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SGI-110 in Combination With Carboplatin in Ovarian Cancer

Phase 2
Completed
Conditions
Ovarian Cancer
Interventions
Drug: Treatment of Choice (topotecan, pegylated liposomal doxorubicin, paclitaxel, or gemcitabine)
Registration Number
NCT01696032
Lead Sponsor
Astex Pharmaceuticals, Inc.
Brief Summary

A 2-part, Phase 2 controlled, open-label, randomized study in participants with platinum-resistant recurrent ovarian cancer. In Part 1, participants received SGI-110 and carboplatin. The optimum dose of SGI-110 (guadecitabine) was identified in Part 1 based on safety and efficacy. In Part 2, participants were randomized to receive the dose identified in Part 1 plus carboplatin or one of four treatment of choice at the discretion of the investigator. The treatment of choice consisted of topotecan, pegylated liposomal doxorubicin, paclitaxel or gemcitabine.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
120
Inclusion Criteria
  1. Participants who are women 18 years of age or older.
  2. Participants who have histologically or cytologically confirmed recurrent high-grade serous epithelial ovarian cancer (Grade 2 or 3), primary peritoneal carcinomatosis or fallopian tube cancer.
  3. Participants who have platinum-resistant disease (defined as having relapsed within 6 months of her last platinum-containing regimen). There is no limit on the number of prior treatment regimens in Part 1. In Part 2, participants may have had no more than 3 prior cytotoxic treatment regimens, excluding adjuvant or maintenance therapy.
  4. Participants must have had prior paclitaxel treatment.
  5. Participants who have measurable disease according to RECIST v1.1 or detectable disease.
  6. Participants with ECOG performance status of 0 or 1.
  7. Participants with acceptable organ function.
  8. Participants must be at least 3 weeks from last chemotherapy.
Exclusion Criteria
  1. Participants who have hypersensitivity to SGI-110 and/or carboplatin or other components of these drug products.
  2. Participants who have received prior therapy with any hypomethylating agents.
  3. Participants who are refractory to platinum treatment i.e., progressed while on platinum treatment.
  4. Participants with abnormal left ventricular ejection fraction.
  5. Participants with Grade 2 or greater neuropathy.
  6. Participants with known brain metastases.
  7. Participants with known history of HIV, HCV or HBV.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SGI-110 + CarboplatinSGI-110Stage 1 was a safety lead-in stage with a dose escalation design. Participants were evaluated with the combination of SGI-110 (guadecitabine) plus carboplatin (G+C), given as 28-day treatment cycles: guadecitabine administered subcutaneous (SC) daily on Days 1-5, at a starting dose of 45 mg/m2/day in Cohort 1, followed by carboplatin intravenous (IV) based on a targeted dose of area under the curve (AUC) 5 on Day 8. After dose limiting toxicities were noted, guadecitabine dose was reduced to 30 mg/m2/day for subsequent cycles for 4 participants. Cohort 2 received 30 mg/m2/day guadecitabine and carboplatin IV AUC 4.
SGI-110 + Carboplatin or TCSGI-110Stage 2 was an open-label, randomized, controlled trial. Eligible participants were randomly assigned in a 1:1 ratio to receive either (1) G+C combination treatment in 28-day cycles at 30 mg/m2 SC once daily on Days 1-5 and carboplatin IV AUC 4 on Day 8, or (2) treatment of choice (TC) of topotecan, pegylated liposomal doxorubicin (PLD), paclitaxel, or gemcitabine based on recommended dosing in 28-day cycles; participants initially randomized to TC were able to cross over to receive 30 mg/m2 G+C due to disease progression.
SGI-110 + Carboplatin or TCTreatment of Choice (topotecan, pegylated liposomal doxorubicin, paclitaxel, or gemcitabine)Stage 2 was an open-label, randomized, controlled trial. Eligible participants were randomly assigned in a 1:1 ratio to receive either (1) G+C combination treatment in 28-day cycles at 30 mg/m2 SC once daily on Days 1-5 and carboplatin IV AUC 4 on Day 8, or (2) treatment of choice (TC) of topotecan, pegylated liposomal doxorubicin (PLD), paclitaxel, or gemcitabine based on recommended dosing in 28-day cycles; participants initially randomized to TC were able to cross over to receive 30 mg/m2 G+C due to disease progression.
SGI-110 + Carboplatin or TCCarboplatinStage 2 was an open-label, randomized, controlled trial. Eligible participants were randomly assigned in a 1:1 ratio to receive either (1) G+C combination treatment in 28-day cycles at 30 mg/m2 SC once daily on Days 1-5 and carboplatin IV AUC 4 on Day 8, or (2) treatment of choice (TC) of topotecan, pegylated liposomal doxorubicin (PLD), paclitaxel, or gemcitabine based on recommended dosing in 28-day cycles; participants initially randomized to TC were able to cross over to receive 30 mg/m2 G+C due to disease progression.
SGI-110 + CarboplatinCarboplatinStage 1 was a safety lead-in stage with a dose escalation design. Participants were evaluated with the combination of SGI-110 (guadecitabine) plus carboplatin (G+C), given as 28-day treatment cycles: guadecitabine administered subcutaneous (SC) daily on Days 1-5, at a starting dose of 45 mg/m2/day in Cohort 1, followed by carboplatin intravenous (IV) based on a targeted dose of area under the curve (AUC) 5 on Day 8. After dose limiting toxicities were noted, guadecitabine dose was reduced to 30 mg/m2/day for subsequent cycles for 4 participants. Cohort 2 received 30 mg/m2/day guadecitabine and carboplatin IV AUC 4.
Primary Outcome Measures
NameTimeMethod
Stage 1: Dose Limiting ToxicitiesUp to 12 months

Number of participants with dose limiting toxicities (DLTs) in Stage 1

Stage 2: Progression Free SurvivalUp to 24 months

Progression free survival (PFS) time was defined as the time interval from the date of the first dose of study medication until the earlier of disease progression or death. Participants were treated with their assigned treatment \[guadecitabine+carboplatin (G+C) or treatment choice (TC)\] until disease progression or unacceptable treatment-related toxicity occurred.

Secondary Outcome Measures
NameTimeMethod
Objective Response RateUp to 24 months

The objective response rate (ORR) was defined as the proportion of participants who experienced an objective response (best overall response of complete response/full response or partial response, which was confirmed by a subsequent assessment at least 28 days later). Response categories were determined based on RECIST v1.1 criteria, or on modified Rustin (CA-125) criteria if response assessment could not be made using RECIST criteria.

Progression Free Survival at 6 Months6 months

Progression free survival rate at 6 months is the proportion of participants who were alive and did not have disease progression at 6 months after start of treatment.

Clinical Benefit RateUp to 24 months

Clinical benefit rate (CBR) was defined as the proportion of subjects who experienced a best overall response of complete response/full response or partial response (confirmed by a subsequent assessment at least 28 days later), or documented stable disease for at least 3 months after the first dose. Response categories were determined based on RECIST v1.1 criteria, then based on modified Rustin (CA-125) criteria if assessment could not be made using RECIST criteria.

CA-125 LevelsUp to 24 months

Percentage of participants with CA-125 reduction by ≥ 50% from baseline

Duration of ResponseUp to 24 months

Duration of response is defined as the time between the date of the first documentation of complete response/full response or partial response, and the date of disease progression or date of death due to any cause, or the last adequate tumor assessment prior to the start of subsequent anti-cancer therapy including crossing over to G+C from TC arm, whichever occurred earlier. Only participants who responded were included in the duration of response calculation.

Overall SurvivalUp to 24 months

Overall survival was defined as the number of days from the day the participant was administered the first dose of study treatment to the date of death (regardless of cause). Survival time was censored on the last date the participant was known to be alive or lost to follow-up before reaching the event of death; in the TC group, time was censored at the date of crossover.

Stage 1: Pharmacokinetic Parameter CmaxPre-dose and up to 8 hours post-dose on Cycle 1 Day 1 for guadecitabine and decitabine and Day 8 for carboplatin (28 day cycles)

Time to maximum plasma concentration for guadecitabine, decitabine and carboplatin

Stage 1: Pharmacokinetic Parameter TmaxPre-dose and up to 8 hours post-dose on Cycle 1 Day 1 for guadecitabine and decitabine and Day 8 for carboplatin (28 day cycles)

Time to last measurable concentration for guadecitabine, decitabine and carboplatin

Stage 1: Pharmacokinetic Parameter AUC0-8Pre-dose and up to 8 hours post-dose on Cycle 1 Day 1 for guadecitabine and decitabine and Day 8 for carboplatin (28 day cycles)

Area under the concentration-time curve from 0 to 8 hours (AUC0-8) for guadecitabine, decitabine and carboplatin

Trial Locations

Locations (24)

Norris Comprehensive Cancer Center- University of Southern California

🇺🇸

Los Angeles, California, United States

University of Chicago

🇺🇸

Chicago, Illinois, United States

Dana Farber Cancer Institute

🇺🇸

Boston, Massachusetts, United States

Duke Cancer Institute- Duke University Medical Center

🇺🇸

Durham, North Carolina, United States

Royal Marsden Foundation Trust

🇬🇧

Sutton, United Kingdom

Johns Hopkins Kimmel Cancer Center

🇺🇸

Baltimore, Maryland, United States

Women's Cancer Care

🇺🇸

Covington, Louisiana, United States

Melvin and Bren Simon Cancer Center- Indiana University

🇺🇸

Indianapolis, Indiana, United States

Mary Crowley Medical Research Center

🇺🇸

Dallas, Texas, United States

University of Cincinnati Cancer Institute

🇺🇸

Cincinnati, Ohio, United States

Princess Margaret Hospital

🇨🇦

Toronto, Ontario, Canada

Bristol Heamatology and Oncology Centre

🇬🇧

Bristol, United Kingdom

St. James Univesity Hospital - St. James Institute of Oncology

🇬🇧

Leeds, United Kingdom

Mount Vernon Cancer Centre

🇬🇧

Middlesex, United Kingdom

Juravinski Cancer Centre

🇨🇦

Hamilton, Ontario, Canada

Georgia Health Sciences University

🇺🇸

Augusta, Georgia, United States

Island Gynecologic Oncology

🇺🇸

Brightwaters, New York, United States

Tom Baker Cancer Centre

🇨🇦

Calgary, Alberta, Canada

Inova Fairfax Hospital

🇺🇸

Falls Church, Virginia, United States

CHUM Gynecologie-Oncologie, Notre Dame Hospital

🇨🇦

Montreal, Quebec, Canada

Cambridge University Hospitals NHS Foundation and Trust

🇬🇧

London, United Kingdom

Univesity College Hospital

🇬🇧

London, United Kingdom

Imperial College Health Care NHS Trust-Garry Weston Centre

🇬🇧

London, United Kingdom

University of Florida Shands Cancer Center

🇺🇸

Gainesville, Florida, United States

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