Statin Therapy to Reduce Progression in Women With Platinum Sensitive Ovarian Cancer

NCT04457089 — Early Phase 1, Completed, 18 participants, Marc Goodman

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RegistryNCT04457089
StatusCompleted
PhaseEarly Phase 1
Study typeInterventional; na, single group, masking: none, treatment
Enrollment18 (Actual)
SponsorMarc Goodman (Other)
ConditionsRecurrent Ovarian Cancer, Platinum-sensitive Ovarian Cancer
InterventionsSimvastatin 40mg (Drug)
Datesstart 2021-01-25, primary completion 2024-11-01, completion 2025-05-12, first posted 2020-07-07, last updated 2026-02-04
Locations1 site in United States

Related Papers Related Patents Related Grants Related Experts
All trials for Recurrent Ovarian Cancer All trials for Platinum-sensitive Ovarian Cancer All trials of Simvastatin 40mg

-Summary

This is a single arm pilot trial to evaluate the feasibility of using a simvastatin intervention, and to evaluate its effects on cancer progression, among 20 patients with platinum-sensitive ovarian cancer, treated with carboplatin and liposomal doxorubicin at Cedars-Sinai Medical Center.

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+Detailed description

This is a pilot study of statin therapy to examine the feasibility of simvastatin use to reduce disease progression in 20 patients with platinum-sensitive ovarian cancer at Cedars-Sinai Medical Center. This study will focus on patients with recurrent platinum sensitive ovarian cancer to increase the likelihood that this population will experience recurrent disease during the 6-month intervention and follow-up. In addition, this population of patients has a narrow range of standard of care carboplatin doublet combinations that are prescribed, enabling the investigators to create a more homogenous study population. Given their high risk of developing recurrent disease, women with platinum sensitive ovarian cancer, have the potential to derive the maximum benefit from an intervention that could delay disease progression and enhance survival.

+Arms and interventions

ArmTypeInterventionsDescription
SimvastatinExperimentalDrug: Simvastatin 40mg
  • Simvastatin 40mg (Drug), also known as Zocor: Simvastatin 40mg by mouth nightly for approximately 6 months during treatment with carboplatin and liposomal doxorubicin

+Outcome measures

Primary outcomes

  • Completion of the simvastatin intervention with at least 85% compliance [From Cycle 1 Day 1 until Cycle 6 Day 28 (each cycle is 28 days)]: Percentage of patients who complete the simvastatin intervention with at least 85% compliance during Carboplatin and Doxil chemotherapy.

Secondary outcomes

  • Response by CA125 [From baseline until 12 months]: Change in serum level of CA125
  • Progression-free survival [From baseline until 12 months]: Duration until disease progression or death

+Eligibility

Sex: Female, ages: 18 Years to any

Inclusion Criteria:

* Recurrent platinum sensitive ovarian cancer, all histologies (serous, endometrioid, mucinous, clear cell). Platinum sensitivity defined as ≥ 6 months since last platinum treatment.
* No contraindication to carboplatin and/or liposomal doxorubicin or simvastatin.

Exclusion Criteria:

* Prior or current use of any statin medication
* Current systemic use of medications known to interact with statins
* Current use of any other investigational agents
* Liver disease, active cirrhosis
* Uncontrolled intercurrent illness
* History of chronic myopathy
* Prior cancer other than ovarian cancer or non-melanomatous skin cancers
* Known active infection with HIV
* Current excessive alcohol consumption (average alcohol consumption of more than 5 drinks per day)
* Prior exposure to doxorubicin or liposomal doxorubicin
* Hemoglobin A1C >8.0%

+Locations (1)

FacilityCityCountryStatus
Cedars Sinai Medical CenterLos Angeles, CaliforniaUnited States

+Investigators