RECIST Response Criteria for Breast Cancer
RECIST (Response Evaluation Criteria In Solid Tumors) is a standardized system that categorizes treatment response in breast cancer into four categories based on unidimensional tumor measurements: Complete Response (CR), Partial Response (PR), Stable Disease (SD), and Progressive Disease (PD). 1
Core RECIST Definitions
The RECIST criteria use the longest diameter only (unidimensional measurement) to assess tumor response, which simplifies the older WHO bidimensional approach 1:
Response Categories
Complete Response (CR): Complete disappearance of all tumor lesions 1
Partial Response (PR): ≥30% decrease in the sum of longest diameters of all target lesions compared to baseline 1
Stable Disease (SD): Insufficient shrinkage to qualify as PR and insufficient increase to qualify as PD 1
Progressive Disease (PD): ≥20% increase in the sum of longest diameters of target lesions from the smallest measurement (nadir) OR appearance of new lesions OR unequivocal progression of non-target lesions 1
Measurement Requirements
Measurable lesions must have a longest diameter ≥2 cm with conventional imaging techniques or ≥1 cm with spiral CT scan 1:
- Only pre-selected "target lesions" are measured serially, while other lesions are recorded but not measured 1
- The sum of the longest diameters of all target lesions determines response status 1
- Response confirmation requires a minimum 4-week interval between assessments 1
Application in Breast Cancer
Neoadjuvant Setting
In the neoadjuvant chemotherapy context for breast cancer, RECIST provides standardized assessment of tumor shrinkage 1:
- Pathologic complete response (pCR) serves as a surrogate endpoint for improved disease-free survival 1
- RECIST measurements guide decisions about switching chemotherapy regimens when response is inadequate 1
- The criteria help determine feasibility of breast conservation versus mastectomy 1
Metastatic Setting
The NCCN explicitly recommends using RECIST or WHO criteria as objective systems for assigning disease activity in metastatic breast cancer 1:
- Serial imaging with the same modality should be used for consistency 1
- Response assessment should integrate clinical symptoms, physical examination, laboratory tests, and imaging 1
Important Caveats and Pitfalls
Bone Lesions
Bone metastases present a significant challenge with RECIST 2:
- Pure osteolytic or osteoblastic bone lesions are generally considered non-measurable 1
- Only bone lesions with identifiable soft tissue components can serve as target lesions 3
- Bone scan "flare" phenomenon can mimic progression when disease is actually responding 1
Measurement Limitations
RECIST may underestimate progressive disease in breast cancer 4:
- The 20% threshold for PD may delay recognition of treatment failure 4
- Changes from tumor necrosis, fibrosis, or fragmentation after treatment can be difficult to assess 1
- Tumors <2 cm, irregular shapes, or ill-defined margins are challenging to measure accurately 1
Functional Imaging Challenges
PET/CT scanning lacks validated standards for RECIST assessment 1:
- According to RECIST, PET can only assess progression when new sites of abnormality appear 1
- PET cannot be used to declare response, stability, or progression in other contexts 1
Practical Implementation
Research demonstrates that measuring the two largest lesions provides excellent concordance with measuring all lesions 5:
- Evaluating more than two target lesions does not significantly improve accuracy 5
- Overall response rates differ by <3% when using two versus all lesions 5
- This simplification reduces cost and time burden without compromising accuracy 5
Comparison with WHO Criteria
RECIST shows 94-97% concordance with older WHO bidimensional criteria in breast cancer 4, 6:
- The kappa statistic for concordance is 0.91, indicating excellent agreement 6
- RECIST is simpler and more reproducible than WHO criteria 6
- However, RECIST may reclassify some progressive disease cases as stable disease 4
Monitoring Frequency
Regular serial assessments are essential, with intervals based on treatment type and disease biology 1: