Flow cytometry cell sorting and T-cell cytotoxicity assay laboratory

CLINICAL APPLICATION & CRITERIA

Immunotherapy & Checkpoint Inhibitors in China

Immunotherapy harnesses the body’s own immune system to recognize and destroy cancer cells. The most widely used class is immune checkpoint inhibitors — antibodies targeting PD-1, PD-L1, or CTLA-4 — that release natural brakes on T cells, enabling them to attack tumors. Unlike chemotherapy or targeted therapy, immunotherapy can produce durable, long-term remissions that persist years after treatment ends, even in advanced metastatic disease. Responses are enriched in patients whose tumors express predictive biomarkers such as PD-L1, high tumor mutational burden (TMB-H), or microsatellite instability (MSI-H/dMMR). Combination approaches with chemotherapy, targeted agents, or radiation continue to expand the受益 patient population.

CLINICAL INDICATIONS

Key Cancers Treated with Immunotherapy

World-leading first-in-class bispecific antibodies, high-affinity PD-1/PD-L1 inhibitors, and synergistic combination protocols across solid tumors:

Lung Cancer

First-in-class PD-1/VEGF bispecifics (Ivonescimab) and validated PD-1 antibodies achieving superior PFS in advanced EGFR-mutant and wild-type NSCLC.

Stomach & Colorectal Cancer

Approved first-line PD-1/CTLA-4 bispecifics (Cadonilimab) and chemo-immunotherapy regimens for esophageal, gastric, and MSI-H colorectal cancer.

Liver Cancer

Standard-of-care PD-1 plus anti-angiogenic combinations (Camrelizumab+Rivoceranib, Sintilimab+Bevacizumab) extending median overall survival.

WHY CHOOSE US

Why Choose China for Immunotherapy

A specialized cross-border continuum connecting international patients directly with China's world-leading immuno-oncology ecosystem.

China has become a global powerhouse in immuno-oncology, with the world’s largest number of clinical trials for PD-1/PD-L1 inhibitors. Multiple domestically developed checkpoint antibodies — sintilimab (Innovent), tislelizumab (BeiGene), camrelizumab (Hengrui), toripalimab (Junshi), and penpulimab — have received NMPA approval, with several now recognized by the FDA and EMA. NRDL negotiations have driven anti-PD-1 prices down to roughly 10–20% of US list prices, making immunotherapy widely accessible to both domestic and international patients.

Chinese companies are pioneering novel bispecific antibodies — including ivonescimab, the world’s first approved PD-1×VEGF bispecific — which demonstrated a statistically significant overall survival benefit over standard PD-1 plus chemotherapy in squamous NSCLC, a result unmatched by any other anti-PD-(L)1 regimen. Fast-track NMPA approvals, a vast patient base for rapid clinical development, and extensive real-world data on high-incidence Chinese cancers (esophageal, gastric, liver, nasopharyngeal) make China a global leader in delivering cutting-edge immunotherapy.

HOW IT WORKS

4 Steps to Treatment in China

A simple, step-by-step process from initial record review to your arrival and treatment in China.

01. Submit Records Online

Upload existing pathology reports, biomarker NGS profiles, and imaging scans through our secure clinical intake portal.

02. Pre-Screen & Doctor Match

Clinical eligibility and contraindication screening, matching your specific case with China's foremost oncology chiefs.

03. Doctor Consultation

One-on-one remote video consultation or written multidisciplinary assessment to confirm treatment protocol before travel.

04. Travel to China & Care

Expedited medical visa support, priority hospital admission, dedicated bilingual bedside escorts, and continuum follow-up.

PATIENT FAQS

Frequently Asked Questions

Key clinical, financial, and logistical insights for international patients considering care in China.
China has approved over 10 distinct domestic PD-1/PD-L1 antibodies and developed world-first bispecifics such as Cadonilimab (PD-1/CTLA-4) and Ivonescimab (PD-1/VEGF), demonstrating superior progression-free survival in Phase III head-to-head trials against global standards.
Standard evaluation includes PD-L1 expression (TPS and CPS scores by validated IHC), Microsatellite Instability (MSI-H/dMMR), and Tumor Mutational Burden (TMB-H). However, novel combination regimens frequently achieve responses even in PD-L1 negative tumors.
Leading Chinese cancer centers maintain standardized multidisciplinary irAE task forces. Patients undergo regular liver, thyroid, endocrine, and pulmonary monitoring, with immediate access to immunosuppressive protocols if necessary.
Immunotherapy is typically administered intravenously once every 2 to 3 weeks. Durable responses are typically maintained for 1 to 2 years, provided tolerance is maintained.

CONFIDENTIAL CASE EVALUATION

Start with a Confidential Clinical Case Review

Submit your basic case details below for an initial eligibility review. Our medical team coordinates directly with chief oncologists at top Chinese cancer centers, returning a preliminary assessment and roadmap within 24–48 hours.

✓ Free initial triage  •  ✓ Direct specialist coordination  •  ✓ 100% Confidential

    Immunotherapy & Checkpoint Inhibitors