Marenco-Hillembrand Lina, Bamimore Michael A, Rosado-Philippi Julio, Perdikis Blake, Abarbanel David N, Quinones-Hinojosa Alfredo, Chaichana Kaisorn L, Sherman Wendy J
Department of Neurological Surgery, Mayo Clinic, Jacksonville, FL 32224, USA.
Department of Neurological Surgery, Cooper University Hospital, Camden, NJ 08103, USA.
Cancers (Basel). 2023 Jan 22;15(3):685. doi: 10.3390/cancers15030685.
Leptomeningeal carcinomatosis (LMC) is a fatal but uncommon complication occurring in 5-15% of patients with stage IV cancer. Current treatment options are ineffective at managing leptomeningeal spread, with a median overall survival (mOS) of 2-6 months. We aimed to conduct a systematic review of the literature to identify past and future therapies for LMC from solid tumors. Forty-three clinical trials (CTs) published between 1982-2022 were identified. Of these, 35 (81.4%) were non-randomized CTs and 8 (18.6%) were randomized CTs. The majority consisted of phase I (16.3%) and phase II CTs (65.1%). Trials enrolled patients with LMC from various primary histology (n = 23, 57.5%), with one CT evaluating LCM from melanoma (2.4%). A total of 21 trials evaluated a single modality treatment. Among CTs, 23.7% closed due to low accrual. Intraventricular (ITV)/intrathecal (IT) drug delivery was the most common route of administration (n = 22, 51.2%) vs. systemic drug delivery (n = 13, 30.3%). Two clinical trials evaluated the use of craniospinal irradiation for LMC with favorable results. LMC continues to carry a dismal prognosis, and over the years, increments in survival have remained stagnant. A paradigm shift towards targeted systemic therapy with continued standardization of efficacy endpoints will help to shed light on promising treatments.
软脑膜癌病(LMC)是一种致命但不常见的并发症,发生在5%-15%的IV期癌症患者中。目前的治疗方案在控制软脑膜扩散方面效果不佳,中位总生存期(mOS)为2-6个月。我们旨在对文献进行系统综述,以确定过去和未来针对实体瘤LMC的治疗方法。共确定了1982年至2022年期间发表的43项临床试验(CT)。其中,35项(81.4%)为非随机CT,8项(18.6%)为随机CT。大多数试验为I期(16.3%)和II期CT(65.1%)。试验纳入了来自各种原发性组织学的LMC患者(n = 23,57.5%),其中一项CT评估了黑色素瘤的LCM(2.4%)。共有21项试验评估了单一模式治疗。在CT中,23.7%因入组率低而终止。脑室内(ITV)/鞘内(IT)给药是最常见的给药途径(n = 22,51.2%),而全身给药(n = 13,30.3%)。两项临床试验评估了颅脊髓照射治疗LMC的效果,结果良好。LMC的预后仍然很差,多年来,生存率的提高一直停滞不前。向靶向全身治疗的模式转变以及疗效终点的持续标准化将有助于揭示有前景的治疗方法。