tailOred dRug repurposIng of dEcitabine in KRAS-dependeNt refracTory pAncreaTic cancEr

Brief summary public domain (ClinicalTrials.gov)

The study is designed to assess the therapeutic efficacy of decitabine repurposing against advanced, refractory, ductal adenocarcinoma (PDAC) with molecular transcriptional signatures indicating dependency on the KRAS oncogene

Detailed description public domain (ClinicalTrials.gov)

TYPE OF STUDY: Phase II study, open label, multicentre, single arm, interventional, Non-randomized  TARGET POPULATION: Advanced (locally advanced or metastatic), pre-treated PDAC patients, progressing after at least one and no more than two lines of systemic therapy, whose tumors express a KRAS-dependency signature.  RATIONALE. BACKGROUND: KRAS gene mutations occur in 95% of PDAC. Inhibitors targeting the prevalent KRASG12V and KRASG12D mutations in PDAC have yet to reach the clinical setting. Oncogenic KRAS-driven signatures have been derived from PDAC cancer models. Based on these, it is possible to identify a subset of PDACs that are highly addicted to oncogenic KRAS, and referred to as KRAS-dependent tumors (dKRAS), in which the direct targeting of KRAS or KRAS-dependent phenotypes reduced tumor growth. Notably, KRAS dependency was associated with a rewiring of nucleotide metabolism and the inhibition of pyrimidine biosynthesis was sufficient to inhibit the growth of dKRAS PDAC cells. In contrast, tumors that, though harboring KRAS mutations, do not display KRAS dependency are resistant to anti-KRAS targeting. Decitabine (DEC) is FDA-approved for the treatment of myelodysplastic syndromes and acute myeloid leukaemia. Importantly, phase-I and -II clinical trials of DEC have defined a recommended phase II dose (RP2D) for DEC monotherapy in solid tumors. HYPOTHESES AND RATIONALE: Preclinical studies show that DEC has cytotoxic activity and inhibits the growth of dKRAS PDAC, whereas KRAS-independent PDACs are not responsive. Based on solid preclinical studies and the scientific literature, the investigators' hypotheses are that: i) DEC is a potent anticancer drug inhibiting pyrimidine homeostasis and eliciting DNA damage in PDAC with a KRAS dependency; ii) The KRAS dependency of tumors can be analytically defined by computational scores based on the analysis of the gene expression signature on tumor biopsy; iii) These genetic scores might have a prognostic value. Based on these hypotheses, the investigators propose a proof-of-concept, biomarker-driven, phase-II clinical trial to explore the activity of DEC repurposing against advanced, refractory KRAS-dependent PDAC. OBJECTIVES: The primary objective of the trial is to provide proof-of-concept of DEC antitumor activity in dKRAS metastatic PDAC. Secondary objectives of the trial are to assess the feasibility of a molecularly tailored approach in advanced, pre-treated PDAC, as well as to assess treatment safety and tolerability, clinical benefit, impact on quality of life, and survival outcomes.

Intervention public domain (ClinicalTrials.gov)

Drug: Decitabine 50 MG [Dacogen]. DACOGEN will be administered i.v. over 1 hour, at the dose of 10 mg/m2/d, daily on days 1-5 and 8-12 of each 4-wk cycle.

Arm public domain (ClinicalTrials.gov)

Experimental group (experimental): A fresh, mandatory, tumor biopsy will be performed at baseline to assess KRAS mutational status and functional dependency and determine the patient's eligibility for the trial. KRAS dependency will be assessed based on computational score and inferred by a transcriptional signature of tumor cells. Transcriptomic data will be generated by using RNAseq data. Sample RNA processing and generation of the gene expression profile will be guaranteed within a maximum of 10 working days from the biopsy. Patients with high L-, S- or both L/S- scores of KRAS-dependency will receive DACOGEN. DACOGEN will be administered i.v. over 1 hour, at the dose of 10 mg/m2/d, daily on days 1-5 and 8-12 of each 4-wk cycle. Patients will continue to receive study treatment until objective radiological disease progression per modified RECIST 1.1, as assessed by the investigator, unacceptable toxicity, physician's decision, patient's refusal, or until they meet any other discontinuation criteria.

Primary outcome public domain (ClinicalTrials.gov)

Best Overall Respone (BOR) according to RECIST1.1. Best response is recorded from the start of the treatment until disease progression. Tumor assessments according to modified RECIST 1.1 criteria will be performed at baseline and every 8 weeks (±1week) up to 40 weeks and then every 12 weeks (±1 week) until objective radiological disease progression according to modified RECIST criteria (evised RECIST guideline (version 1.1). Eur J Cancer 2009. DOI:10.1016/j.ejca.2008.10.026). Time frame: From registration to date of documented best response, assessed up to 24 months.

Secondary outcome public domain (ClinicalTrials.gov)

Disease Control Rate (DCR). Time frame: Every 8 weeks (±1 week) from enrolment for the first 40 weeks, then every 12 weeks (±1 week) up to discontinuation the treatment.

Secondary outcome public domain (ClinicalTrials.gov)

Clinical Benefit Rate (CBR). Time frame: Every 8 weeks (±1 week) from enrolment for the first 40 weeks, then every 12 weeks (±1 week) up to discontinuation the treatment.

Secondary outcome public domain (ClinicalTrials.gov)

tumor marker (Ca19.9) response. Time frame: On day 1 of every cycle and at the treatment discontinuation.

Secondary outcome public domain (ClinicalTrials.gov)

Number of participants with treatment-related adverse events as assessed by CTCAE version 5.0. Time frame: Adverse Events will be collected from time of signature of informed consent throughout the treatment period up to and including the 30-day follow-up period..

Secondary outcome public domain (ClinicalTrials.gov)

PFS (progression free survival). Time frame: Every 8 weeks (±1 week) from enrolment for the first 40 weeks, then every 12 weeks (±1 week) and at the treatment discontinuation.

Secondary outcome public domain (ClinicalTrials.gov)

OS (overall survival). Time frame: Every 8 weeks (±1 week) from enrolment for the first 40 weeks, then every 12 weeks (±1 week) and at the treatment discontinuation.

Eligibility public domain (ClinicalTrials.gov)

Inclusion Criteria: 1. Age ≥ 18 years; 2. Histologically or cytologically proven, advanced, inoperable (metastatic or locally advanced), PDAC; 3. Eastern Cooperative Oncology Group (ECOG) Performance Status 0-2; 4. Life expectancy of at least 12 weeks; 5. At least one and no more than two lines of systemic treatment for advanced disease; 6. At least one metastatic lesion(s) and/or primary tumor amenable to pre-treatment biopsy; 7. KRAS dependency, as assessed by molecular analysis of RNA isolated from a fresh tumor biopsy; 8. Imaging-documented progressive disease (PD), according to modified RECIST 1.1 criteria; 9. Imaging-documented measurable disease, according to modified RECIST 1.1 criteria; 10. Adequate organ and marrow function; 11. Postmenopausal status or evidence of non-childbearing status (negative urine or serum pregnancy test) for women of childbearing potential; 12. Women of childbearing potential (defined as not post- menopausal for 12 months or no previous surgical sterilization) and fertile men must agree to use two highly effective forms of contraception while they are receiving Exclusion Criteria: 1. Uncontrolled intercurrent illness(es); 2. Pregnancy or lactation; 3. Active and uncontrolled bacterial, viral, or fungal infection(s) requiring systemic therapy; 4. Major surgical intervention within 4 weeks prior to enrollment; 5. Radiotherapy, surgery, chemotherapy, or an investigational therapy within 2 weeks prior to signing the treatment ICF; 6. Any previous treatment with DEC; 7. Patients with second primary cancers, except for adequately treated non- melanoma skin cancer, curatively treated in-situ cancer of the cervix, stage 1 grade 1 endometrial carcinoma, or other solid tumours including lymphomas (without bone marrow involvement) treated with curative intent and with no evidence of active disease at \>1 year from the completion of curative treatment prior to study entry; 8. Persistent toxicities (≥CTCAE grade 2) caused by previous cancer therapy, excluding alopecia; 9. Serious medical risk factors involving any of the major organ systems such that the investigator considers it unsafe for the patient to receive an experimental research drug; 10. Serious psychiatric or medical conditions that could interfere with a valid informed consent.

Enrollment public domain (ClinicalTrials.gov)

Enrollment: 7 participants (actual).

Why stopped public domain (ClinicalTrials.gov)

Unexpected toxicity events were documented during interim safety evaluations of the investigational drug.