Hyperthermia Combined With Immune Checkpoint Inhibitor Therapy for Advanced Gastrointestinal Tumours

Gastrointestinal Tumor Clinical Trial

— HEAIS001  

Official title:

Water-filtered Infrared A Radiation Whole-body Hyperthermia Combined With Immune Checkpoint Inhibitor Therapy for Advanced Gastrointestinal Tumours: A Prospective Open-label Single-arm Phase 2 Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06022692
• Other study ID #: ZhejiangH
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: June 1, 2020
• Est. completion date: August 1, 2023

Study information

• Verified date: September 2023
• Source: Zhejiang Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Gastrointestinal tumours (GITs) are the most common and fatal cancers worldwide; 96% of GITs show the microsatellite-stable (MSS)/proficient mismatch repair (pMMR) phenotype, and these tumours have a poor response to immune checkpoint inhibitor (ICI) therapy. Hyperthermia combined with ICI treatment (HIT) has been reported to show a synergistic sensitisation effect in numerous basic studies. This study aimed to validate the effectiveness, safety, and feasibility of water-filtered infrared A radiation (WIRA) whole-body hyperthermia combined with PD-1 inhibitor therapy and evaluate the real-world clinical application prospects of HIT. This open-label single-arm phase 2 clinical trial aimed to enrol advanced GIT patients with the MSS/pMMR phenotype in the East Asian population who had received third-line or higher treatment. The patients were treated with whole-body hyperthermia on days 1 and 8 of each HIT cycle along with administration of tislelizumab 200 mg on day 2 (24 h after the hyperthermia at day 1). The primary outcome was the disease control rate (DCR), while the secondary outcomes were progression-free survival (PFS), overall survival (OS), safety, and improvement in quality of life.

Description:

The specific treatment process is shown in the trial flow diagram. The patients underwent WIRA whole-body hyperthermia on days 1 and 8 of each HIT cycle. On day 2 (24 h after hyperthermia on day 1), 200 mg of tislelizumab prepared with 100 mL of normal saline was intravenously administered for less than 30 min. After six HIT cycles, tislelizumab was administered intravenously every 21 days until drop-out. For quality control of hyperthermia, the core temperature was set to 38·5-39·5 °C and measured using a rectal temperature-sensing probe. Hyperthermia was considered to have been achieved when this temperature range was recached and maintained for 60 min. Each hyperthermia session lasted for 2 h, including a 30-min heating stage, a 60-min insulation stage, and a 30-min cooling stage. Clinical data were collected every two HIT treatment cycles and evaluated using the RECIST version 1.1 standard.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: August 1, 2023
• Est. primary completion date: May 31, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Patients with advanced GIT who have previously received third-line or above treatment.

• Patients are aged 18-75.

• Patients with at least one measurable tumor lesion.

• Patients' all physiological indexes meet the HIT requirements.

Exclusion Criteria:

• Patients have participated in other clinical trials within 4 weeks before enrollment.

• Patients contraindicate to whole-body hyperthermia.

• Patients contraindicate to immunotherapy.

• Patients cannot fully cooperate with HIT and follow-up.

• Pregnant or lactating women.

• Other circumstances may affect the results.

Related Conditions & MeSH terms

• Digestive System Neoplasms
• Fever
• Gastrointestinal Neoplasms
• Gastrointestinal Tumor
• Hyperthermia

Intervention

Device:
• Water-filtered infrared A radiation whole-body hyperthermia (HECKEL 3000MT-4T, Germany)
The patients were treated with whole-body hyperthermia (HECKEL 3000MT-4T, Germany)) on days 1 and 8 of each hyperthermia combined with immune checkpoint inhibitor treatment cycle along with administration of tislelizumab (BeiGene, China) 200 mg on day 2 (24 hours after the hyperthermia at day 1).

Drug:
• tislelizumab (BeiGene, China) combined with PD-1 inhibitor
The patients were treated with whole-body hyperthermia (HECKEL 3000MT-4T, Germany)) on days 1 and 8 of each hyperthermia combined with immune checkpoint inhibitor treatment cycle along with administration of tislelizumab (BeiGene, China) 200 mg on day 2 (24 hours after the hyperthermia at day 1).

Locations

Country	Name	City	State
China	Zhejiang Hospital	Hangzhou

Sponsors (2)

Lead Sponsor	Collaborator
Pengyuan Liu	Zhejiang Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	disease control rate (DCR)	DCR=(PR+CR) / (PD+SD+PR+CR) * 100%	up to 6 months
Secondary	progression-free survival (PFS)	The time between enrollment and tumor progression (in any aspect) or death (for any reason).	up to 36 months
Secondary	overall survival (OS)	The time between enrollment and death (for any reason).	up to 36 months