Camrelizumab combined with FOLFOX as neoadjuvant therapy for resectable locally advanced gastric and gastroesophageal junction adenocarcinoma.

Authors

null

Ying Liu

Department of Medical Oncology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China

Ying Liu , Guangsen Han , Hongle Li , Yuzhou Zhao , Jing Zhuang , Gangcheng Wang , Baodong Li , Jinbang Wang , Zhimeng Li , Qingxin Xia , Jie Ma , Chengjuan Zhang , Juan Yu , Ke Li , Shuning Xu , Lei Qiao , Gaizhen Kuang , Danyang Li

Organizations

Department of Medical Oncology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China, Department of Surgical Oncology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China, Department of Molecular Pathology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China, Department of Pathology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China, Department of Endoscopy Center, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China

Research Funding

Pharmaceutical/Biotech Company
Jiangsu Hengrui Medicine Co., Ltd.

Background: Neoadjuvant chemotherapy has been demonstrated to improve the pathological complete response(pCR) and 5-year survival rate of patients with locally advanced gastric and gastroesophageal junction adenocarcinoma (GC/GEJC). Immunotherapy has become a new promising treatment for advanced GC/GEJC. Therefore, we intended to evaluate the safety and efficacy of Camrelizumab (anti-PD-1 antibody) combined with FOLFOX as the neoadjuvant therapy for patients with locally advanced GC/GEJC. Methods: Eligiblepatients were locally advanced GC/GEJC with clinical stage≥T2 and/or positive lymphoglandula confirmed by endoscopic ultrasonography (EUS) and imaging. They received 4 cycles neoadjuvant therapy which including Camrelizumab(200mg ivgtt D1), FOLFOX(Oxaliplatin 85mg/m2 ivgtt D1, 5-Fu 400mg/m2 iv D1, LV 200mg/m2 ivgtt D1, 5-Fu 2.4mg/m2 CIV 46 hours) every 14 days. Imaging evaluation was performed in 2-4 weeks after neoadjuvant therapy. Patients without progression disease (PD) received D2 radical gastrectomy. The primary endpoint was pCR, the secondary endpoints were R0 resection rate and safety. Results: From July 24 2019 to January 31 2020, 16 patients were eligible. The median age was 57 years (29-72 years). A total of 11(69%) males and 5(31%) females, ECOG PS 0 (n=9, 56%), ECOG PS 1 (n=7, 44%). All the patients completed 4 cycles treatment and none of them was confirmed PD by image. One of the patients refused gastrectomy and withdraw from the study. The other 15 patients underwent operation. Unfortunately, intraperitoneal metastases were confirmed in 2 patients during operation. 13 patients received D2 radical gastrectomy and all of them experienced R0 resection. Among the 13 evaluable patients, 1 patient (8%) was observed pCR, 3 patients (23%) experienced TRG1, 10 patients (77%) achieved stage reduction. Notably, 8 patients (62%) had lymphonodus pCR. The grade 3-4 treatment-related AEs were neutropenia (n=3, 19%), leukopenia (n=2, 13%) and anorexia (n=1, 6%). No serious AEs resulted in termination of treatment. Either severe immune-related AEs or treatment-related death was not observed. Conclusions: Camrelizumab combined with FOLFOX as neoadjuvant regimen in patients with locally advanced GC/GEJC showed promising pCR with good tolerance. Clinical trial information: NCT03939962.

Patient characteristics.

CharacteristicsN%
Clinical stage (T≥3)16100
Clinical stage (N≥1)16100
HER-2 postive00
MMR deficient00
EBV postive213
PD-L1 CPS<1744
PD-L1 5<CPS≥1425
PD-L1 CPS≥5531

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

Session Type

Poster Session

Session Title

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Track

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Sub Track

Esophageal or Gastric Cancer

Clinical Trial Registration Number

NCT03939962

Citation

J Clin Oncol 38: 2020 (suppl; abstr 4536)

DOI

10.1200/JCO.2020.38.15_suppl.4536

Abstract #

4536

Poster Bd #

144

Abstract Disclosures