4.7 Article

Management of metastatic melanoma: improved survival in a national cohort following the approvals of checkpoint blockade immunotherapies and targeted therapies

期刊

CANCER IMMUNOLOGY IMMUNOTHERAPY
卷 67, 期 12, 页码 1833-1844

出版社

SPRINGER
DOI: 10.1007/s00262-018-2241-x

关键词

Melanoma; Metastasis; Immune checkpoint blockade; Targeted therapy; Immunotherapy

资金

  1. NATIONAL CANCER INSTITUTE [U24CA224331] Funding Source: NIH RePORTER
  2. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [T32HL007627] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM007205] Funding Source: NIH RePORTER

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BackgroundImmune checkpoint blockade (ICB) and BRAF(V600)-targeted therapy have demonstrated substantial clinical efficacy for patients with stage 4 melanoma in clinical trials; however, their impact on survival and barriers to treatment in the real-life setting remains unknown.MethodsPatients who presented with cutaneous melanoma during 2004-2015 using the National Cancer Database, which comprises>70% of all newly diagnosed cancers in the U.S., were evaluated for predictors of presenting with stage 4 disease and receiving ICB, and fortheir associated unadjusted and risk-adjusted overall survival (OS).Results17,975 patients presented with stage 4 metastatic cutaneous melanoma. Overall, patients who presented after the FDA's initial approvals (starting in 2011) for ICB and BRAF(V600)-targeted therapy demonstrated a 31% relative improvement in 4-year OS (p<0.001), compared to pre-2011. Following the initial approvals in 2011, improved OS was associated in risk-adjusted analyses with ICB (HR 0.57, 95CI 0.52-0.63). ICB demonstrated improved median and 4-year OS of 16.9 months (95CI 15.6-19.3; vs. 7.7months, 95CI 7.2-8.4) and 32.4% (95CI 29.5-35.3; vs. 21.0%, 95CI 19.6-22.2, all p<0.001), respectively; improved OS was persistent in unadjusted and risk-adjusted landmark survival analyses. Uninsured patients and management in the community setting were less likely to receive ICB in multivariable analyses.ConclusionsIn a national real-life treatment population, we show that the wide availability of the novel treatment modalities ICB and BRAF(V600)-targeted therapy has significantly improved the survival of patients with stage 4 melanoma. Our findings additionally suggest that there are opportunities for expanding coverage and access to these novel immunotherapies in community practice.

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