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NCT05844813Enrolling by invitationPhase 4

Neoadjuvant Chemotherapy Combined With Targeted Treatment in High-risk Retroperitoneal Sarcoma

Neoadjuvant Chemotherapy Combined With Targeted Treatment in High-risk Retroperitoneal Sarcoma-- A Nationwide Multicentered Prospective Controlled Study

Source: ClinicalTrials.gov · Last updated 12 May 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this clinical trial is to explore the potential survival benefits of neoadjuvant chemotherapy combined with target treatments followed by radical surgery in patients with primary high-risk/grade retroperitoneal sarcoma. The main questions it aims to answer are: * Whether the 1,3-year progression-free survival time(PFS) is prolonged in the neoadjuvant therapy group, compared with the surgery-only group. * The Overall survival time in the two groups. * The safety and tolerance in the neoadjuvant therapy group. Participants will be allocated into two groups once they meet the inclusion criteria. * Surgery-only Group: Patients will directly undergo surgeries after the confirmation of diagnosis through pre-operative biopsy. * Neoadjuvant therapy group: Patients will receive the neoadjuvant chemotherapy combined with target treatment for three circles before the following sarcoma resectional surgeries.

Status (registry)
Enrolling by invitation
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
102 (estimated)
First submitted
16 Apr 2023
Start date
1 Nov 2022
Primary completion date
1 Nov 2025
Lead sponsor
Peking University International Hospital
Diseases
Sarcoma
NCT number
NCT05844813

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 102
  • From 1 Nov 2022 to the primary completion date, 1 Nov 2025
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Sarcoma protruded into the chest cavity evaluated through preoperative imaging or surgical reports.
  • Persistent one or more organ or system dysfunctions, could not be recovered prior to the study.

Other illness

  • Severe contradiction to surgery and chemotherapies, including persistent myelosuppression, myocardial/cerebral/pulmonary infarction, uncontrolled cardiac arrhythmia, etc within the last 6 months
  • Indication of severe infection or undergoing surgeries with high-risk hemorrhages in one month.
  • Patients with psychological conditions

Other

  • Sarcoma confirmed originating from the GI tract, uterus, or urinal tract.
  • Patients included in the study through preoperative biopsy or MDT discussion, with WDLPS, grade 1 LPS, or other types of tumors not mentioned in the Inclusion criteria evaluating through final pathological findings.
  • Metastasis confirmed pathologically or highly suspicious metastatic lesions through radiological findings, PET-CT(Positron emission tomography) is highly recommended, MDT discussion and evaluation are needed.
  • Histories of administration of Anthracyclines, Ifosfamide, and targeted agents.
  • Female patients who are pregnant or breastfeeding or female and male patients of reproductive potential who are not willing to employ effective birth control methods.

Who the study is looking for

  • Histologically proven primary high-risk Retroperitoneal sarcoma(RPS) (Including Dedifferentiated liposarcoma (DDLPS), leiomyosarcoma(LMS), Undifferentiated pleomorphic sarcoma(UPS), Solitary fibrous tumor(SFT)).
  • Primary localized RPS without histories of surgical resection, chemo- or radio-therapy, targeted therapy. Patients who underwent laparotomy with biopsy only will also be considered as primary cases.
  • Without histories of second malignant tumors.
  • In DDLPS
    • Diagnosis should be confirmed based on MDM2(Mouse double minute 2 homolog) and CDK4(Cyclin-dependent kinase 4) expression on IHC (immunohistochemistry), while MDM2 amplification in the Fish test is highly recommended.
    • All grade 2-3 DDLPS can be included.
  • In LMS
    • All grades of LMS can be included.
    • Tumor size ≥10cm
  • In UPS or SFT
    • All grades of UPS can be included.
    • High-risk SFT with a score ≥6 in 'Risk stratification of SFT for development of metastasis' introduced in The 5th edition of the WHO(World Health Organization) Soft tissue sarcoma classification.
  • Sarcoma without protruding across the diaphragm
  • Possibility of R0/R1 resection evaluated through preoperative MDT(multi-disciplinary team) discussion
  • No multi-organ or system dysfunction/failure or patients with slight dysfunction of organ/system could be easily recovered
  • Tolerable of chemotherapy and surgery through MDT evaluation and tests.
  • American Society of Anesthesiologist (ASA) ≤3
  • Fully understand the informs and consent to participate in the study.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University First Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status
Beijing Friendship Hospital
Coordinator of this site? Confirm its status
BeijingChinaUnknown status
The Affiliated Hospital of Qingdao University
Coordinator of this site? Confirm its status
QingdaoChinaUnknown status
Shanghai Cancer Hospital, Minhang Branch
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status
Shanghai Zhongshan Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status
First Affiliated Hospital Xi'an Jiaotong University
Coordinator of this site? Confirm its status
Xi’anChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.