Pathologic response evaluation of localized or locally advanced esophageal carcinoma to induction chemotherapy followed by preoperative concurrent chemotherapy and hypofractionated radiotherapy: a clinical trial.

Autor:	Emadi Torghabeh A; Cancer Research Center, Mashhad University of Medical Sciences, Mashhad, Iran., Aledavood SA; Cancer Research Center, Mashhad University of Medical Sciences, Mashhad, Iran., Soltani E; Surgical Oncology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran., Akbari Oryani M; Department of Pathology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran., Akhlaghi S; Department of Biostatistics, School of Health, Mashhad University of Medical Sciences, Mashhad, Iran., Hosseini S; Cancer Research Center, Mashhad University of Medical Sciences, Mashhad, Iran., Fani Pakdel A; Cancer Research Center, Mashhad University of Medical Sciences, Mashhad, Iran., Taghizadeh Kermani A; Cancer Research Center, Mashhad University of Medical Sciences, Mashhad, Iran., Anvari K; Cancer Research Center, Mashhad University of Medical Sciences, Mashhad, Iran., Shahidsales S; Cancer Research Center, Mashhad University of Medical Sciences, Mashhad, Iran., Bahadorian S; Department of Pathology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran., Mashreghi Moghaddam S; Cancer Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Jazyk:	angličtina
Zdroj:	Frontiers in oncology [Front Oncol] 2024 Aug 19; Vol. 14, pp. 1439730. Date of Electronic Publication: 2024 Aug 19 (Print Publication: 2024).
DOI:	10.3389/fonc.2024.1439730
Abstrakt:	Objective: Esophageal cancer is a therapeutic challenge in most healthcare systems. Most patients present with locally advanced disease at diagnosis. Concurrent chemoradiotherapy (CRT) is the standard treatment for locally advanced esophageal carcinoma. Since achieving a complete pathological response in postoperative specimens following neoadjuvant therapy is associated with improved patient survival, this study was designed to evaluate the pathologic response of localized or locally advanced esophageal carcinoma to induction chemotherapy followed by preoperative concurrent chemotherapy and hypofractionated radiotherapy (HFR). Methods: This single-arm clinical trial (IRCT20210623051676N1) evaluated patients with squamous cell carcinoma or adenocarcinoma of the esophagus, stage cT2-T4a N0 M0 or cT1-T4a N+ M0. Patients received 3-5 cycles of weekly induction chemotherapy with the paclitaxel (50 mg/m2) and carboplatin (AUC=2) regimen, followed by weekly concurrent CRT with the same chemotherapy regimen. The radiation dose was 40 Gy, delivered over 16 fractions, 5 days per week (2.5 Gray/fraction). Patients underwent surgery 4-6 weeks after completion of CRT. The surgical specimens were evaluated for pathological response. A p-value of < 0.05 was considered significant in all analyses. Results: Out of 54 patients enrolled in this study, 45 completed the neoadjuvant protocol. Of these 45 patients, 32 underwent surgery and were finally analyzed. The mean age of the patients was 59.9 ± 8.6 years (range, 37-75 years). The location of the tumor was in the mid-thoracic esophagus in most patients (21, 65.6%) and the most common histological type was SCC (29, 90.6%). The median number of induction and concurrent chemotherapy cycles was 5 (4.8 ± 1.3 course, range, 1-10) and 3 (2.6 ± 0.8 course, range, 0-4), respectively. Among 45 patients who completed the neoadjuvant protocol, the most common toxicities were grade 3 neutropenia (15.6%), acute renal failure (4.4%), and odynophagia (37.8%). Nearly two-thirds of the patients experienced complete or near-complete responses (71.9%, 23 patients). Partial response was reported in 6 patients (18.8%) and poor response in 3 patients (9.4%). Conclusion: Preoperative induction chemotherapy followed by HFR with concurrent chemotherapy has low toxicity and side effects, good tolerance, and significant efficacy in the treatment of patients with esophageal cancer. Clinical Trial Registration: https://irct.behdasht.gov.ir/trial/59930, identifier NCT05745545. Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. (Copyright © 2024 Emadi Torghabeh, Aledavood, Soltani, Akbari Oryani, Akhlaghi, Hosseini, Fani Pakdel, Taghizadeh Kermani, Anvari, Shahidsales, Bahadorian and Mashreghi Moghaddam.)
Databáze:	MEDLINE
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