A Phase 2 interventional study of Sintilimab Combined with Ramucirumab and Paclitaxel in Gastric Cancer (Diagnosis), sponsored by The First Affiliated Hospital with Nanjing Medical University. Not yet recruiting at 1 site in China. Open to participants aged 15 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-06-25.
Sponsored by The First Affiliated Hospital with Nanjing Medical University · Phase 2, Interventional, and Treatment
To explore the efficacy and safety of sintilimab combined with ramucirumab and paclitaxel in the treatment of advanced gastric cancer patients with short-term recurrence after postoperative adjuvant therapy, and to identify efficacy-related biomarkers to guide subsequent individualized treatment.
The treatment of gastric cancer relies first on surgical resection. Especially for patients with early-stage and locally advanced gastric cancer, surgical resection of the tumor and regional lymph nodes constitutes the most effective therapeutic approach. The goal of surgery is to maximize survival rates and prolong patients' disease-free survival (DFS) by completely eradicating cancer cells . However, due to the high metastatic potential of gastric cancer-particularly lymph node metastasis and peritoneal metastasis-the postoperative recurrence rate remains considerable . Therefore, postoperative adjuvant therapy has become crucial for reducing recurence and improving survival outcomes.
According to the clinical guidelines of the Chinese Society of Clinical Oncology (CSCO) and the European Society for Medical Oncology (ESMO), postoperative adjuvant therapy typically adopts chemotherapy regimens, such as oxaliplatin plus S-1 (SOX), oxaliplatin plus capecitabine (CAPOX), and oxaliplatin plus 5-fluorouracil plus leucovorin (FOLFOX) . These chemotherapy regimens have achieved remarkable results by inhibiting residual micrometastatic tumor cells and reducing the risk of postoperative recurrence.
Nonetheless, despite the certain success of postoperative adjuvant therapy, some patients still experience recurrence either during adjuvant treatment or within 6 months after its completion. Once recurrence occurs, tumor treatment becomes more challenging. Such recurrence usually indicates resistance of the gastric cancer to initial therapy, and the treatment strategy post-recurrence is more complex. For patients with short-term recurrence after postoperative adjuvant therapy, the adjuvant therapy is defined as first-line treatment, and recurrence signifies progression to the second-line treatment phase.The choice of second-line treatment for this specific patient population is generally based on the patients' HER2 expression status. For HER2-positive gastric cancer patients, the trastuzumab plus chemotherapy regimen is usually administered . Multiple clinical trial results have demonstrated that trastuzumab combined with chemotherapy can significantly enhance the efficacy and survival rates of HER2-positive gastric cancer patients . For HER2-negative patients, the RAINBOW study has provided a novel therapeutic regimen of paclitaxel combined with ramucirumab for gastric cancer. The study indicated that the combination of paclitaxel and ramucirumab can significantly prolong patients' median overall survival (OS) and improve their progression-free survival (PFS). This treatment regimen has been recommended by guidelines as the standard second-line treatment option .
In recent years, the emergence of immune checkpoint inhibitors (ICIs)-especially those targeting programmed cell death protein 1 (PD-1) and programmed death-ligand 1 (PD-L1)-has brought revolutionary changes to cancer treatment. Immunotherapy activates the patients' own immune system to recognize and eliminate tumor cells, and it has exhibited significant clinical efficacy in various malignancies, including non-small cell lung cancer, melanoma, and hepatocellular carcinoma . Clinical trials such as ORIENT-16, CheckMate-649, and ATTRACTION-4 have shown that immunotherapy combined with chemotherapy can significantly improve the OS and PFS of patients with PD-L1-positive tumors.The choice of second-line treatment for this specific patient population is generally based on the patients' HER2 expression status. For HER2-positive gastric cancer patients, the trastuzumab plus chemotherapy regimen is usually administered . Multiple clinical trial results have demonstrated that trastuzumab combined with chemotherapy can significantly enhance the efficacy and survival rates of HER2-positive gastric cancer patients . For HER2-negative patients, the RAINBOW study has provided a novel therapeutic regimen of paclitaxel combined with ramucirumab for gastric cancer. The study indicated that the combination of paclitaxel and ramucirumab can significantly prolong patients' median overall survival (OS) and improve their progression-free survival (PFS). This treatment regimen has been recommended by guidelines as the standard second-line treatment option .
In recent years, the emergence of immune checkpoint inhibitors (ICIs)-especially those targeting programmed cell death protein 1 (PD-1) and programmed death-ligand 1 (PD-L1)-has brought revolutionary changes to cancer treatment. Immunotherapy activates the patients' own immune system to recognize and eliminate tumor cells, and it has exhibited significant clinical efficacy in various malignancies, including non-small cell lung cancer, melanoma, and hepatocellular carcinoma . Clinical trials such as ORIENT-16, CheckMate-649, and ATTRACTION-4 have shown that immunotherapy combined with chemotherapy can significantly improve the OS and PFS of patients with PD-L1-positive tumors
2,851 studies on the registry are indexed under Stomach Neoplasms; 864 are open to participants now.
This study's planned enrollment of 30 is below the median of 67 across 2,096 interventional studies indexed under Stomach Neoplasms.
Browse Stomach Neoplasms studies →The First Affiliated Hospital with Nanjing Medical University is the lead sponsor of 543 studies on the registry; 301 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
A Study on the Efficacy and Safety of Sintilimab Combined with Ramucirumab and Paclitaxel in the Treatment of Gastric Cancer Patients with Short-term Recurrence after Adjuvant Therapy
Drug: Sintilimab Combined with Ramucirumab and Paclitaxel
Sintilimab Combined with Ramucirumab and Paclitaxel in the Treatment of Gastric Cancer Patients with Short-term Recurrence after Adjuvant Therapy
Objective Response Rate (ORR)
Proportion of patients achieving complete response (CR) or partial response (PR) according to RECIST v1.1.
Time frame: From baseline until disease progression or study completion, assessed up to 24 months
Progression-Free Survival (PFS)
Progression-free survival is defined as the time from baseline to the first documented disease progression according to RECIST v1.1 or death from any cause, whichever occurs first.
Time frame: From treatment initiation until disease progression or death, whichever occurs first, assessed up to 24 months
Plan to share: Yes
Supporting information: Study protocol, Sap, Icf
No publications or documents are linked to this record.
This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
The First Affiliated Hospital with Nanjing Medical University