TY - JOUR
T1 - Utility of PET/CT in assessing early treatment response in patients with newly diagnosed multiple myeloma
AU - Charalampous, Charalampos
AU - Goel, Utkarsh
AU - Broski, Stephen M.
AU - Dingli, David
AU - Kapoor, Prashant
AU - Gertz, Morie A.
AU - Lacy, Martha Q.
AU - Dispenzieri, Angela
AU - Hayman, Suzanne R.
AU - Buadi, Francis
AU - Hwa, Lisa
AU - Leung, Nelson
AU - Lin, Yi
AU - Gonsalves, Wilson I.
AU - Kourelis, Taxiarchis V.
AU - Warsame, Rahma
AU - Fonder, Amie
AU - Hobbs, Miriam
AU - Binder, Moritz
AU - Kyle, Robert A.
AU - Rajkumar, S. Vincent
AU - Kumar, Shaji K.
N1 - Publisher Copyright:
© 2022 by The American Society of Hematology.
PY - 2022/5/10
Y1 - 2022/5/10
N2 - Multiple myeloma (MM) is a plasma cell malignancy that is characterized by diverse clinical presentations. Although biochemical assessment of disease activity is commonly used to monitor treatment response, findings on magnetic resonance imaging and positron emission tomography (PET)/computed tomography (CT), among other imaging modalities, have proven to harbor prognostic value. We sought to corroborate these findings by examining the prognostic significance of fluorodeoxyglucose PET/CT scanning in the setting of newly diagnosed MM. We retrospectively analyzed 195 patients with a PET/CT available at diagnosis and at 6 months posttreatment to examine their value as an adjuvant metric to conventional hematologic responses in terms of time to next treatment (TTNT) and overall survival (OS). The median TTNT and OS for the entire cohort were 24.6 months (95% confidence interval [CI], 20.4-29.1) and 79 months (95% CI, 63.1-119.1), respectively. When comparing PET/CT negative (2) with PET/CT positive (1) patients, we found significantly prolonged median TTNT (55.2 vs 17.8 months, P, .0001) and OS (unreached vs 60.8 months, P, .0001) in the former group. We then examined the additive value of PET/CT on the hematologic response achieved at 6 months and found that PET/CT (2) is associated with significantly increased median TTNT and OS for the very good partial response (VGPR) group and the less than VGPR group. Importantly, PET/CT retained prognostic significance after adjusting for multiple other predictive variables. We conclude that a PET/CT (2) at 6 months confers a significant prognostic advantage for patients with newly diagnosed MM and adds significant value to the hematologic response assessment.
AB - Multiple myeloma (MM) is a plasma cell malignancy that is characterized by diverse clinical presentations. Although biochemical assessment of disease activity is commonly used to monitor treatment response, findings on magnetic resonance imaging and positron emission tomography (PET)/computed tomography (CT), among other imaging modalities, have proven to harbor prognostic value. We sought to corroborate these findings by examining the prognostic significance of fluorodeoxyglucose PET/CT scanning in the setting of newly diagnosed MM. We retrospectively analyzed 195 patients with a PET/CT available at diagnosis and at 6 months posttreatment to examine their value as an adjuvant metric to conventional hematologic responses in terms of time to next treatment (TTNT) and overall survival (OS). The median TTNT and OS for the entire cohort were 24.6 months (95% confidence interval [CI], 20.4-29.1) and 79 months (95% CI, 63.1-119.1), respectively. When comparing PET/CT negative (2) with PET/CT positive (1) patients, we found significantly prolonged median TTNT (55.2 vs 17.8 months, P, .0001) and OS (unreached vs 60.8 months, P, .0001) in the former group. We then examined the additive value of PET/CT on the hematologic response achieved at 6 months and found that PET/CT (2) is associated with significantly increased median TTNT and OS for the very good partial response (VGPR) group and the less than VGPR group. Importantly, PET/CT retained prognostic significance after adjusting for multiple other predictive variables. We conclude that a PET/CT (2) at 6 months confers a significant prognostic advantage for patients with newly diagnosed MM and adds significant value to the hematologic response assessment.
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U2 - 10.1182/bloodadvances.2022007052
DO - 10.1182/bloodadvances.2022007052
M3 - Article
C2 - 35235951
AN - SCOPUS:85130173291
SN - 2473-9529
VL - 6
SP - 2763
EP - 2772
JO - Blood advances
JF - Blood advances
IS - 9
ER -