Pathological Response

3

Review clinical trials related to Pathological Response. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Objective Sleep Characteristics and Neoadjuvant Immunotherapy Response in Gastric/GEJ Cancer

This prospective observational study will enroll 120 patients with locally advanced gastric or gastroesophageal junction adenocarcinoma who are scheduled to receive neoadjuvant immunotherapy followed by radical surgery. Non-invasive objective sleep monitoring will be performed during the neoadjuvant treatment period to assess sleep characteristics, including sleep duration, sleep efficiency, device-estimated deep sleep proportion, nocturnal awakenings, sleep regularity, heart rate, and heart rate variability. The primary objective is to evaluate the association between objective sleep characteristics and major pathological response (MPR) after neoadjuvant immunotherapy. This study will not alter standard treatment decisions, surgical procedures, or perioperative management.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: West China Second University HospitalUpdated: Jun 23, 2026Duration: 3 Years
Eligibility criteria

Age greater than 18 years, regardless of sex. [+6]

Presence of distant metastasis, peritoneal metastasis, or disease considered no... [+7]

Status: Recruiting

Circulating microRNAs and Response to Neoadjuvant Chemotherapy in Breast Cancer

This prospective observational study aims to investigate subtype-specific circulating microRNAs (miRNAs) and their association with response to neoadjuvant chemotherapy (NAC) in patients with breast cancer. Serum samples will be collected before NAC and prior to surgery, and changes in miRNA expression levels will be evaluated. Pathological complete response (pCR) and Miller-Payne scoring will be used to assess treatment response after NAC. The study also explores whether changes in circulating miRNA profiles can predict treatment response across different breast cancer subtypes. The findings may help identify biomarkers that support treatment planning and personalized therapy strategies.

Participants needed: 80
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Atlas UniversityUpdated: Mar 31, 2026Locations: 1
Eligibility criteria

Histologically confirmed breast cancer [+5]

Presence of metastatic disease at diagnosis [+4]

Status: Recruiting

Camrelizumab Plus Apatinib and Temozolomide as Neoadjuvant in High Risk Acral Melanoma

Neoadjuvant therapy is feasible in stage Ⅱ-Ⅲ melanoma, Carrelizumab combined with apatinib and temozolomide has synergistic antitumor effects and may improve pathological response.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Peking University Cancer Hospital & InstituteUpdated: Mar 3, 2025Locations: 1
Eligibility criteria

age:18-75 years, male or female. [+7]

Patients who have or are currently undergoing additional chemotherapy, radiation... [+7]