Survival improvement in patients with medullary thyroid carcinoma who undergo pretargeted anti-carcinoembryonic-antigen radioimmunotherapy:: A collaborative study with the French Endocrine Tumor Group

被引:137
作者
Chatal, JF
Campion, L
Kraeber-Bodéré, F
Bardet, S
Vuillez, JP
Charbonnel, B
Rohmer, V
Chang, CH
Sharkey, RM
Goldenberg, DM
Barbet, J
机构
[1] Univ Nantes, INSERM, U601, Res Unit, F-44093 Nantes 1, France
[2] Inst Reg Canc, Dept Nucl Med, Nantes, France
[3] Univ Hosp, Dept Endocrinol, Nantes, France
[4] Ctr Francois Baclesse, Dept Nucl Med, F-14021 Caen, France
[5] Univ Hosp, Dept Nucl Med, Grenoble, France
[6] Univ Hosp, Dept Endocrinol, Angers, France
[7] IBC Pharmaceut Inc, Morris Plains, NJ USA
[8] Immunomedics Inc, Morris Plains, NJ USA
[9] Garden State Canc Ctr, Ctr Mol Med & Immunol, Belleville, NJ USA
关键词
D O I
10.1200/JCO.2005.04.4917
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose No effective therapy is currently available for the management of patients with metastatic medullary thyroid carcinoma (MTC). The efficacy of pretargeted radioimmunotherapy (pBAIT) with bispecific monoclonal antibody (BsMAb) and a iodine-131 (I-131) -labeled bivalent hapten is evaluated. Patients and Methods Twenty-nine patients with advanced, progressive MTC, as documented by short serum calcitonin doubling times (Ct DTs), received an anti-carcinoembryonic antigen (CEA)/anti-diethylenetriamine pentaacetic acid (DTPA) -indium BsMAb, followed 4 days later by a I-131-labeled bivalent hapten. Overall survival (OS) was compared with 39 contemporaneous untreated MTC patients with comparable prognostic indicators. Results OS was significantly longer in high-risk, treated patients (Ct DT < 2 years) than in high-risk, untreated patients (median OS, 110 v 61 months; P <.030). Forty-seven percent of patients, defined as biologic responders by a more than 100% increase in CtDT, experienced significantly longer survival than nonresponders (median OS, 159 v 109 months; P <.035) and untreated patients (median OS, 159 v 61 months; P <.010). Treated patients with bone/bone-marrow disease had a longer survival than patients without such involvement (10-year OS, 83% v 14%; P <.023). Toxicity was mainly hematologic and related to bone/bone-marrow tumor spread. Conclusion pRAIT against CEA induced long-term disease stabilization and a significantly longer survival in high-risk patients with Ct DTs less than 2 years, compared with similarly high-risk, untreated patients. Ct DT and bone-marrow involvement appear to be prognostic indicators in MTC patients who undergo pRAIT.
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收藏
页码:1705 / 1711
页数:7
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