A phase I study of DS-8201a in combination with olaparib in HER2-expressing malignancies

NOT ENROLLING
Protocol # :
21-151
Conditions
Endometrial Serous Adenocarcinoma
Metastatic Malignant Solid Neoplasm
Unresectable Malignant Solid Neoplasm
Phase
I
Disease Sites
Healthy volunteer
Transplanted organ and tissue status, unspecified
Disease not specified
Neuroendocrine/Carcinoid
Gastroesophageal Junction
Gallbladder/Biliary
Other specified personal risk factors, not elsewhere classified
Lip, Oral Cavity and Pharynx
Esophagus
Stomach
Small Intestine
Colon
Rectum
Anus
Liver
Pancreas
Other Digestive Organ
Larynx
Lung
Other Respiratory and Intrathoracic Organs
Bones and Joints
Soft Tissue
Mycosis Fungoides
Other Skin
Breast
Cervix
Corpus Uteri
Ovary
Other Female Genital
Prostate
Other Male Genital
Urinary Bladder
Kidney
Other Urinary
Eye and Orbit
Brain and Nervous System
Thyroid
Unknown Sites
Ill-Defined Sites
Other Endocrine System
Donors
Kaposi's Sarcoma
Melanoma, Skin
Principal Investigator
Lee, Elizabeth
Site Research Nurses
Hindenach, Sarah
Hurley-Whalen, Christin
Keis, Rylee
Morrissey, Stephanie, C.
Neals, Allison
Thistle, Katrina, M.

Trial Description

This phase I trial identifies the side effects and best dose of DS-8201a and olaparib in
treating patients with HER2-expressing cancers that have spread to other places in the
body or cannot be removed by surgery or endometrial cancer. Olaparib is a drug that
blocks an enzyme involved in many cell functions, including the repair of
deoxyribonucleic acid (DNA) damage. Blocking this enzyme may help keep tumor cells from
repairing their damaged DNA, causing them to die. DS-8201a is an antibody-drug conjugate.
This agent has two components: an antibody component and a chemotherapy component. The
antibody component is attached to the chemotherapy molecules. Upon administration of
DS-8201a, the antibody targets and binds to tumor cells that have abundant HER2
(human-epidermal growth factor receptor 2), which is a protein on the surface of some
tumor cells. The chemotherapy then enters the cells and blocks DNA replication in the
tumor cells with abundant HER2, causing them to die. Giving DS-8201a and olaparib may
shrink or stabilize the cancer.

Eligibility Requirements

Inclusion Criteria:

- DOSE ESCALATION PHASE

- Patients must have histologically confirmed malignancy that is metastatic or
unresectable and for which standard curative or palliative measures do not exist or
are no longer effective

- DOSE EXPANSION PHASE

- Patients must have histologically confirmed uterine serous carcinoma with at least
one lesion suitable for biopsy without significant risk to the patient. This lesion
may also be used for evaluation for the criterion below

- Patient disease must be evaluable or measurable by Response Evaluation Criteria in
Solid Tumors (RECIST) version 1.1. Biopsiable lesion can be same as evaluable lesion

- DOSE ESCALATION AND DOSE EXPANSION PHASES

- Patients must have had at least one prior line of cytotoxic chemotherapy

- Patients can have received an unlimited number of additional lines of chemotherapy,
targeted therapy, biologic therapy, or hormonal therapy

- Patients must have HER2-positive or HER2-expressing tumors determined by a Clinical
Laboratory Improvement Act (CLIA)-certified laboratory. Specific requirement of HER2
status is outlined below:

- HER2 1-3+ expression by IHC OR

- HER2 amplification by next generation sequencing panel (NGS) or in situ
hybridization (ISH) OR

- If local testing is not feasible, patients will submit archival tissue for
central HER2 testing to determine eligibility. Patients with unknown or
negative HER2 testing will not be eligible

- Patients must have archival formalin-fixed paraffin-embedded (FFPE) tissue available
for central confirmation of HER2 testing

- Age >= 18 years. Because no dosing or adverse event data are currently available on
the use of DS-8201a in combination with olaparib in patients < 18 years of age,
children are excluded from this study

- Eastern Cooperative Oncology Group (ECOG) performance status =< 1 (Karnofsky >= 70%)

- Hemoglobin >= 10.0 g/dL (within 14 days of randomization/enrollment)

- No transfusions with red blood cells or platelets are allowed within 1 week
prior to screening assessment

- Absolute neutrophil count >= 1,000/mcL (within 14 days of randomization/enrollment)

- No administration of granulocyte colony-stimulating factor (G-CSF) is allowed
within 1 week prior to screening assessment

- Platelets >= 100,000/mcL (within 14 days of randomization/enrollment)

- No transfusions with red blood cells or platelets are allowed within 1 week
prior to screening assessment

- Total bilirubin =< 1.5 x institutional upper limit of normal (ULN), (< 3 x ULN in
the presence of documented Gilbert's syndrome or liver metastases at baseline)
(within 14 days of randomization/enrollment)

- Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase
[SGOT])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase
[SGPT]) =< 3 x institutional ULN (within 14 days of randomization/enrollment)

- International normalized ratio (INR)/prothrombin time (PT) and activated partial
thromboplastin time (aPTT) =< 1.5 x ULN (within 14 days of randomization/enrollment)

- Creatinine =< 1.5 x institutional ULN (within 14 days of randomization/enrollment)
OR

- Glomerular filtration rate (GFR) >= 51 mL/min/1.73 m^2 unless data exists supporting
safe use at lower kidney function values, no lower than 30 mL/min/1.73 m^2 (using
the Cockcroft-Gault Equation) (within 14 days of randomization/enrollment)

- Patients must have left ventricular ejection fraction (LVEF) >= 50% by either an
echocardiogram (ECHO) or multigated acquisition (MUGA) scan within 28 days before
randomization/enrollment

- Patients who are human immunodeficiency virus (HIV) positive may participate IF they
meet the following eligibility requirements:

- They must be stable on their anti-retroviral regimen, and they must be healthy
from an HIV perspective

- They must have an undetectable viral load and a CD4 count >= 250 cells/uL
within 7 days of enrollment

- They must not be currently receiving prophylactic therapy for an opportunistic
infection and must not have had an opportunistic infection within the past 6
months

- HIV-infected patients should be monitored every 12 weeks for viral load and CD4
counts

- For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV
viral load must be undetectable on suppressive therapy, if indicated

- Patients with a history of hepatitis C virus (HCV) infection must have been treated
and cured. For patients with HCV infection who are currently on treatment, they are
eligible if they have an undetectable HCV viral load

- Patients with brain metastases should be stable and off steroids and at least 4
weeks from radiation at the time of registration

- Patients with a prior or concurrent malignancy whose natural history or treatment
does not have the potential to interfere with the safety or efficacy assessment of
the investigational regimen are eligible for this trial

- Patients with known history or current symptoms of cardiac disease, or history of
treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac
function using the New York Heart Association Functional Classification. To be
eligible for this trial, patients should be better than class 2B

- The effects of DS-8201a and olaparib on the developing human fetus are unknown. For
this reason and because HER2 antibody conjugated to a topoisomerase 1 inhibitor
agents as well as PARP inhibitors are known to be teratogenic; thus, women of
child-bearing potential and men must agree to use highly effective contraception
(hormonal or barrier method of birth control; abstinence) prior to study entry, for
the duration of study participation, and for at least 7 months (women of
childbearing potential [WOCBP] only) after the last dose of study drug. Should a
woman become pregnant or suspect she is pregnant while she or her partner is
participating in this study, she should inform her treating physician immediately.
Men treated or enrolled on this protocol must also agree to use adequate
contraception prior to the study, for the duration of study participation, and 4
months after completion of DS-8201a and olaparib administration

- Women of non-child-bearing potential defined as pre-menopausal females with a
documented tubal ligation or hysterectomy; or postmenopausal defined as 12 months of
spontaneous amenorrhea (in questionable cases, a blood sample with simultaneous
follicle-stimulating hormone [FSH] > 40 mIU/mL and estradiol < 40 pg/mL [< 147
pmol/L] is confirmatory) are eligible. Females on hormone replacement therapy (HRT)
and whose menopausal status is in doubt will be required to use one of the
contraception methods outlined for women of child-bearing potential if they wish to
continue their HRT during the study. Otherwise, they must discontinue HRT to allow
confirmation of post-menopausal status prior to study enrollment. For most forms of
HRT, at least 2-4 weeks will elapse between the cessation of therapy and the blood
draw; this interval depends on the type and dosage of HRT. Following confirmation of
their post-menopausal status, they can resume use of HRT during the study without
use of a contraceptive method

- Male subjects must not freeze or donate sperm starting at screening and throughout
the study period, and at least 4 months after the final study drug administration.
Preservation of sperm should be considered prior to enrollment in this study

- Female subjects must not donate, or retrieve for their own use, ova from the time of
screening and throughout the study treatment period, and for at least 7 months after
the final study drug administration

- Ability to understand and the willingness to sign a written informed consent
document. Participants with impaired decision-making capacity (IDMC) who have a
legally-authorized representative (LAR) and/or family member available will also be
eligible

Exclusion Criteria:

- Patients who have had chemotherapy (including antibody drug therapy) within 4 weeks
with the following exceptions: 1 week for weekly paclitaxel; 2 weeks or five
half-lives, whichever is longer, for small-molecule targeted agents such as
5-fluorouracil-based agents, folinate agents, hormonal agents; or 6 weeks for
nitrosoureas or mitomycin C

- Patients who have had radiation therapy within 4 weeks

- Patients who have had a major surgery within 4 weeks

- Patients who are receiving any other investigational agents

- For the dose expansion cohort: Patients who have received prior PARP inhibitors

- Patients with a history of (non-infectious) interstitial lung disease
(ILD)/pneumonitis that required steroids, has current ILD/pneumonitis, or where
suspected ILD/pneumonitis cannot be ruled out by imaging at screening

- Patients with clinically severe pulmonary compromise resulting from intercurrent
pulmonary illnesses including, but not limited to, any underlying pulmonary disorder
(i.e. pulmonary emboli within three months of the study enrollment, severe asthma,
severe chronic obstructive pulmonary disease [COPD], restrictive lung disease,
pleural effusion, etc.), and any autoimmune, connective tissue or inflammatory
disorders with potential pulmonary involvement (i.e. rheumatoid arthritis,
Sjogren's, sarcoidosis, etc.), or prior pneumonectomy

- History of allergic reactions attributed to compounds of similar chemical or
biologic composition to DS-8201a, the inactive ingredients in the drug product,
olaparib, or severe hypersensitivity to other monoclonal antibodies

- Patients receiving any medications or substances that are moderate or strong
inhibitors or inducers of CYP3A are ineligible. Because the lists of these agents
are constantly changing, it is important to regularly consult a frequently-updated
medical reference. As part of the enrollment/informed consent procedures, the
patient will be counseled on the risk of interactions with other agents, and what to
do if new medications need to be prescribed or if the patient is considering a new
over-the-counter medicine or herbal product

- Patients with a medical history of myocardial infarction within 6 months before
randomization/enrollment, symptomatic congestive heart failure (CHF) (New York Heart
Association class IIb to IV), troponin levels consistent with myocardial infarction
as defined according to the manufacturer 28 days prior to randomization

- Patients with a corrected QT interval (QTc) prolongation to > 470 ms (females) or >
450 ms (males) based on average of the screening triplicate 12-lead
electrocardiogram (ECG)

- Patients with multiple primary malignancies within 3 years, except adequately
resected non-melanoma skin cancer, curatively treated in-situ disease, and other
solid tumors curatively treated

- Patients with an uncontrolled infection requiring IV antibiotics, antivirals, or
antifungals

- Patients receiving chloroquine or hydroxychloroquine will require a washout period
of >= 14 days to be eligible for the study

- Patients with unresolved toxicities from previous anticancer therapy, defined as
toxicities (other than alopecia) not yet resolved to grade =< 1 or baseline.
Subjects with chronic grade 2 toxicities may be eligible per the discretion of the
investigator after consultation with the sponsor medical monitor or designee (e.g.,
grade 2 chemotherapy-induced neuropathy)

- Patients with psychiatric illness/social situations that would limit compliance with
study requirements

- Pregnant women are excluded from this study because DS-8201a is a HER2 antibody
conjugated to a topoisomerase 1 inhibitor agent with the potential for teratogenic
or abortifacient effects. Because there is an unknown but potential risk for adverse
events in nursing infants secondary to treatment of the mother with DS-8201a,
breastfeeding should be discontinued if the mother is treated with DS-8201a. These
potential risks may also apply to other agents used in this study

21-151