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BRIEF TITLE: Combination Therapy With Pemetrexed and Avelumab in Previously Treated Patients With MTAP-Deficient Advanced Urothelial Cancer

A Phase II Trial to Evaluate Combination Therapy With Pemetrexed and Avelumab in Previously Treated Patients With MTAP-Deficient Advanced Urothelial Cancer


  • Org Study ID: 2018-0576
  • Secondary ID: NCI-2018-02517,2018-0576,P30CA016672
  • NCT ID: NCT03744793
  • NCT Alias:
  • Sponsor: M.D. Anderson Cancer Center - Other
  • Source: M.D. Anderson Cancer Center

Brief Summary

This phase II trial studies how well pemetrexed and avelumab work in treating patients with MTAP-deficient urothelial cancer that has spread to other places in the body. Pemetrexed may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such as avelumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving pemetrexed and avelumab may work better in treating patients with MTAP-deficient urothelial cancer.

Detailed Description


PRIMARY OBJECTIVES:

I. To evaluate the response rate (RR) in patients with (methylthioadenosine phosphorylase)
MTAP-deficient metastatic urothelial cancer treated sequentially with pemetrexed and
avelumab.

SECONDARY OBJECTIVES:

I. To estimate the progression-free survival (PFS) and overall survival (OS) in patients with
MTAP-deficient metastatic urothelial cancer treated sequentially with pemetrexed and
avelumab.

II. To explore the effect of pemetrexed +/- avelumab on the immune system and tumor
microenvironment including peripheral T-cells, tumor-infiltrating T-cells, macrophages, and
myeloid-derived suppressor cells (MDSCs).

OUTLINE:

Patients receive pemetrexed intravenously (IV) over 10 minutes on day 1. Starting cycle 2,
patients also receive avelumab IV over 60 minutes. Cycles repeat every 21 days in the absence
of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 30 and 120 days, and then
every 3 months for 2 years.

Overal Status Start Date Phase Study Type
Recruiting April 11, 2019 Phase 2 Interventional

Primary Outcomes:

Primary Outcome 1 - Measure: Overall response rate

Primary Outcome 1 - Time Frame: Up to 2 years

Condition:

  • Infiltrating Bladder Urothelial Carcinoma Sarcomatoid Variant
  • Infiltrating Bladder Urothelial Carcinoma With Glandular Differentiation
  • Infiltrating Bladder Urothelial Carcinoma With Squamous Differentiation
  • Infiltrating Bladder Urothelial Carcinoma, Micropapillary Variant
  • Infiltrating Bladder Urothelial Carcinoma, Plasmacytoid Variant
  • Metastatic Urothelial Carcinoma
  • MTAP Negative

Eligibility

Criteria:
Inclusion Criteria:

- Patients must have histologic confirmation of MTAP-deficient metastatic urothelial
carcinoma. MTAP-deficiency must be verified by institutional Clinical Laboratory
Improvement Act (CLIA)-certified immunohistochemistry (IHC). Histological variants
such as glandular, squamous, sarcomatoid, micropapillary, plasmacytoid, and small cell
changes will be allowed for this trial if these tumors are MTAP-deficient.

- Patients can be considered for second line of therapy (after chemotherapy or immune
checkpoint inhibitor with PD-[L]1 agent) or for third line of therapy (can have
previously received chemotherapy and immune checkpoint inhibitor with PD-[L]1
blockade). Any prior intravesical therapy is allowed and does not count as a prior
line of therapy.

- Patients who received methotrexate-containing chemotherapy (e.g.
methotrexate/vinblastine/adriamycin/cisplatin [MVAC]) as neoadjuvant therapy or
first-line systemic therapy at least 12 months prior will be allowed for this trial.

- All patients must have measurable disease by Response Evaluation Criteria in Solid
Tumors (RECIST) version (v)1.1 and tumors of sufficient sizes for biopsy. In general,
liver and lung lesions should be at least 1.0 cm, and patients with lymph node-only
disease should have lesions of >= 1.5 cm in shortest dimension. Patients with disease
confined to bone may be eligible if a measurable lytic defect is present. The study
principal investigator (PI) is the final arbiter in questions related to
measurability. Patients with a three-dimensional mass or pelvic sidewall fixation on
bladder examination under anesthesia are considered to have measurable disease.

- Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status =<
2.

- Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) =< 2.5 x upper
limit of normal (ULN), or =< 5 ULN if documented liver metastases are present.

- Total bilirubin =< 1.5 x ULN, except subjects with Gilbert's syndrome or liver
metastases, who must have a baseline total bilirubin =< 3.0 mg/dL.

- Absolute neutrophil count (ANC) >= 1.5 x 10^9/L.

- Hemoglobin >= 9 g/dL (may have been transfused).

- Platelets >= 100 x 10^9/L.

- Normal serum creatinine, or a creatinine clearance >= 40 ml/min [either measured using
a 24 hour urine, calculated using Cockcroft-Gault, or estimated using the MDRD method
from the National Kidney Disease Education Program (NKDEP) (the method reported by MD
Anderson Cancer Center [MDACC] laboratories).

- Negative serum or urine pregnancy test at screening for women of child-bearing
potential.

- Females of childbearing potential who are sexually active with a non-sterilized male
partner and non-sterilized males must use a highly effective method of contraception
for 28 days prior to the first dose of investigational product, and must agree to
continue using such precautions for 180 days after the final dose of investigational
product; cessation of contraception after this point should be discussed with a
responsible physician. They must also refrain from egg cell donation for 180 days
after the final dose of investigational product.

- Non-sterilized males who are sexually active with a female partner of childbearing
potential must use a highly effective method of contraception from days 1 through 180
post last dose. In addition, they must refrain from sperm donation for 180 days after
the final dose of investigational product.

- The ability to interrupt nonsteroidal anti-inflammatory drugs (NSAIDS) 2 days before
(5 days for long-acting NSAIDs), the day of, and 2 days following administration of
pemetrexed.

- The ability to take folic acid, vitamin B12, and dexamethasone according to protocol.

- Mild autoimmune conditions (such as localized psoriasis) requiring minimal treatment
or systemic autoimmune conditions well controlled by target agents such as an
anti-IL-17 that do not affect overall immune system. Patients with a history of
Hashimoto's thyroiditis only requiring hormone replacement, type I diabetes, or
conditions not expected to recur in the absence of an external trigger are allowed to
participate.

Exclusion Criteria:

- Primary central nervous system (CNS) malignancies or CNS metastases, including
leptomeningeal metastases, are not allowed. Subjects with previously treated brain
metastases will be allowed if the brain metastases have been stable for at least 4
weeks following prior treatment and no ongoing steroid requirement.

- Any other malignancy from which the patient has been disease-free for less than 2
years, except for non-melanomatous skin cancer, controlled localized prostate cancer,
in situ carcinoma of any site.

- Women who are pregnant or breastfeeding or intend to become pregnant during their
participation in the study.

- Presence of third space fluid which cannot be controlled by drainage. For patients who
develop or have baseline clinically significant pleural or peritoneal effusions (on
the basis of symptoms or clinical examination) before or during initiation of
pemetrexed therapy, consideration should be given to draining the effusion prior to
dosing. However, if, in the investigator's opinion, the effusion represents
progression of disease, the patient should be discontinued from study therapy.

- Known or suspected autoimmune disease. Patients with a history of inflammatory bowel
disease (including Crohn's disease and ulcerative colitis) and autoimmune disorders
such as rheumatoid arthritis, systemic progressive sclerosis (scleroderma), systemic
lupus erythematosus or autoimmune vasculitis (e.g., Wegener's granulomatosis) are
excluded from this study.

- Any condition requiring systemic treatment with corticosteroids (> 10 mg daily
prednisone equivalents) or other immunosuppressive medications within 14 days prior to
first dose of study drug. Inhaled steroids and adrenal replacement steroids doses > 10
mg daily prednisone equivalents are permitted in the absence of active autoimmune
disease.

- History of primary immunodeficiency.

- Patients who have prior organ transplantation, including allogeneic stem-cell
transplant.

- Vaccinations within 4 weeks of the first dose of avelumab and while on trials is
prohibited except for administration of inactivated vaccines.

- True positive test results for hepatitis A, B, or C during screening.

- Known history of testing positive for human immunodeficiency virus (HIV) or known
acquired immunodeficiency syndrome (AIDS).

- Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, current pneumonitis, symptomatic congestive heart failure, unstable angina
pectoris, symptomatic cardiac arrhythmia, or interstitial lung disease.

- Clinically significant (i.e., active) cardiovascular disease: cerebral vascular
accident/stroke (< 6 months prior to enrollment), myocardial infarction (< 6 months
prior to enrollment), unstable angina, congestive heart failure (>= New York Heart
Association Classification class II), or serious cardiac arrhythmia requiring
medication.

- Persisting toxicity related to prior therapy (National Cancer Institute [NCI] Common
Terminology Criteria for Adverse Events [CTCAE] version [v.] 5.0 grade > 1); however,
alopecia, sensory neuropathy grade =< 2, or other grade =< 2 not constituting a safety
risk based on investigator's judgment are acceptable.

- Uncontrolled psychiatric illness/social situations that would limit compliance with
study requirements or compromise the ability of the subject to give written informed
consent.

- Known allergy or hypersensitivity to study drug formulations.

- Major surgical procedure (as defined by the PI or co-PIs within 28 days prior to the
first dose of therapy) or still recovering from prior surgery.

- Patient currently on dialysis.
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Gender: All

Minimum Age: 18 Years

Maximum Age: N/A

Healthy Volunteers: No

Official Information

Name: Amishi Y Shah

Role: Principal Investigator

Affiliation: M.D. Anderson Cancer Center

Overall Contact

Name: Amishi Shah

Phone: 713-745-7575

Email: ayshah@mdanderson.org

Link: MD Anderson Cancer Center Website

Location

Facility Status Contact
M D Anderson Cancer Center
Houston, Texas 77030
United States
Recruiting Amishi Y. Shah
713-792-2830