To hear about similar clinical trials, please enter your email below
Trial Title:
Local Therapy for Oligometastatic ESCC Patients Treated With PD-1 Inhibitor
NCT ID:
NCT06190782
Condition:
Esophageal Squamous Cell Carcinoma
Oligometastatic Disease
Radiotherapy
Conditions: Official terms:
Carcinoma
Carcinoma, Squamous Cell
Esophageal Squamous Cell Carcinoma
Immune Checkpoint Inhibitors
Conditions: Keywords:
esophageal squamous cell carcinom
Oligometastatic
Radiotherapy
pd-1 inhibitor
Study type:
Interventional
Study phase:
Phase 3
Overall status:
Recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Combination Product
Intervention name:
PD-1 inhibitor+/- chemotherapy combined with local therapy
Description:
1. PD-1 inhibitor +/- Chemotherapy PD-1 inhibitor: all FDA approved PD-1 inhibitor
producter is suitable
First line:
i. TP: paclitaxel 135-175mg/m2,d1+ DDP25mg/m2, d1-3 or 75mg/m2,d1;q21d
(albumin-bound paclitaxel or paclitaxel liposomes as alternative of paclitaxel
permitted as alternative) or ii. PF: DDP Second line (other platinum-based agents
permitted as alternative such as carboplatin, nedaplatin, oxaliplatin, lobaplatin,
etc.) i. Docetaxel or ii. Irinotecan or iii. Paclitaxel (albumin-bound paclitaxel or
paclitaxel liposomes as alternative of paclitaxel permitted as alternatives)
2. Local therapy i. Radiotherapy GTV=all suspected lesions. SBRT: for lung, liver,
adrenal gland, celiac lymphnode metatstases 48Gy/6fx; for spine metastatic disease
30Gy/10Fx; for brain metastases 24Gy/30fx; IMRT: for bone metastatic disease
30Gy/10fx; for esophageal lesion or lesion unsuitable of SBRT 50.4Gy/28fx; ii.
Surgery iii. Radiofrequency/microwave ablation
Arm group label:
PD-1 inhibitor+/- chemotherapy combined with local therapy
Intervention type:
Drug
Intervention name:
systemic therapy alone
Description:
1.PD-1 inhibitor +/- Chemotherapy PD-1 inhibitor: all FDA approved PD-1 inhibitor
producter is suitable
First line:
i. TP: paclitaxel 135-175mg/m2,d1+ DDP25mg/m2, d1-3 or 75mg/m2,d1;q21d (albumin-bound
paclitaxel or paclitaxel liposomes as alternative of paclitaxel permitted as alternative)
or ii. PF: DDP Second line (other platinum-based agents permitted as alternative such as
carboplatin, nedaplatin, oxaliplatin, lobaplatin, etc.) i. Docetaxel or ii. Irinotecan or
iii. Paclitaxel (albumin-bound paclitaxel or paclitaxel liposomes as alternative of
paclitaxel permitted as alternatives)
Arm group label:
PD-1 inhibitor +/- chemotherapy alone
Other name:
the systemic therapy only
Summary:
Patients with oligometastatic squamous cell carcinoma were enrolled and randomly assigned
to receive either PD-1 inhibitor +/- chemotherapy combined with local therapy or PD-1
inhibitor +/- chemotherapy alone.
The primary end point was progression-free survival (PFS). The secondary end points
included overall survival, side effects and local control.
Detailed description:
Patients with oligometastatic squamous cell carcinoma were enrolled and 2:1 randomly
assigned to receive either PD-1 inhibitor +/- chemotherapy combined with local therapy
(radiotherapy, surgery, radiofrequency/microwave ablation, etc.) or PD-1 inhibitor +/-
chemotherapy alone. Different local therapy techniques are allowed to be used on
different lesions in the same patient.All suspected malignant lesion should be included
in local treatment planning in principle.
The primary end point was progression-free survival (PFS). The second end points included
overall survival, side effects and local control.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
-
1. ≥18 years old; 2. ECOG 0-1; 3. Esophageal squamous cell carcinoma 4.
ASTRO/ESTRO defined genuine oligometastatic disease and consistent with: i. ≤4
distant metastases, ii. ≤3 metastatic lesions within a single organ, iii.
maximum diameter of each metastatic lesion ≤5cm; 5. ≥1 pathologically diagnosed
metastases
Exclusion Criteria:
-
1. History of disseminated metastases or ASTRO/ESTRO defined induced
oligometastatic disease 2.Esophageal perforation/hemorrhage 3.Progression
disease after PD-1 inhibitor treatment 4.In-field recurrence 5.Intolerance to
chemotherapy or immunotherapy 6.lung V20>25%
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Fudan University Shanghai cancer center
Address:
City:
Shanghai
Country:
China
Status:
Recruiting
Contact:
Last name:
Kuaile Zhao, MD
Phone:
86-18017312534
Email:
kuaile_z@sina.com
Start date:
September 27, 2022
Completion date:
September 27, 2027
Lead sponsor:
Agency:
Fudan University
Agency class:
Other
Source:
Fudan University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06190782