Preoperative IMRT With Anlotinib and Penpulimab for Localized Sarcoma (SPARE-01)

Recruiting Phase 2 Interventional Study
Sarcoma,Soft Tissue Extremity Trunk Anlotinib Intensity-modulated Radiotherapy Major Wound Complications
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
30 (estimated)
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences · Other
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About This Trial
To investigate the safety and efficacy of preoperative IMRT and concurrent Anlotinib Hydrochloride for primary truncal or extremity soft tissue sarcoma; To investigate the Quality of life and extremity function post-combination treatment; To study the mechanism of radio-sensitizing effects of Anlotinib Hydrochloride and Penpulimab for primary truncal or extremity soft tissue sarcoma; To assess the…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age older than 18-yo * Histology proven soft tissue sarcoma of truncal or extremity, deemed appropriate for preoperative radiotherapy and conservative surgery by multidisciplinary discussion. * ECOG 0-3 * Histology reviewed by reference pathologist * Lesion can be assessed * C…
Contacts

Ning-Ning Lu

+868611804268

Ning-Ning.Lu@hotmail.com

CONTACT