Khanmammadov Nijat, Ferhatoglu Ferhat, Paksoy Nail, Dogan İzzet, Khishigsuren Bayarmaa, Nizam Nihan, Saip Pinar, Aydiner Adnan
Department of Medical Oncology, Istanbul University Institute of Oncology, Istanbul, Turkey.
Medicine (Baltimore). 2025 Feb 7;104(6):e41404. doi: 10.1097/MD.0000000000041404.
Kaposi sarcoma (KS) is a rare angioproliferative malignancy linked to human herpesvirus 8 infection. While systemic therapy is often unnecessary for classic and iatrogenic KS, advanced cases may require chemotherapy. This study aims to evaluate the efficacy and safety of weekly paclitaxel or oral etoposide as second-line treatments for classical and iatrogenic Kaposi sarcoma. We retrospectively analyzed clinicopathological characteristics and treatment outcomes of 32 patients diagnosed with classical and iatrogenic KS at a tertiary cancer center between December 2000 and November 2022. Patients received oral etoposide (50 mg every 3 weeks for 10 days) or weekly paclitaxel (80 mg/m²). The cohort comprised 23 males (71.9%) and 9 females (28.1%), with a mean age of 63 years. Most patients (87.5%) had classical KS, while 12.5% had iatrogenic KS. The objective response rate (ORR) was 75%, with a disease control rate (DCR) of 87.5%. Median progression-free survival (PFS) was 32.1 months, and median overall survival (OS) was 110.2 months. No significant differences in PFS (P = .633) and OS (P = .456) were observed between paclitaxel and etoposide treatments. The treatment regimen was generally well tolerated. Severe hematological toxicities were less frequent, with febrile neutropenia in 1 patient (3.1%), while severe non-hematological side effects included neuropathy in 2 patients (6.2%). Two patients (6.2%) were hospitalized due to complications, with no treatment-related deaths. Weekly paclitaxel and oral etoposide regimens are effective and well-tolerated second-line treatments for classical and iatrogenic Kaposi sarcoma. Given the high ORR and DCR, these therapies represent viable options for patients who progress after initial treatment. Further studies with larger patient populations are needed to confirm these findings.
卡波西肉瘤(KS)是一种与人类疱疹病毒8感染相关的罕见血管增殖性恶性肿瘤。虽然经典型和医源性KS通常无需全身治疗,但晚期病例可能需要化疗。本研究旨在评估每周使用紫杉醇或口服依托泊苷作为经典型和医源性卡波西肉瘤二线治疗的疗效和安全性。我们回顾性分析了2000年12月至2022年11月期间在一家三级癌症中心确诊为经典型和医源性KS的32例患者的临床病理特征和治疗结果。患者接受口服依托泊苷(每3周50mg,共10天)或每周紫杉醇(80mg/m²)治疗。该队列包括23名男性(71.9%)和9名女性(28.1%),平均年龄为63岁。大多数患者(87.5%)为经典型KS,而12.5%为医源性KS。客观缓解率(ORR)为75%,疾病控制率(DCR)为87.5%。无进展生存期(PFS)中位数为32.1个月,总生存期(OS)中位数为110.2个月。紫杉醇和依托泊苷治疗之间在PFS(P = 0.633)和OS(P = 0.456)方面未观察到显著差异。该治疗方案总体耐受性良好。严重血液学毒性较少见,1例患者(3.1%)出现发热性中性粒细胞减少,而严重非血液学副作用包括2例患者(6.2%)出现神经病变。2例患者(6.2%)因并发症住院,无治疗相关死亡。每周紫杉醇和口服依托泊苷方案是经典型和医源性卡波西肉瘤有效的且耐受性良好的二线治疗方法。鉴于高ORR和DCR,这些疗法是初始治疗后病情进展患者的可行选择。需要更大患者群体的进一步研究来证实这些发现。