The Combination of Immunotherapy and Stereotactic Ablative Radiotherapy in Oligometastatic Gastrointestinal Cancer

NCT ID: NCT04625894

Last Updated: 2020-11-12

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 21 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-12-31
• Study Completion Date: 2023-06-30

Brief Summary

This is a single-center, open-label, single-arm phase I clinical study to exploratory observe and evaluate the efficacy and safety of anti-PD-1 antibody (Camrelizumab for Injection) combined with multisite stereotactic ablative radiotherapy (SABR) in patients with oligometastatic gastrointestinal cancer.

According to the origin site of metastases, this study will consist of three subgroups, including gastric carcinoma group, colorectal carcinoma group and hepatocellular carcinoma group. For each of the subgroup, seven eligible patients with oligometastatic cancer originating from stomach, colon and liver, respectively will be recruited. All patients will receive multisite SABR followed by immunotherapy of Camrelizumab within one week from completion. Camrelizumab will be administered at a fixed dose of 200 mg intravenously (iv) on D1 in a 14-day cycle. The treatment will continue for up to two years until disease progression, unacceptable toxicity or patient withdrawal.

Tumor tissue samples, sections, paraffin blocks or biopsy blocks, and biomarkers, including but not limited to PD-L1 expression level and the proportion of positive cells, TMB level and MMR status, will be collected from subjects.

Conditions

Oligometastatic Gastrointestinal Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment Arm

Patients with oligometastatic gastrointestinal cancer will receive multisite SABR, followed by Camrelizumab within one week from completion of radiation. Camrelizumab for injection at 200 mg, d1, q2w, 14-day cycle will continue for up to two years until disease progression, unacceptable toxicity or patient withdrawal.

Group Type: EXPERIMENTAL

Stereotactic Ablative Radiotherapy (SABR)

Intervention Type: RADIATION

To irradiate as many metastatic lesions as possible, in the precondition that normal tissues can tolerate. Target dose will be adjusted depending on site of the lesion and organs at risk (BED \> 100Gy). Sequence of irradiation for multiple metastases will be at the discretion of the investigators based on their experience.

Camrelizumab for injection (200 mg, iv), D1, Q2W, 14-day cycle

Intervention Type: DRUG

Administration of Carrelizumab will be started within one week upon SABR completion, and will be continued for up to two years until disease progression, unacceptable toxicity or patient withdrawal.

Interventions

Stereotactic Ablative Radiotherapy (SABR)

To irradiate as many metastatic lesions as possible, in the precondition that normal tissues can tolerate. Target dose will be adjusted depending on site of the lesion and organs at risk (BED \> 100Gy). Sequence of irradiation for multiple metastases will be at the discretion of the investigators based on their experience.

Intervention Type: RADIATION

Camrelizumab for injection (200 mg, iv), D1, Q2W, 14-day cycle

Administration of Carrelizumab will be started within one week upon SABR completion, and will be continued for up to two years until disease progression, unacceptable toxicity or patient withdrawal.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Aged 18-70 years old, regardless of gender;

2. Fully informed and willing to provide written informed consent for the trial;

3. ECOG performance status 0-1;

4. Expected survival time ≥ 6 months;

5. Has gastric carcinoma /colorectal carcinoma / hepatocellular carcinoma, confirmed by histopathology (or pathology consultation in our hospital) and measurable oligometastatic lesions on imaging (RECIST version 1.1); pathological diagnosis confirmation of oligometastatic lesions using biopsy tissue samples (e.g. obtained by hollow core needle, biopsy, excision, etc.) is recommended but not required;

6. Has undergone curative treatment on the primary lesion at least three months ago, without local progression;

7. Has received standard treatment prior to enrolment, except for any type of immunotherapy;

8. Has no more than three metastatic lesions detected on imaging in single organ (e.g. lung, liver, brain, bone, etc.), and the total number of metastases is no more than five;

9. Multiple sites of lesions can be safely treated by SABR; and the maximum diameter of each lesion for irradiation is no more than 5cm.

10. Contraindicated for surgery or the participant refuses to receive surgery.

11. Has adequate organ function to tolerate the regimen:

12. Bone marrow function: neutrophils ≥ 1.5 × 109/L, platelets ≥ 100 × 109/L, hemoglobin ≥ 90 g/L;

13. Liver and kidney function: serum creatinine ≤ 1.5 times the upper limit of normal; AST and ALT ≤ 2.5 times the upper limit of normal or the presence of liver metastasis ≤ 5 times the upper limit of normal; total bilirubin ≤ 1.5 times the upper limit of normal, or patients with Gilbert's syndrome ≤ 2.5 times the upper limit of normal;

14. Subject is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up

15. Non-lactating patients.

Exclusion Criteria

1. Pregnant or lactating women

2. Serious medical comorbidities precluding radiotherapy

3. Prior radiotherapy to a site requiring treatment

4. Malignant pleural effusion

5. Inability to treat all sites of active disease

6. Has clinical or radiologic evidence of spinal cord compression or tumor within 3mm of spinal cord on MRI.

7. Dominant brain metastasis requiring surgical decompression

8. Has prior treatment with cancer immunotherapy including, but not limited to immune checkpoint inhibitors.

9. Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy at a dose of >10 mg Prednisone daily or equivalent at time of trial treatment.

10. Has a known history of active Bacillus Tuberculosis

11. Has active autoimmune disease that has required systemic treatment in the past 2 years

12. Hypersensitivity to PD-1 inhibitor or any of its excipients.

13. Has had prior chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to study day 1 or who has not recovered from adverse events due to a previously administered agent.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fudan University

OTHER

Sponsor Role: lead

Responsible Party

Zhen Zhang

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

Countries

China

Central Contacts

Zhen Zhang, MD, PhD

Role: CONTACT

Phone: 18801735029

Email: zhen_zhang@fudan.edu.cn

Other Identifiers

MA-CRC-I-002

Identifier Type: -

Identifier Source: org_study_id