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HIPEC Priming Followed by Serplulimab Plus SOX/XELOX in Locally Advanced Gastric Cancer

2 lipca 2026 zaktualizowane przez: weijun wang, Shanghai Changzheng Hospital

A Prospective Exploratory Study of a HIPEC Priming Strategy Followed by Serplulimab Combined With SOX/XELOX as Neoadjuvant Therapy for Locally Advanced Gastric Cancer

Patients with locally advanced gastric cancer (LAGC), particularly those with serosal invasion, remain at high risk of peritoneal recurrence despite standard perioperative treatment. Hyperthermic intraperitoneal chemotherapy (HIPEC) may eradicate free intraperitoneal tumor cells and microscopic peritoneal disease while potentially enhancing systemic anti-tumor immune activation.

This is a prospective, single-center, single-arm exploratory study evaluating a HIPEC priming strategy followed by serplulimab-based neoadjuvant therapy in patients with locally advanced gastric cancer (cT3-4aN+M0). Eligible patients will undergo diagnostic laparoscopy confirming no visible peritoneal metastasis (P0) and negative peritoneal cytology (CY0), followed by docetaxel-based HIPEC.

After recovery from HIPEC, patients will initially receive one cycle of serplulimab combined with fluoropyrimidine monotherapy (S-1 or capecitabine), followed by subsequent cycles of serplulimab combined with SOX/XELOX chemotherapy prior to radical gastrectomy.

The primary endpoints are pathological complete response (pCR) rate and major pathological response (MPR) rate. Secondary endpoints include R0 resection rate, objective response rate (ORR), peritoneal recurrence-free survival (PRFS), overall survival (OS), and safety.

Przegląd badań

Szczegółowy opis

Locally advanced gastric cancer (LAGC) remains associated with a high risk of recurrence after curative-intent treatment, particularly peritoneal recurrence in patients with serosal invasion. Although perioperative chemotherapy improves survival outcomes, current systemic treatment strategies remain insufficient for controlling microscopic peritoneal dissemination.

Hyperthermic intraperitoneal chemotherapy (HIPEC) delivers heated chemotherapeutic agents directly into the peritoneal cavity, resulting in enhanced regional drug exposure and hyperthermia-mediated cytotoxicity. In addition to direct anti-tumor effects, accumulating evidence suggests that HIPEC may induce immunogenic cell death, enhance tumor antigen release, and activate systemic anti-tumor immune responses.

Serplulimab is a humanized anti-programmed cell death protein 1 (PD-1) monoclonal antibody that restores T-cell-mediated anti-tumor immunity through blockade of the PD-1/PD-L1 signaling pathway. The sequential administration of HIPEC followed by PD-1 blockade-based neoadjuvant therapy may therefore provide synergistic anti-tumor activity in locally advanced gastric cancer.

This prospective, single-center, single-arm exploratory study is designed to evaluate the efficacy and safety of HIPEC followed by serplulimab-based neoadjuvant therapy in patients with HER2-negative locally advanced gastric or gastroesophageal junction adenocarcinoma.

Approximately 48 patients with clinically staged cT3-4aN+M0 disease will be enrolled. After screening and informed consent, all eligible patients will undergo diagnostic laparoscopy with peritoneal lavage cytology. Patients confirmed to have no visible peritoneal metastasis (P0) and negative cytology (CY0) will receive docetaxel-based HIPEC.

Following postoperative recovery, patients will receive one induction cycle of serplulimab combined with fluoropyrimidine monotherapy (S-1 or capecitabine). Subsequent neoadjuvant treatment will consist of serplulimab combined with SOX or XELOX administered every 3 weeks for a total of 3-4 treatment cycles. Patients considered resectable after radiologic reassessment will undergo standard radical gastrectomy with D2 lymphadenectomy.

The primary endpoints are pathological complete response (pCR) and major pathological response (MPR). Secondary endpoints include R0 resection rate, objective response rate (ORR), peritoneal recurrence-free survival (PRFS), overall survival (OS), and treatment-related safety assessed according to NCI-CTCAE criteria.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

48

Faza

  • Faza 2

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  • Aged 18 to 75 years (inclusive); gender unrestricted.
  • Histologically confirmed gastric or gastroesophageal junction adenocarcinoma via endoscopic biopsy.
  • Clinical stage cT3-4a (imaging evidence of tumor invasion into or penetration through the serosa), N+ (lymph node positive), M0 (no distant organ metastasis), based on the 8th Edition of the AJCC Staging Manual.
  • HER2-negative disease, defined as HER2 IHC 0 or 1+, or IHC 2+ with negative ISH.
  • Diagnostic laparoscopy confirms the absence of macroscopic peritoneal metastasis (P0) and negative peritoneal lavage cytology (CY0).
  • Adequate cardiac function, rendering the patient eligible for curative-intent resection. If clinically indicated, patients with underlying ischemic heart disease, valvular heart disease, or other severe cardiac conditions must undergo a preoperative cardiac evaluation by a cardiologist.
  • ECOG Performance Status (PS) score of 0 or 1 within 7 days prior to enrollment.
  • Anticipated survival time of ≥ 6 months.
  • Hepatitis B surface antigen (HBsAg) negative (-) and Hepatitis B core antibody (HBcAb) negative (-). If HBsAg is positive (+) or HBcAb is positive (+), the Hepatitis B virus DNA (HBV-DNA) level must be < 1000 copies/mL, < 200 IU/mL, or below the upper limit of normal (ULN) at the study center to be eligible for enrollment.
  • HCV antibody negative (-).
  • Major organ function is normal, defined as meeting the following criteria (having not received transfusions of blood products, albumin, recombinant human thrombopoietin, or colony-stimulating factors [CSF] within 14 days prior to randomization):

Hematologic System Absolute Neutrophil Count (ANC) ≥ 1.5×10⁹/L Platelets (PLT) ≥ 100×10⁹/L Hemoglobin (Hb) ≥ 90 g/L Liver Function Total Bilirubin (TBIL) ≤ 1.5×Upper Limit of Normal (ULN) Alanine Aminotransferase (ALT) ≤ 2.5×ULN; ≤ 5.0×ULN for patients with liver metastases Aspartate Aminotransferase (AST) ≤ 2.5×ULN; ≤ 5.0×ULN for patients with liver metastases Alkaline Phosphatase (ALP) ≤ 2.5×ULN; ≤ 5.0×ULN for patients with liver and/or bone metastases Albumin ≥ 25 g/L Renal Function Creatinine Clearance (CrCl) ≥ 50 mL/min (calculated using the Cockcroft-Gault formula) Coagulation Function Activated Partial Thromboplastin Time (APTT) ≤ 1.5×ULN Prothrombin Time (PT) ≤ 1.5×ULN International Normalized Ratio (INR) ≤ 1.5×ULN -Female patients must meet the following criteria:

Be in a postmenopausal state (defined as having had no menstruation for at least 1 year, with no other confirmed cause for amenorrhea other than menopause), or have undergone surgical sterilization (removal of ovaries and/or uterus); alternatively, patients with reproductive potential must simultaneously meet the following requirements:

  • A serum pregnancy test result must be negative within 7 days prior to randomization;
  • Agree to use a contraceptive method with an annual failure rate of < 1% or practice abstinence (avoidance of heterosexual intercourse) (from the time of signing the informed consent form until at least 120 days after the last dose of the investigational drug, and at least 6 [months] after the last dose of the chemotherapy drug ...months (contraceptive methods with an annual failure rate of < 1% include bilateral tubal ligation, vasectomy, correct use of ovulation-suppressing hormonal contraceptives, hormone-releasing intrauterine devices [IUDs], and copper-containing IUDs);
  • Must not be breastfeeding. -Male patients must meet the following criteria: Agree to practice abstinence (avoid heterosexual intercourse) or use contraception, as specified below: If the partner is a female of childbearing potential or is pregnant, the male patient must practice abstinence or correctly use condoms for contraception-to prevent drug exposure to the embryo-during the chemotherapy treatment period and for at least 6 months after the last dose of chemotherapy medication, and for at least 120 days after the last dose of the investigational drug. The reliability of sexual abstinence should be evaluated with reference to the duration of the clinical study, patient preference, and lifestyle. Periodic abstinence (e.g., calendar-based, ovulation-based, basal body temperature, or post-ovulation methods) and withdrawal (coitus interruptus) are not considered acceptable methods of contraception.

Exclusion Criteria:

  • History of other active malignancies within the past 5 years, or the presence of other active malignancies at the time of enrollment. Patients with cured localized tumors-such as basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, carcinoma in situ of the prostate, carcinoma in situ of the cervix, or carcinoma in situ of the breast-are eligible for enrollment.
  • Presence of documented distant metastases (e.g., liver, lung, or bone metastases) or laparoscopically confirmed peritoneal seeding (P1).
  • Patients scheduled to undergo, or with a history of having undergone, organ or bone marrow transplantation.
  • Occurrence of myocardial infarction or poorly controlled arrhythmias (including a QTc interval ≥ 450 ms for males or ≥ 470 ms for females; QTc interval calculated using the Fridericia formula) within 6 months prior to enrollment.
  • Presence of NYHA Class III or IV heart failure, or a cardiac ultrasound result showing a Left Ventricular Ejection Fraction (LVEF) < 50%.
  • Human Immunodeficiency Virus (HIV) infection.
  • Presence of active pulmonary tuberculosis.
  • History of, or current presence of, interstitial pneumonia, pneumoconiosis, radiation pneumonitis, drug-induced pneumonitis, or severe impairment of pulmonary function that could interfere with the detection or management of suspected drug-related pulmonary toxicity.
  • Presence of a known active or suspected autoimmune disease. Exceptions are made for patients whose disease is in a stable state at the time of enrollment (defined as requiring no systemic immunosuppressive therapy).
  • Receipt of a live vaccine within 28 days prior to enrollment; inactivated viral vaccines for seasonal influenza are permitted.
  • Patients requiring systemic corticosteroid therapy (at a prednisone-equivalent dose > 10 mg/day) or other immunosuppressive medications within 14 days prior to enrollment or during the study period. However, the following exceptions are permitted: in the absence of active autoimmune disease, patients may use topical or inhaled corticosteroids, or receive adrenal replacement therapy at a prednisone-equivalent dose ≤ 10 mg/day.
  • Presence of any active infection requiring systemic anti-infective treatment within 14 days prior to enrollment; prophylactic antibiotic treatment (e.g., for the prevention of urinary tract infections or chronic obstructive pulmonary disease) is an exception.
  • Prior receipt of any anti-tumor therapy for the current gastric cancer, including chemotherapy, radiotherapy, targeted therapy, or immunotherapy.
  • Currently receiving treatment in another clinical study, or the planned start date of the treatment in this study is less than 14 days after the completion of treatment in a previous clinical study.
  • Known history of severe allergy to any monoclonal antibody or excipients of the investigational drug.
  • Known history of substance abuse (including drug abuse); patients who have ceased alcohol consumption are eligible for enrollment.
  • Presence of any condition that may increase the risks associated with study participation or the investigational drug, or presence of other severe, acute, or chronic diseases that, in the investigator's judgment, render the patient unsuitable for participation in the clinical study.

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Experimental
Participants will undergo diagnostic laparoscopy with peritoneal lavage cytology followed by docetaxel-based hyperthermic intraperitoneal chemotherapy (HIPEC). After recovery from HIPEC, patients will receive one induction cycle of serplulimab combined with fluoropyrimidine monotherapy (S-1 or capecitabine), followed by subsequent cycles of serplulimab combined with SOX/XELOX neoadjuvant chemotherapy prior to radical gastrectomy with D2 lymphadenectomy
Docetaxel-based hyperthermic intraperitoneal chemotherapy administered after diagnostic laparoscopy in patients with P0/CY0 locally advanced gastric cancer
Serplulimab administered intravenously every 3 weeks as part of neoadjuvant treatment
Oral S-1 administered during neoadjuvant treatment.
Oral capecitabine administered during neoadjuvant treatment.
Intravenous oxaliplatin administered as part of SOX/XELOX neoadjuvant chemotherapy.
Standard radical gastrectomy with D2 lymphadenectomy performed after completion of neoadjuvant therapy.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Pathological Complete Response (pCR) Rate
Ramy czasowe: At the time of surgery
Proportion of patients achieving pathological complete response, defined as the absence of residual viable tumor cells in both the primary tumor and regional lymph nodes after neoadjuvant treatment and radical gastrectomy.
At the time of surgery

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Major Pathological Response (MPR) Rate
Ramy czasowe: At the time of surgery
Proportion of patients achieving major pathological response, defined as ≤10% residual viable tumor cells in the resected primary tumor specimen following neoadjuvant treatment.
At the time of surgery
Objective Response Rate (ORR)
Ramy czasowe: Perioperative
Proportion of patients achieving complete response (CR) or partial response (PR) according to RECIST version 1.1.
Perioperative
R0 Resection Rate
Ramy czasowe: At surgery
Proportion of patients achieving microscopically margin-negative (R0) resection.
At surgery
Peritoneal Recurrence-Free Survival (PRFS)
Ramy czasowe: Up to 3 years after surgery
Time from enrollment to the occurrence of peritoneal metastasis (peritoneal metastasis detected by PET/CT and/or diagnostic laparoscopy).
Up to 3 years after surgery
Overall Survival (OS)
Ramy czasowe: Up to 3 years
Time from study enrollment to death from any cause.
Up to 3 years
Incidence of Treatment-Related Adverse Events
Ramy czasowe: From the date of informed consent signing until the end of the safety follow-up period (30 days after the last dose of study treatment)
Incidence and severity of treatment-related adverse events assessed according to NCI-CTCAE version 6.0.
From the date of informed consent signing until the end of the safety follow-up period (30 days after the last dose of study treatment)

Współpracownicy i badacze

Tutaj znajdziesz osoby i organizacje zaangażowane w to badanie.

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 lipca 2026

Zakończenie podstawowe (Szacowany)

9 maja 2028

Ukończenie studiów (Szacowany)

9 maja 2028

Daty rejestracji na studia

Pierwszy przesłany

18 maja 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

31 maja 2026

Pierwszy wysłany (Rzeczywisty)

2 czerwca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

7 lipca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

2 lipca 2026

Ostatnia weryfikacja

1 lipca 2026

Więcej informacji

Terminy związane z tym badaniem

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Nie

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .

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