Starting soon
Phase 1
HS-IT101 Injection for Advanced NSCLC
Condition(s) studied
Advanced Non-Small Cell Lung Cancer
Investigational drug(s) / intervention(s)
CyclophosphamideFludarabineIL-2 (interleukin 2)HS-IT101 monotherapy
Cyclophosphamide: Cyclophosphamide administered via intravenous infusion once daily for 3 consecutive days.
Fludarabine: Fludarabine is administered once daily via intravenous infusion for 4 consecutive days.
IL-2 (interleukin 2): IL-2 administered subcutaneously once daily. Dosing may be adjusted based on subject tolerance, including modifications to dose quantity, administration frequency, or complete treatment discontinuation, with a maximum treatment duration of 3 days.
HS-IT101 monotherapy: TIL Injection administered by intravenous infusion over 30-60 minutes.
Study summary
An Open-Label, Single-Arm Phase Ib Clinical Trial Evaluating the Safety, Tolerability, and Preliminary Efficacy of HS-IT101 Injection in Subjects with Advanced NSCLC.
Eligibility
Inclusion Criteria:
* Age: 18-70 years (inclusive).
Diagnosis:
Histologically/cytologically confirmed advanced, recurrent, or metastatic non-small cell lung cancer (NSCLC) .
Tumor Sampling:
≥1 lesion untreated with radiotherapy/local therapy within 28 days for TIL preparation (tissue weight ≥0.050 g).
Target Lesion:
≥1 measurable lesion per RECIST v1.1, untreated with radiotherapy/local therapy (unless treatment occurred \>28 days before sampling with documented progression).
Performance Status: ECOG score ≤1. Survival: Life expectancy ≥3 months.
Organ Function:
Hematology: ANC ≥1.5×10⁹/L, PLT ≥90×10⁹/L, HGB ≥90 g/L (no transfusion/erythropoietin within 14 days).
Liver: ALT/AST ≤2.5×ULN (≤5×ULN if liver metastases); TBil ≤1.5×ULN (≤3×ULN for Gilbert syndrome).
Kidney: Serum Cr ≤1.5×ULN or Ccr ≥60 mL/min (Cockcroft-Gault formula). Coagulation: APTT ≤1.5×ULN; INR/PT ≤1.5×ULN.
Cardiac Function:
LVEF ≥50% by echocardiography; QTcF ≤470 ms (Fridericia formula: QTcF = QT/RR⁰·³³).
Baseline SpO₂ \>91% (room air). Note: If QTcF is abnormal initially, repeat twice at ≥5-minute intervals and use mean value for eligibility.
Toxicity Recovery: All treatment-related adverse events resolved to CTCAE v5.0 ≤Grade 1 (except alopecia/non-risk toxicities per investigator) before tumor sampling.
Contraception: Effective non-pharmacological contraception from informed consent until 1 year post-TIL infusion.
Compliance: Capable of understanding the trial, voluntarily signing informed consent, and adhering to protocol visits/procedures.
Exclusion Criteria:
* Severe Hypersensitivity: History of severe hypersensitivity to drugs used in the study (including but not limited to cyclophosphamide, fludarabine, IL-2, gentamicin, amphotericin B, or components of TIL infusion).
Uncontrolled Comorbidities:
Poorly controlled hypertension (resting SBP ≥160 mmHg or DBP ≥100 mmHg despite medication).
Congestive heart failure (NYHA Class III/IV).
Cardiovascular Events (within 6 months):
Deep vein thrombosis, pulmonary embolism, myocardial infarction, severe/unstable arrhythmia, angina, PCI, ACS, CABG, stroke, TIA, or cerebral embolism.
Active Autoimmune Disease:
Requires systemic therapy during the study period (Exceptions: Eczema, vitiligo, psoriasis, alopecia, or Graves' disease stable without systemic therapy for 2 years; hypothyroidism on hormone replacement; type 1 diabetes on insulin).
Transplantation History: Solid organ or hematopoietic stem cell transplantation.
Immunosuppressive Therapy:
Use of immunosuppressants (e.g., steroids) within 4 weeks before tumor sampling (Allowed: Physiologic glucocorticoid doses ≤12 mg/m²/day hydrocortisone equivalent; topical/nasal steroids).
Recent Anticancer Therapy:
Systemic anticancer treatment within 4 weeks before preconditioning (including investigational drugs; washout \<5 half-lives if \<4 weeks).
Planned participation in other interventional trials.
Active Infections:
HIV/syphilis antibody-positive; active HBV/HCV (Allowed: HBsAg/HBeAg+ if HBV DNA below LLN; HCV Ab+ if HCV RNA below LLN).
Active systemic infection or tuberculosis requiring treatment. Recent Surgery/Trauma: Major surgery or significant trauma within 4 weeks before screening; elective surgery planned during the study.
Poor Wound Healing: Surgery-related complications or delayed healing increasing risks of TIL therapy (per investigator judgment).
Other Malignancies: Additional primary malignancy within 5 years (Exceptions: Curatively treated basal/squamous cell carcinoma or carcinoma in situ).
Severe Respiratory Disease: History of severe ILD, COPD, pulmonary insufficiency, or symptomatic bronchospasm.
Gastrointestinal Complications: Surgical-required GI bleeding, bowel ischemia, or perforation.
CNS Involvement:
Leptomeningeal metastasis; uncontrolled/untreated CNS metastases (Exceptions: Asymptomatic lesions \<1 cm, stable for ≥4 weeks without steroids/anticonvulsants).
Prior Cell Therapy: Previous treatment with similar cellular products. Pregnancy/Lactation: Pregnant or breastfeeding women.
Other Exclusions:
Psychiatric disorders, alcoholism, drug abuse, or other conditions deemed unsuitable by the investigator.
Primary outcome measure(s)
- Adverse Events (AE) — 12 months
To characterize the safety profile of HS-IT101 in patients with advanced solid tumor as assessed by incidence of adverse events
- Serious Adverse Events (SAE) — 12 months
To characterize the safety profile of HS-IT101 in patients with advanced solid tumor as assessed by incidence of serious adverse events
- Objective Response Rate (ORR) — Up to 36 months
To evaluate the efficacy of HS-IT101 in patients with advanced solid tumor, based on the objective response rate (ORR) as assessed by the Independent Review Committee (IRC) per RECIST v1.1
- Time-to-response (TTR) — Up to 36 months
To evaluate the efficacy of HS-IT101 in patients with advanced solid tumor by assessing the time-to-response (TTR) as assessed by the Investigator per RECIST v1.1
- Duration of Response (DOR) — Up to 36 months
To evaluate the efficacy of HS-IT101 in patients with advanced solid tumor by assessing the duration of response (DOR) as assessed by the Investigator per RECIST v1.1
- Disease Control Rate (DCR) — Up to 36 months
To evaluate the efficacy of HS-IT101 in patients with advanced solid tumor, based on the disease control rate (DCR) as assessed by the Independent Review Committee (IRC) per RECIST v1.1
Trial sites (1)
| Facility | City | Region | Status |
| Guangdong Provincial People's Hospital |
Guangzhou |
Guangdong |
|
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