Viewing Study NCT06587802


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Study NCT ID: NCT06587802
Status: RECRUITING
Last Update Posted: 2025-04-29
First Post: 2024-08-29
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Phase II Study of PD-1 Antibody Combined With Radiotherapy in Recurrent or Metastatic Adrenal Cortical Carcinoma
Sponsor: Sun Yat-sen University
Organization:

Study Overview

Official Title: Phase II Study of PD-1 Antibody Combined With Radiotherapy in Recurrent or Metastatic Adrenal Cortical Carcinoma
Status: RECRUITING
Status Verified Date: 2025-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Adrenal cortical cancer is an extremely rare and highly aggressive malignancy with an incidence of 0.7-2 per million people · year and a 5-year overall survival rate of 15-44%, among which the 5-year survival rate of stage IV cortical cancer is only 13% and the prognosis is poor. Complete surgical resection is one of the most important ways to cure cortical cancer, but the surgical trauma is large, the complications are high, the postoperative recovery of patients is slow, and the tumor is difficult to achieve complete resection, and the postoperative recurrence and metastasis rate of patients is high, even for localized cortical cancer (stage I-III), the recurrence and metastasis rate is still close to 60%.

Recurrent or metastatic cortical cancer is mainly treated with drugs. However, the current first-line drug therapy is only 22.3% effective, the tumor progression-free time is 5.6 months, and the serious adverse reaction rate is as high as 58.1%.

The effective rate of second-line treatment with chemotherapy and targeted drugs was less than 10%, and the tumor progression-free time was only 2.8 months.

The Phase II study of PD-1 monoclonal antibody in the treatment of cortical cancer showed that the treatment effective rate was 23%, and the tumor progression-free survival time was 2.1 months, which was comparable to the first-line regimen, and has been approved by the guidelines for advanced cortical cancer.

Radiation therapy has high efficiency and local control rate, small side effects, and can inhibit tumor growth, relieve local pressure and pain. However, it only has a good effect on the irradiated site, and it is difficult to inhibit the progression of non-radiotherapy lesions and the generation of other new lesions.

The synergistic effect of immunotherapy combined with radiation therapy for metastatic stoves has been confirmed in many solid tumors such as kidney cancer, which can improve the local control rate of solid tumors and prolong the time of tumor progressive-free.

In the early stage, this research team applied PD-1 monoclonal antibody combined with radiotherapy to treat recurrent or metastatic adrenal cortical cancer in many cases after receiving first-line drug therapy regimen, which not only achieved local control of the radiotherapy focus, but also inhibited the progression of other metastases, and achieved longer disease control effect.
Detailed Description: Adrenocortical Carcinoma (ACC) is an extremely rare and highly aggressive malignant tumor with an incidence of 0.7-2 per million people and poor prognosis. The 5-year overall survival rate is 15-44%, and the 5-year survival rate of stage IV ACC is only 13%. Surgical complete resection (R0) is one of the most important ways to cure ACC. However, even for localized ACC (stage I-III), there is still a recurrence and metastasis rate of nearly 60%, due to reasons including surgical failure to achieve R0 resection, tumor rupture, and postoperative hematologic and lymphatic metastasis. Recurrent or metastatic ACC is mainly treated with systemic drugs, mitotan monotherapy or mitotan combined with cisplatin based chemotherapy (mitotan ± etoposide, adriamycin and cisplatin: EDP-M protocol is currently the first-line protocol for advanced ACC, but the objective response rate (ORR) of EDP-M is only 22.3%, the progression-free survival (PFS) is 5.6 months, and the grade 3-4 adverse reactions are as high as 58.1%. Treatment options for patients with recurrent or metastatic ACC after first-line treatment progress are more limited and less effective. The ORR of second-line chemotherapy for advanced ACC was less than 10%. Targeted drugs such as Sunitinib for second-line treatment of advanced ACC had an ORR of 0, and PFS was only 2.8 months. Five clinical studies have been conducted to investigate the efficacy of immunotherapy for adrenal cortical cancer. The results of a phase II study on the treatment of ACC with PD-1 monoclonal antibody showed that ORR could reach 23%, which is the regimen with the highest objective response rate at present. Therefore, the guidelines recommend PD-1 monoclonal antibody for advanced ACC, but the PFS of PD-1 monoclonal antibody is only 2.1 months. Therefore, how to prolong PFS with high ORR is a difficult problem in the treatment of advanced ACC.

For recurrent or metastatic ACC, surgical palliative resection of metastasis can reduce tumor or alleviate symptoms. However, due to large surgical trauma, high complications, slow postoperative recovery of patients, difficult R0 resection of tumors, and high postoperative recurrence and metastasis rate of patients, it is still controversial whether palliative surgery for advanced ACC can bring survival benefits to patients. The guidelines also recommend that radiotherapy can be used for advanced ACC, with high ORR and local control rate, small side effects, inhibiting tumor growth, relieving local pressure and pain. However, radiotherapy is a local treatment that only has a good effect on the irradiated site, and it is difficult to inhibit the progression of non-radiotherapy lesions and the emergence of other new lesions. Therefore, the effect of radiotherapy alone on the overall disease control of patients with advanced ACC recurrence or metastasis is still unsatisfactory.

The synergistic effect of immunotherapy combined with radiotherapy for metastatic stoves has been demonstrated in many solid tumors such as kidney cancer. The ORR of advanced renal clear cell carcinoma treated with PD-1 monoclonal antibody alone was only 36.5%, the median PFS time was 7.1 months, and the 2-year PFS rate was 22.3%, while the ORR of advanced renal clear cell carcinoma treated with PD-1 monoclonal antibody combined with radiotherapy was 63%, PFS was 15.6 months, and the 2-year PFS rate was 45%. Therefore, immunotherapy combined with radiotherapy can improve the local control rate and prolong the PFS time of metastatic renal carcinoma. The ORR of PD-1 monoclonal antibody monotherapy for advanced ACC was 23% and PFS was 2.1 months. Although the ORR was similar to that of EDP-M first-line regimen, the PFS was shorter. Therefore, it is of great clinical significance to explore whether PD-1 monoclonal antibody combined with radiotherapy for advanced ACC can obtain higher ORR and longer PFS.

In the early stage, this research team applied PD-1 monoclonal antibody combined with SBRT to treat recurrent or metastatic adrenal cortical cancer in multiple cases of recurrent or metastatic ACC after treatment with first-line EDP-M protocol, which not only achieved local control of radiotherapy lesions, but also inhibited the progression of other metastasies, and achieved longer disease control effect (ORR: 4/7, PFS: July). On the basis of previous practice, our team plans to further conduct prospective exploratory clinical research on the efficacy and safety of PD-1 monoclonal antibody combined with radiotherapy in the treatment of recurrent or metastatic adrenal cortical carcinoma, so as to provide more safe and effective treatment options for this rare tumor.

Main purpose:

To observe and evaluate the progression-free survival time of PD-1 monoclonal antibody combined with radiotherapy in the treatment of recurrent or metastatic adrenal cortical carcinoma

Secondary purpose:

To observe and evaluate the secondary efficacy indexes and safety of PD-1 monoclonal antibody combined with radiotherapy in the treatment of recurrent or metastatic adrenal cortical carcinoma

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: