Nomogram for predicting pathologic complete response following preoperative chemoradiotherapy in patients with esophageal squamous cell carcinoma

Author:

Shin Young Seob1ORCID,Jang Jeong Yun1,Yoo Ye Jin1,Yu Jesang2,Song Kye Jin1,Jo Yoon Young3,Kim Sung-Bae4,Park Sook Ryun4,Song Ho June5,Kim Yong-Hee6ORCID,Kim Hyeong Ryul6,Kim Jong Hoon1

Affiliation:

1. Department of Radiation Oncology, Asan Medical Center, University of Ulsan College of Medicine , Seoul, Korea

2. Department of Radiation Oncology, Kosin University Gospel Hospital, Kosin University College of Medicine , Busan, Korea

3. Department of Radiation Oncology, Yeungnam University Medical Centre, University of Yeungnam College of Medicine , Daegu, Korea

4. Department of Medical Oncology, Asan Medical Center, University of Ulsan College of Medicine , Seoul, Korea

5. Department of Gastroenterology, Asan Medical Center, University of Ulsan College of Medicine , Seoul, Korea

6. Department of Thoracic and Cardiovascular Surgery, Asan Medical Center, University of Ulsan College of Medicine , Seoul, Korea

Abstract

Abstract Background In patients with esophageal squamous cell carcinoma (ESCC), accurately predicting a pathologic complete response (pCR) to preoperative chemoradiotherapy (PCRT) has the potential to enable an active surveillance strategy without esophagectomy. We aimed to establish a reliable multiparameter nomogram model that combines tumor characteristics, imaging modalities, and hematologic markers to predict pCR in patients with ESCC who underwent PCRT and esophagectomy. Methods We retrospectively reviewed the medical records of 457 patients with ESCC who received PCRT followed by esophagectomy between January 2005 and October 2020. The nomogram model was developed using logistic regression analysis with a training cohort and externally validated with a validation cohort. Results In the training and validation cohorts, 44.2% (126/285) and 48.3% (83/172) of patients, respectively, achieved pCR after PCRT. The 5-year rates of overall survival, progression-free survival, and freedom from local progression in the training cohort were 51.6%, 48.5%, and 77.6%, respectively. The parameters included in the nomogram were histologic grade, clinical N stage, maximum standardized uptake value on positron emission tomography, and post-PCRT biopsy. Hematologic markers were significantly associated with survival outcomes but not with pCR. The area under the receiver operating characteristic curve of the nomogram was 0.717, 0.704, and 0.707 for the training cohort, internal validation cohort, and external validation cohort, respectively. Conclusion Our nomogram model based on four parameters obtained from standard clinical practice demonstrated good performance in both the training and validation cohorts and could be useful to aid clinical decision-making to determine whether surgery or active surveillance strategy should be pursued.

Publisher

Oxford University Press (OUP)

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