Department of Surgical Oncology, The Institute for Cancer Care, Mercy Medical Center, Baltimore, MD, USA.
Ann Surg Oncol. 2021 Dec;28(13):9126-9135. doi: 10.1245/s10434-021-10298-2. Epub 2021 Jul 15.
Peritoneal surface malignancies (PSM) can disseminate into the pleural cavity, increasing morbidity and mortality. While cytoreductive surgery with hyperthermic intraperitoneal chemoperfusion (CRS/HIPEC) improves outcomes for PSM with intra-abdominal spread, the optimal approach for patients with pleural dissemination from PSM remains unclear. It seems reasonable to apply peritoneal carcinomatosis management principles to patients with pleural lesions using CRS and hyperthermic intrathoracic chemotherapy (HITHOC).
We conducted a descriptive study to evaluate outcomes of PSM patients who underwent CRS/HITHOC for pleural dissemination using a high-volume PSM center's prospective database from October 1994-June 2020. CRS/HITHOC was performed via either diaphragmatic window during CRS/HIPEC (CRS/HIPEC+HITHOC) or thoracotomy as a separate procedure (CRS/HITHOC).
Of 852 completed CRS/HIPECs, 18 HITHOCs in 15 patients were identified: 10 CRS/HIPEC+HITHOCs, and 8 CRS/HITHOCs. CRS/HIPEC+HITHOC primary tumors included: 4 appendix, 4 ovary, 1 colon, and 1 unknown. All (n = 8) CRS/HITHOC patients had recurrent appendiceal neoplasms. Complete cytoreduction was achieved in 90% of CRS/HIPEC+HITHOCs and 75% of CRS/HITHOCs. Major complications occurred in 20% of CRS/HIPEC+HITHOCs and 13% of CRS/HITHOCs with no 30-day mortality in either group. After median follow-up of 22 months, overall survival at 1, 3, and 5 years was 93.3%, 67.9%, and 67.9%, while 1-, 3-, and 5-year progression-free survival was 70.9%, 20.3%, and 20.3%. Intrapleural recurrence occurred in 1 CRS/HIPEC+HITHOC and 2 CRS/HITHOC patients.
CRS/HITHOC performed via diaphragm or thoracotomy at high-volume centers is a safe option for PSM with pleural dissemination. Further comparative studies with longer follow-up are needed to evaluate survival by tumor type.
腹膜表面恶性肿瘤(PSM)可播散至胸腔,增加发病率和死亡率。虽然细胞减灭术联合腹腔内热灌注化疗(CRS/HIPEC)可改善腹膜内扩散的 PSM 患者的预后,但对于来自 PSM 的胸膜播散患者的最佳治疗方法仍不清楚。应用腹膜肿瘤转移治疗原则,对胸膜病变患者行 CRS 并给予胸腔内热化疗(HITHOC)似乎是合理的。
我们对 1994 年 10 月至 2020 年 6 月,高容量 PSM 中心前瞻性数据库中接受 CRS/HITHOC 治疗胸膜播散的 PSM 患者的结局进行了描述性研究。CRS/HITHOC 通过 CRS/HIPEC 期间的膈肌窗进行(CRS/HIPEC+HITHOC)或作为单独的手术进行(CRS/HITHOC)。
在 852 例完成的 CRS/HIPEC 中,确定了 15 例患者的 18 例 HITHOC:10 例 CRS/HIPEC+HITHOC 和 8 例 CRS/HITHOC。CRS/HIPEC+HITHOC 的主要肿瘤包括:4 例阑尾、4 例卵巢、1 例结肠和 1 例未知。所有(n=8)CRS/HITHOC 患者均为复发性阑尾肿瘤。90%的 CRS/HIPEC+HITHOC 和 75%的 CRS/HITHOC 达到完全肿瘤减灭。20%的 CRS/HIPEC+HITHOC 和 13%的 CRS/HITHOC 发生主要并发症,两组均无 30 天死亡率。中位随访 22 个月后,1、3 和 5 年的总生存率分别为 93.3%、67.9%和 67.9%,而 1、3 和 5 年无进展生存率分别为 70.9%、20.3%和 20.3%。1 例 CRS/HIPEC+HITHOC 和 2 例 CRS/HITHOC 患者出现胸膜内复发。
在高容量中心,通过膈肌或胸腔镜进行的 CRS/HITHOC 是 PSM 伴胸膜播散的安全选择。需要进一步进行比较研究,以评估不同肿瘤类型的生存情况,并进行更长期的随访。