Department of Medical Oncology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, 3-18-22 Hon-komagome, Bunkyo-ku, Tokyo, 113-8677, Japan.
Department of Clinical Research Support, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.
BMC Cancer. 2022 Jun 11;22(1):640. doi: 10.1186/s12885-022-09734-7.
Synchronous multiple primary malignant tumors (sMPMTs) are sometimes diagnosed in patients with malignant lymphoma. We herein investigated the prognostic impact of sMPMT in lymphoma patients and the optimal treatment strategy.
Seventy-five patients with sMPMTs (5.8%) among 1285 patients with lymphoma newly diagnosed between August 2004 and April 2020 were enrolled.
In patients with indolent lymphoma, those with sMPMTs had a worse prognosis than those without sMPMTs (5-year overall survival [OS]: 73.4% and 87.8%, respectively; P = 0.047). Among those with high and low tumor burden, the cumulative rate of death due to solid tumors was significantly higher in patients with sMPMTs than those without sMPMTs (high tumor burden: 26.7% vs. 1.6%, P < 0.001; low tumor burden: 12.7% vs. 1.0%, P = 0.003). The presence of sMPMTs did not have a significant impact on outcomes in patients with diffuse large B-cell lymphoma (DLBCL) (5-year OS: 65.4% and 66.9%, respectively; P = 0.74; 5-year progression-free survival [PFS]: 65.5% and 59.9%, respectively; P = 0.65). However, the cumulative rate of death from solid tumor in patients with sMPMTs was significantly higher than in patients without sMPMTs (5-year cumulative rate: 7.4% and 2.1%, respectively; P = 0.004). The treatment sequence did not have a significant effect on outcomes or the relative dose intensity of chemotherapy.
In patients with indolent lymphoma, those with sMPMTs had a significantly worse prognosis than those without sMPMTs, mainly because of high mortality due to solid tumors. The presence of sMPMTs was not a significant prognostic factor in patients with DLBCL. It is important to assess the status and need for early treatment of each type of malignancy in patients with sMPMTs.
同步性多原发恶性肿瘤(sMPMT)有时会在恶性淋巴瘤患者中被诊断出来。本研究旨在探讨 sMPMT 对淋巴瘤患者的预后影响以及最佳治疗策略。
纳入 2004 年 8 月至 2020 年 4 月期间新诊断的 1285 例淋巴瘤患者中 75 例(5.8%)sMPMT 患者。
在惰性淋巴瘤患者中,sMPMT 患者的预后明显差于无 sMPMT 患者(5 年总生存[OS]率:73.4%和 87.8%;P=0.047)。在高肿瘤负荷和低肿瘤负荷患者中,sMPMT 患者死于实体瘤的累积率明显高于无 sMPMT 患者(高肿瘤负荷:26.7%比 1.6%,P<0.001;低肿瘤负荷:12.7%比 1.0%,P=0.003)。sMPMT 对弥漫性大 B 细胞淋巴瘤(DLBCL)患者的结局无显著影响(5 年 OS 率:分别为 65.4%和 66.9%;P=0.74;5 年无进展生存[PFS]率:分别为 65.5%和 59.9%;P=0.65)。然而,sMPMT 患者死于实体瘤的累积率明显高于无 sMPMT 患者(5 年累积率:分别为 7.4%和 2.1%;P=0.004)。治疗顺序对结局或化疗的相对剂量强度无显著影响。
在惰性淋巴瘤患者中,sMPMT 患者的预后明显差于无 sMPMT 患者,主要是因为实体瘤死亡率较高。sMPMT 对 DLBCL 患者的预后不是一个显著的预后因素。重要的是要评估 sMPMT 患者每种恶性肿瘤的状态和治疗需求。