Skip to content

A single-arm, observational, single-center, open label study for Toripalimab with or without Paclitaxel (albumin bound) plus Tegafur, Gimeracil and Oteracil Potassium Capsules as a Neoadjuvant therapy for esophageal cancer before operation

A single-arm, observational, single-center, open label study for Toripalimab with or without Paclitaxel (albumin bound) plus Tegafur, Gimeracil and Oteracil Potassium Capsules as a Neoadjuvant therapy for esophageal cancer before operation

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027160
Enrollment
Unknown
Registered
2019-11-02
Start date
2019-11-01
Completion date
Unknown
Last updated
2019-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

esophageal cancer

Interventions

Case series:Toripalimab with or without Paclitaxel (albumin bound) plus Tegafur, Gimeracil and Oteracil Potassium Capsules

Sponsors

The General Hospital of People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) aged >= 18 years; (2) esophageal squamous carcinoma or adenocarcinoma was diagnosed by histology and related examination; (3) it is a resectable tumor; (4) patients who can be operated after preoperative evaluation; (5) did not receive any systematic treatment of esophageal cancer before participating in the study; (6) TNM was divided into stage II or stage IIIa; (7) ECOG PS score 0-1; (8) the urine pregnancy test of women of childbearing age must be negative. From the beginning of the screening period to the last use of the study drug, fertile women and men must voluntarily use recognized and effective contraceptive measures; (9) be able to read, understand and give written informed consent.

Exclusion criteria

Exclusion criteria: (1) patients with definite stage IV and part of stage III (T4 lesions involving aorta and trachea); (2) patients who have been previously treated with PD-1, PD-L1, PD-L2, CTLA-4, or directly treated with another stimulating or co inhibiting T cell receptor (such as CTLA-4, ox 40, CD137); (3) patients with active autoimmune diseases who need systemic treatment or who have immune deficiency; (4) patients who were vaccinated within 30 days before admission; (5) for patients with serious heart, liver, kidney and other important organs, blood and endocrine system diseases, the evaluation criteria are as follows: 1) heart disease: Patients with decompensated cardiac insufficiency or refractory hypertension (hypertension who can not control systolic and diastolic blood pressure at the target level after sufficient dose, reasonable combination and at least three antihypertensive drugs combined treatment, including lifestyle improvement and diuretic use); abnormal ECG during screening, which is considered clinically significant by the researchers And it may bring unacceptable risk to patients to participate in this study; 2) liver function: alanine aminotransferase (ALT) and / or aspartate aminotransferase (AST) >= 2 times of upper limit of normal reference value (ULN); 3) renal function: with renal tubules and / or renal interstitial lesions, or renal insufficiency: blood creatinine >= ULN or glomerular filtration rate (EGFR) < 60ml / min / 1.73m2; 4) WBC < 3 x 10^9 / L and / or HB < 100g / L and / or PLT < 80 x 10^9 / L; (6) patients who participated in another clinical study 4 weeks before or during the study; (7) in the past two years, there are known patients with other malignant tumors other than esophageal cancer that are developing or need active treatment, or are expected to need active treatment within two years; (8) history of previous (non infectious) pneumonia; (9) there are active infections that need to be treated, which can aggravate the disease; (10) patients with HIV or hepatitis B or C; (11) patients who have received organ transplantation; (12) uncontrolled patients with complicated diseases, including but not limited to uncontrolled infection, congestive heart failure, unstable angina, arrhythmia, etc; (13) patients who could not tolerate surgery; (14) patients whose distance from the tumor site to the incisor was less than 23cm; (15) patients who were unable to swallow liquid food or who were unable to take tegio orally were assessed by researchers; (16) pregnant and lactating women, or those of childbearing age who cannot guarantee effective contraception; (17) mental illness or other reasons can not cooperate with the treatment; (18) people with allergic constitution or multiple drug allergy or PD-1 allergy or intolerance.

Design outcomes

Primary

MeasureTime frame
MPR;

Secondary

MeasureTime frame
PCR;OS;DFS;ORR;DCR;dADL;dStooler;

Countries

China

Contacts

Public ContactGuoqing Zhang

The General Hospital of People's Liberation Army

23188133@qq.com+86 13810996462

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026