RECRUITING

A Study of Alpelisib and Fulvestrant to Treat Endometrial Cancer

Conditions

Endometroid Endometrial Cancer advanced persistent recurrent PIK3CA-mutated ER-postive

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a 2 stage multi-center study designed to evaluate the efficacy of the combination of alpelisib and fulvestrant in patients with PIK3CA-mutated ER-positive endometrioid endometrial cancers by estimating the objective response rate (ORR). Treatment will continue until either unacceptable toxicity, progression of disease, or investigator/patient request for withdrawal.

Official Title

Phase 2 Study of Alpelisib and Fulvestrant for PIK3CA-mutated Estrogen Receptor (ER)-Positive Endometrioid Endometrial Cancers

Quick Facts

Study Start:2024-09-30

Study Completion:2026-04-01

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05154487

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:FEMALE

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Patient must have advanced (FIGO 2014 Stage III or IV), persistent, or recurrent endometrial carcinoma, which is not likely to be curable by surgery or radiotherapy. Histologic confirmation of recurrent disease is required. For cases of persistent disease, histologic confirmation of the primary disease with radiologic evidence of progression is required. 2. Patients must have endometrioid histology (all grades allowed) based on hysterectomy or biopsy specimen and have positive expression of ER and oncogenic PIK3CA mutation per criteria below. 3. All patients must have measurable disease. Measurable disease is defined by RECIST version 1.1. Measurable disease is defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded). Each lesion must be greater than or equal to 10mm when measured by CT, MRI or caliper measurement by clinical exam; or greater than or equal to 20mm when measured by chest x-ray. Lymph nodes must be greater than or equal to 15mm in short axis when measured by CT or MRI. 4. Prior chemotherapy in the adjuvant setting for Stage I, II, or III or metastatic/recurrent/Stage IV is permitted. Prior chemoradiotherapy for a pelvic recurrence is permitted. 5. Patient must be able to swallow oral medications. 6. Patient must have an ECOG performance status of 0 to 2. 7. Patients must have adequate glucose control as defined by the following (both criteria must be met): * Fasting blood glucose (FBG) ≤140/dL (7.7mmol/L) AND * Hemoglobin A1c (HbA1c) ≤6.4% 8. Patients must have adequate organ and marrow function as defined below NOTE: Institutional/laboratory upper limit of normal = ULN Institutional/laboratory lower limit of normal = LLN * Absolute neutrophil count (ANC) greater than or equal to 1000/mcl * Platelets greater than or equal to 100,000 cells/mcl * Hemoglobin greater than or equal to 8 g/dL (Patients may receive erythrocyte transfusions to achieve this hemoglobin level at the discretion of the investigator. Initial treatment must not begin earlier than the day after erythrocyte transfusion). * Fasting Serum amylase ≤ 2 × ULN * Fasting Serum lipase ≤ ULN * Bilirubin less than or equal to 1.5 x ULN (Patients with Gilbert's syndrome with a total bilirubin ≤2 times ULN and direct bilirubin within normal limits are permitted). * ALT (alanine aminotransferase) and AST (aspartate aminotransferase) less than or equal to 3 x ULN * Albumin greater than or equal to 2.8 g/dL 9. Patients must have signed an approved informed consent and authorization permitting release of personal health information. 10. Patients must be at least 18 years of age. 11. Patients of childbearing potential must have a negative serum pregnancy test prior to the study entry and be practicing a highly effective form of contraception during the study treatment and for 8 weeks after stopping the treatment. * Use of oral, injected, or implanted hormonal contraceptives or; * Placement of an intrauterine device (IUD) or intrauterine system (IUS); * Barrier methods of contraception: condom or occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/vaginal suppository; * Total abstinence or; * Male/female sterilization. Women are considered post-menopausal and not of child-bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g., age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks prior to registration. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment is she considered not of child-bearing potential.	1. Patients who have previously received fulvestrant or any PIK3CA, PI3K, mTOR, or AKT inhibitor. 2. Patients with clear cell, serous, carcinosarcoma, mixed histology endometrial cancers, or uterine sarcomas. 3. Patients with known intolerance or hypersensitivity to alpelisib or fulvestrant, or any of their excipients. 4. Patient has had major surgery within 14 days prior to study treatment start and/or has not recovered from major side effects. 5. Patients with an established diagnosis of diabetes mellitus type I or uncontrolled type II (based on fasting blood glucose \[FBG\] and HemoglobinA1c \[HbA1c\], see inclusion criterion 67). 6. Patients with history of osteonecrosis of the jaw. 7. Patients with concomitant invasive malignancy or a history of other invasive malignancies, with the exception of non-melanoma skin cancer, are excluded if there is any evidence of other malignancy being present within the past five years. Patients are also excluded if their previous cancer treatment contraindicates this protocol. 8. Patients with active bacterial infection (requiring intravenous \[IV\] antibiotics at time of initiating study treatment, fungal infection, or detectable viral infection (such as known human immunodeficiency virus (HIV) positivity or with known active hepatitis B or C \[for example, hepatitis B surface antigen positive\]). Screening is not required for enrollment. 9. Patients with a serious pre-existing medical condition(s) that would preclude participation in this study (for example: interstitial lung disease or pneumonitis, severe dyspnea at rest or requiring oxygen therapy, severe renal impairment (i.e. estimated creatinine clearance \<30ml/min), history of major surgical resection involving the stomach or small bowel, or preexisting Crohn's disease or ulcerative colitis or pre-existing chronic condition resulting in baseline grade 2 or higher diarrhea). 10. Patients with a known history of cardiac disease. This includes: * Uncontrolled hypertension, defined as systolic greater than 150mm Hg or diastolic greater than 90mm Hg despite antihypertensive medications * Myocardial infarction, unstable angina, symptomatic pericarditis, or coronary artery bypass graft (CABG) within 6 months prior to registration. * New York Heart Association (NYHA) Class II or greater congestive heart failure. * History of clinically significant cardiac arrhythmias (i.e. ventricular tachycardia or ventricular fibrillation, complete left bundle branch block, high grade AV block (e.g. bifascicular block, Mobitz type II and third degree AV block without pacemaker in place) or serious cardiac arrhythmia requiring medication. This does not include asymptomatic atrial fibrillation with controlled ventricular rate. * Long QT syndrome, family history of idiopathic sudden death or congenital long QT syndrome, or Fridericia QT correction formula (QTcF) \> 470 msec at screening. * Cerebrovascular accident (CVA, stroke), transient ischemic attack (TIA) within 6 months prior to the first date of study therapy. * Syncope of cardiovascular etiology, * Sudden cardiac arrest. 11. Patient is currently receiving any of the following medications and cannot be discontinued 7 days prior to the start of the treatment: * Strong CYP3A4 inducers * Inhibitors of BCRP. 12. Patients who are pregnant or breast-feeding. 13. Patients with known central nervous system metastases which was not previously treated and not fulfilling the following 3 criteria to be eligible for the study: * Completed prior therapy (including radiation and/or surgery) for CNS metastases ≥ 28 days prior to the start of study entry and * CNS tumor is clinically stable at the time of screening and * Participant is not receiving steroids and/or enzyme inducing anti-epileptic medications for brain metastases. 14. Patients with an impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of the study drugs (i.e. ulcerative disease; uncontrolled nausea, vomiting and/or diarrhea; malabsorption syndrome; clinical signs and symptoms of gastrointestinal obstruction; and/or patients who require parenteral hydration and/or nutrition). 15. Patients who plan to receive live attenuated vaccines within 1 week of start of alpelisib and during the study. Patients should also avoid close contact with others who have received live attenuated vaccines. Examples of live attenuated vaccines include intranasal influenza, measles, mumps, rubella, oral polio, BCG\< yellow fever, varicella, and TY21a typhoid vaccines. 16. Patients with active bleeding or pathologic conditions that carry high risk of bleeding such as known bleeding disorder or coagulopathy. 17. Patients who are currently part of or have participated in any clinical investigation with an investigational drug within 30 days prior to dosing, or within 5 half-lives of the investigational product, whichever is longer. 18. Patient is not able to understand and to comply with study instructions and requirements, including oral administration of study treatment

Inclusion Criteria

Exclusion Criteria

1. Patient must have advanced (FIGO 2014 Stage III or IV), persistent, or recurrent endometrial carcinoma, which is not likely to be curable by surgery or radiotherapy. Histologic confirmation of recurrent disease is required. For cases of persistent disease, histologic confirmation of the primary disease with radiologic evidence of progression is required.
2. Patients must have endometrioid histology (all grades allowed) based on hysterectomy or biopsy specimen and have positive expression of ER and oncogenic PIK3CA mutation per criteria below.
3. All patients must have measurable disease. Measurable disease is defined by RECIST version 1.1. Measurable disease is defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded). Each lesion must be greater than or equal to 10mm when measured by CT, MRI or caliper measurement by clinical exam; or greater than or equal to 20mm when measured by chest x-ray. Lymph nodes must be greater than or equal to 15mm in short axis when measured by CT or MRI.
4. Prior chemotherapy in the adjuvant setting for Stage I, II, or III or metastatic/recurrent/Stage IV is permitted. Prior chemoradiotherapy for a pelvic recurrence is permitted.
5. Patient must be able to swallow oral medications.
6. Patient must have an ECOG performance status of 0 to 2.
7. Patients must have adequate glucose control as defined by the following (both criteria must be met):
* Fasting blood glucose (FBG) ≤140/dL (7.7mmol/L) AND
* Hemoglobin A1c (HbA1c) ≤6.4%
8. Patients must have adequate organ and marrow function as defined below NOTE: Institutional/laboratory upper limit of normal = ULN Institutional/laboratory lower limit of normal = LLN
* Absolute neutrophil count (ANC) greater than or equal to 1000/mcl
* Platelets greater than or equal to 100,000 cells/mcl
* Hemoglobin greater than or equal to 8 g/dL (Patients may receive erythrocyte transfusions to achieve this hemoglobin level at the discretion of the investigator. Initial treatment must not begin earlier than the day after erythrocyte transfusion).
* Fasting Serum amylase ≤ 2 × ULN
* Fasting Serum lipase ≤ ULN
* Bilirubin less than or equal to 1.5 x ULN (Patients with Gilbert's syndrome with a total bilirubin ≤2 times ULN and direct bilirubin within normal limits are permitted).
* ALT (alanine aminotransferase) and AST (aspartate aminotransferase) less than or equal to 3 x ULN
* Albumin greater than or equal to 2.8 g/dL
9. Patients must have signed an approved informed consent and authorization permitting release of personal health information.
10. Patients must be at least 18 years of age.
11. Patients of childbearing potential must have a negative serum pregnancy test prior to the study entry and be practicing a highly effective form of contraception during the study treatment and for 8 weeks after stopping the treatment.
* Use of oral, injected, or implanted hormonal contraceptives or;
* Placement of an intrauterine device (IUD) or intrauterine system (IUS);
* Barrier methods of contraception: condom or occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/vaginal suppository;
* Total abstinence or;
* Male/female sterilization. Women are considered post-menopausal and not of child-bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g., age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks prior to registration. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment is she considered not of child-bearing potential.

1. Patients who have previously received fulvestrant or any PIK3CA, PI3K, mTOR, or AKT inhibitor.
2. Patients with clear cell, serous, carcinosarcoma, mixed histology endometrial cancers, or uterine sarcomas.
3. Patients with known intolerance or hypersensitivity to alpelisib or fulvestrant, or any of their excipients.
4. Patient has had major surgery within 14 days prior to study treatment start and/or has not recovered from major side effects.
5. Patients with an established diagnosis of diabetes mellitus type I or uncontrolled type II (based on fasting blood glucose \[FBG\] and HemoglobinA1c \[HbA1c\], see inclusion criterion 67).
6. Patients with history of osteonecrosis of the jaw.
7. Patients with concomitant invasive malignancy or a history of other invasive malignancies, with the exception of non-melanoma skin cancer, are excluded if there is any evidence of other malignancy being present within the past five years. Patients are also excluded if their previous cancer treatment contraindicates this protocol.
8. Patients with active bacterial infection (requiring intravenous \[IV\] antibiotics at time of initiating study treatment, fungal infection, or detectable viral infection (such as known human immunodeficiency virus (HIV) positivity or with known active hepatitis B or C \[for example, hepatitis B surface antigen positive\]). Screening is not required for enrollment.
9. Patients with a serious pre-existing medical condition(s) that would preclude participation in this study (for example: interstitial lung disease or pneumonitis, severe dyspnea at rest or requiring oxygen therapy, severe renal impairment (i.e. estimated creatinine clearance \<30ml/min), history of major surgical resection involving the stomach or small bowel, or preexisting Crohn's disease or ulcerative colitis or pre-existing chronic condition resulting in baseline grade 2 or higher diarrhea).
10. Patients with a known history of cardiac disease. This includes:
* Uncontrolled hypertension, defined as systolic greater than 150mm Hg or diastolic greater than 90mm Hg despite antihypertensive medications
* Myocardial infarction, unstable angina, symptomatic pericarditis, or coronary artery bypass graft (CABG) within 6 months prior to registration.
* New York Heart Association (NYHA) Class II or greater congestive heart failure.
* History of clinically significant cardiac arrhythmias (i.e. ventricular tachycardia or ventricular fibrillation, complete left bundle branch block, high grade AV block (e.g. bifascicular block, Mobitz type II and third degree AV block without pacemaker in place) or serious cardiac arrhythmia requiring medication. This does not include asymptomatic atrial fibrillation with controlled ventricular rate.
* Long QT syndrome, family history of idiopathic sudden death or congenital long QT syndrome, or Fridericia QT correction formula (QTcF) \> 470 msec at screening.
* Cerebrovascular accident (CVA, stroke), transient ischemic attack (TIA) within 6 months prior to the first date of study therapy.
* Syncope of cardiovascular etiology,
* Sudden cardiac arrest.
11. Patient is currently receiving any of the following medications and cannot be discontinued 7 days prior to the start of the treatment:
* Strong CYP3A4 inducers
* Inhibitors of BCRP.
12. Patients who are pregnant or breast-feeding.
13. Patients with known central nervous system metastases which was not previously treated and not fulfilling the following 3 criteria to be eligible for the study:
* Completed prior therapy (including radiation and/or surgery) for CNS metastases ≥ 28 days prior to the start of study entry and
* CNS tumor is clinically stable at the time of screening and
* Participant is not receiving steroids and/or enzyme inducing anti-epileptic medications for brain metastases.
14. Patients with an impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of the study drugs (i.e. ulcerative disease; uncontrolled nausea, vomiting and/or diarrhea; malabsorption syndrome; clinical signs and symptoms of gastrointestinal obstruction; and/or patients who require parenteral hydration and/or nutrition).
15. Patients who plan to receive live attenuated vaccines within 1 week of start of alpelisib and during the study. Patients should also avoid close contact with others who have received live attenuated vaccines. Examples of live attenuated vaccines include intranasal influenza, measles, mumps, rubella, oral polio, BCG\< yellow fever, varicella, and TY21a typhoid vaccines.
16. Patients with active bleeding or pathologic conditions that carry high risk of bleeding such as known bleeding disorder or coagulopathy.
17. Patients who are currently part of or have participated in any clinical investigation with an investigational drug within 30 days prior to dosing, or within 5 half-lives of the investigational product, whichever is longer.
18. Patient is not able to understand and to comply with study instructions and requirements, including oral administration of study treatment

Contacts and Locations

Study Contact

Jennifer Klein, MEd

CONTACT

215-854-0770

jklein@gog.org

Principal Investigator

Stephanie Gaillard, MD

STUDY_CHAIR

GOG Foundation

Study Locations (Sites)

City of Hope

Duarte, California, 91010

United States

AdventHealth Gynecologic Oncology

Orlando, Florida, 32804

United States

Tampa General Hospital

Tampa, Florida, 33606

United States

Ascension St. Vincent

Indianapolis, Indiana, 46260

United States

Johns Hopkins Medicine

Baltimore, Maryland, 21287

United States

Kettering Health Cancer Center

Kettering, Ohio, 45429

United States

Oklahoma Cancer Specialists and Research Institute, LLC

Tulsa, Oklahoma, 74146

United States

Legacy Good Samaritan Medical Center

Portland, Oregon, 97210

United States

Legacy Meridian Park Medical Center

Tualatin, Oregon, 97062

United States

Legacy Salmon Creek Medical Center

Vancouver, Washington, 98686

United States

University of Wisconsin Clinical Science Center

Madison, Wisconsin, 53792

United States

Collaborators and Investigators

Sponsor: GOG Foundation

Stephanie Gaillard, MD, STUDY_CHAIR, GOG Foundation

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-09-30

Study Completion Date2026-04-01

Study Record Updates

Study Start Date2024-09-30

Study Completion Date2026-04-01

Terms related to this study

Keywords Provided by Researchers

advanced
persistent
recurrent
PIK3CA-mutated
ER-postive

Additional Relevant MeSH Terms

Endometroid Endometrial Cancer