Treatment strategies for post-epidermal growth factor receptor () tyrosine kinase inhibitor (TKI) therapy in -mutant non-small cell lung cancer (NSCLC) is an ongoing challenge. Previously, the IMPRESS trial comparing platinum doublet chemotherapy with or without -TKI did not demonstrate any progression-free survival (PFS) benefit. The retrospective subgroup analysis of IMpower150 indicated that the quad regimen (carboplatin, paclitaxel, bevacizumab, atezolizumab) improved PFS and overall survival (OS) in patients with -mutant NSCLC who progressed on first-generation -TKIs. Given the retrospective nature of the analysis, the IMpower150 regimen is not approved in the US for post--TKI treatment. Currently, osimertinib or other third-generation (3G) -TKIs is the first-line standard of care for advanced -mutant NSCLC. MARIPOSA-2 provided the first randomized trial post-osimertinib in -mutant NSCLC patients with another quad regimen (platinum, pemetrexed, lazertinib, amivantamab). The IMpower150 and MARIPOSA-2 quad regimens differ in the principle of whether to continue or even "double-down" on inhibition. Recently, three prospective randomized trials conducted in Asia offered promising results, showing that a quad regimen of doublet platinum chemotherapy plus anti-angiogenesis agent and ICI may be as efficacious as MARIPOSA-2 with a lower rate of toxicities and accounting for the PFS difference if 1L chemotherapy plus osimertinib instead of osimertinib monotherapy. In particular, the median PFS achieved by the quad regimens of ATTLAS and IMpower151 is 8.5 months. However, only 8.2% and 17.9% of the -mutant NSCLC patients who received the quad regimens progressed on 3G -TKI, respectively. Here, we discuss how the results of IMpower151 and ATTLAS may rejuvenate interest in a non- containing quad regimen as a potential post-osimertinib monotherapy treatment. Randomized trials comparing the results of these studies, including the quad regimen of MARIPOSA-2 versus the quad regimen of IMpower151/Impower150/ATTLAS in post-osimertinib (or other 3G -TKI) progression, are urgently needed.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11137922 | PMC |
http://dx.doi.org/10.2147/LCTT.S460870 | DOI Listing |
Case Rep Oncol Med
October 2024
Radiation Oncology Unit College of Medicine King Saud University, Riyadh, Saudi Arabia.
Eur J Haematol
October 2024
Bone Marrow Transplant Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Introduction: Triple- and quad-refractory multiple myeloma patients usually have an aggressive course and a poor prognosis. Available therapeutic options are scarce.
Methods: The objective of the current study was to evaluate responses and toxicities of VDTPACE or mCBAD with hematopoietic stem-cell support as a bridge to subsequent therapies in patients with refractory/relapsed multiple myeloma.
Lung Cancer (Auckl)
May 2024
Division of Hematology-Oncology, Department of Medicine, Chao Family Comprehensive Cancer Center, University of California Irvine School of Medicine, Orange, California, USA.
Head Neck
June 2024
Department of Radiation Oncology, Tata Medical Center, Kolkata, West Bengal, India.
Background: This study assessed a palliative radiotherapy regimen using daily radiation over 4 days for three courses in inoperable head and neck cancers, emphasizing oral primary cancers.
Methods: Retrospective data of 116 patients treated with a daily dose of 3.6-3.
Oral Oncol
April 2024
Department of Radiation Oncology, Faculty of Life Sciences, Kumamoto University, 1-1-1 Honjo, Chuo-ku, Kumamoto 860-8556, Japan. Electronic address:
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