PI-RADS · Próstata
Sistemas/Próstata

PI-RADS Prostate Imaging Reporting and Data System v2.1

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Assessment of clinically significant prostate cancer likelihood on multiparametric MRI, with the dominant sequence depending on zone.

Índice de referência, não é suporte à decisão clínica. O RadCommons apresenta conteúdo de referência reescrito a partir de critérios publicados e com link para a fonte primária. Confira sempre a publicação primária vigente. Não é um dispositivo médico nem substitui o julgamento clínico. O radiologista responsável pelo laudo permanece o autor e o responsável.
Escala de categorias
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Procedência e vigência

Órgão emissor
ACR, ESUR, AdMeTech
Versão
v2.1
Ano
2019
Família
léxico
Tipo de lógica
matrix
Modalidade
MRI
Fonte primária
Prostate Imaging Reporting and Data System Version 2.1: 2019 Update of Prostate Imaging Reporting and Data System Version 2 · doi:10.1016/j.eururo.2019.02.033
Última verificação
2026-07-24
Última checagem
2026-07-24

Lógica de decisão

Forma estruturada (matrix). Uma futura calculadora a lê; as categorias abaixo são a superfície legível.

Use DWI/ADC as the dominant sequence in the peripheral zone and T2W in the transition zone. DCE only upgrades a peripheral-zone DWI score 3 to overall category 4 when positive; category and clinical management are separate decisions.

Mostrar a lógica estruturada (JSON)
{
  "applicability": {
    "purpose": "Detect, localize, characterize, and risk-stratify clinically significant prostate cancer on pretreatment prostate MRI.",
    "clinically_significant_cancer": "Gleason score >=3+4 (grade group >=2), and/or tumor volume >=0.5 cc, and/or extraprostatic extension.",
    "assessment_inputs": "Assign the category from mpMRI findings only; do not incorporate PSA, digital rectal examination, clinical history, or planned treatment into the imaging category."
  },
  "axes": {
    "zone": [
      "peripheral",
      "transition"
    ],
    "dominant_sequence": {
      "peripheral": "DWI_ADC",
      "transition": "T2W"
    },
    "DCE": [
      "positive",
      "negative",
      "inadequate_or_absent"
    ],
    "component_quality": [
      "diagnostic",
      "X_inadequate_or_absent"
    ]
  },
  "sequence_scores": {
    "DWI_ADC": [
      {
        "score": 1,
        "finding": "No abnormality on ADC or high-b-value DWI."
      },
      {
        "score": 2,
        "finding": "Linear or wedge-shaped ADC hypointensity and/or linear or wedge-shaped high-b-value DWI hyperintensity."
      },
      {
        "score": 3,
        "finding": "Focal abnormality discrete from background with ADC hypointensity and/or high-b-value DWI hyperintensity, but not marked on both."
      },
      {
        "score": 4,
        "finding": "Focal markedly low ADC and markedly high high-b-value DWI signal, greatest dimension <15 mm."
      },
      {
        "score": 5,
        "finding": "Same diffusion pattern as score 4 with greatest dimension >=15 mm, or definite extraprostatic extension/invasive behavior."
      }
    ],
    "T2W_transition_zone": [
      {
        "score": 1,
        "finding": "Normal-appearing transition zone or a round completely encapsulated typical nodule."
      },
      {
        "score": 2,
        "finding": "Mostly encapsulated nodule, homogeneous circumscribed nodule without encapsulation, or homogeneous mildly hypointense area between nodules."
      },
      {
        "score": 3,
        "finding": "Heterogeneous signal with obscured margins, including findings that do not qualify as 2, 4, or 5."
      },
      {
        "score": 4,
        "finding": "Lenticular or noncircumscribed homogeneous moderately T2-hypointense focus, greatest dimension <15 mm."
      },
      {
        "score": 5,
        "finding": "Same morphology as score 4 with greatest dimension >=15 mm, or definite extraprostatic extension/invasive behavior."
      }
    ],
    "T2W_peripheral_zone": [
      {
        "score": 1,
        "finding": "Uniform T2 hyperintense signal (normal)."
      },
      {
        "score": 2,
        "finding": "Linear or wedge-shaped hypointensity, or diffuse mild hypointensity, usually with indistinct margins."
      },
      {
        "score": 3,
        "finding": "Heterogeneous signal or a noncircumscribed rounded moderately hypointense focus that does not qualify as 2, 4, or 5."
      },
      {
        "score": 4,
        "finding": "Circumscribed homogeneous moderately T2-hypointense focus confined to the prostate, greatest dimension <15 mm."
      },
      {
        "score": 5,
        "finding": "Same morphology as score 4 with greatest dimension >=15 mm, or definite extraprostatic extension/invasive behavior."
      }
    ],
    "DCE": {
      "positive": "Focal enhancement earlier than or contemporaneous with adjacent normal prostate that corresponds to a suspicious T2W and/or DWI finding.",
      "negative": "No early enhancement, or diffuse/noncorresponding enhancement, or focal enhancement matching a T2W feature of BPH."
    }
  },
  "categories": [
    "1",
    "2",
    "3",
    "4",
    "5"
  ],
  "cells": {
    "peripheral_zone": [
      {
        "DWI_ADC_score": 1,
        "DCE": "any",
        "outcome_code": "1"
      },
      {
        "DWI_ADC_score": 2,
        "DCE": "any",
        "outcome_code": "2"
      },
      {
        "DWI_ADC_score": 3,
        "DCE": "negative",
        "outcome_code": "3"
      },
      {
        "DWI_ADC_score": 3,
        "DCE": "positive",
        "outcome_code": "4"
      },
      {
        "DWI_ADC_score": 4,
        "DCE": "any",
        "outcome_code": "4"
      },
      {
        "DWI_ADC_score": 5,
        "DCE": "any",
        "outcome_code": "5"
      }
    ],
    "transition_zone": [
      {
        "T2W_score": 1,
        "DWI_ADC_score": "any",
        "outcome_code": "1"
      },
      {
        "T2W_score": 2,
        "DWI_ADC_score": "<=3",
        "outcome_code": "2"
      },
      {
        "T2W_score": 2,
        "DWI_ADC_score": ">=4",
        "outcome_code": "3"
      },
      {
        "T2W_score": 3,
        "DWI_ADC_score": "<=4",
        "outcome_code": "3"
      },
      {
        "T2W_score": 3,
        "DWI_ADC_score": 5,
        "outcome_code": "4"
      },
      {
        "T2W_score": 4,
        "DWI_ADC_score": "any",
        "outcome_code": "4"
      },
      {
        "T2W_score": 5,
        "DWI_ADC_score": "any",
        "outcome_code": "5"
      }
    ]
  },
  "inadequate_components": {
    "DWI_ADC_X": {
      "warning": "Usually repeat DWI if the cause can be remedied; otherwise acknowledge the substantial limitation in the report.",
      "fallback_cells": [
        {
          "T2W_score": 1,
          "DCE": "any",
          "outcome_code": "1"
        },
        {
          "T2W_score": 2,
          "DCE": "any",
          "outcome_code": "2"
        },
        {
          "T2W_score": 3,
          "DCE": "negative",
          "outcome_code": "3"
        },
        {
          "T2W_score": 3,
          "DCE": "positive",
          "outcome_code": "4"
        },
        {
          "T2W_score": 4,
          "DCE": "any",
          "outcome_code": "4"
        },
        {
          "T2W_score": 5,
          "DCE": "any",
          "outcome_code": "5"
        }
      ]
    },
    "DCE_X": {
      "peripheral_zone": "Determine the category from the DWI assessment category.",
      "transition_zone": "Use the standard T2W-by-DWI transition-zone matrix."
    },
    "DWI_ADC_and_DCE_X": "Limit assessment to staging for extraprostatic extension; do not infer a lesion PI-RADS category from missing components."
  },
  "management_scope": {
    "rule": "PI-RADS v2.1 does not prescribe management; decisions must incorporate laboratory and clinical history, local expertise, and standards of care.",
    "category_1_2": "The document says biopsy should not be based on PI-RADS 1 or 2 alone.",
    "category_3": "Biopsy may or may not be appropriate depending on factors outside mpMRI.",
    "category_4_5": "Biopsy should be considered, but the final decision remains clinical.",
    "forbidden_inference": "Do not invent PSA-density cutoffs, follow-up intervals, or a biopsy mandate from PI-RADS alone."
  },
  "source_locator": "ACR/ESUR/AdMeTech PI-RADS v2.1 (2019), assessment categories and management scope p 10; zone matrices p 11; inadequate-component tables pp 15-16; T2W scoring p 18; DWI scoring pp 20-21; DCE definition and caveats pp 22-23."
}

Categorias num relance

Cat.SignificadoCondutaRiscoFonte
1
Very low likelihood of clinically significant cancer
Very low likelihood. With diagnostic sequences, a peripheral-zone lesion maps here when DWI/ADC score is 1; a transition-zone finding maps here when T2W score is 1, meaning a normal-appearing transition zone or a round completely encapsulated typical nodule.
PI-RADS v2.1 says biopsy should not be based on category 1 alone, but it does not prescribe management. Final action must incorporate PSA and other laboratory data, clinical history, examination, local expertise, and standards of care.Clinically significant prostate cancer is highly unlikely to be present. This is a qualitative imaging likelihood, not a numeric patient-level probability or guarantee of absence.
ACR/ESUR/AdMeTech PI-RADS v2.1 pp 10-11, 18, and 20-21; assessment-category meaning and management-scope paragraph p 10.
2
Low
Low likelihood. In the peripheral zone, DWI/ADC score 2 determines overall category 2. In the transition zone, T2W score 2 remains category 2 when DWI/ADC is 3 or lower; T2W score 2 with DWI/ADC 4 or 5 instead upgrades to category 3.
PI-RADS v2.1 says biopsy should not be based on category 2 alone, but it does not prescribe management. A clinically discordant negative MRI still requires patient-level assessment rather than automatic reassurance.Clinically significant prostate cancer is unlikely to be present. The category reflects mpMRI appearance only and must not absorb PSA, digital rectal examination, history, or treatment plans.
ACR/ESUR/AdMeTech PI-RADS v2.1 pp 10-11, 18, and 20-21; transition-zone matrix p 11 and management-scope paragraph p 10.
3
Intermediate, equivocal
Intermediate or equivocal likelihood. In the peripheral zone, DWI/ADC score 3 remains category 3 when DCE is negative and upgrades to category 4 when DCE is positive. In the transition zone, category 3 results from T2W score 2 with DWI/ADC at least 4, or T2W score 3 with DWI/ADC no greater than 4.
Biopsy may or may not be appropriate. PI-RADS v2.1 supplies no PSA-density cutoff or fixed follow-up interval; the decision must use factors outside mpMRI, including laboratory and clinical history, local expertise, and standards of care.The presence of clinically significant prostate cancer is equivocal. Category 3 is deliberately an uncertainty state and does not itself justify a deterministic biopsy or surveillance instruction.
ACR/ESUR/AdMeTech PI-RADS v2.1 assessment-category and management-scope text p 10; peripheral- and transition-zone matrices p 11; DCE definition/caveats pp 22-23.
4
High
High likelihood. In the peripheral zone, DWI/ADC score 4 maps to category 4, as does DWI/ADC score 3 with positive focal DCE. In the transition zone, T2W score 4 maps here, and T2W score 3 upgrades here only when DWI/ADC is 5. Score-4 morphology or diffusion restriction is under 15 mm unless definite extraprostatic extension is present.
Biopsy should be considered, but PI-RADS v2.1 does not make it mandatory and does not prescribe the biopsy strategy. Final management must incorporate laboratory and clinical history, local expertise, and standards of care.Clinically significant prostate cancer is likely to be present. The category is a qualitative imaging likelihood and should remain separate from patient-level pretest probability and management.
ACR/ESUR/AdMeTech PI-RADS v2.1 pp 10-11, 18, and 20-23; management-scope paragraph p 10 and zone matrices p 11.
5
Very high
Very high likelihood. In the peripheral zone, DWI/ADC score 5 determines category 5; in the transition zone, T2W score 5 determines category 5. The defining score-5 lesion is at least 15 mm in greatest dimension with score-4 features, or shows definite extraprostatic extension or invasive behavior.
Biopsy should be considered, but PI-RADS v2.1 does not make it mandatory and does not prescribe downstream treatment. Final management must incorporate laboratory and clinical history, local expertise, and standards of care.Clinically significant prostate cancer is highly likely to be present. This is the highest qualitative PI-RADS likelihood category, not a histopathologic diagnosis or a fixed percentage.
ACR/ESUR/AdMeTech PI-RADS v2.1 pp 10-11, 18, and 20-21; assessment-category meaning and management-scope paragraph p 10.

Referências cruzadas

fronteira compartilhadaBI-RADS. Breast Imaging Reporting and Data System, 5th editionShares the Reporting and Data System framework that BI-RADS established.

Histórico de versões

DataEventoDetalheSituação
2019-03-01revisedPI-RADS v2.1 published, updating v2 (2015). evidênciaconfirmado
Quickstart da APIGET /api/v1/systems/pi-rads-v2-1aberto
curl -s "https://radcommons.laudos.ai/api/v1/systems/pi-rads-v2-1"
Ver documentação completa
PI-RADS. Prostate Imaging Reporting and Data System v2.1. RadCommons