Real-world outcomes of the CROSS regimen in patients with resectable esophageal or gastro-esophageal junction adenocarcinoma: a nationwide cohort study in the Netherlands.

IF 10 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL EClinicalMedicine Pub Date : 2025-01-22 eCollection Date: 2025-02-01 DOI:10.1016/j.eclinm.2024.103067
Hanneke van Laarhoven, Rob Verhoeven, Mark van Berge Henegouwen, Nadia Haj Mohammad, Richard van Hillegersberg, Marije Slingerland, Christina T Muijs, Bas Wijnhoven, Bianca Mostert, Laurens Beerepoot, Grard Nieuwenhuijzen, Sarah Derks, Peter S N van Rossum
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Abstract

Background: Recent studies in patients with resectable adenocarcinoma of the esophagus or gastroesophageal junction (GEJ)-Neo-AEGIS and ESOPEC-have explored the comparison of neoadjuvant chemoradiotherapy (nCRT) with chemotherapy, with conflicting results. To contextualize the findings from these studies using nCRT as a comparator, we aimed to investigate contemporary real-world outcomes of nCRT in patients with adenocarcinoma of the esophagus or GEJ.

Methods: From the Netherlands Cancer Registry, patients were selected who were diagnosed between 1 January 2015 and 31 December 2022 with a resectable (cT1N+M0 or cT2-4aNanyM0) esophageal, GEJ or gastric cardia adenocarcinoma and started treatment with nCRT according to the CROSS regimen, that is 5 weekly cycles of carboplatin (AUC 2 mg/mL per minute) and paclitaxel (50 mg/m2) combined with concurrent radiotherapy (41.4 Gy in 23 fractions of 1.8 Gy). Pathologic complete response (pCR) according to Mandard was the primary outcome of this study and defined as complete tumor regression of the primary tumor (Mandard grade I) irrespective of residual nodal involvement.

Findings: Of the 4765 included patients, 4170 (87.5%) completed the full CROSS regimen of radiotherapy and chemotherapy. A pCR was observed in 704 (20.5%) of 3439 patients who underwent surgical resection within 16 weeks after completing the CROSS regimen. In the complete study population, the median overall survival (OS) was 33.7 months (95% CI 32.0-35.6), with a 3-year OS rate of 48.1%.

Interpretation: Although survival rates in real-world settings are often lower compared to clinical trials, in our real-world cohort the 3-year OS was only 2.6% lower compared to that reported for the group that underwent nCRT in ESOPEC. These real-world results underscore the potential of the CROSS regimen in daily clinical practice.

Funding: None.

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CROSS方案在可切除食管或胃-食管交界腺癌患者中的实际结果:荷兰的一项全国性队列研究
背景:最近对食管或胃食管连接处可切除腺癌(GEJ)患者的研究-Neo-AEGIS和esopec -探讨了新辅助放化疗(nCRT)与化疗的比较,结果相互矛盾。为了将这些研究的结果与nCRT作为比较,我们的目的是研究nCRT在食管腺癌或GEJ患者中的当代现实结果。方法:从荷兰癌症登记处选择2015年1月1日至2022年12月31日期间诊断为可切除(cT1N+M0或cT2-4aNanyM0)食管、GEJ或贲门腺癌的患者,并根据CROSS方案开始使用nCRT治疗,即卡铂(AUC 2mg /mL /分钟)和紫杉醇(50mg /m2) 5周周期联合同步放疗(41.4 Gy, 1.8 Gy的23个部分)。根据标准,病理完全缓解(pCR)是本研究的主要结果,并定义为原发肿瘤的完全消退(标准I级),无论残余淋巴结是否受累。结果:在纳入的4765例患者中,4170例(87.5%)完成了完整的CROSS放疗和化疗方案。在完成CROSS方案后16周内接受手术切除的3439例患者中,有704例(20.5%)观察到pCR。在整个研究人群中,中位总生存期(OS)为33.7个月(95% CI 32.0-35.6), 3年OS率为48.1%。解释:尽管与临床试验相比,现实环境中的生存率通常较低,但在我们的现实世界队列中,3年OS仅比在ESOPEC中接受nCRT的组低2.6%。这些实际结果强调了CROSS方案在日常临床实践中的潜力。资金:没有。
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来源期刊
EClinicalMedicine
EClinicalMedicine Medicine-Medicine (all)
CiteScore
18.90
自引率
1.30%
发文量
506
审稿时长
22 days
期刊介绍: eClinicalMedicine is a gold open-access clinical journal designed to support frontline health professionals in addressing the complex and rapid health transitions affecting societies globally. The journal aims to assist practitioners in overcoming healthcare challenges across diverse communities, spanning diagnosis, treatment, prevention, and health promotion. Integrating disciplines from various specialties and life stages, it seeks to enhance health systems as fundamental institutions within societies. With a forward-thinking approach, eClinicalMedicine aims to redefine the future of healthcare.
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