Thalidomide Prevention or Treatment of Camrelizumab-induced Reactive Cutaneous Capillary Endothelial Proliferation (RCCEP)

Esophageal Carcinoma Clinical Trial

Official title:

A Prospective, Randomized Clinical Study of the Prevention or Treatment of Camrelizumab-induced Reactive Cutaneous Capillary Endothelial Proliferation (RCCEP) With Thalidomide

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06231680
• Other study ID #: MA-RCCEP-II-001
• Status: Recruiting
• Phase: Phase 2
• Start date: January 19, 2024
• Est. completion date: September 30, 2025

Study information

• Verified date: January 2024
• Source: Henan Cancer Hospital
• Contact: Ying Liu, MD
• Phone: +86 137 8360 4602
• Email: yaya7207[@]126.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To explore the dose and safety of thalidomide for the prevention and treatment of camrelizumab-induced reactive cutaneous capillary endothelial proliferation (RCCEP)

Description:

1. To increase the evidence of thalidomide for the prevention of RCCEP, the investigators will explore the dose of thalidomide for the prevention of RCCEP in participants with esophageal squamous cell carcinoma and non-small cell lung cancer who were scheduled to receive camrelizumab combined with platinum-based chemotherapy;

2. To increase the evidence of thalidomide for the treatment of RCCEP, the investigators will explore the dose of thalidomide for the treatment of ≥G2 RCCEP in participants with esophageal squamous cell carcinoma and non-small cell lung cancer with camrelizumab

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 132
• Est. completion date: September 30, 2025
• Est. primary completion date: June 30, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Prevention cohort 1:

1. Histopathology or cytology confirmed advanced non-small cell lung cancer or esophageal squamous cell carcinoma; no previous systemic therapy (patients who had progressed =6 months after [neo] adjuvant therapy were eligible).

2. A treatment regimen of Camrelizumab combined with platinum-containing chemotherapy is planned.

3. ECOG: 0-1;

4. Age =18 years old;

5. Have a life expectancy of at least 12 weeks;

6. No prior therapy with anti-PD-1, anti-PD-L1, or anti-CTLA-4 antibody (including any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways).

7. Can swallow pills normally;

8. Adequate organ and bone marrow function:Standard of blood routine examination (without transfusion within 14 days) : Hemoglobin (HB) =80 g/L; Neutrophil absolute value (ANC) =1.5×10^9/L; Platelet (PLT) =90×10^9/L;Biochemical examination should meet the following criteria: Total bilirubin (TBIL) =1.5 times the upper limit of normal value (ULN); Alanine aminotransferase (ALT), aspartate aminotransferase (AST) =3×ULN; Serum creatinine (Cr) =1.5 ULN;

9. Female Subjects of childbearing potential must have a negative serum pregnancy test within 72 hours before the first dose and must be willing to use very efficient barrier methods of contraception for the course of the study through 2 months after the last dose of study treatment. Male Subjects with a female partner(s) of child-bearing potential must be willing to use very efficient barrier methods of contraception for the course of the study through 2 months after the last dose of study treatment;

10. Subjects has voluntarily agreed to participate by giving written informed consent/assent for the trial.

• Treatment cohort 2:

1. Histopathology or cytology confirmed advanced lung cancer or esophageal carcinoma;

2. Subjects had=G2 grade RCCEP for the first time after treatment with a Camrelizumab based regimen;

3. ECOG: 0-2;

4. Age =18 years old;

5. Have a life expectancy of at least 12 weeks;

6. Can swallow pills normally;

7. No ongoing grade 3 or higher adverse events except for RCCEP (according to CTCAE version 5.0).

8. Female Subjects of childbearing potential must have a negative serum pregnancy test within 72 hours before the first dose and must be willing to use very efficient barrier methods of contraception for the course of the study through 2 months after the last dose of study treatment. Male Subjects with a female partner(s) of child-bearing potential must be willing to use very efficient barrier methods of contraception for the course of the study through 2 months after the last dose of study treatment;

9. Subjects have voluntarily agreed to participate by giving written informed consent/assent for the trial.

Exclusion Criteria:

• Prevention cohort 1:

1. Known allergy to the investigational drug or excipient, history of severe hypersensitivity reactions to other monoclonal antibodies.

2. Subjects with a condition requiring systemic treatment with other immunosuppressive medications within 14 days of first administration of study treatment.

3. Subjects had administration of a live, attenuated vaccine within 4 weeks of the first dose of study treatment or anticipation that such a live attenuated vaccine will be required during the study.

4. Advanced patients who have symptoms, have spread to the internal organs, and are at risk of developing life-threatening complications in the short term;

5. Subjects with a history of interstitial lung disease, or other disease may interfere with the detection or treatment of suspected drug-related lung toxicity.

6. Subjects with active, known or suspected autoimmune disease. Subjects in conditions not expected to recur in the absence of an external trigger, or not requiring systemic treatment are permitted to enroll.

7. HIV infection; Combined hepatitis B and hepatitis C co-infection

8. Subjects with active CNS metastases are excluded.

9. Subjects with clinically significant cardiovascular and cerebrovascular diseases.

10. Coagulation abnormalities, with bleeding tendency or are receiving thrombolytic or anticoagulant therapy;

11. Disposition evidence of hemoptysis in 2 months (bright red blood, 1/2 teaspoon).

12. History of hemorrhage within 3 months prior to the start of study treatment or clear tendency of hemorrhage

13. Thrombosis or thromboembolic event within 6 months prior to the start of study treatment;

14. Active infection (CTCAE> Grade 2)

15. Subjects had or plan to have allogeneic bone marrow transplantation or solid organ transplant.

16. Subjects are currently participating and receiving study therapy or had participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks or 5 half-value period life of the agent, before the first dose of trial treatment.

17. Subjects have known psychiatric or substance abuse disorder

18. Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the subject's participation for the full duration of the study, or is not in the best interest of the subject to participate, in the opinion of the treating Investigator.

• Treatment cohort 2:

1. Known allergy to the investigational drug or excipient

2. Advanced patients who have symptoms, have spread to the internal organs, and are at risk of developing life-threatening complications in the short term;

3. Subjects with a history of interstitial lung disease, or other disease may interfere with the detection or treatment of suspected drug-related lung toxicity.

4. HIV infection; Combined hepatitis B and hepatitis C co-infection

5. Active infection (CTCAE> Grade 2)

6. Subjects have known psychiatric or substance abuse disorder

7. Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the subject's participation for the full duration of the study, or is not in the best interest of the subject to participate, in the opinion of the treating Investigator

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Esophageal Carcinoma
• Esophageal Neoplasms
• Lung Cancer, Nonsmall Cell

Intervention

Drug:
• Camrelizumab
Camrelizumab 200mg intravenous (IV) on Day 1 of each 21-day cycle,until progression or unacceptable toxicity
• Thalidomide 50mg
Thalidomide 50mg,po qd;
• Thalidomide 100mg
Thalidomide 100mg,po qd;
• Thalidomide 200mg
Thalidomide 200mg,po qd;
• Chemotherapy
Platinum-based chemotherapy: Esophageal squamous cell carcinoma: cisplatin/carboplatin/nedaplatin/lobaplatin+ paclitaxel/albumin-bound paclitaxel/fluorouracil on Day 1 of each 21-day cycle for 4-6 cycles; Non-small cell lung cancer (non-squamous cell carcinoma): pemetrexed plus carboplatin/cisplatin on Day 1 of each 21-day cycle for 4-6 cycles,pemetrexed every three weeks (Q3W) maintenance for the remainder of the study or until documented PD; Non-small cell lung cancer (squamous cell carcinoma) : paclitaxel/albumin-bound paclitaxel + carboplatin/cisplatin on Day 1 of each 21-day cycle for 4-6 cycles.

Locations

Country	Name	City	State
China	The First Affiliated Hospital of Xi'an Jiaotong University	Xi'an	Shaanxi
China	Ying Liu	Zhengzhou	Henan

Sponsors (2)

Lead Sponsor	Collaborator
Henan Cancer Hospital	First Affiliated Hospital Xi'an Jiaotong University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence rate of RCCEP	Incidence rate of RCCEP	2 years
Primary	RCCEP response rate at 3 weeks	RCCEP response rate at 3 weeks	3 weeks
Secondary	Incidence rate of =G3 grade RCCEP	Incidence rate of =G3 grade RCCEP	2 years
Secondary	Median time to RCCEP	Median time to RCCEP	2 years
Secondary	Incidence rate of RCCEP at 6 weeks	Incidence rate of RCCEP at 6 weeks	6 weeks
Secondary	Incidence rate of RCCEP at 9 weeks	Incidence rate of RCCEP at 9 weeks	9 weeks
Secondary	Median time to response of RCCEP	Median time to response of RCCEP	2 years
Secondary	Thalidomide treatment-related adverse events	Thalidomide treatment-related adverse events	2 years