The role of dacarbazine and temozolomide therapy after treatment with immune checkpoint inhibitors in malignant melanoma patients: A case series and meta-analysis Show others and affiliations
2024 (English) In: Pigment Cell & Melanoma Research, E-ISSN 1755-148X, Vol. 37, no 3, p. 352-362Article in journal (Refereed) Published
Abstract [en]
Dacarbazine (DTIC) and its oral counterpart temozolomide (TMZ) have been the most used agents in advanced malignant melanoma (MM) patients and they are still used routinely. The preferred first line treatment, immune checkpoint inhibitors (CPIs) might shape the tumor and the tumor microenvironment, possibly affecting the response to subsequent therapies. The aim of this study was to investigate the treatment effect of DTIC/TMZ in MM patients after CPI therapy in a consecutive patient cohort and through systematic literature review and meta-analysis. Thirty-five patients with advanced MM treated with DTIC/TMZ after previous CPI therapy in three Swedish regions between 2017 and 2021 were recognized and seven case series studies were identified through systematic database review. Pooled data from all 345 patients showed a median real-world progression-free survival (rwPFS) of 1.9 months and overall survival (OS) of 6.0 months. Three of these studies were included in a meta-analysis comparing DTIC/TMZ after CPI treatment, versus no previous immunotherapy, showing no statistically significant differences in rwPFS or OS but higher real-world response rate to chemotherapy for the prior-CPI treated group (Odds Ratio: 2.24; 95% Confidence Interval: 1.04-4.86). The current study supports consideration of DTIC/TMZ in later line of treatment in the immunotherapy era.
Place, publisher, year, edition, pages John Wiley & Sons, 2024. Vol. 37, no 3, p. 352-362
Keywords [en]
Dacarbazine, Temozolomide, immune checkpoint inhibitors, malignant melanoma, meta-analysis
National Category
Cancer and Oncology
Identifiers URN: urn:nbn:se:oru:diva-110617 DOI: 10.1111/pcmr.13156 ISI: 001133714300001 PubMedID: 38158376 Scopus ID: 2-s2.0-85180832000 OAI: oai:DiVA.org:oru-110617 DiVA, id: diva2:1825255
Funder Stiftelsen Onkologiska Klinikens i Uppsala Forskningsfond
Note This study was supported by grants to G.J. Ullenhag and V. Rydén from The Research Foundation Stiftelsen Onkologiska Klinikens i Uppsala Forskningsfond and Uppsala University Hospital (ALF).
2024-01-092024-01-092024-05-02 Bibliographically approved