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实体瘤疗效评介标准-快速查阅-RECIST.pdf
Response Evaluation Criteria in Solid Tumors (RECIST) Quick Reference:
Eligibility
Only patients with measurable disease at baseline should be included in protocols where
objective tumor response is the primary endpoint.
Measurable disease - the presence of at least one measurable lesion. If the measurable
disease is restricted to a solitary lesion, its neoplastic nature should be confirmed by
cytology/histology.
Measurable lesions - lesions that can be accurately measured in at least one dimension
with longest diameter 20 mm using conventional techniques or 10 mm with spiral CT
scan.
Non-measurable lesions - all other lesions, including small lesions (longest diameter 20
mm with conventional techniques or 10 mm with spiral CT scan), i.e., bone lesions,
leptomeningeal disease, ascites, pleural/pericardial effusion, inflammatory breast disease,
lymphangitis cutis/pulmonis, cystic lesions, and also abdominal masses that are not
confirmed and followed by imaging techniques; and.
All measurements should be taken and recorded in metric notation, using a ruler or calipers.
All baseline evaluations should be performed as closely as possible to the beginning of
treatment and never more than 4 weeks before the beginning of the treatment.
The same method of assessment and the same technique should be used to characterize each
identified and reported lesion at baseline and during follow-up.
Clinical lesions will only be considered measurable when they are superficial (e.g., skin
nodules and palpable lymph nodes). For the case of skin lesions, documentation by color
photography, including a ruler to estimate the size of the lesion
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