BACKGROUND. The severity of myelotoxicity after radioimmunotherapy has
been predicted from body and blood radiation doses to marrow. However
, marrow radiation can be increased substantially if the marrow or ske
leton contains the malignancy targeted by the radiolabeled monoclonal
antibodies. A study of 29 patients treated with iodine-131 (I-131)-Lym
-1 showed that radiation doses to marrow from body and blood had littl
e correlation with myelotoxicity. The purpose of the present study was
to assess the significance of marrow targeting and other factors for
prediction of myelotoxicity. METHODS. Injected radioactivity and nonta
rgeted radiation doses to marrow were compared with peripheral blood c
ell counts after the first therapy dose of I-131-Lym-1 in 16 heavily p
retreated patients with non-Hodgkin's lymphoma (NHL). Bone marrow biop
sy, targeted marrow radiation doses, marrow image uptake scores, age,
Kamofsky performance score (KPS), previous chemotherapy, and tumor bur
den were also compared with blood counts. RESULTS. Myelotoxicity was n
ot predicted well by injected radioactivity, total body radiation, or
body and blood radiation doses contributed to marrow (P > 0.1). Biopsy
-proven bone marrow lymphoma also failed to predict myelotoxicity (P >
0.1). Thrombocytopenia and leukopenia were predicted well by targeted
radiation dose to marrow (P < 0.05) obtained by I-131 imaging. Simila
rly, marrow image scores predicted decreases in platelets and white bl
ood cells (WBCs; P < 0.05). Prediction of myelotoxicity using marrow r
adiation dose methods was slightly improved when serum lactic dehydrog
enase (LDH), age, KPS, and prior chemotherapy were included in the ana
lysis (P less than or equal to 0.01). CONCLUSIONS. Prediction of myelo
toxicity was improved in this group of patients by assessment of the t
argeting component of marrow radiation and was better predicted and ob
tained more easily by semiquantitative marrow image scores. Further im
provement in prediction was slight when other factors were considered.
(C) 1997 American Cancer Society.