WSD0922-FU for the Treatment of Glioblastoma, Anaplastic Astrocytoma, or Non-small Cell Lung Cancer With Central Nervous System Metastases

Inclusion Criteria:

Pre-registration - Inclusion Criteria Specific to Dose Escalation Cohort:

Histopathological and/or molecular confirmation of either glioblastoma, IDH wildtype (GBM) (as defined by either the 2016 or 2021 WHO classifications), anaplastic astrocytoma, IDH wildtype (AA) (as defined by the 2016 WHO classification) or non-small cell lung cancer (NSCLC).

EGFR Status:

GBM/AA must have either EGFR amplification and/or any activating EGFR mutation (e.g. A289T, EGFRvIII, etc.);
NSCLC must have a confirmed activating EGFR mutation [e.g. Del19, L858R, EGFRvIII, G719A, L861Q, T790M, C797S, etc]..
Pre-Registration - Inclusion Criteria Specific to Dose Expansion Cohorts

Glioblastoma, IDH wildtype/Anaplastic astrocytoma, IDH wildtype (GBM/AA) Cohort:

Diagnosis: Histological confirmation of either glioblastoma, IDH wildtype (GBM) or anaplastic astrocytoma, IDH wildtype (AA)
EGFR status: GBM/AA must have EGFR amplification and/or any activating EGFRvIII mutation

Brain Tumor Penetration (BTP) Cohort:

Diagnosis: Histological confirmation of either glioblastoma, IDH wildtype (GBM) or anaplastic astrocytoma, IDH wildtype (AA)
EGFR status: GBM/AA must have been previously demonstrated to have EGFR amplification and/or any activating EGFRvIII mutation based on any prior resection

Non-Small Cell Lung Cancer Leptomeningeal Metastases (NSCLC LM) cohort:

Diagnosis: Histological confirmation of non-small cell lung cancer (NSCLC)
EGFR status: NSCLC must have confirmed activating EGFR mutation (including Del19, L858R, EGFRvIII, G719A, L861Q)
Registration -Inclusion Criteria Specific to Dose Escalation Cohort

Previous treatments:

Patients with GBM/AA must have been previously treated with radiation and temozolomide
Patients with NSCLC must have been previously treated with at least one line of single-agent therapy with an EGFR TKI e.g. gefitinib, erlotinib, afatinib, or osimertinib)

Radiographic progression:

Patients with GBM/AA must have radiographic progression based on RANO criteria
Patients with NSCLC must have new or radiographic progression in the central nervous system (brain metastases and/or leptomeningeal metastases). Positive confirmation of CSF cytology is both necessary and sufficient to define the presence of leptomeningeal metastases for patients in this study. Patients with positive CSF cytology and brain metastases will be categorized as "leptomeningeal metastases."
Measurable disease
Eastern Cooperative Oncology Group (ECOG) 0 or 1. For patients with NSCLC with leptomeningeal metastases, ECOG 2 is also acceptable
Registration - Inclusion Criteria Specific to Dose Expansion Cohorts

Glioblastoma, IDH wildtype/Anaplastic astrocytoma, IDH wildtype (GBM/AA) Cohort:

Previous treatments: Patients must have been previously treated with radiation and temozolomide
Radiographic progression: Patients with GBM/AA must have radiographic progression based on RANO criteria
Measurable disease
Performance status: ECOG 0 or 1 for patients with GBM/AA

Brain Tumor Penetration (BTP) Cohort:

Previous treatments: Patients must have been previously treated with radiation and temozolomide
Radiographic progression: Patients with GBM/AA must have radiographic progression based on RANO criteria
Therapeutic surgical resection of GBM/AA required as part of routine clinical care
Performance status: ECOG 0 or 1

Non-Small Cell Lung Cancer Leptomeningeal Metastases (NSCLC LM) cohort:

Previous treatments: Patients must have had either:

No prior treatment with an EGFR TKI, or
Previous EGFR TKI treatment (e.g. gefitinib, erlotinib, afatinib, or osimertinib) followed by central nervous system (CNS) disease progression without extra-CNS progression
Radiographic progression: Patients must have new or radiographic progression of leptomeningeal metastases. Positive confirmation of CSF cytology is both necessary and sufficient to define the presence of leptomeningeal metastases for patients in this study
For the NSCLC LM expansion cohort, patients must have both positive confirmation of CSF cytology and at least one site of leptomeningeal disease that can be assessed by magnetic resonance imaging (MRI) and which is suitable for repeat assessments as per the investigator's discretion
Performance Status: ECOG 0, 1, or 2
Registration - Inclusion Criteria Common to Dose Escalation and Dose Expansion Cohorts:
Age >/equal to 18 years
Ability to understand and the willingness to sign a written informed consent document
Hemoglobin >= 9.0 g/dL (obtained =< 14 days prior to registration)
Leukocytes >= 3.0 x 10^9/L (obtained =< 14 days prior to registration)
Absolute neutrophil count >= 1.5 x 10^9/L (obtained =< 14 days prior to registration)
Platelets >= 100 x 10^9/L (obtained =< 14 days prior to registration)

International normalized ratio (INR) =< 1.5 x upper limit of normal (ULN) (obtained =< 14 days prior to registration)

Patients on a stable dose of anti-coagulation therapy will be allowed to participate if they have no signs of bleeding or clotting and the INR/prothrombin time (PT) and partial thromboplastin time (PTT)/activated (a)PTT results are compatible with an acceptable risk-benefit ratio as per the investigator's discretion

aPTT =< 1.5 x ULN (obtained =< 14 days prior to registration)

Patients on a stable dose of anti-coagulation therapy will be allowed to participate if they have no signs of bleeding or clotting and the INR/PT and PTT/aPTT results are compatible with an acceptable risk-benefit ratio as per the investigator's discretion
Total bilirubin =< 1.5 x ULN and < 3 mg/dL for patients with Gilbert's disease (obtained =< 14 days prior to registration)
Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 3 x ULN or =< 5 x ULN if due to liver involvement by tumor (obtained =< 14 days prior to registration)
Creatinine =< 1.5 x ULN or estimated glomerular filtration rate (estimated glomerular filtration rate [eGFR]) >= 60 mL/minute (obtained =< 14 days prior to registration)
Negative pregnancy test done =< 7 days prior to registration, for persons of childbearing potential only
Provision of signed and dated written informed consent prior to any study specific procedures, sampling, and analyses
Willingness to provide mandatory blood specimens and mandatory tissue specimens for correlative research
Willingness to return to enrolling institution for follow-up (during the active monitoring phase of the study i.e., active treatment and clinical follow-up)
Male and female patients of child bearing potential must be willing to use contraception, (i.e., condoms, birth control) while on study and until 3 months after the last dose of study drug is taken
Must be willing to take light-protective measures during the study and for 2 weeks after their last dose of WSD0922-FU
Must have a minimum life expectancy of >= 3 months
Must be stable on no more than 2 mg of dexamethasone (or equivalent steroids) per day. Steroid dose should not be adjusted during cycle 1 of therapy
Must not take enzyme-inducing anticonvulsants treatment for at least 2 weeks prior to enrollment. Patients on enzyme-inducing anticonvulsants will be changed to non-enzyme inducing anticonvulsants. Drug-drug interactions (DDI) with proton pump inhibitor (PPI), H2 blockers or antacids have not been assessed; therefore it is suggested to avoid taking those drugs together with WSD0922-FU
Strong inducers and strong inhibitors of CYP3A should be discontinued at least 14 days prior to registration
Willingness to provide mandatory tissue specimens for correlative research (BTP cohort only).
Willingness to provide mandatory CSF specimens for correlative research (NSCLC LM cohort only).

Exclusion Criteria:

Registration - Exclusion Criteria for Dose Escalation and Dose Expansion

Any of the following because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown:

Pregnant persons
Nursing persons
Persons of childbearing potential who are unwilling to employ adequate contraception

Any of the following prior therapies:

Any cytotoxic chemotherapy or other anticancer drugs for the treatment of advanced NSCLC from a previous treatment regimen =< 14 days prior to registration
In patients with NSCLC, treatment with an EGFR TKI (e.g., erlotinib, gefitinib, afatinib or osimertinib) within 8 days or approximately 5 x half-life, whichever is the longer, prior to registration (if sufficient wash-out time has not occurred due to schedule or PK properties, an alternative appropriate wash-out time based on known duration and time to reversibility of drug related adverse events could be agreed upon by the Investigator and Wayshine)
Radiation therapy to the brain =< 12 weeks prior to registration
Patients with GBM/AA must not have received (i) nitrosoureas within 42 days of registration, (ii) any chemotherapy or experimental therapy within 28 days or 5 half-lives, whichever is longer, prior to registration
Patients with GBM/AA must not have received prior anti-EGFR or EGFRvIII therapies (erlotinib, gefitinib, afatinib, osimertinib, ABT-414, ABBV-221, AMG-595, AMG-596 etc.)
Patients with GBM/AA who have been treated with bevacizumab within the last four months are not eligible.
Received prior systemic biologic therapy (CAR-T, anti-PD-1 / anti-PD-L1, anti-CTLA-4, etc.) within 28 days prior to registration.
Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens including uncontrolled hypertension and active bleeding diatheses, which in the investigator's opinion makes it undesirable for the patient to participate in the trial or which would jeopardize compliance with the protocol. Screening for chronic conditions is not required
Subjects who are human immunodeficiency virus (HIV), hepatitis virus B (HBV), and/or hepatitis virus C (HCV) positive

Uncontrolled inter-current illness including, but not limited to:

Symptomatic CNS complications that require urgent neurosurgical or medical (e.g. mannitol) intervention
Seizures requiring a change in anti-epileptic medications (addition of new anti-epileptic or increase in dose) =< 2 weeks of registration
Known intracranial hemorrhage which is unrelated to tumor
Significant medical or psychiatric illness that would interfere with compliance and ability to tolerate treatment as outlined in the protocol
Illness/social situations that would limit compliance with study requirements
Receiving any other investigational agent which would be considered as a treatment for the primary neoplasm
Patients with a "currently active" second malignancy other than non-melanoma skin cancers and carcinoma-in-situ of the cervix. Patients are not considered to have a "currently active" malignancy if they have completed therapy and are free of disease for more than three years prior to registration

Any of the following cardiac criteria:

A marked baseline prolongation of QT/corrected QT (QTc) interval
(e.g., repeated demonstration of a QTc interval > 480 milliseconds (ms) (Common Terminology Criteria for Adverse Events [CTCAE] grade 1) using Fridericia's QT correction formula
A history of additional risk factors for torsade de pointes (TdP) (e.g., heart failure, hypokalemia, family history of long QT syndrome)
The use of concomitant medications that prolong the QT/QTc interval
Patients confirmed to have a cis double mutation (Del19/T790M or L858R/T790M) or cis triple mutation (Del19/T790m/C797S or L858R/T790M/C797S)
Past medical history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis which required steroid treatment, or any evidence of clinically active interstitial lung disease. History of hypersensitivity to active or inactive excipients of WSD0922-FU or drugs with a similar chemical structure or class to WSD0922-FU
Refractory nausea and vomiting if not controlled by supportive therapy, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection that would preclude adequate absorption of WSD0922-FU
Inadequate bone marrow reserve or organ function
Patients with NSCLC LM who are unable to undergo collection of CSF
Patients who are unable to tolerate dairy (GBM/AA cohort only). This is to ensure that patients on this cohort can participate in the food effect study.