Opitz Isabelle, Lauk Olivia, Werner Raphael, Matter Alessandra, Hebeisen Monika, Battilana Bianca, Batirel Hasan, Pass Harvey, Flores Raja, Wolf Andrea, de Perrot Marc, Hoda Mir Alireza, Klepetko Walter, Klikovits Thomas, Hashimoto Masaki, Hasegawa Seiki, Richards William G, Bueno Raphael
Department of Thoracic Surgery, University Hospital Zurich, Zurich, Switzerland.
Department of Thoracic Surgery, University Hospital Zurich, Zurich, Switzerland.
Ann Thorac Surg. 2025 Jul;120(1):108-116. doi: 10.1016/j.athoracsur.2024.10.004. Epub 2024 Oct 22.
Pleural mesothelioma (PM) is a cancer with a usually dismal prognosis. However, long-term survivors do exist. Herein, we analyzed long-term survivors (>5 years after surgery) from high-volume centers around the world.
This is a multicenter retrospective descriptive analysis of long-term survivors (overall survival ≥5 years from surgery) treated within a multimodality therapy approach, including macroscopic complete resection. Overall survival was calculated with Kaplan-Meier analysis, and patients were matched by center and surgery year and compared with a control group of short-term survivors (<2 years) in a conditional logistic regression analysis.
There were 276 long-term survivors (166 men [63%]), with a median age of 59 years (range 21-83 years) at the time of diagnosis. The histology was epithelioid for 246 patients and nonepithelioid for 30 patients. The disease was on the right side in 58% of the patients. As of this analysis, 148 patients had died, 104 were alive, and 10 were lost to follow-up. Pathologic tumor stages were: pT1 (n = 50), pT2 (n = 63), pT3 (n = 90), or pT4 (n = 16) and pN0 (n = 150), pN1 (n = 20), and pN2 (n = 39). The matched control data set included 333 patients, 95 cases and 238 controls. Comparing short- with long-term survivors, we found moderate evidence that a low white blood cell count before surgery was more often observed in long-term survivors.
The data show that long-term survival in PM is possible in a subgroup of surgically treated patients. Histologic subtype and white blood cell count seem to be prognosticators for longer survival.
胸膜间皮瘤(PM)是一种预后通常较差的癌症。然而,长期存活者确实存在。在此,我们分析了来自世界各地大型医疗中心的长期存活者(术后超过5年)。
这是一项对采用多模式治疗方法(包括宏观完全切除)治疗的长期存活者(术后总生存期≥5年)进行的多中心回顾性描述性分析。采用Kaplan-Meier分析计算总生存期,并按中心和手术年份对患者进行匹配,在条件逻辑回归分析中与短期存活者(<2年)的对照组进行比较。
有276名长期存活者(166名男性[63%]),诊断时的中位年龄为59岁(范围21 - 83岁)。组织学类型为上皮样的患者有246例,非上皮样的有30例。58%的患者病变位于右侧。截至本次分析,148例患者已死亡,104例存活,10例失访。病理肿瘤分期为:pT1(n = 50)、pT2(n = 63)、pT3(n = 90)或pT4(n = 16)以及pN0(n = 150)、pN1(n = 20)和pN2(n = 39)。匹配的对照数据集包括333例患者,95例病例和238例对照。比较短期和长期存活者,我们发现有适度证据表明长期存活者术前白细胞计数较低的情况更为常见。
数据表明,在接受手术治疗的患者亚组中,PM患者有可能实现长期存活。组织学亚型和白细胞计数似乎是更长生存期的预后因素。