Depth of metabolic response at interim PET and survival outcomes among patients with primary refractory and early relapsing diffuse large B-cell lymphoma (DLBCL).

Authors

null

Allison Marie Bock

Mayo Clinic, Rochester, MN

Allison Marie Bock , Raphael Mwangi , Fatemah Ataei , Matthew Thorpe , Matthew J. Maurer , Joshua Pritchett , Jacob Tyler Shreve , Jonas Paludo , Arushi Khurana , James Robert Cerhan , Thomas E. Witzig , Thomas Matthew Habermann , Yucai Wang , Jason R. Young , Grzegorz S. Nowakowski

Organizations

Mayo Clinic, Rochester, MN, Mayo Clinic, Jacksonville, FL, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, Division of Hematology, Mayo Clinic, Rochester, MN, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, Department of Radiology, Mayo Clinic, Rochester, MN

Research Funding

No funding received
None.

Background: Total metabolic tumor volume (TMTV) and maximum standardized uptake value (SUVmax) may improve upon standard 18F-fluorodeoxyglucose positron emission tomography/computed tomography (PET-CT)-based assessment of advanced DLBCL during treatment. We report the association of TMTV and SUVmax changes at interim PET-CT (PET2) on survival outcomes in patients with primary refractory DLBCL (prDLBCL) and early relapsing DLBCL (erDLBCL). Methods: Adult patients with prDLBCL (less than a complete response (CR) or progression by the end of treatment (EOT)) or erDLBCL (CR at EOT with relapse within 12 months) between 2005 and 2019 at Mayo Clinic Rochester were included. The % change (Δ) from baseline to PET2 (after 2 cycles of 1L therapy) of TMTV and SUVmax were measured. A PET segmentation threshold of 1.5 liver mean SUV + two standard deviations with a minimum volume constraint of 0.5 mL was utilized (MIM Software, Inc., Cleveland OH, USA) with manual input as needed. Functional splines analysis determined SUVmax and TMTV threshold for analysis. Results: 131 patients had complete PET-CT data (N=79 prDLBCL, N=52 erDLBCL). Baseline median TMTV and SUVmax were 767.4 cm3 (range 0.9-6840.4) and 20.5 (2.0-52.6), respectively. At a median follow up of 77.6 months, 81 patients had died. 2-year OS rate was 53% (95% CI: 42-67) for patients with a PET2 ΔSUVmax decline ≥65% compared to 15% (95% CI: 7-29) for patients with a PET2 ΔSUVmax decline <65%(p<0.001). PrDLBCL had a 2-year OS rate of 48% (95% CI: 31-74) for a ΔSUVmax ≥65% compared to 7% (95% CI: 2-21) for a ΔSUVmax <65%(p<0.001), which captured 58% of prDLBCL patients (N=46). Two-year OS rate was 43% (95% CI: 34-54) for patients with a ΔTMTV ≥75% compared to 5% (95% CI: 1-35) for patients with ΔTMTV <75% (p<0.001). All patients with a ΔTMTV <75% had prDLBCL. PrDLBCL had a 2-year OS rate of 28% (95% CI: 18-44) for a ΔTMTV ≥75%. The outcomes for ΔSUVmax <65% and ΔTMTV <75% at PET2 remained significant in a cox regression model adjusted for IPI and bulky disease (>10cm)(Table). Conclusions: A ΔTMTV decline <75% or a ΔSUVmax decline <65% at PET2 identified an ultra-high-risk subgroup of DLBCL with particularly poor outcomes, that captured a high percentage of prDLBCL patients, and was significant after adjusting for IPI and bulky baseline disease. These patients may benefit from clinical trials evaluating alternative PET-adapted treatment strategies, but further evaluation among all patients with DLBCL is needed.

Multivariate analysis of TMTV and SUVmax response at interim PET (PET2) on OS from time of relapse after 1L therapy, adjusted for baseline bulky disease and IPI.

PET2
Overall Survival (OS)
2-Year RateHR (95% CI)P-Value
ΔSUVmax >= 65%53%(reference)
ΔSUVmax < 65%15%3.58 (2.15-5.97)<0.001
ΔTMTV >= 75%43%(reference)
ΔTMTV < 75%5%2.97 (1.69 - 5.20)<0.001

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Abstract Details

Meeting

2023 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Hematologic Malignancies—Lymphoma and Chronic Lymphocytic Leukemia

Track

Hematologic Malignancies

Sub Track

Non-Hodgkin Lymphoma

Citation

J Clin Oncol 41, 2023 (suppl 16; abstr 7543)

DOI

10.1200/JCO.2023.41.16_suppl.7543

Abstract #

7543

Poster Bd #

94

Abstract Disclosures