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Clinical trial information and results are updated daily from ClinicalTrials.gov. The latest data update was conducted on 06/14/2021.

Androgen Deprivation Therapy (ADT) and Pembrolizumab for Advanced Stage Androgen Receptor-positive Salivary Gland Carcinoma

Clinicaltrials.gov identifier NCT03942653

Recruitment Status Recruiting

First Posted May 8, 2019

Last update posted November 17, 2020

Study Description

Brief summary:

A Phase II, multi-center, single-arm, non-blinded study combining androgen deprivation therapy (ADT) and pembrolizumab for patients with metastatic or locally recurrent androgen receptor-positive salivary gland carcinoma, not amenable to surgery or radiation.

  • Condition or Disease:Salivary Gland Carcinoma
  • Intervention/Treatment: Drug: Goserelin Acetate
    Drug: Pembrolizumab
  • Phase: Phase 2
Detailed Description

This is a Phase II multi-center, single-arm, non-blinded study combining androgen deprivation therapy (ADT) and pembrolizumab for patients with metastatic or locally recurrent androgen receptor-positive salivary gland carcinoma, not amenable to surgery or radiation. Eligible patients will include both those with no prior systemic therapy and those who have failed prior systemic therapy. Patients who have received previous ADT or immunotherapy will be excluded. ADT will consist of goserelin acetate every 4 weeks with the first injection given approximately 2 weeks prior to the first dose of pembrolizumab. Pembrolizumab 200 mg will be given on day 1 of 21-day cycles, starting 2 weeks after initiation of goserelin acetate. Each 21-day period is considered a treatment cycle with therapy continuing for up to 35 cycles, until disease progression, significant toxicity, or patient refusal. Except for fatigue, we do not expect overlapping toxicities with pembrolizumab and ADT, thus the starting doses will be the FDA-approved doses. This study will use a Simon 2-stage phase II trial design. The first stage of the Simon 2-stage design will have a sample size of nine patients. If at least two patients have an objective response by RECIST 1.1 then enrollment will proceed to stage 2 with an additional 11 patients, to a goal of 20 patients. If less than 4 patients out of 20 respond, then the combination treatment will be rejected. Patients will be staged with CT of neck, chest, abdomen, and pelvis at baseline and every 12 weeks while on study. Treatment with both ADT and pembrolizumab will continue until disease progression or intolerable side effects. Archival tumor biopsy tissue must be available at baseline to evaluate for expression of androgen receptor (AR), PD-L1, and tumor-infiltrating lymphocytes (TIL). An optional biopsy will be performed after 4 doses of pembrolizumab to evaluate immune response to combined therapy. Blood will be collected at baseline, cycle 1 day 1, cycle 2 day 1 and cycle 3 day 1 to evaluate for change in lymphocyte subsets by flow cytometry.

Study Design
  • Study Type: Interventional
  • Estimated Enrollment: 20 participants
  • Intervention Model: Single Group Assignment
  • Masking: None (Open Label) ()
  • Primary Purpose: Treatment
  • Official Title: Phase II Trial of Androgen Deprivation Therapy (ADT) and Pembrolizumab for Advanced Stage Androgen Receptor-positive Salivary Gland Carcinoma: Big Ten Cancer Research Consortium BTCRC-HN17-111
  • Actual Study Start Date: May 2019
  • Estimated Primary Completion Date: January 2022
  • Estimated Study Completion Date: January 2023
Arms and interventions
Arm Intervention/treatment
Experimental: Goserelin Acetate + Pembrolizumab
Goserelin Acetate, 3.6 mg, every four weeks, SQ Pembrolizumab, 200mg, every three weeks, IV
Drug: Goserelin Acetate
Goserelin Acetate, SQ, Q4W

Drug: Pembrolizumab
Pembrolizumab, IV, Q3W
Outcome Measures
  • Primary Outcome Measures: 1. Objective Response Rate [ Time Frame: 35 months ]
    Determine the objective response rate (ORR) of pembrolizumab when given with goserelin in patients with locally recurrent or metastatic androgen receptor-positive salivary gland carcinoma not amenable to curative-intent treatment with surgery or radiation, per RECIST 1.1 Criteria
  • Secondary Outcome Measures: 1. Number of participants with grade 3, 4, 5 adverse events [ Time Frame: 35 months ]
    To evaluate the safety and tolerability of pembrolizumab when given with goserelin, grade 3,4,5 adverse events will be summarized according to CTCAE v5 criteria.
  • 2. Progression Free Survival [ Time Frame: 12 Months ]
    Determine progression free survival (PFS) at 12 months, according to RECIST 1.1 criteria
  • 3. Disease Control Rate [ Time Frame: 35 Months ]
    Disease control rate as defined by stable disease plus objective response (SD+PR+CR), according to RECIST 1.1 criteria
  • 4. Overall Survival [ Time Frame: 12 Months ]
    Determine overall survival (OS) at 12 months, according to RECIST 1.1 criteria
Eligibility Criteria
  • Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
  • Sexes Eligible for Study: All
  • Accepts Healthy Volunteers: No

Inclusion Criteria:

- Written informed consent and HIPAA authorization for release of personal health
information. NOTE: HIPAA authorization may be included in the informed consent or
obtained separately.

- Age ≥ 18 years at the time of consent.

- Locally advanced, recurrent, or metastatic salivary gland carcinoma that is not
amenable to curative surgery or radiation

- ECOG Performance Status of 0 or 1 within 28 days prior to registration.

- Local, pathologic testing of androgen receptor-positive salivary gland carcinoma will
be performed as standard of care. Archival tissue must be available for central
confirmation of androgen receptor-positive disease and for correlative studies. AR
positivity will be defined according to IHC staining of tumor tissue with at least 20%
of tumor staining positive with moderate intensity (1+ or greater).

- Measurable disease according to RECIST v1.1 for solid tumors within 28 days prior to

- For patients who have been treated with prior therapy, patients must have documented
progression of disease on their prior therapy for entry into the study.

- Patients with prior chemotherapy, radiation, or surgery as part of curative intent
therapy are allowed. Any number of prior lines of systemic therapy is permitted for
entry into this study so long as prior therapy did not include anti-androgen therapy
or immune checkpoint blockade.

- If prior cancer treatment, the subject must have recovered from toxic effects of prior
cancer treatment (other than alopecia) to ≤ Grade 1.

- Adequate organ function as defined below; all screening labs to be obtained within 28
days prior to registration.

- Absolute neutrophil count (ANC) ≥1500/µL

- Platelets ≥75,000/µL

- Hemoglobin ≥8.0 g/dL or ≥5 mmol/L

- Creatinine (Cr) OR Measured or calculated creatinine clearance (GFR can also be
used in place of Cr or creatinine clearance) ≤1.5 × ULN OR

≥30 mL/min for participant with creatinine levels >1.5 × institutional ULN

- Total bilirubin ≤1.5 ×ULN OR direct bilirubin ≤ULN for participants with total
bilirubin levels >1.5 × ULN

- AST (SGOT) and ALT (SGPT) ≤2.5 × ULN (≤5 × ULN for participants with liver
metastases) o International normalized ratio (INR) OR prothrombin time (PT) &
aPTT ≤1.5 × ULN unless participant is receiving anticoagulant therapy as long as
PT or aPTT is within therapeutic range of intended use of anticoagulants

- A male participant must agree to use contraception during the treatment period and for
at least 8 months after the last dose of study treatment and refrain from donating
sperm during this period.

- Females of childbearing potential must have a negative serum pregnancy test within 72
hours prior to registration. NOTE: Females are considered of child bearing potential
unless they are surgically sterile (have undergone a hysterectomy, bilateral tubal
ligation, or bilateral oophorectomy) or they are naturally postmenopausal for at least
12 consecutive months

- Females of childbearing potential and males with partners of childbearing potential
must be willing to abstain from heterosexual activity or to use a highly effect form
of contraception from the time of informed consent until 8 months after treatment

- As determined by the enrolling physician or protocol designee, ability of the subject
to understand and comply with study procedures for the entire length of the study

Exclusion Criteria:

- Women of childbearing age with a positive serum pregnancy test within 72 hours prior
to study registration.

- Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with
an agent directed to another stimulatory or co-inhibitory T-cell receptor (eg, CTLA-4,
OX40, CD137).

- Has received prior androgen deprivation therapy including orchiectomy,
gonadotropin-releasing hormone (GnRH) agonists/antagonists, androgen receptor blocker,
abiraterone, or enzalutamide.

- Has received prior systemic anti-cancer therapy including investigational agents
within 14 days prior to registration.

- Has received prior palliative radiotherapy within 7 days of start of study treatment.
Participants must have recovered from all radiation-related toxicities and require
less than 10mg of prednisone (or equivalent corticosteroid) daily.

- Has received a live vaccine within 28 days prior to the first dose of study drug.
Examples of live vaccines include, but are not limited to, the following: measles,
mumps, rubella (MMR), varicella/zoster (chicken pox), yellow fever, rabies, Bacillus
Calmette-Guérin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection
are generally killed virus vaccines and are allowed; however, intranasal influenza
vaccines (eg, FluMist®) are live attenuated vaccines and are not allowed.

- Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy
(in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of
immunosuppressive therapy within 7 days prior to the first dose of study drug.

- Has a known additional malignancy that is progressing or has required active treatment
within the past 2 years. Note: Participants with basal cell carcinoma of the skin,
squamous cell carcinoma of the skin, or carcinoma in situ (e.g. breast ductal
carcinoma in situ, cervical cancer in situ) that have undergone potentially curative
therapy are not excluded.

- Has known active CNS metastases and/or carcinomatous meningitis. Participants with
previously treated brain metastases may participate provided they are radiologically
stable, i.e. without evidence of progression for at least 14 days by repeat imaging
(note that the repeat imaging should be performed during study screening), clinically
stable, and without requirement of steroid treatment for at least 14 days prior to
first dose of study treatment.

- Has ≥Grade 3 hypersensitivity to pembrolizumab and/or any of its excipients.

- Has active autoimmune disease that has required systemic treatment in the past 2 years
(i.e. with use of disease modifying agents, corticosteroids or immunosuppressive
drugs). Replacement therapy (eg, levothyroxine, insulin, or physiologic corticosteroid
replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
form of systemic treatment.

- Has a history of (non-infectious) pneumonitis that required steroids or has current

- Has an active infection requiring systemic therapy.

- Has a known history of Human Immunodeficiency Virus (HIV).

- Has a known history of active TB (Bacillus Tuberculosis).

- Has a history or current evidence of any condition, therapy, or laboratory abnormality
that might confound the results of the study, interfere with the subject's
participation for the full duration of the study, or is not in the best interest of
the subject to participate, in the opinion of the treating investigator.

- Has known psychiatric or substance abuse disorders that would interfere with
cooperation with the requirements of the trial.

- Is pregnant or breastfeeding or expecting to conceive or father children within the
projected duration of the study, starting with the screening visit through 120 days
after the last dose of trial treatment.

Contacts and Locations

Contact: Manish Patel, MD 6126246940 Patel069@umn.edu

Contact: Julia Beck 3176345842 ext 62 jbeck@hoosiercancer.org


United States, Illinois
Northwestern University Feinberg School of Medicine

United States, Illinois
University of Illinois Cancer Center

United States, Iowa
University of Iowa Hospitals and Clinics
Iowa City

United States, Michigan
University of Michigan Health System
Ann Arbor

United States, Minnesota
University of Minnesota: Masonic Cancer Center

United States, Wisconsin
University of Wisconsin

Sponsors and Collaborators

Manish Patel

Merck Sharp & Dohme Corp.

TerSera Therapeutics


Principal Investigator: Manish Patel University of Minnesota

More Information
  • Responsible Party: Manish Patel
  • ClinicalTrials.gov Identifier: NCT03942653 History of Changes
  • Other Study ID Numbers: BTCRC-HN17-111
  • First Posted: May 8, 2019 Key Record Dates
  • Last Update Posted: November 17, 2020
  • Last Verified: November 2020
  • Individual Participant
    Data (IPD) Sharing
  • Plan to Share IPD: No
  • Studies a U.S. FDA-regulated Drug Product: Yes
  • Studies a U.S. FDA-regulated Device Product: No
  • Product Manufactured in and Exported from the U.S.: Yes
  • Additional relevant MeSH terms: Carcinoma Salivary Gland Neoplasms