Genetic Exploration of the Molecular Basis of Malignancy in Adults

This protocol is not designed as a treatment protocol. Patients enrolled on this study will
be treated according to the treating physician's plan of care, independent of enrollment into
the study. Once enrolled, the physician may proceed with the appropriate plan of care during
the period of specimen analysis if indicated. Upon return of the results, therapy may or may
not be altered based upon the patient's pathology, pertinent medical and treatment history,
imaging studies, available clinical trials, and on the CLIA validated clinical molecular
profiling results. Regardless of the results, the patient will be offered a treatment
selected on an empirical basis by the treating physician at the individual site. All patients
enrolled in the study will be followed for clinical outcome. Clinical molecular profiling
results will expire 14 weeks following the date the Foundation One report is received. No
investigational agents will be administered as part of this study. However, patients may be
referred to open clinical trials based on the results of profiling. Patients referred for
clinical trial may receive investigational agents under a separate clinical trial in
accordance with the written protocol for which they are subsequently enrolled. All
anti-neoplastic drugs used while participating in this study, whether used on-label or
off-label, will be administered to the patient by the route of administration published in
the FDA approved package insert. In addition, the dosing of the agent (including dose
modifications) will be calculated based upon what is published in the FDA approved package
insert.

Inclusion Criteria:

- Understand and provide written informed consent and HIPAA Authorization prior to
initiation of any study-specific procedures.

- Have a life expectancy of >3 months.

- Have a diagnosis of metastatic, incurable cancer and have progressed on at least one
line of systemic therapy OR a cancer with no standard 1st-line systemic therapy shown
to prolong survival (or where a clinical trial recommended as the 1st-line option).
Patients do not have to be off-treatment when enrolled on this trial. However, please
see section 6.4.8 regarding the required wash-out period before starting any FDA
approved on-label or off-label treatment.

- Measurable disease (RECIST 1.1).

- Be ≥18 years of age.

- ECOG Performance status 0 or 1.

- In the opinion of the investigator, be medically suitable for and willing to undergo a
biopsy or surgical procedure to obtain tissue as a part of routine care for their
malignancy OR have adequate archival tissue from a previous biopsy, performed no more
than 14 weeks prior to enrollment, available for profiling.

- Have adequate organ and bone marrow function as defined below: Bone marrow: absolute
neutrophil count (ANC) ≥ 1.5 x 109/L; hemoglobin ≥ 9 g/dL; platelets >100 x 109/L
Renal: creatinine clearance ≥ 60 mL/min (calculated according to Cockcroft and Gault
formula) or creatinine ≤ 1.5 mg/dL Hepatic: bilirubin ≤ 2.5 x the upper limit of
normal (ULN); aspartate transaminases (AST/SGOT); alanine transaminases (ALT/SGPT) ≤
2.5 x ULN (or ≤ 5 x ULN if due to underlying liver metastases)

- Female patients of childbearing potential must have a negative pregnancy test and
agree to use at least two forms of contraception during the study and for at least one
month after treatment discontinuation. For the purposes of this study, a female with
child- bearing potential is defined as: any woman who meets the following criteria.

Has not undergone a hysterectomy or bilateral oophorectomy. Has not been naturally
postmenopausal for at least 24 months (i.e. has had a menses at any time in the preceding
24 consecutive months).

- Male patients must use a form of barrier contraception that contains spermicide and is
approved by the investigator / treating physician during the study and for at least
one month after treatment discontinuation.

- No more than one prior screening attempt for SH GEMMA.

Exclusion Criteria:

- Have lesions that are not accessible to biopsy or not planned for biopsy as part of
routine care OR if archival tissue will be used for profiling, an insufficient amount
is available OR archival tissue was obtained ≥ 14 weeks prior to enrollment.

- Have diagnosis of a hematologic malignancy.

- Diagnosis of astrocytoma, glioblastoma multiforme, or any other primary brain cancer.

- Have concurrent uncontrolled malignancy.

- Have symptomatic CNS metastasis. Patients with a history of CNS metastases who have
been treated with whole brain irradiation must be stable without symptoms for 4 weeks
after completion of treatment, with image documentation required, and must be either
off steroids or on a stable dose of steroids for ≥ 2 weeks prior to enrollment.

- Have uncontrolled concurrent illness including, but not limited to, ongoing or active
serious infection, symptomatic congestive heart failure, unstable angina pectoris,
unstable cardiac arrhythmias, psychiatric illness, or situations that would limit
compliance with the study requirements or the ability to willingly give written
informed consent.

- Have known HIV, HBV, HCV infection.

- Previous enrollment in the SH GEMMA study. Patients are allowed one prior screening
attempt.

- Are pregnant or breast-feeding patients or any patient with childbearing potential not
using adequate contraception.