About this trial

The purpose of this study is to find out whether giving the study drug pembrolizumab in combination with the chemotherapy drugs melphalan and dactinomycin, delivered directly to the affected arm or leg using a technique called isolated limb infusion (ILI), is a safe treatment that can delay the time before your disease gets worse (progresses).

Eligibility criteria

Qualifiers

Age >/= 12 years at the time of informed consent

Willing and able to provide written informed consent/assent for the trial

Willing to comply with treatment protocol

Have a histologically confirmed metastatic and/or locally advanced sarcoma

Disqualifiers

Have any other malignancy that requires active treatment

Ineligible for ILI because of underlying physical conditions (e.g. coronary artery disease with inability to tolerate anesthesia) as determined by treating physician

Has previously experienced hypersensitivity to pembrolizumab or any of its excipients

Has uncontrolled intercurrent illness including active infection requiring systemic therapy or symptomatic congestive heart failure within the past 6 months

Trial design

Treatments tested in this trial

  • Isolated Limb Infusion
  • Pembrolizumab
  • infusion of melphalan and dactinomycin

Treatment groups

30 Participants
are divided into 1 treatment group

Locations

7
Memorial Sloan Kettering Basking Ridge (Limited protocol activities)07920, Basking RidgeNew Jersey, United States
Memorial Sloan Kettering Monmouth (Limited protocol activities)07748, MiddletownNew Jersey, United States
Memorial Sloan Kettering Bergen (Limited Protocol Activities)07645, MontvaleNew Jersey, United States
Memorial Sloan Kettering Cancer Center @ Suffolk - Commack (Limited Protocol Activities)11725, CommackNew York, United States

Sponsors and collaborators

Memorial Sloan Kettering Cancer Center

Lead sponsor