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Nimotuzumab Concurrent With Chemoradiotherapy for Esophageal Cancer Patients

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status and phase

Enrolling
Phase 2

Conditions

Chemotherapy
Esophageal Cancer
Immunotherapy
Chemoradiotherapy
Nimotuzumab

Treatments

Combination Product: Nimotuzumab with chemoradiotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06429839
NCC4571

Details and patient eligibility

About

Elderly or malnourished patients diagnosed with locally advanced esophageal squamous cell carcinoma (ESCC) had poor prognosis. Radiotherpy was an important and effective treatment in treating ESCC. The present study is a one-arm trial that seeks to evaluate the efficacy in patients with unresectable ESCC. The study objectives include R0 resection rate, complete pathological response and treatment toxicity, etc.

Nimotuzumab is a recombinant humanized monoclonal antibody against EGFR. Its efficacy and safety in patients with esophageal cancer have been confirmed by many studies.

The current prospective phase II study aimed to evaluate the efficacy and safety of a combination regimen comprising chemotherapy with nimotuzumab with a dose of 800mg per week and S-1 and concurrent radiotherapy for patients who are elderly or malnourished.

Enrollment

55 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histologically confirmed esophageal squamous cell carcinoma.
  • No previous treatment for the esophageal carcinoma.
  • KPS score ≥70.
  • NRS-2002 score≥2.
  • Main organs and bone marrow function are normal: routine blood tests: hemoglobin (Hb) ≥100g/L ; absolute neutrophil count (NEUT)≥1.5×109/L; platelets (PLT) ≥100×109/L; white blood cell (WBC)≥3.5×109/L,biochemical examination: alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤1.5×UNL; serum total bilirubin (TBIL) ≤1.5×UNL; serum creatinine ( Cr) 1.0×1.5UNL, and BUN≤1.0×UNL;

Exclusion criteria

  • Previous treatment of the esophageal cancer with surgery, radiation, or chemotherapy.
  • Those combined with other primary malignant tumors other than esophageal cancer (except cured basal cell carcinoma of the skin and carcinoma in situ of the cervix);
  • At the time of diagnosis, there were distant and hematogenous metastases beyond the supraclavicular lymph node region, including retroperitoneal multiple lymph node metastasis, bone metastasis, brain metastasis, lung metastasis, liver metastasis, malignant pleural effusion and ascites
  • There are active infections, such as active tuberculosis and hepatitis
  • There are contraindications to targeted therapy.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

55 participants in 1 patient group

Nimotuzumab concurrent with chemordiotherapy followed by surgery
Experimental group
Treatment:
Combination Product: Nimotuzumab with chemoradiotherapy

Trial contacts and locations

1

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Central trial contact

Xin Wang, Doctor; Guojie Feng, B.M

Data sourced from clinicaltrials.gov

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