Quantifying Systemic Immunosuppression to Personalize Cancer Therapy

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorFondazione IRCCS Istituto Nazionale dei Tumori, Milano

About this trial

The Serpentine (Stratify cancER PatiENTs by ImmuNosupprEssion) project, represents the most consistent effort so far attempted to translate MDSC into clinical practise by producing an off-the-shelf compliant assay for quantifying these cells in peripheral blood.

Eligibility criteria

Qualifiers

Histologically documented diagnosis of metastatic/locally advanced melanoma, hormone-refractory breast cancer, RCC and UC, SCCHN, SCC or NSCLC, stage III resectable NSCLC will also be included

Will and ability to comply with the protocol

Willingness and ability to provide an adequate archival Formalin-Fixed Paraffin-Embedded (FFPE) tumor sample available for exploratory biomarker analysis

Age from 18 to 90 years at the time of recruitment

Disqualifiers

Known history of HIV infection

Serious neurological or psychiatric disorders

Pregnancy or lactation

Inability or unwillingness of participant to give written informed consent

Trial design

Treatments tested in this trial

  • MDSC quantification

Treatment groups

1,000 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.