Di Pietro Francesca Romana, Marinelli Daniele, Verkhovskaia Sofia, Poti Giulia, Falcone Rosa, Carbone Maria Luigia, Morelli Maria Francesca, Zappalà Albina Rita, Di Rocco Zorika Christiana, Morese Roberto, Piesco Gabriele, Chesi Paolo, Marchetti Paolo, Failla Cristina Maria, De Galitiis Federica
Department of Oncology and Dermatological Oncology, IDI-IRCCS, Rome, Italy.
Department of Experimental Medicine, Sapienza University, Rome, Italy.
BMC Cancer. 2024 Oct 1;24(1):1220. doi: 10.1186/s12885-024-12961-9.
Immunotherapy with anti-PD-1 antibodies significantly improved the prognosis in advanced melanoma patients, but most of them develop primary or secondary resistance to the treatment. In this study, we evaluated efficacy and safety of a chemotherapy regimen with weekly carboplatin plus paclitaxel (wCP) in patients previously treated with anti-PD-1 antibodies. We retrospectively identified 30 patients with advanced melanoma treated at our Institute over the last eight years with wCP. The co-primary endpoints of the study were overall survival (OS) and progression-free survival (PFS). In addition, we evaluated treatment tolerability. For this patient cohort, median PFS and OS were 3.25 and 7.69 months, respectively. All included patients had previously received anti-PD-1 immunotherapy, most of them had ECOG PS 0-1, and only 5 patients had a BRAF V600 mutation. In univariable analysis, we observed shorter OS in patients with > 2 involved metastatic sites, superficial spreading histology, and serum lactate dehydrogenase (LDH) values above the median. Liver metastases were associated with worse outcomes, while radiotherapy treatment of brain metastases was associated with improved OS. However, in a multivariable Cox regression model, only LDH above the median, superficial spreading histology, and female sex were significantly associated with worse OS. We reported grade 3 and 4 treatment-related toxicities in 4 and 0 patients, respectively. In conclusion, chemotherapy with wCP is a valid palliative treatment in advanced melanoma who progressed with anti-PD-1 antibodies.
抗程序性死亡蛋白1(PD-1)抗体免疫疗法显著改善了晚期黑色素瘤患者的预后,但其中大多数患者会对该治疗产生原发性或继发性耐药。在本研究中,我们评估了每周使用卡铂联合紫杉醇(wCP)的化疗方案对先前接受过抗PD-1抗体治疗的患者的疗效和安全性。我们回顾性确定了过去八年在我院接受wCP治疗的30例晚期黑色素瘤患者。该研究的共同主要终点为总生存期(OS)和无进展生存期(PFS)。此外,我们评估了治疗耐受性。对于该患者队列,中位PFS和OS分别为3.25个月和7.69个月。所有纳入患者均先前接受过抗PD-1免疫治疗,其中大多数患者东部肿瘤协作组(ECOG)体能状态评分为0-1,只有5例患者存在BRAF V600突变。在单变量分析中,我们观察到转移部位>2个、浅表扩散组织学类型以及血清乳酸脱氢酶(LDH)值高于中位数的患者OS较短。肝转移与较差的预后相关,而脑转移的放射治疗与OS改善相关。然而,在多变量Cox回归模型中,只有LDH高于中位数、浅表扩散组织学类型以及女性与较差的OS显著相关。我们分别报告了4例和0例3级和4级治疗相关毒性反应。总之,对于因抗PD-1抗体治疗进展的晚期黑色素瘤患者,wCP化疗是一种有效的姑息治疗方法。