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Predicting response to neoadjuvant chemotherapy in patients with oesophageal adenocarcinoma

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DataCite Commons2022-12-20 更新2024-07-28 收录
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https://tandf.figshare.com/articles/dataset/Predicting_response_to_neoadjuvant_chemotherapy_in_patients_with_oesophageal_adenocarcinoma/16752592/1
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Neoadjuvant chemotherapy is often used prior to surgical resection for oesophageal adenocarcinoma but remains ineffective in a high proportion of patients. The histological Mandard tumour regression grade is used to determine chemoresponse but is not available at the time of treatment decision-making. The aim of this cohort study was to identify factors that predict chemotherapy response prior to surgery. A prospectively collected database of patients undergoing surgical resection for oesophageal adenocarcinoma from a high-volume UK institution was used. Patients were subcategorised using pathological tumour response into ‘responders’ (Mandard grade 1–3) and ‘non-responders’ (Mandard grade 4 and 5). Multivariable logistic regression analysis was performed to calculate crude and adjusted odds ratios (OR) with 95% confidence intervals (CI) for responder status adjusting for a variety of parameters. Receiver operating characteristic (ROC) curves were calculated. Among 315 patients included, 102 (32%) were responders and 213 (68%) non-responders. A decrease in radiological tumour volume (OR 1.92 95%CI 1.02–3.62; <i>p</i> = 0.05), a ‘partial response’ RECIST score (OR 7.16 95%CI 1.49–34.36; <i>p</i> = 0.01), a clinically improved dysphagia score (OR 2.79 95%CI 1.05–7.04; <i>p</i> = 0.04) and lymphovascular invasion (OR 0.06 95%CI 0.02–0.13; <i>p</i> = 0.000) influenced responder status. ROC curve analysis for responder status utilising all available parameters had an area under the curve (AUC) of 0.86. This study has highlighted the potential for using pre-defined factors to identify those patients who have responded to neoadjuvant chemotherapy, prior to surgical resection, potentially facilitating a more individualised therapeutic approach.
提供机构:
Taylor & Francis
创建时间:
2021-10-06
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