Inclusion Criteria

Inclusion criteria:

- Subjects eligible for enrolment in the study must meet all of the following criteria:

- Patients who have consent to this study participation and signed into Informed
consent form.

- Subjects must have histologically confirmed invasive breast cancer with stage IIIB,
stage IIIC with T4 lesion, or stage IV disease.

- Documentation of ErbB2 overexpression [IHC3+ or IHC2+ with FISH confirmation] is
required based on local laboratory.

- Subjects must have documented progressive advanced or metastatic breast cancer.

- Subjects must have refractory breast cancer defined as progression in the locally
advanced or metastatic setting or relapse within 6 months of completing adjuvant
therapy. Prior therapies must include, but are not limited to:

- Taxane containing regimen for at least 4 cycles or 2 cycles provided disease
progression occurred while on taxane.

- Anthracycline containing regimen for at least 4 cycles or 2 cycles provided disease
progression occurred while on anthracycline.

- Subjects who relapse >6 months after completion of adjuvant anthracycline-containing
chemotherapy, and for whom further anthracycline is not indicated, will be considered
to have met the anthracycline prior exposure requirement.

- Taxanes and anthracyclines may have been administered concurrently or separately.

- Prior treatment with capecitabine is not permitted.

- Prior treatment must have contained trastuzumab alone or in combination with other
chemotherapy for at least 6 weeks of standard doses in the adjuvant or
advanced/metastatic setting.

- Subjects with hormone receptor positive tumors must have disease progression
following hormonal therapy unless intolerant to hormonal therapy or hormonal therapy
is not considered to be clinically appropriate.

- Subjects with stable CNS metastases (asymptomatic, and off systemic steroids and
anticonvulsants for at least 3 months) are eligible.

- Measurable disease according to modified RECIST (Response Evaluation Criteria in
Solid Tumors) (see Section 6.2, Efficacy p.49).

- Subjects must have archived tumor tissue available for biomarker assessment.

- Female subjects must be ≥20

- ECOG Performance Status of 0 or 1.

- Life expectancy of ≥12 weeks.

- Measurable lesions may be in the field of prior irradiation. However, there must be
at least a 4-week period between the last radiation treatment and the baseline scan
documenting disease status for the lesion to be measurable.

- Cardiac ejection fraction within the institutional range of normal as measured by
ECHO (or MUGA if ECHO is not available). If no institutional range is available,
cardiac ejection fraction must be ≥50%.

- Adequate hematologic value, hepatic and renal function as defined below. Hematologic
ANC (absolute neutrophil count) ≥1.5×109/L Hemoglobin ≥9 g/dL Platelets ≥100× 109/L
Hepatic Serum bilirubin ≤1.5×ULN

- 2.5×ULN if subject has Gilbert's syndrome AST and ALT ≤5×ULN if documented liver
metastases

- 3×ULN without liver metastases Renal Serum creatinine Creatinine clearance* ≤50
mL/min

- Calculated by the Cockcroft and Gault Method

Exclusion criteria:

Subjects meeting any of the following criteria must not be enrolled in the study:

- Pregnant or lactating females.

- Malabsorption syndrome, disease significantly affecting gastrointestinal function, or
resection of the stomach or small bowel. In addition, subjects with ulcerative
colitis are excluded.

- History of other malignancy. Subjects who have been disease-free for at least 5 years
or subjects with a history of completely resected non-melanoma skin cancer or
successfully treated in situ carcinoma are eligible.

- Unresolved or unstable, serious toxicity from prior administration of another
investigational drug and/or of prior anticancer therapy.

- Active or uncontrolled infection.

- Dementia, altered mental status, or any psychiatric condition that would prohibit the
understanding or rendering of informed consent.

- Known history of uncontrolled or symptomatic angina, arrhythmia or congestive heart
failure.

- No prior anti-ErbB1/ErbB2 inhibitor for breast cancer other than trastuzumab.

- Known history or clinical evidence of leptomeningeal carcinomatosis.

- Concurrent anticancer therapy (chemotherapy, radiation therapy, surgery,
immunotherapy, biologic therapy, or tumor embolization) other than capecitabine.

- Bisphosphonates for the treatment of bone metastases should not be initiated
following the first dose of study medication. Prophylactic use of bisphosphonate in
subjects without bone disease is not permitted, except for prevention of
osteoporosis.

- Use of an investigational drug within 30 days or 5 half-lives, whichever is longer,
preceding the first dose of study medication.

- Participation in other studies or use of other investigational drugs during this
study.

- Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs
chemically related to lapatinib or excipients of lapatinib.

- Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs
chemically related to capecitabine, fluorouracil or any excipients.

- Known dihydropyrimidine dehydrogenase (DPD) deficiency.

- Patients who an investigator judges ineligible to this study in consideration of
patient's safety (e.g., complications).