ASCO GUIDELINES Bundle

Treatment of Locally Advanced Esophageal Carcinoma

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Treatment ➤ Preoperative CRT or CRT without surgery (definitive CRT) should be offered to patients with locally advanced esophageal squamous cell carcinoma. (Strong Recommendation; EB-B-M) Subgroup considerations: • Historical studies suggest that in patients who respond completely to CRT, the addition of surgery may offer minimal benefit. In patients with squamous cell carcinoma who appear to have a complete response to CRT, the option of surveillance and salvage surgery upon progression may be considered, where salvage esophagectomy is practiced. At this time, randomized controlled trials are exploring the question of surveillance and salvage surgery after CRT compared to planned surgery after CRT. • In patients for whom radiation is not an option, preoperative CT (without radiation) may be considered. • Definitive CRT is recommended for patients with tumors located in the cervical esophagus; surgery should be considered in the event of persistent or recurrent disease. • While CRT and surgery are preferred, definitive CRT is an option for patients who cannot tolerate or choose not to undergo surgery. Practice Statement ➤ For patients with esophageal squamous cell carcinoma, the decision to undertake surgery should be considered in the context of shared decision making, considering age, comorbidities, patient preference, caregiver support, and other factors. (CB-H) ASCO Recommendation Update – August 2021 ➤ Following neoadjuvant CRT and surgery, nivolumab should be offered to patients with locally advanced esophageal carcinoma with Eastern Cooperative Oncology Group status 0-1 who did not experience a pathological complete response (i.e., with residual disease of at least ypT1 or ypN1 in resected specimens). (Strong Recommendation; EB-B-M) Qualifying statements: ▶ Data are not available to support any recommendation for nivolumab following treatment with perioperative chemotherapy. ▶ A post-hoc analysis showed an HR for disease-free survival of 0.62 (95% CI, 0.46 to 0.83, median DFS 29.4 vs. 10.2 months) in the subgroup of patients with programmed death-ligand 1 (PD-L1) combined positive score (CPS) of at least 5 (n=371) and 0.89 (95% CI, 0.65 to 1.22, median DFS 16.3 vs. 11.1 months) in the subgroup of patients with PD-L1 CPS of less than 5 (n=295). This exploratory analysis suggests that future studies may define biomarkers, such as PD-L1 CPS, and/or a subgroup that will benefit from adjuvant nivolumab.

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