT have been recognized by other authors [17–19].
A comprehensive review of the literature regarding adjuvant chemoRT for resectable carcinoma of the esophagus is provided as an online supplement (Additional file 1).
Adjuvant chemoRT with IMRT-SIB has become our new institutional standard of care for patients with resectable carcinoma of the distal esophagus and GEJ. Our IMRT-SIB technique represents a modern revision of our historical technique . We developed our IMRT-SIB technique for several reasons. In general, IMRT-SIB provides efficiency and convenience relative to 3DCRT. Instead of 2 separate phases of treatment, we need to plan only a single course of treatment, while quality assurance is more efficient than with 2 separate 3DCRT plans. As well, because IMRT had already become established for the treatment of several other disease sites at our institution, we were familiar with its application, delivery and potential clinical and dosimetric benefits, and we were hopeful that IMRT would extend those same benefits to our patients with resected high-risk carcinoma of the esophagus.
Nonetheless, a new technique is not necessarily better simply because it is more technologically advanced. In order to be a true improvement, it must also confer a demonstrable benefit in terms of dosimetry and clinical outcomes, and of course it must be able to do so safely.
Comparison of observed clinical outcomes: IMRT-SIB cohort and published 3DCRT cohort
(n = 18)
(n = 15)
570 days (19 months)
690 days (23 months)
DFS (1 year)
DFS (2 years)
3 years (36 months)
1.8 years (21 months)
OS (1 year)
OS (2 years)
pulmonary toxicity (≤90 days)
esophageal toxicity (≤90 days)
pulmonary toxicity (>90 days)
esophageal toxicity (>90 days)
One of the potential detriments with our IMRT-SIB technique is the fact that the target volume encompasses the anastomosis, thereby potentially treating a substantial amount of normal lung. It is intriguing that our modern cohort seemed to experience more acute pulmonary toxicity than our historical cohort (Table 4). If the results of our dosimetric comparison (Table 3) are in fact correct, then our 3DCRT technique would have treated the normal lung to a much higher V20 than with IMRT-SIB, correspondingly raising the risk of radiation-induced lung injury. It is possible that the incidence of radiation-induced lung injury was simply under-reported in our original cohort. On the other hand, the significantly increased V10 that we identified for IMRT-SIB over 3DCRT might actually precipitate acute radiation-induced lung injury at a faster rate than would 3DCRT. Interestingly, a recently published series from China did not identify a single case of acute radiation-induced pulmonary toxicity in a cohort of 78 patients receiving adjuvant chemoRT . In that series, 30 of 78 patients were treated to 50 Gy to the lower mediastinum and upper abdomen, while an additional 48 patients were treated to this same dose using an extended field, encompassing the sixth cervical vertebra to the first lumbar vertebra. Although their technique was not thoroughly described, it appears that they delivered all treatment using 3DCRT as opposed to IMRT.
Much of our observed toxicity was either expected (hematologic toxicity in response to chemotherapy) or was clinically insignificant (low-grade pulmonary toxicity). The three most significant observed toxicities were an acute TEF, a late grade 5 aspiration pneumonitis, and a late TEF with simultaneous grade 5 aspiration pneumonitis. The acute TEF occurred within low-dose PTV1, in a patient who required almost-weekly endoscopic dilatation, implying the role of mechanical injury. The late grade 5 aspiration pneumonitis occurred nearly 1 year after the start of RT, in a debilitated patient with widely metastatic recurrent disease. Finally, the late grade 5 aspiration pneumonitis occurred more than 2 years after days after the start of RT, while the TEF was again within low-dose PTV1.
The occurrence of two grade 5 toxicity events is clearly a cause for concern. However, it is not possible to ascertain the significance of this observation from our small, retrospective cohort. We note that grade 5 toxicity was not observed in our previously reported series using 3DCRT . Given the similarity of surgical techniques between our current cohort and our previously reported series, and given the radiobiological similarity between our current and previous dose-fractionation regimes, at the very least we expect IMRT-SIB to be comparable in terms of acute and late toxicity to our previous technique, with comparable survival.
Additional study is therefore required to characterize the efficacy and potential toxicity of our adjuvant IMRT-SIB technique more fully. To this end, we are assessing IMRT-SIB as part of a randomized-controlled clinical trial comparing adjuvant chemoRT and neoadjuvant chemoRT directly, using quality of life as our primary endpoint .
We presented the results of a modern cohort of patients with resected, high-risk adenocarcinoma of the distal esophagus and GEJ, treated with adjuvant chemoRT using IMRT-SIB. Our approach is novel and feasible. Although our approach is associated with acceptable local control and reasonable survival, long-term safety and efficacy still need to be defined. To our knowledge, our study is the first to report the use of IMRT techniques and SIB techniques in this clinical setting. We hope that our experience, as reported here, will be useful to other clinicians when treating this challenging patient population.
Permissions are unnecessary as all content herein was generated by the authors themselves.
- Pera M: Epidemiology of esophageal cancer, especially adenocarcinoma of the esophagus and esophagogastric junction. Recent results in cancer research Fortschritte der Krebsforschung Progres dans les recherches sur le cancer. 2000, 155: 1-14.Google Scholar
- Saito H, Sato T, Miyazaki M: Extramural lymphatic drainage from the thoracic esophagus based on minute cadaveric dissections: fundamentals for the sentinel node navigation surgery for the thoracic esophageal cancers. Surg Radiol Anat 2007,29(7):531-542. Epub 2007/08/22 10.1007/s00276-007-0257-6View ArticlePubMedGoogle Scholar
- Barbour AP, Rizk NP, Gonen M, Tang L, Bains MS, Rusch VW: Adenocarcinoma of the gastroesophageal junction: influence of esophageal resection margin and operative approach on outcome. Annals of Surgery 2007,246(1):1-8. Epub 2007/06/27 10.1097/01.sla.0000255563.65157.d2View ArticlePubMedPubMed CentralGoogle Scholar
- Heeren PA, Kelder W, Blondeel I, van Westreenen HL, Hollema H, Plukker JT: Prognostic value of nodal micrometastases in patients with cancer of the gastro-oesophageal junction. Eur J Surg Oncol: Eur J Soc Surg Oncol British Assoc Surg Oncol 2005,31(3):270-276. Epub 2005/03/23View ArticleGoogle Scholar
- Allum WH, Stenning SP, Bancewicz J, Clark PI, Langley RE: Long-term results of a randomized trial of surgery with or without preoperative chemotherapy in esophageal cancer. J Clin Oncol 2009,27(30):5062-5067. 10.1200/JCO.2009.22.2083View ArticlePubMedGoogle Scholar
- Gebski V, Burmeister B, Smithers BM, Foo K, Zalcberg J, Simes J: Survival benefits from neoadjuvant chemoradiotherapy or chemotherapy in oesophageal carcinoma: a meta-analysis. Lancet Oncol 2007,8(3):226-234. Epub 2007/03/03 10.1016/S1470-2045(07)70039-6View ArticlePubMedGoogle Scholar
- Graham AJ, Shrive FM, Ghali WA, Manns BJ, Grondin SC, Finley RJ: Defining the optimal treatment of locally advanced esophageal cancer: a systematic review and decision analysis. Ann Thorac Surg 2007,83(4):1257-1264. Epub 2007/03/27 10.1016/j.athoracsur.2006.11.061View ArticlePubMedGoogle Scholar
- Greer SE, Goodney PP, Sutton JE, Birkmeyer JD: Neoadjuvant chemoradiotherapy for esophageal carcinoma: a meta-analysis. Surgery 2005,137(2):172-177. Epub 2005/01/28 10.1016/j.surg.2004.06.033View ArticlePubMedGoogle Scholar
- Bedard EL, Inculet RI, Malthaner RA, Brecevic E, Vincent M, Dar R: The role of surgery and postoperative chemoradiation therapy in patients with lymph node positive esophageal carcinoma. Cancer 2001,91(12):2423-2430. Epub 2001/06/20 10.1002/1097-0142(20010615)91:12<2423::AID-CNCR1277>3.0.CO;2-1View ArticlePubMedGoogle Scholar
- Yu E, Dar R, Rodrigues GB, Stitt L, Videtic GM, Truong P: Is extended volume external beam radiation therapy covering the anastomotic site beneficial in post-esophagectomy high risk patients? Radiother Oncol: Eur J Soc Therapeutic Radiol Oncol 2004,73(2):141-148. Epub 2004/11/16 10.1016/j.radonc.2004.08.024View ArticleGoogle Scholar
- Cooper JS, Guo MD, Herskovic A, Macdonald JS, Martenson JA Jr, Al-Sarraf M: Chemoradiotherapy of locally advanced esophageal cancer: long-term follow-up of a prospective randomized trial (RTOG 85–01). Radiation Therapy Oncology Group. Jama 1999,281(17):1623-1627. Epub 1999/05/11 10.1001/jama.281.17.1623View ArticlePubMedGoogle Scholar
- Emami B, Lyman J, Brown A, Coia L, Goitein M, Munzenrider JE: Tolerance of normal tissue to therapeutic irradiation. Int J Radiat Oncol Biol Phys 1991,21(1):109-122. 10.1016/0360-3016(91)90171-YView ArticlePubMedGoogle Scholar
- Bentzen SM, Constine LS, Deasy JO, Eisbruch A, Jackson A, Marks LB: Quantitative Analyses of Normal Tissue Effects in the Clinic (QUANTEC): an introduction to the scientific issues. Int J Radiat Oncol Biol Phys 2010,76(3 Suppl):S3-S9. Epub 2010/03/05View ArticlePubMedPubMed CentralGoogle Scholar
- Services USDoHaH: Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0. In Edited by: Services DoHaH. 2010.Google Scholar
- Yu E, Tai P, Younus J, Malthaner R, Truong P, Stitt L: Postoperative extended-volume external-beam radiation therapy in high-risk esophageal cancer patients: a prospective experience. Curr Oncol 2009,16(4):48-54. Epub 2009/08/13View ArticlePubMedPubMed CentralGoogle Scholar
- Yu E, Tai P, Malthaner R, Stitt L, Rodrigues G, Dar R: What are the factors that predict outcome at relapse after previous esophagectomy and adjuvant therapy in high-risk esophageal cancer? Curr Oncol 2010,17(6):46-51. Epub 2010/12/15View ArticlePubMedPubMed CentralGoogle Scholar
- Wu SD, Zhang P, Xie C, Zhang X, Jin Z: Phase II study of postoperative chemoradiotherapy for esophageal carcinoma. J Clin Oncol 2009,27(suppl):abstr e15606.Google Scholar
- Adelstein DJ, Rice TW, Rybicki LA, Saxton JP, Videtic GM, Murthy SC: Mature results from a phase II trial of postoperative concurrent chemoradiotherapy for poor prognosis cancer of the esophagus and gastroesophageal junction. J Thorac Oncol 2009,4(10):1264-1269. Epub 2009/08/12 10.1097/JTO.0b013e3181b26f8eView ArticlePubMedGoogle Scholar
- Rice TW, Adelstein DJ, Chidel MA, Rybicki LA, DeCamp MM, Murthy SC: Benefit of postoperative adjuvant chemoradiotherapy in locoregionally advanced esophageal carcinoma. J Thorac Cardiovasc Surg 2003,126(5):1590-1596. 10.1016/S0022-5223(03)01025-0View ArticlePubMedGoogle Scholar
- Lv J, Cao X-F, Zhu B, Ji L, Tao L, Wang D-D: Long-term efficacy of perioperative chemoradiotherapy on esophageal squamous cell carcinoma. World J Gastroenterol 2010,16(13):1649-1654. 10.3748/wjg.v16.i13.1649View ArticlePubMedPubMed CentralGoogle Scholar
- Malthaner R: Quality of Life in Neoadjuvant Versus Adjuvant Therapy of Esophageal Cancer Treatment Trial (QUINTETT). ClinicalTrialsgov Identifier: NCT009075432009Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.