Capovilla Giovanni, Pierobon Elisa Sefora, Moletta Lucia, Scarton Alessia, Sciuto Maria Elisa, Tagkalos Evangelos, Uzun Eren, De Pasqual Carlo Alberto, Turolo Cecilia, Zanchettin Gianpietro, Riccio Federica, Provenzano Luca, Salvador Renato, Berlth Felix, Weindelmayer Jacopo, Lonardi Sara, Galuppo Sara, Giacopuzzi Simone, De Manzoni Giovanni, Grimminger Peter, Valmasoni Michele
Department of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, Padua, Italy.
Unit of Chirurgia Generale 1, University Hospital of Padova, Padua, Italy.
Ann Surg Oncol. 2025 May 5. doi: 10.1245/s10434-025-17264-2.
The higher rate of pathological complete response (pCR) after neoadjuvant chemoradiotherapy (NACRT) is an argument to support this treatment. However, previous studies have not demonstrated a survival benefit of NACRT for adenocarcinoma (ADC) compared with neoadjuvant chemotherapy (NACT) and the correlation between pathological tumor response (pTR) and survival is unclear. We aimed to verify whether the prognostic value of pTRis influenced by the type of neoadjuvant treatment performed.
Patients with ADC who underwent NACT or NACRT and surgery between 2015 and 2020 were included. The correlation between pTR and overall survival (OS) and disease-free survival (DFS) after both treatments was evaluated by using Kaplan-Meier analysis. pTR was assessed by using the Mandard tumor regression grade (TRG).
Overall, 563 patients were included; 278 received NACT, and 285 NACRT. The incidence of pCR was significantly higher after NACRT (24.6% vs. 11.2%, p < 0.0001). The TRG of both node-negative (pN0) and node-positive (pN+) patients significantly correlated with the 5 years OS after NACT (pN0 p = 0.03, pN+ p = 0.01). The same result was not detected in NACRT patients (pN0 p = 0.98, pN+ p = 0.23). The 5-year DFS of the patients with pCR was higher in the NACT group (84% vs. 66.5%, p = 0.05). The proportion of patients showing distant recurrences was significantly higher in the NACRT group (35.4% vs. 23.8%, p = 0.009).
Tumor regression grade was significantly associated with survival after NACT, but not with NACRT. Despite a lower rate of pCR, both OS and, especially, DFS of patients with pCR improved after NACT compared with NACRT.
新辅助放化疗(NACRT)后较高的病理完全缓解(pCR)率是支持这种治疗方法的一个依据。然而,既往研究尚未证实与新辅助化疗(NACT)相比,NACRT对腺癌(ADC)有生存获益,且病理肿瘤反应(pTR)与生存之间的相关性尚不清楚。我们旨在验证pTR的预后价值是否受所进行的新辅助治疗类型的影响。
纳入2015年至2020年间接受NACT或NACRT及手术的ADC患者。采用Kaplan-Meier分析评估两种治疗后pTR与总生存期(OS)和无病生存期(DFS)之间的相关性。使用Mandard肿瘤退缩分级(TRG)评估pTR。
总体而言,共纳入563例患者;278例接受NACT,285例接受NACRT。NACRT后pCR的发生率显著更高(24.6%对11.2%,p<0.0001)。淋巴结阴性(pN0)和淋巴结阳性(pN+)患者的TRG与NACT后的5年OS均显著相关(pN0 p=0.03,pN+ p=0.01)。在接受NACRT的患者中未发现相同结果(pN0 p=0.98,pN+ p=0.23)。NACT组pCR患者的5年DFS更高(84%对66.5%,p=0.05)。NACRT组远处复发患者的比例显著更高(35.4%对23.8%,p=0.009)。
肿瘤退缩分级与NACT后的生存显著相关,但与NACRT无关。尽管pCR率较低,但与NACRT相比,NACT后pCR患者的OS,尤其是DFS有所改善。