Radiotherapy Combined With Realgar-Indigo Naturalis Formula (RIF) in the Treatment of Rhabdomyosarcoma(RMS) in Children

Trial Title: Radiotherapy Combined With Realgar-Indigo Naturalis Formula (RIF) in the Treatment of Rhabdomyosarcoma(RMS) in Children

NCT ID: NCT05708391

Condition: Rhabdomyosarcoma, Child

Conditions: Official terms:
Rhabdomyosarcoma

Study type: Interventional

Study phase: Phase 2

Overall status: Not yet recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Realgar-Indigo Naturalis Formulation
Description: Radiotherapy: after 4 courses of chemotherapy, radiotherapy was started 13 weeks later. The radiotherapy was performed by three-dimensional conformal intensity modulated radiation (IMRT) technique with a dose of 45-50.4 grey, and radiotherapy was performed 5 times per week for 5-6 weeks. Oral administration of Realgar-Indigo naturalis formula from 1 week before radiotherapy to the whole radiotherapy period. Dosage: oral, according to body weight, 3 times a day.Because the patient constitution is different, may first start from the half dose, within 3 days gradually increases the dose.In this study, the dosage of Realgar-Indigo naturalis formula (250mg per tablet) was determined according to the patient's weight stage.In each body weight segment, 60 mg/kg realgar-indigo naturalis formula were given according to the upper limit of body weight
Arm group label: Experimental arm: Radiotherapy, Realgar-Indigo naturalis formula

Intervention type: Radiation
Intervention name: Radiotherapy
Description: Radiotherapy
Arm group label: Experimental arm: Radiotherapy, Realgar-Indigo naturalis formula

Summary: The goal of this clinical trial]is to evaluate the efficacy, safety and feasibility of radiotherapy combined with Realgar-Indigo naturalis formula（An oral arsenic agent）in the treatment of rhabdomyosarcoma in children. Including the occurrence of adverse events and the improvement of quality of life.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Eastern Cooperative Oncology Group performance status score（ECOG PS）: 0-2, and the expected survival time is ≥3 months; - At least one measurable lesion according to RECIST version 1.1; - Postoperative pathological diagnosis of rhabdomyosarcoma, pathological staging of Group II-III patients; - Patients who have not previously received radiotherapy, have received chemotherapy or whose legal guardian refuses to receive chemotherapy, and may have received surgical treatment for the initial diagnosis; - Normal major organ function, i.e., meeting the following criteria: 1. Blood routine examination standards shall meet:(No transfusion within 14 days) 1. Hemoglobin(HB)≥90g/L; 2. Absolute Neutrophil Count（ANC）≥1.5×109/L; 3. Platelet count(PLT)≥80×109/L 2. Biochemical examination shall meet the following standards: 1. Bilirubin（BIL）<1.25 times the upper limit of normal (ULN); 2. Alaninetransaminase(ALT) and aspartate transaminase（AST）<2.5 ULN; 3. Serum creatinine≤1ULN, endogenous creatinine clearance 50ml/min (Cockcroft-Gault formula) - The subject voluntarily participates in the study, and the patient or legal guardian signs the informed consent form with the consent of the patient, with good compliance and cooperation in follow-up; - Patients whose physician believes the treatment will benefit. Exclusion Criteria: - Previous or concurrent with other malignancies; - Persons who have been proved to be allergic to Realgar-Indigo naturalis formula and/or its excipients; - Has a number of factors affecting oral medication (such as inability to swallow, nausea, vomiting, chronic diarrhea and intestinal obstruction, etc.) ; - Abnormal coagulation function (international normalized ratio(INR) > 1.5, Activated Partial Thromboplastin Time(APTT) > 1.5 uln) , the patients with bleeding tendency (such as active ulcer lesion in stomach, occult blood in stool (+ +) , black stool and/or hematemesis within 3 months, hemoptysis) or the lesion located near the great vessels; - Tumors involving the skin and/or pharyngeal mucosa with ulceration; - Have a history of psychotropic substance abuse and can not quit or have mental disorders; - patients who had participated in clinical trials of other drugs within 4 weeks; - The patients whose organ function had not recovered more than 35 days after the previous chemotherapy and could not be treated with the next course of chemotherapy; - No other anti-cancer treatment may be used during radiotherapy except for the treatment prescribed in the protocol; - According to the researchers' judgment, there are other patients with concomitant diseases that seriously compromise patient safety or affect the patient's ability to complete the study.

Gender: All

Minimum age: 3 Years

Maximum age: 18 Years

Healthy volunteers: No

Start date: January 31, 2023

Completion date: December 30, 2024

Lead sponsor:
Agency: Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Agency class: Other

Source: Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05708391