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SBRT Combined With Reduced-Dose Anthracycline Chemotherapy and Toripalimab as Neoadjuvant Therapy for Localized High-Risk Undifferentiated Pleomorphic Sarcoma (SPARK)

A Single-Arm Phase II Exploratory Study of Neoadjuvant Immunotherapy Plus Chemotherapy Plus SBRT Triplet Therapy and Postoperative Stratified Maintenance Therapy for Undifferentiated Pleomorphic Sarcoma

This is a prospective, single-center, single-arm, open-label phase II exploratory study to evaluate the efficacy, safety, and immune remodeling effects of stereotactic body radiotherapy (SBRT) combined with reduced-dose anthracycline chemotherapy and the PD-1 inhibitor toripalimab as neoadjuvant therapy, followed by postoperative stratified maintenance therapy, in patients with localized high-risk undifferentiated pleomorphic sarcoma (UPS). A Simon two-stage design will be used, with 39 patients planned (stage 1: 13 patients; 35 patients in total, including a 10% dropout rate). Treatment consists of SBRT (8-10 Gy in 5 fractions) followed by toripalimab (240 mg intravenously every 3 weeks, 3 cycles in the neoadjuvant phase) combined with liposomal doxorubicin (30-40 mg/m² intravenously every 3 weeks, 2 cycles in the neoadjuvant phase). After response evaluation, radical surgery is performed. Postoperative stratified maintenance therapy is delivered according to pathological response: patients achieving major pathologic response (MPR) or hyalinized pathologic response (HPR) receive toripalimab monotherapy (240 mg every 3 weeks, up to 14 cycles), while those not achieving MPR/HPR receive toripalimab combined with liposomal doxorubicin (2-4 cycles). The primary endpoint is the rate of major pathologic response (MPR). Secondary endpoints include the rate of hyalinized pathologic response (HPR), radiologic objective response rate (ORR), R0 resection rate, limb salvage rate, and safety.

研究概览

详细说明

Undifferentiated pleomorphic sarcoma (UPS) accounts for 5-10% of soft tissue sarcomas. For localized high-risk UPS of the extremities, the standard of care is preoperative radiotherapy plus radical surgery; however, even with R0 resection, the risk of distant metastasis is 30-40% and 2-year disease-free survival is approximately 50%. The SARC028 study showed an objective response rate of 23% in UPS with pembrolizumab, and SU2C-SARC032 demonstrated that adding perioperative pembrolizumab to preoperative radiotherapy improved 2-year DFS (67% vs 52%, HR 0.61). Preclinical and clinical data suggest that stereotactic body radiotherapy (SBRT) with high dose per fraction better synergizes with immune checkpoint blockade than conventional fractionation; sparing the tumor-draining lymph nodes is critical for preserving immune priming.

This phase II study evaluates the triplet neoadjuvant regimen of SBRT, reduced-dose anthracycline chemotherapy, and toripalimab followed by postoperative stratified maintenance in patients with localized high-risk UPS. The fixed treatment schedule is: weeks 1-3 SBRT (8-10 Gy in 5 fractions, on alternate days or consecutively) plus first dose of toripalimab; week 4 first chemotherapy cycle plus second dose of toripalimab; weeks 5-6 recovery; week 7 second chemotherapy cycle plus third dose of toripalimab; weeks 8-9 recovery and response assessment; weeks 10-12 radical surgery. Postoperative maintenance begins within 4-8 weeks after surgery. Patients achieving MPR or HPR receive toripalimab monotherapy 240 mg every 3 weeks for up to 14 cycles; patients not achieving MPR/HPR receive toripalimab for 14 cycles combined with liposomal doxorubicin (2-4 cycles; 2 cycles for HPR >30%).

The sample size uses Simon's two-stage Minimax design with one-sided alpha of 0.05 and 80% power, assuming P0 = 60% and P1 = 80%. The first stage enrolls 13 patients (stop if <=8 responders); the second stage expands to 35 patients total (declare regimen ineffective if <=25 responders overall). Allowing for a 10% dropout rate, the planned total enrollment is 39 patients.

Efficacy assessment: pathologic response (MPR defined as <=10% residual viable tumor cells; HPR defined as >30% hyalinization) is evaluated using a standardized pathology SOP, with confirmation by an independent central pathology laboratory. Radiologic response is evaluated by RECIST v1.1 every 12 weeks. Safety: adverse events are graded per NCI CTCAE v5.0; all adverse events are recorded up to at least 100 days after the last dose. Major wound complications are monitored within 90 days after surgery. Follow-up: visits at 30 days and 84 days after surgery, then every 3 months for survival; imaging every 12 weeks in the first year, every 24 weeks in the second year, and every 6-12 months in years 3-5; ctDNA and peripheral blood immune monitoring every 3 months for at least 2 years.

研究类型

介入性

注册 (估计的)

39

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

      • Tianjin、中国
        • Tianjin Medical University Cancer Institute & Hospital
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

Inclusion Criteria:

  1. Male or female, aged 18 to 75 years.
  2. Histologically confirmed UPS, screened locally and confirmed by central pathology before enrollment. Adequate IHC (at least CK, S100, SOX10, SMA, desmin, MDM2, CDK4) and NGS when feasible (MDM2/CDK4 amplification mandatory) to exclude dedifferentiated liposarcoma and other differentiated tumors.
  3. UPS of extremities or trunk. Max diameter >5 cm, or <=5 cm with any of: encasement of major neurovascular bundle >180 degrees; expected limb functional loss >50% after resection; MDT deems R0 difficult. SBRT-feasible anatomy with >3 mm margin to critical neurovascular structures or joint.
  4. Regional nodes evaluated by imaging (US/CT/MRI/PET-CT). Suspicious nodes (short axis >=10 mm, abnormal morphology, or high FDG) require pathology. Uninvolved nodes must not be irradiated; involved nodes included with radical dose or resected.
  5. Treatment-naive: no prior chemotherapy, targeted therapy, immunotherapy, or local radiotherapy.
  6. At least one measurable lesion per RECIST v1.1.
  7. ECOG 0-1.
  8. Adequate organ function.
  9. Signed ICF, good compliance, willing to provide fresh tumor and blood for translational research.

Exclusion Criteria:

  1. Other malignancy, except completed treatment with no recurrence/metastasis within 2 years.
  2. Major surgery within 4 weeks, or systemic steroids (>10 mg/day prednisone equivalent) or immunosuppressants within 2 weeks.
  3. Active infection requiring systemic therapy; active HBV (DNA >=2000 IU/mL), HCV, syphilis, or HIV positive.
  4. Active or relapsing autoimmune disease.
  5. Severe comorbidity: NYHA >=III, ischemic heart disease, uncontrolled hypertension/diabetes; interstitial lung disease or severe pulmonary impairment.
  6. Known active brain metastases.
  7. Pregnancy/breastfeeding, or refusal of effective contraception.
  8. Any investigator-judged risk to safety or completion.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Experimental Arm
Single-arm. All enrolled patients receive triplet neoadjuvant therapy: SBRT (8-10 Gy in 5 fractions, alternate days or consecutively) first, with concurrent toripalimab (240 mg IV q3w, 3 neoadjuvant cycles) plus liposomal doxorubicin (30-40 mg/m2 IV q3w, 2 neoadjuvant cycles). Radical surgery at weeks 10-12. Postoperative stratified maintenance within 4-8 weeks: MPR/HPR -> toripalimab 240 mg q3w up to 14 cycles; non-MPR/HPR -> toripalimab q3w 14 cycles plus liposomal doxorubicin 2-4 cycles (2 cycles if HPR >30%).
Toripalimab 240 mg IV q3w; 3 neoadjuvant doses from SBRT start; maintenance up to 14 cycles until progression, death, or unacceptable toxicity.
Liposomal doxorubicin 30-40 mg/m2 IV q3w; 2 neoadjuvant cycles. Non-MPR/HPR: 2-4 adjuvant cycles (2 cycles if HPR >30%).
SBRT 8-10 Gy x 5 (median 8 Gy x 5), over 5-10 days in weeks 1-3, IGRT required.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Rate of Major Pathologic Response (MPR)
大体时间:At surgery
At surgery

次要结果测量

结果测量
大体时间
Rate of Hyalinized Pathologic Response (HPR)
大体时间:At surgery
At surgery
Objective Response Rate (ORR)
大体时间:After completion of neoadjuvant therapy, before surgery (approximately weeks 8-9 after enrollment)
After completion of neoadjuvant therapy, before surgery (approximately weeks 8-9 after enrollment)
R0 Resection Rate
大体时间:At surgery
At surgery
Limb Salvage Rate
大体时间:At surgery
At surgery
Adverse Events
大体时间:From the first dose of study treatment until at least 100 days after the last dose
From the first dose of study treatment until at least 100 days after the last dose

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年9月1日

初级完成 (估计的)

2029年1月1日

研究完成 (估计的)

2030年9月1日

研究注册日期

首次提交

2026年9月8日

首先提交符合 QC 标准的

2026年9月8日

首次发布 (实际的)

2026年9月14日

研究记录更新

最后更新发布 (实际的)

2026年9月14日

上次提交的符合 QC 标准的更新

2026年9月8日

最后验证

2026年9月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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