Heery Christopher R, Madan Ravi A, Stein Mark N, Stadler Walter M, Di Paola Robert S, Rauckhorst Myrna, Steinberg Seth M, Marté Jennifer L, Chen Clara C, Grenga Italia, Donahue Renee N, Jochems Caroline, Dahut William L, Schlom Jeffrey, Gulley James L
Laboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Genitourinary Malignancies Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Oncotarget. 2016 Oct 18;7(42):69014-69023. doi: 10.18632/oncotarget.10883.
PSA-TRICOM is a therapeutic vaccine in late stage clinical testing in metastatic castration-resistant prostate cancer (mCRPC). Samarium-153-ethylene diamine tetramethylene phosphonate (Sm-153-EDTMP; Quadramet®), a radiopharmaceutical, binds osteoblastic bone lesions and emits beta particles causing local tumor cell destruction. Preclinically, Sm-153-EDTMP alters tumor cell phenotype facilitating immune-mediated killing. This phase 2 multi-center trial randomized patients to Sm-153-EDTMP alone or with PSA-TRICOM vaccine. Eligibility required mCRPC, bone metastases, prior docetaxel and no visceral disease. The primary endpoint was the proportion of patients without radiographic disease progression at 4 months. Secondary endpoints included progression-free survival (PFS), overall survival (OS), and immune responses. Forty-four patients enrolled. Eighteen and 21 patients were evaluable for the primary endpoint in Sm-153-EDTMP alone and combination arms, respectively. There was no statistical difference in the primary endpoint, with two of 18 (11.1%) and five of 21 (23.8%) in Sm-153-EDTMP alone and combination arms, respectively, having stable disease at approximately the 4-month evaluation time point (P = 0.27). Median PFS was 1.7 vs. 3.7 months in the Sm-153-EDTMP alone and combination arms (P = 0.041, HR = 0.51, P = 0.046). No patient in the Sm-153-EDTMP alone arm achieved prostate-specific antigen (PSA) decline > 30% compared with four patients (of 21) in the combination arm, including three with PSA decline > 50%. Toxicities were similar between arms and related to number of Sm-153-EDTMP doses administered. These results provide the rationale for clinical evaluation of new radiopharmaceuticals, such as Ra-223, in combination with PSA-TRICOM.
PSA-TRICOM是一种用于转移性去势抵抗性前列腺癌(mCRPC)晚期临床试验的治疗性疫苗。放射性药物钐-153-乙二胺四亚甲基膦酸盐(Sm-153-EDTMP;Quadramet®)可结合成骨性骨病变并发射β粒子,导致局部肿瘤细胞破坏。临床前研究表明,Sm-153-EDTMP可改变肿瘤细胞表型,促进免疫介导的杀伤作用。这项2期多中心试验将患者随机分为单独使用Sm-153-EDTMP或联合使用PSA-TRICOM疫苗两组。入选标准为mCRPC、骨转移、既往接受过多西他赛治疗且无内脏疾病。主要终点是4个月时无影像学疾病进展的患者比例。次要终点包括无进展生存期(PFS)、总生存期(OS)和免疫反应。44名患者入组。单独使用Sm-153-EDTMP组和联合使用组分别有18名和21名患者可评估主要终点。主要终点无统计学差异,单独使用Sm-153-EDTMP组18名患者中有2名(11.1%)、联合使用组21名患者中有5名(23.8%)在大约4个月评估时间点病情稳定(P = 0.27)。单独使用Sm-153-EDTMP组和联合使用组的中位PFS分别为1.7个月和3.7个月(P = 0.041,HR = 0.51,P = 0.046)。单独使用Sm-153-EDTMP组没有患者的前列腺特异性抗原(PSA)下降> 30%,而联合使用组21名患者中有4名(包括3名PSA下降> 50%)。两组的毒性相似,且与Sm-153-EDTMP给药剂量有关。这些结果为评估新型放射性药物(如Ra-223)与PSA-TRICOM联合使用的临床效果提供了理论依据。