دورية أكاديمية

Real-World Evidence of Systemic Therapy Sequencing on Overall Survival for Patients with Metastatic BRAF-Mutated Cutaneous Melanoma.

التفاصيل البيبلوغرافية
العنوان: Real-World Evidence of Systemic Therapy Sequencing on Overall Survival for Patients with Metastatic BRAF-Mutated Cutaneous Melanoma.
المؤلفون: Kartolo A; Department of Oncology, Queen's University, Kingston, ON K7L 2V7, Canada., Deluce J; Department of Oncology, University of Western Ontario, London, ON N6A 5W9, Canada., Hopman WM; Department of Public Health Sciences, Queen's University, Kingston, ON K7L 2V7, Canada., Liu L; Pulse Infoframe, London, ON N5X 4E7, Canada., Baetz T; Department of Oncology, Queen's University, Kingston, ON K7L 2V7, Canada., Ernst S; Department of Oncology, University of Western Ontario, London, ON N6A 5W9, Canada., Lenehan JG; Department of Oncology, University of Western Ontario, London, ON N6A 5W9, Canada.
المصدر: Current oncology (Toronto, Ont.) [Curr Oncol] 2022 Mar 01; Vol. 29 (3), pp. 1501-1513. Date of Electronic Publication: 2022 Mar 01.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 9502503 Publication Model: Electronic Cited Medium: Internet ISSN: 1718-7729 (Electronic) Linking ISSN: 11980052 NLM ISO Abbreviation: Curr Oncol Subsets: MEDLINE
أسماء مطبوعة: Publication: 2021- : Basel, Switzerland : MDPI
Original Publication: Toronto : Multimed, c1994-
مواضيع طبية MeSH: Melanoma*/drug therapy , Melanoma*/genetics , Melanoma*/pathology , Neoplasms, Second Primary* , Skin Neoplasms*/drug therapy , Skin Neoplasms*/genetics, Canada ; Humans ; Prospective Studies ; Proto-Oncogene Proteins B-raf/genetics ; Melanoma, Cutaneous Malignant
مستخلص: Aim: To evaluate optimal systemic therapy sequencing (first-line targeted therapy (1L-TT) vs. first-line immunotherapy (1L-IO)) in patients with BRAF-mutated metastatic melanoma. Methods: Nation-wide prospective data of patients with newly diagnosed BRAF-mutated metastatic melanoma were retrieved from the Canadian Melanoma Research Network. Results: Our study included 79 and 107 patients in the 1L-IO and 1L-TT groups, respectively. There were more patients with ECOG 0−1 (91% vs. 72%, p = 0.023) in the 1L-IO group compared to the 1L-TT group. Multivariable Cox analysis suggested no OS differences between the two groups (HR 0.838, 95%CI 0.502−1.400, p = 0.500). However, patients who received 1L-TT then 2L-IO had the longest OS compared to 1L-IO without 2L therapy, 1L-IO then 2L-TT, and 1L-TT without 2L therapy (38.3 vs. 32.2 vs. 16.9 vs. 6.3 months, p < 0.001). For patients who received 2L therapy, those who received 2L-IO had a trend towards OS improvement compared with the 2L-TT group (21.7 vs. 8.9 months, p = 0.053). Conclusions: Our nation-wide prospective study failed to establish any optimal systemic therapy sequencing in advanced BRAF-mutant melanoma patients. Nevertheless, we provided evidence that immunotherapy has durable efficacy in advanced BRAF-mutant melanoma patients, regardless of treatment line, and that Canadian medical oncologists were selecting the appropriate treatment sequences in a real-world setting, based on patients’ clinical and tumour characteristics.
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فهرسة مساهمة: Keywords: BRAF mutant; immunotherapy; melanoma; targeted therapy; therapy sequencing
المشرفين على المادة: EC 2.7.11.1 (BRAF protein, human)
EC 2.7.11.1 (Proto-Oncogene Proteins B-raf)
تواريخ الأحداث: Date Created: 20220324 Date Completed: 20220414 Latest Revision: 20231213
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC8947206
DOI: 10.3390/curroncol29030126
PMID: 35323326
قاعدة البيانات: MEDLINE
الوصف
تدمد:1718-7729
DOI:10.3390/curroncol29030126