Systemic Therapy

7

Review clinical trials related to Systemic Therapy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Cytoreductive Gastrectomy After Systemic Therapy Versus Systemic Therapy Alone For Limited Metastasis Gastric Cancer

The results of the current studies to determine the optimal strategy for metastatic gastric cancer remain contrversial worldwide. Hypothesis: Cytoreductive Gastrectomy After Systemic Therapy will improve survival time for metastasis gastric cancer compared to Systemic Therapy alone.

Participants needed: 250
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: University Medical Center Ho Chi Minh City (UMC)Updated: Aug 27, 2025Locations: 1
Eligibility criteria

Age 18-75 [+18]

Any extra-abdominal metastasis at diagnosis or during systemic treatment. [+20]

Status: Recruiting

Continuation of First-line Therapy With Radiotherapy Versus Early Switch to Second-line Therapy in Oligoprogressive HCC

This multicenter, prospective, randomized, controlled, open-label, two-arm Phase III clinical trial is designed to evaluate whether adding radiotherapy to oligoprogressive lesions while continuing first-line systemic therapy at the time of oligoprogression can effectively prolong progression-free survival compared to early switching to second-line systemic therapy in oligoprogressive hepatocellular carcinoma.

Participants needed: 132
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: Shandong Cancer Hospital and InstituteUpdated: Aug 1, 2025Locations: 1
Eligibility criteria

1. Histological or cytological confirmation of primary hepatocellular carcinoma... [+9]

1. Patients who received FLST as adjuvant treatment after curative surgery for H... [+16]

Status: Recruiting

Prospective Collection of Therapeutic Efficacy and Safety Data in Patients with Unresectable Hepatocellular Carcinoma

The malignant degree of middle and advanced liver cancer is very high, and the survival prognosis of patients is very poor. TACE is currently the standard treatment for unresectable liver cancer recommended by several international authoritative guidelines. However, TACE can only extend survival from 8 months to 13 months, and the prognosis for patients with unresectable liver cancer is still not optimistic. In recent years, some studies have suggested that the combination of TACE and systemic therapy can prolong OS and PFS, but a number of prospective studies have found that the combination of TACE and targeted therapy can not improve the prognosis of unresectable liver cancer. However, TACE as a non-radical treatment is difficult to achieve complete tumor necrosis, so it is still unknown which treatment combination can best improve the prognosis. This trial is an observational clinical trial to explore the efficacy and safety of TACE combined targeting/immunotherapy for unresectable hepatocellular carcinoma. Clinical data of patients with unresectable liver cancer treated in our hospital from March 2023 to March 2025 are intended to be collected to evaluate the efficacy and safety of TACE combined with different systems for unresectable liver cancer.

Participants needed: 500
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Sun Yat-sen UniversityUpdated: Jan 23, 2025Locations: 1Duration: 24 Months
Eligibility criteria

Preoperative imaging examination assessed tumor load >50%; [+5]

Status: Recruiting

TIPS Combined With Lenvatinib and PD-1 Inhibitor for Advanced HCC With Main Trunk PVTT

Hepatocellular carcinoma (HCC) with main trunk portal vein tumor thrombus (PVTT) has poor prognosis. The main lethiferous factor is the upper gastrointestinal hemorrhage by PVTT-related portal hypertension, then the second is the tumor-caused death. It is vital to prevent the portal hypertension by PVTT.

Participants needed: 42
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Sun Yat-sen UniversityUpdated: Jan 13, 2025Locations: 1
Eligibility criteria

diagnosis of primary HCC, confirmed histologically or clinically according to th... [+10]

recurrent HCC; [+6]

Status: Recruiting

Ablation of Pulmonary Oligometastasis Combined With System for Advanced Hepatocellular Carcinoma

Ablation has been an effective therapy in treating intrathoracic metastases. However, for hepatocellular carcinoma with pulmonary oligometastasis, ablation of metastases remains relatively unexplored and still needs clinical evidence.

Participants needed: 470
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: Sun Yat-sen UniversityUpdated: Dec 3, 2024Locations: 1
Eligibility criteria

diagnosis of primary HCC, confirmed histologically or clinically according to th... [+9]

intermediate HCC; [+5]

Status: Recruiting

The Comparison of TACE-Lenvatinib With TACE-Lenvatinib-ablation for Intermediate Recurrent Hepatocellular Carcinoma

Studies have shown that combination therapy of TACE with Lenvatinib could achieve better survival outcomes than TACE alone for hepatocellular carcinoma (HCC) at BCLC B stage. However, whether patients could benefit from the ablation for intermediate recurrent HCC (RHCC) is still need high quality clinical evidence. This study is to evaluate the efficacy of ablation combined with TACE and Lenvatinib for the intermediate-stage RHCC.

Participants needed: 116
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Sun Yat-sen UniversityUpdated: Dec 3, 2024Locations: 1
Eligibility criteria

18-75 years; [+7]

under 18 years or over 75 years of age; [+2]

Status: Recruiting

HAIC in Combination with PD-1 Inhibitors and Lenvatinib for Intermediate and Advanced HCC After the Failure of Systemic Therapy Recommended by BCLC

The purpose of this study is to evaluate the safety and efficacy of hepatic arterial infusion chemotherapy (HAIC) in combination with PD-1 inhibitors and Lenvatinib in patients with intermediate or advanced-stage hepatocellular carcinoma (HCC) after failure of systemic therapy recommended by BCLC.

Participants needed: 84
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: First Hospital of China Medical UniversityUpdated: Oct 8, 2024Locations: 1
Eligibility criteria

Has a diagnosis of HCC confirmed by radiology, histology, or cytology; [+7]

The interval between the failure of systemic therapy and the beginning of combin... [+2]