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Page 1 of 6 Esophageal Cancer This practice algorithm has been specifically developed for MD Anderson using a multidisciplinary approach and taking into consideration circumstances particular to MD Anderson, including the following: MD Anderson’s specific patient population; MD Anderson’s services and structure; and MD Anderson’s clinical information. Moreover, this algorithm is not intended to replace the independent medical or professional judgment of physicians or other health care providers. This algorithm should not be used to treat pregnant women. Note: Consider Clinical Trials as treatment options for eligible patients. Consider referral to a Comprehensive Cancer Center WORK UP PRIMARY TREATMENT ADDITIONAL EVALUATION CLINICAL STAGE Endoscopic mucosal resection (EMR) and/or Ablation or Esophagectomy cTis to less than or equal to cT1b ● History and Physical Swallow (optional) ● Esophagogastroduodenoscopy (EGD) to visualize entire upper GI tract ● Biopsy confirmation and histologic subtyping1 ● CBC & chemistry profile ● Chest/abdominal CT with contrast ● Bronchoscopy, if tumor is at or above the carina with no evidence of M1 disease ● Endoscopic ultrasound, if no evidence of M1 disease and tumor is at Gastroesophageal (GE) junction ● Biopsy confirmation of suspected metastatic disease ● PET/CT ● HER2-neu evaluation by Immunohistochemistry (IHC)2 in patients with advanced, metastatic cancer (not localized cancer) ● Barium ● Multidisciplinary cTis – cT4, N0-1 evaluation is required for all localized cases (not for metastatic patients) ● Nutritional assessment (for preoperative nutritional support, consider nasogastric or J-tube [PEG is not recommended] ● Barium enema or colonoscopy if colon interposition or bypass planned ● Arteriogram (optional) consider if performing colon interposition 1 Confirmation should be completed on outside MDACC specimen and inside MDACC specimen Consider HER2-neu evaluation initially by IHC and later with FISH if clinically indicated cT1b, AnyN Yes Esophagectomy3 No Definitive chemoradiation Medically Operable ? cT2, N0 Surgery or combined modality therapy Not medically operable or patient declining surgery Definitive chemoradiation Medically operable Preoperative chemoradiation ● RT, 50-50.4 Gy plus concurrent chemotherapy cT1b-T2, N+ cT3-T4, N0-3 Stage IV Metastatic cancer Follow-up, See page 3 Salvage Surgery4 Surgery4 Palliative treatment as clinically indicated 2 See MDA Approved Biomarkers - https://www.mdanderson.org/education-and-research/resources-for-professionals/clinical-tools-and-resources/practice-algorithms/clin-management-biomarkers-web-algorithm.pdf 3 Preferred for noncervical cT1b disease Patients who receive preoperative chemoradiation should be followed after surgery. 4 Copyright 2016 The University of Texas MD Anderson Cancer Center Department of Clinical Effectiveness V4 Approved by The Executive Committee of the Medical Staff 06/28/2016 Esophageal Cancer Page 2 of 6 This practice algorithm has been specifically developed for MD Anderson using a multidisciplinary approach and taking into consideration circumstances particular to MD Anderson, including the following: MD Anderson’s specific patient population; MD Anderson’s services and structure; and MD Anderson’s clinical information. Moreover, this algorithm is not intended to replace the independent medical or professional judgment of physicians or other health care providers. This algorithm should not be used to treat pregnant women. Note: Consider Clinical Trials as treatment options for eligible patients. Consider referral to a Comprehensive Cancer Center SURGICAL OUTCOMES AFTER ESOPHAGECTOMY CLINICAL PATHOLOGIC FINDINGS POSTOPERATIVE TREATMENT Tis,T1,N0 Observe as clinically indicated Adenocarcinoma T2,N0 T3, N0 Yes Surgery as primary therapy Squamous ● Observe or chemoradiation (Fluoropyrimidine based) for selected patients. ● Adjuvant chemotherapy if patient received chemotherapy preoperatively ● Chemoradiation (Fluoropyrimidine based). ● Adjuvant chemotherapy if patient received chemotherapy preoperatively Observe as clinically indicated Node negative? Proximal or mid esophagus Adenocarcinoma Observe or chemoradiation (Fluoropyrimidine based) for selected patients No Distal esophagus, GE junction Squamous Macroscopic residual cancer Copyright 2016 The University of Texas MD Anderson Cancer Center ● Chemoradiation ● Adjuvant (Fluoropyrimidine based). chemotherapy if patient received chemotherapy preoperatively Observe as clinically indicated Chemoradiation (Flouropyrimidine-based) or palliative therapy Department of Clinical Effectiveness V4 Approved by The Executive Committee of the Medical Staff 06/28/2016 Esophageal Cancer Page 3 of 6 This practice algorithm has been specifically developed for MD Anderson using a multidisciplinary approach and taking into consideration circumstances particular to MD Anderson, including the following: MD Anderson’s specific patient population; MD Anderson’s services and structure; and MD Anderson’s clinical information. Moreover, this algorithm is not intended to replace the independent medical or professional judgment of physicians or other health care providers. This algorithm should not be used to treat pregnant women. Note: Consider Clinical Trials as treatment options for eligible patients. Consider referral to a Comprehensive Cancer Center FOLLOW - UP ● If asymptomatic: History and Physical every 4 months for 1 year, every 6 months for 2 years, then annually ● Chemistry profile and CBC, as clinically indicated ● Imaging as clinically indicated ● Upper GI as clinically indicated1 ● Dilatation for anostomotic stenosis ● Nutritional counseling ● Vitamin D level check PALLIATIVE THERAPY RECURRENCE Concurrent chemoradiation (Fluoropyrimidine-based preferred and/or best supportive care or surgery or chemotherapy Local/regional only recurrence: prior surgery, no prior chemoradiation Yes Esophageal recurrence: (prior chemoradiation, no prior surgery) Salvage surgery Resectable and medically operable No Palliative therapy Metastatic cancer 1 Patient with Tis or T1a who undergo EMR should have endoscopic surveillance every 3 months for one year, then annually. Copyright 2016 The University of Texas MD Anderson Cancer Center Department of Clinical Effectiveness V4 Approved by The Executive Committee of the Medical Staff 06/28/2016 Esophageal Cancer Page 4 of 6 This practice algorithm has been specifically developed for MD Anderson using a multidisciplinary approach and taking into consideration circumstances particular to MD Anderson, including the following: MD Anderson’s specific patient population; MD Anderson’s services and structure; and MD Anderson’s clinical information. Moreover, this algorithm is not intended to replace the independent medical or professional judgment of physicians or other health care providers. This algorithm should not be used to treat pregnant women. Note: Consider Clinical Trials as treatment options for eligible patients. Consider referral to a Comprehensive Cancer Center SUGGESTED READINGS PRINCIPLES OF MULTIDISCIPLINARY TEAM APPROACH FOR GASTROESOPHAGEAL CANCERS Cooper JS, Guo MD, Herskovic A, et al. (1999). Chemoradiotherapy of locally advanced esophageal cancer: long-term follow-up of a prospective randomized trial (RTOG 85-01). Radiation Therapy Oncology Group. JAMA; 281(17):1623-1627. Macdonald JS, Smalley SR, Benedetti J, et al. (2001). Chemoradiotherapy after surgery compared with surgery alone for adenocarcinoma of the stomach or gastroesophageal junction. N Engl J Med; 345(10):725-730. PRINCIPLES OF SURGERY Birkmeyer JD, Siewers AE, Finlayson EVA, et at. (2002). Hospital volume and surgical mortality in the United States. N Engl J Med; 346:1128-1137. Hofstetter WL. (2004). Lymph Node Dissection in Esophageal Cancer. Current Therapies in Thoracic and Cardiovascular Surgery, edited by SC Yang and DE Cameron. Mosby, Inc., Philadelphia, Pennsylvania, pp. 360-363. Hulscher JBF, van Sandick JW, de Boer AG, et al. (2002). Extended transthoracic resection compared with limited transhiatal resection for adenocarcinoma of the esophagus. N Engl J Med; 347:1662-1669. Risk NP, Ishwaran H, Rice T, et al. (2010). Optimum lymphadenectomy for esophageal cancer. Ann Surg; 25(1):46-50. Swisher SG, Wynn P, Putnam JB, et al. (2002). Salvage esophagectomy for recurrent tumors after definitive chemotherapy and radiotherapy. J Thorac Cardiovasc Surg; 123:175-183. CONTINUED ON NEXT PAGE Copyright 2016 The University of Texas MD Anderson Cancer Center Department of Clinical Effectiveness V4 Approved by The Executive Committee of the Medical Staff 06/28/2016 Esophageal Cancer Page 5 of 6 This practice algorithm has been specifically developed for MD Anderson using a multidisciplinary approach and taking into consideration circumstances particular to MD Anderson, including the following: MD Anderson’s specific patient population; MD Anderson’s services and structure; and MD Anderson’s clinical information. Moreover, this algorithm is not intended to replace the independent medical or professional judgment of physicians or other health care providers. This algorithm should not be used to treat pregnant women. Note: Consider Clinical Trials as treatment options for eligible patients. Consider referral to a Comprehensive Cancer Center SUGGESTED READINGS - CONTINUED PRINCIPLES OF SYSTEMIC THERAPY FOR ESOPHAGEAL OR GASTROESOPHAGEAL JUNCTION CANCER Al-Batran SE Hartmann JT, Probst S, et al. (2008). Phase III trial in metastatic gastroesophageal adenocarcinoma with fluorouracil, leucovorin plus either oxaliplatin or cisplatin: a study of the Arbeitsgemeinschaft Internistische Onkologie. J Clin Oncol; 26(9):1435-42. Cunningham D, Starling, N., Rao, S., et al. (2008). Capecitabine and oxaliplatin for advanced esophagogastric cancer. N Engl J Med; 358:36-46. Dank M, Zatuski J, Barone C, et al. (2008). Randomized phase III study comparing irinotecan combined with 5-fluorouracil and folinic acid to cisplatin combined with 5-fluorouracil in chemotherapy naive patients with advanced adenocarcinoma of the stomach or esophagogastric junction. Ann Oncol; 19(8):1450-1457. Kang Y, Kang WK, Shin DB, et al. (2006). Randomized phase III trial of capecitabine/cisplatin (XP) vs. continuous infusion of 5-FU/cisplatin (FP) as first-line therapy in patients (pts) with advanced gastric cancer (AGC): Efficacy and safety results. J Clin Oncol (Meeting Abstracts); 24(18_suppl):LBA4018. Minsky BD, Pajak TF, Ginsberg RJ, et al. (2002). 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; 20: 1167-1174. Van Cutsem E, Moiseyenko VM, Tjulandin S, et al. (2006). Phase III study of docetaxel and cisplatin plus fluorouracil compared with cisplatin and fluorouracil as first-line therapy for advanced gastric cancer: a report of the V325 Study Group. J Clin Oncol; 24(31 ):4991-4997. OTHER SUPPORTIVE READINGS Peterson LA, Zeng X, Caufield-Noll CP, Schweitzer MA, Magnuson TH, & Steele KE. (2016). Vitamin D status and supplementation before and after bariatric surgery: a comprehensive literature review. Surg Obes Relat Dis, pii: S1550-7289(16)00004-6. doi: 10.1016/j.soard.2016.01.001. [Epub ahead of print] Copyright 2016 The University of Texas MD Anderson Cancer Center Department of Clinical Effectiveness V4 Approved by The Executive Committee of the Medical Staff 06/28/2016 Esophageal Cancer Page 6 of 6 This practice algorithm has been specifically developed for MD Anderson using a multidisciplinary approach and taking into consideration circumstances particular to MD Anderson, including the following: MD Anderson’s specific patient population; MD Anderson’s services and structure; and MD Anderson’s clinical information. Moreover, this algorithm is not intended to replace the independent medical or professional judgment of physicians or other health care providers. This algorithm should not be used to treat pregnant women. Note: Consider Clinical Trials as treatment options for eligible patients. Consider referral to a Comprehensive Cancer Center DEVELOPMENT CREDITS This practice algorithm is based on majority expert opinion of the Gastrointestinal Center Faculty at the University of Texas, MD Anderson Cancer Center. A multidisciplinary approach was used and included input from the following medical oncologists, radiation oncologists, surgical oncologists, and pathologists: Ŧ Jaffer, Ajani , MD Manoop Bhutani, MBBS Prajnan Das, MD, MPH Keith Fournier, MD Ŧ Linus Ho, MD Wayne Hofstetter, MD Jeffrey H. Lee, MD Steven Lin, MD, PHD Ŧ Paul Mansfield, MD Dipen Maru, MD William A. Ross, MD Heath Skinner, MD Stephen Swisher, MD, BS Dongfeng Tan, MD James Welsh, MD Core Development Team Copyright 2016 The University of Texas MD Anderson Cancer Center Department of Clinical Effectiveness V4 Approved by The Executive Committee of the Medical Staff 06/28/2016