Cisplatin and Etoposide With or Without Veliparib in Treating Patients With Extensive Stage Small Cell Lung Cancer

PRIMARY OBJECTIVES:

I. To determine the recommended phase II dose (RP2D) of veliparib to use in combination with
cisplatin and etoposide (CE). (Phase I) II. To determine whether the addition of ABT-888
(veliparib) to cisplatin etoposide (CE) results in improved progression free survival (PFS)
over CE with placebo in the frontline therapy of newly diagnosed extensive stage small cell
lung cancer. (Phase II)

SECONDARY OBJECTIVES:

I. To determine the overall survival (OS) associated with the combination of CE plus ABT-888.
(Phase II) II. To assess the overall response rate (ORR) as well as complete response rate
(CRR) associated with the combination of CE plus ABT-888. (Phase II) III. To determine the
toxicity profile of the combination of ABT-888 and CE chemotherapy in this patient
population. (Phase II)

OTHER PRE-SPECIFIED OBJECTIVES:

I. To conduct exploratory correlative analysis of the impact of the select biomarkers. (Phase
II) II. To compare the overall toxicity profile and specifically the incidence and severity
of chemotherapy-induced peripheral neuropathy with the addition of ABT-888 to CE. (Phase II)

OUTLINE: This is a phase I, dose-escalation study of veliparib followed by a phase II study.

Phase I: Patients receive veliparib orally (PO) twice daily (BID) on days 1-7, etoposide
intravenously (IV) over 60-120 minutes on days 1-3, and cisplatin IV over 60-120 minutes on
day 1. Treatment repeats every 21 days for 4 courses in the absence of disease progression or
unacceptable toxicity.

Phase II: Patients are randomized to 1 of 2 treatment arms.

ARM D: Patients receive veliparib PO BID on days 1-7, etoposide IV over 60-120 minutes on
days 1-3, and cisplatin IV over 60-120 minutes on day 1. Treatment repeats every 21 days for
4 courses in the absence of disease progression or unacceptable toxicity.

ARM E: Patients receive placebo PO BID on days 1-7, etoposide IV over 60-120 minutes on days
1-3, and cisplatin IV over 60-120 minutes on day 1. Treatment repeats every 21 days for 4
courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up every 3 months for 2 years and
then every 6 months for 1 year.

PHASE I

Inclusion Criteria (phase I):

- Women must not be pregnant or breastfeeding; breastfeeding must be discontinued or the
subject is not eligible for the study

- All females of childbearing potential must have a blood test within 2 weeks prior to
randomization to rule out pregnancy; a female of childbearing potential is any woman,
regardless of sexual orientation or whether they have undergone tubal ligation, who
meets the following criteria: 1) has not undergone a hysterectomy or bilateral
oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive
months (i.e., has had menses at any time in the preceding 24 consecutive months)

- Women of childbearing potential and sexually active males must be strongly advised to
use an accepted and effective method of contraception

- Patients must have histologically or cytologically confirmed:

- Extensive stage small cell lung cancer (SCLC) or

- Stage IV (M1a or M1b according to American Joint Committee on Cancer [AJCC]
Staging Manual, 7th edition) large cell neuroendocrine non-small cell lung cancer
(NSCLC) or

- Small cell carcinoma of unknown primary or extrapulmonary origin and must be a
candidate for systemic therapy

- NOTE: The extensive disease SCLC classification for this protocol includes
all patients with disease sites not defined as limited stage; limited stage
disease category includes patients with disease restricted to one hemithorax
with regional lymph node metastases, including hilar, ipsilateral and
contralateral mediastinal, and/or ipsilateral supraclavicular nodes;
extensive disease patients are defined as those patients with extrathoracic
metastatic disease, malignant pleural effusion, bilateral or contralateral
supraclavicular adenopathy

- Patients must have measurable or non-measurable disease based on Response Evaluation
Criteria in Solid Tumors (RECIST) 1.1; baseline measurements and evaluations of all
sites of disease must be obtained =< 4 weeks prior to registration (Phase I)

- Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1

- Absolute neutrophil count >= 1,500/mm^3

- Platelets >= 100,000/mm^3

- Leukocytes >= 3,000/mm^3

- Hemoglobin >= 9 g/dL

- Total bilirubin =< 1.5 times institutional upper limit of normal (ULN)

- Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) and
alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase[SGPT]) =< 3
times institutional ULN (=< 5 times if liver function test [LFT] elevations due to
known liver metastases)

- Creatinine =< 1.5 X ULN OR creatinine clearance >= 60 mL/min/1.73 m^2 for patients
with creatinine levels > 1.5 x ULN

- Patients with central nervous system (CNS) metastases or a history of CNS metastases
are ineligible

- Patients cannot have had prior chemotherapy or biologic therapy for SCLC or large cell
neuroendocrine NSCLC, or small cell carcinoma of unknown primary or extrapulmonary
origin; patients receiving prior radiation cannot register within 7 days after
completion of radiation, and must have resolved adverse events attributed to radiation
to =< grade 1; no previous irradiation to the only site of measurable or evaluable
disease, unless that site had subsequent evidence of progression

- Patients receiving prior radiation cannot register within 7 days after completion of
radiation, and must have resolved adverse events attributed to radiation to =< grade
1; no previous irradiation to the only site of measurable or evaluable disease, unless
that site had subsequent evidence of progression

- Patients must NOT have uncontrolled intercurrent illness including, but not limited
to, ongoing or active infection, symptomatic congestive heart failure, unstable angina
pectoris, uncontrolled cardiac arrhythmia, or psychiatric illness/social situations
that would limit compliance with study requirements

- Human immunodeficiency virus (HIV)-positive patients on combination antiretroviral
therapy are ineligible

- Patient must be able to swallow pills

Exclusion Criteria (phase I):

- Patients have active seizure(s) or history of seizure(s)

- Patients have history of allergic reactions attributed to compounds of similar
chemical or biologic composition to veliparib or other agents used in the study

PHASE II

Inclusion Criteria (phase II):

- Women must not be pregnant or breastfeeding; breastfeeding must be discontinued or the
subject is not eligible for the study

- All females of childbearing potential must have a blood test within 2 weeks prior to
randomization to rule out pregnancy; a female of childbearing potential is any woman,
regardless of sexual orientation or whether they have undergone tubal ligation, who
meets the following criteria: 1) has not undergone a hysterectomy or bilateral
oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive
months (i.e., has had menses at any time in the preceding 24 consecutive months) with
the current month counted as month 1

- Women of childbearing potential and sexually active males must be strongly advised to
use an accepted and effective method of contraception

- Patients must have extensive stage, histologically or cytologically confirmed small
cell lung cancer; NOTE: the extensive disease classification for this protocol
includes all patients with disease sites not defined as limited stage; limited stage
disease category includes patients with disease restricted to one hemithorax with
regional lymph node metastases, including hilar, ipsilateral and contralateral
mediastinal, and/or ipsilateral supraclavicular nodes; extensive disease patients are
defined as those patients with extrathoracic metastatic disease, malignant pleural
effusion, bilateral or contralateral supraclavicular adenopathy

- Patients must have measurable disease based on RECIST 1.1; baseline measurements and
evaluations of all sites of disease must be obtained =< 4 weeks prior to registration

- ECOG performance status 0 or 1

- Absolute neutrophil count >= 1,500/mm^3

- Platelets >= 100,000/mm^3

- Leukocytes >= 3,000/mm^3

- Hemoglobin >= 9 g/dL

- Total bilirubin =< 1.5 times institutional upper limit of normal (ULN)

- AST (SGOT) and ALT (SGPT) =< 3 times institutional ULN (=< 5 times if LFT elevations
due to known liver metastases)

- Creatinine =< 1.5 X ULN OR creatinine clearance >= 60 mL/min/1.73 m^2 for patients
with creatinine levels > 1.5 x ULN

- Patients cannot have had prior chemotherapy or biologic therapy for small cell lung
cancer; patients receiving prior radiation cannot register within 7 days after
completion of radiation, and must have resolved adverse events attributed to radiation
to =< grade 1; no previous irradiation to the only site of measurable or evaluable
disease, unless that site had subsequent evidence of progression

- Patient must be able to swallow pills

- Patients may not be receiving any other investigational agents while on study

Exclusion Criteria (phase II):

- Patients with CNS metastases or a history of CNS metastases are ineligible

- Patients have history of allergic reactions attributed to compounds of similar
chemical or biologic composition to veliparib or other agents used in the study

- Patients have active seizure(s) or history of seizure(s)

- Patients must NOT have uncontrolled intercurrent illness including, but not limited
to, ongoing or active infection, symptomatic congestive heart failure, unstable angina
pectoris, uncontrolled cardiac arrhythmia, or psychiatric illness/social situations
that would limit compliance with study requirements

- HIV-positive patients on combination antiretroviral therapy are ineligible because of
the potential for pharmacokinetic interactions with veliparib; in addition, these
patients are at increased risk of lethal infections when treated with
marrow-suppressive therapy; appropriate studies will be undertaken in patients
receiving combination antiretroviral therapy when indicated