Printed on 7/20/2026
For informational purposes only. This is not medical advice.
The Deauville 5-point score is a standardized PET response grading framework widely used in FDG-avid lymphoma. It anchors lesion uptake to physiologic reference uptake in mediastinum and liver, helping communicate metabolic response during and after therapy.
Formula: Ordinal 5-point PET uptake scale referenced to mediastinum and liver background uptake.
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The Deauville score is assigned after FDG-PET-CT imaging, typically performed at interim staging (after 2–4 cycles of chemotherapy) or at end-of-treatment. The nuclear medicine physician or radiologist reviews each residual lesion and assesses the intensity of FDG uptake compared to physiologic reference organs. A minimum uptake fasting period of 4–6 hours is required, and blood glucose must be controlled, as hyperglycemia reduces FDG uptake and causes false-negative results. The scan timing after chemotherapy also matters — too early (within 10 days) may show false-negative results from treatment-related stunning; too late may allow viable tumor to reduce uptake. Most protocols recommend interim PET at 2–4 cycles and end-of-treatment PET ≥3 weeks after last chemotherapy.
The Deauville scale uses two reference organs to standardize assessment: (1) Mediastinal blood pool: the FDG uptake in the mediastinal vessels (typically the aorta or superior vena cava), which defines the lower boundary. Uptake ≤ mediastinum = score 1–2. (2) Liver parenchyma: the normal hepatic FDG background, which defines the upper reference. Uptake between mediastinum and liver = score 3; uptake moderately above liver = score 4; markedly above liver or new lesions = score 5. The liver is chosen as the upper reference because it has higher baseline FDG uptake than blood pool and serves as a more sensitive discriminator for residual disease. Assign the score based on the hottest residual lesion in the previously involved lymphoma sites.
Apply the Deauville score within the appropriate clinical protocol: Scores 1–2 (complete metabolic response, CMR): No residual uptake or minimal uptake ≤ mediastinum. Excellent prognosis. In Hodgkin lymphoma ABVD trials, score ≤2 at interim PET supports de-escalation or continuation. Scores 3: Uptake above mediastinum but ≤ liver. Treated as CMR in most Hodgkin lymphoma trials (RAPID, RATHL), allowing bleomycin omission. In DLBCL (per Lugano), score 3 may be classified as partial response (PR) or CMR depending on protocol. Scores 4–5 (partial or no response): Indicates significant residual metabolic activity. In Hodgkin lymphoma: escalation to BEACOPP or addition of radiotherapy is typically recommended. In DLBCL: indicates treatment failure; salvage chemotherapy (R-ICE, R-DHAP) and stem cell transplant planning may be initiated. Score X: New areas of FDG uptake not related to lymphoma (e.g., infection, inflammation, secondary malignancy) — requires separate clinical management.
Hematologic oncologists and lymphoma specialists
Apply Deauville scoring to interim PET-CT (typically after 2 cycles of ABVD) in classical Hodgkin lymphoma to guide treatment adaptation. The RATHL trial (NEJM 2016) demonstrated that Deauville ≤3 at interim PET safely permits omission of bleomycin from subsequent ABVD cycles, reducing pulmonary toxicity without compromising outcomes. The RAPID trial showed that Deauville ≤3 at interim PET could support omission of consolidation radiotherapy in early-stage favorable disease. Use Deauville score to present findings at multidisciplinary tumor board and document treatment modification rationale in the medical record.
Medical oncologists treating diffuse large B-cell lymphoma
Use Deauville scoring as part of the Lugano Classification (2014) for end-of-treatment PET assessment in diffuse large B-cell lymphoma (DLBCL). A Deauville score of 1–2 represents complete metabolic response (CMR) and is associated with excellent long-term outcomes. Score 3 requires clinical judgment — some protocols classify as CMR, others as PR. Scores 4–5 indicate treatment failure and should prompt early discussion of salvage therapy (R-ICE or R-DHAP) and autologous stem cell transplant planning. End-of-treatment PET should be performed ≥6 weeks after completion of R-CHOP.
Clinical research oncologists and trial coordinators
Deauville score is the standard response endpoint in modern lymphoma clinical trials, replacing older IHP (International Harmonization Project) criteria. Trials require independent central radiology review with Deauville scoring for complete metabolic response (CMR) determination, progression-free survival (PFS), and event-free survival (EFS) endpoints. Ensure PET-CT protocols comply with EANM guidelines (minimum scanner standards, fasting requirements, acquisition parameters) to ensure Deauville scores are valid and reproducible across sites. Document Deauville scores with supporting images in the trial case report form.
Cellular therapy oncologists
Assess metabolic response after CD19-directed CAR-T cell therapy (axicabtagene ciloleucel, tisagenlecleucel, lisocabtagene maraleucel) using Deauville scoring at day 30 and day 90 post-infusion. Deauville-based CMR (score 1–3) at day 30 is associated with durable remission in relapsed/refractory DLBCL. Score 4–5 at day 30–90 indicates treatment failure and should prompt assessment for consolidation strategies. Be aware that early post-CAR-T PET (within 2–4 weeks) may show inflammatory uptake from cytokine release syndrome (CRS) — correlation with clinical context and serial imaging is essential.
Hematologic oncologists and radiation oncologists
Use Deauville score to support treatment de-escalation (reducing toxicity) or escalation (improving disease control) decisions in lymphoma management. In early-stage favorable Hodgkin lymphoma, Deauville ≤2 after 2 cycles supports consideration of 2 additional cycles ABVD alone without radiotherapy (HD17 trial approach). Deauville 4–5 supports escalation to BEACOPP intensified or addition of consolidation ISRT (involved-site radiotherapy). For DLBCL, score 3–5 at end of treatment supports clinical trial enrollment for consolidation strategies or salvage immunotherapy. Present Deauville-based decisions at weekly tumor board with PET imaging review.
Radiology, nuclear medicine, and oncology teams
Standardize PET response reporting using Deauville score to improve communication between nuclear medicine, radiology, and oncology. When reporting lymphoma PET studies, always include: (1) the reference organ comparisons (mediastinum, liver), (2) the assigned Deauville score for each previously involved site and overall, (3) any score X areas requiring separate clinical correlation, and (4) the clinical context (interim vs end-of-treatment, lymphoma subtype, treatment regimen). This format ensures oncologists have actionable information for treatment decisions and aligns with Lugano Classification reporting standards.
Unlike older response criteria that used SUVmax thresholds, Deauville scoring is based on visual comparison of lesion uptake to reference organs (mediastinum and liver). This makes it reproducible across different scanner types and protocols without requiring standardized uptake value (SUV) calculations. The key reference boundaries are: uptake ≤ mediastinum (scores 1–2), uptake between mediastinum and liver (score 3), moderately above liver (score 4), markedly above liver or new lesions (score 5). Always compare visually at the same window/level settings as the reference organs.
The most important protocol-specific distinction: in most Hodgkin lymphoma clinical trials (RAPID, RATHL, HD17), Deauville score 3 is treated as 'negative' (equivalent to CMR) and supports de-escalation. In DLBCL (Lugano Classification), score 3 at end-of-treatment is ambiguous — it may represent CMR or partial response depending on the clinical context. When score 3 is the determining factor for treatment decisions, discuss with the multidisciplinary team and consider correlation with CT morphology (size reduction) to guide classification.
A Deauville score of 4–5 at interim or end-of-treatment PET indicates persistent significant metabolic activity and should prompt treatment escalation rather than watchful waiting. In Hodgkin lymphoma (interim PET positive): switch from ABVD to escalated BEACOPP or add radiotherapy. In DLBCL (end-of-treatment positive): consider salvage chemotherapy (R-ICE, R-DHAP) with intent for autologous stem cell transplant if the patient is eligible. Early escalation based on interim PET positivity has been validated in multiple randomized trials and reduces the risk of relapse.
Granulocyte colony-stimulating factor (G-CSF, filgrastim, pegfilgrastim) administered after chemotherapy stimulates bone marrow FDG uptake, which can appear markedly increased (score 5) in the axial skeleton and spleen on PET-CT. This is a false-positive pattern that can mimic marrow involvement or relapse. To avoid misinterpretation: (1) note G-CSF use before PET acquisition, (2) recognize symmetric diffuse marrow uptake as G-CSF effect vs focal asymmetric uptake suggesting true marrow disease, (3) ideally, perform PET ≥3 weeks after last G-CSF. When in doubt, biopsy the suspicious site before escalating treatment.
The distinction between Deauville scores 3 and 4 hinges on whether lesion uptake is at/below liver or moderately above liver. This is the boundary where inter-reader variability is highest (κ 0.61–0.73). To standardize: draw a region of interest (ROI) in normal liver parenchyma (avoiding biliary structures, hemangiomas, or metastatic areas) and compare visually. SUV ratios (lesion SUVmax / liver SUVmean) can provide objective support — most centers use a ratio >1.0 as score ≥3 and ratio >2.0 as score ≥4 — but visual assessment remains the standard per consensus criteria.
Deauville PET response should always be correlated with CT findings (size change) per Lugano Classification. A residual mass that is FDG-negative (Deauville 1–3) but large on CT (>2 cm) may represent fibrotic scar tissue (common in Hodgkin lymphoma) — this is still CMR by PET criteria. A residual mass that shows Deauville 4–5 uptake but is also growing on CT represents progressive disease. When PET and CT findings are discordant (e.g., new uptake in area without CT change), consider biopsy to confirm disease vs inflammatory cause.
PET-CT timing relative to chemotherapy completion significantly affects Deauville score accuracy. For end-of-treatment PET: recommended ≥6 weeks after last R-CHOP in DLBCL, ≥3 weeks after last ABVD in Hodgkin lymphoma. PET performed too early (within 2 weeks of chemotherapy) can show false-negative results due to metabolic stunning of viable tumor cells, or false-positive results from treatment-related inflammatory changes. After radiotherapy, wait ≥3 months to reduce radiation pneumonitis or esophagitis causing false-positive uptake. Document the date of last treatment and date of PET in all reports.
Deauville score X is assigned when PET reveals new areas of FDG uptake that are not related to lymphoma — for example, a new FDG-avid lung nodule (possible primary lung cancer or infection), colonic hypermetabolism (possible colon cancer or inflammatory bowel disease), or FDG-avid lymphadenopathy in a non-lymphoma distribution. Score X does not affect the lymphoma response assessment but requires separate clinical investigation. Always highlight score X findings prominently in the PET report and recommend biopsy or clinical follow-up as appropriate.
The Deauville 5-point scale superseded the IHP criteria (published 2007) for lymphoma PET response assessment. IHP used liver as the only reference organ and lacked the mediastinum anchor, making it less reproducible. Lugano Classification (2014) formally adopted Deauville as the standard for all FDG-avid lymphomas. When reviewing older trial data or reports, be aware that IHP 'complete response' (CR) criteria may differ slightly from Lugano CMR — context matters for longitudinal comparison.
Reported inter-reader agreement for Deauville scoring has a kappa (κ) of approximately 0.61–0.73, which is 'substantial' but not 'near-perfect.' The most common source of disagreement is the score 3/4 boundary (is lesion uptake at or moderately above liver?). For high-stakes clinical decisions (treatment escalation in positive interim PET, CMR determination for clinical trial enrollment), consider independent review by two experienced nuclear medicine readers and consensus interpretation. Many academic centers also use central radiology review for trial patients.
Deauville criteria were consensus-defined at a meeting in Deauville, France (2009) and published by Barrington et al. (J Nucl Med 2010). Validated in Hodgkin lymphoma: RAPID trial (Radford et al., NEJM 2015) used Deauville ≤3 for RT omission. RATHL trial (Johnson et al., NEJM 2016) used score 1–3 for bleomycin omission. Lugano Classification 2014 (Cheson et al., J Clin Oncol 2014) incorporated Deauville as standard response criteria for lymphoma. Inter-rater κ 0.61–0.73.
Higher Deauville scores indicate higher relative metabolic activity and may reflect poorer treatment response depending on timing and lymphoma subtype.
Use in FDG-avid lymphoma response assessment when PET-CT findings are being standardized for treatment decisions or multidisciplinary discussion.
Deauville scoring is semi-quantitative and observer dependent. False-positive uptake from inflammation or infection can reduce specificity.
Disclaimer: This tool is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider with questions about your health.
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