Summary & Overview
HCPCS G9072: Invasive Breast Cancer, ER/PR Negative Disease Status
HCPCS Level II code G9072 denotes a disease-status classification for invasive female breast cancer characterized by adenocarcinoma histology, early-stage disease (stage I, stage IIA–IIB, or T3, N1, M0), and negative estrogen and progesterone receptors, with no evidence of progression, recurrence, or metastasis. The code is designated for use within a Medicare-approved demonstration project and captures a precise clinical subgroup of breast cancer important for trial enrollment, reporting, and outcome measurement. Nationally, a standardized code for this disease status supports consistent reporting across oncology providers and demonstrations that inform Medicare policy.
Key payers referenced in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find benchmarks and policy context related to the code’s intended use in demonstration projects, an explanation of the clinical criteria embedded in the code description, and guidance on typical sites of service and service type for billing and reporting purposes. The summary outlines limitations where supplemental data elements (such as associated taxonomies, ICD-10 mappings, and related codes) are not provided in the input.
Billing Code Overview
HCPCS Level II code G9072 identifies a specific oncology disease-status classification for female breast cancer. The description specifies invasive female breast cancer with adenocarcinoma as the predominant cell type, limited to early-stage disease (stage I, stage IIA–IIB, or T3, N1, M0) and estrogen receptor (ER) and progesterone receptor (PR) negative, with no evidence of disease progression, recurrence, or metastases. The code is intended for use within a Medicare-approved demonstration project.
Service type: Oncology disease-status classification and reporting.
Typical site of service: Oncology clinic or cancer center outpatient setting, or other clinical settings where disease-status assessments and reporting for breast cancer are performed, including facilities participating in Medicare demonstration projects.
Clinical & Coding Specifications
Clinical Context
A 58-year-old female with a prior diagnosis of invasive female breast cancer presents to a participating Medicare-approved demonstration project clinic for routine disease-status assessment. Her tumor was originally staged as Stage IIA (T2 N0 M0) with adenocarcinoma predominant histology and estrogen receptor (ER) and progesterone receptor (PR) negative status. She completed definitive local therapy (lumpectomy with sentinel lymph node biopsy and radiotherapy) and systemic chemotherapy, and currently has no clinical or radiographic evidence of progression, recurrence, or metastasis. The visit consists of a focused oncology disease-status evaluation including review of symptoms, physical exam of the breasts and regional nodes, review of recent imaging (mammogram +/- diagnostic views, chest imaging if indicated), review of pathology and receptor status, and documentation of current surveillance plan. Relevant documentation includes staging, receptor status (ER/PR negative), prior treatments, current performance status, and confirmation of no evidence of disease progression. Typical workflow: oncology nurse schedules visit and obtains recent imaging reports; medical oncologist or breast surgical oncologist performs the clinical assessment, documents disease-free status and surveillance plan, and completes billing for the demonstration project service using G9072 with appropriate modifier(s). Typical site of service is an outpatient oncology clinic or breast center within a hospital outpatient department or freestanding oncology practice. Typical patient scenario involves routine surveillance visits at regular intervals following completion of active treatment, with coordination of imaging and lab results as needed.
Coding Specifications
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