Anti-PD-1 Monoclonal Antibodies (mAbs) Are Superior to Anti-PD-L1 mAbs When Combined with Chemotherapy in First-Line Treatment for Metastatic Non-Small Cell Lung Cancer (mNSCLC): A Network Meta-Analysis.

anti-PD-1 anti-PD-L1 chemoimmunotherapy immunotherapy non-small cell lung cancer

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
26 Jun 2023
Historique:
received: 15 05 2023
revised: 16 06 2023
accepted: 21 06 2023
medline: 29 7 2023
pubmed: 29 7 2023
entrez: 29 7 2023
Statut: epublish

Résumé

Platinum-based chemotherapy combined with anti-PD-1 or PD-L1 monoclonal antibodies (mAbs) is now standard first-line therapy for mNSCLC patients without sensitizing driver mutations. Anti-PD-1 and anti-PD-L1 mAbs are considered to be equivalent in efficacy. In the absence of head-to-head randomized control trials (RCTs), we utilized network meta-analysis (NWM) to provide an indirect comparison of their efficacy. A systematic literature review and NWM were performed using RCTs that investigated anti-PD-1 or PD-L1 mAbs ± chemotherapy in patients with mNSCLC in the first-line setting. The primary outcome was comparative overall survival (OS), while secondary outcomes were comparative progression-free survival (PFS), objective response rate (ORR), and rate of grade 3 and higher toxicities. We identified 24 RCTs. Patients treated with anti-PD-1 mAb + chemotherapy compared with anti-PD-L1 mAb + chemotherapy showed superior mOS, mPFS, and ORR with a similar rate of grade 3 and higher toxicities. This difference in mOS was most pronounced in the PD-L1 TPS 1-49% population. The two mAbs were equivalent as single agents. Anti-PD-1 mAb + chemotherapy improved mOS when compared to anti-PD-1 mAb monotherapy, whereas anti-PD-L1 mAbs + chemotherapy did not when compared to anti-PD-L1 mAb monotherapy. Head-to-head RCTs are warranted in the future.

Identifiants

pubmed: 37509467
pii: biomedicines11071827
doi: 10.3390/biomedicines11071827
pmc: PMC10376908
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Joe Q Wei (JQ)

Royal North Shore Hospital, St Leonards, NSW 2065, Australia.
Northern Clinical School, University of Sydney, St Leonards, NSW 2065, Australia.

Alexander Yuile (A)

Royal North Shore Hospital, St Leonards, NSW 2065, Australia.
Northern Clinical School, University of Sydney, St Leonards, NSW 2065, Australia.

Malinda Itchins (M)

Royal North Shore Hospital, St Leonards, NSW 2065, Australia.
Northern Clinical School, University of Sydney, St Leonards, NSW 2065, Australia.

Benjamin Y Kong (BY)

Royal North Shore Hospital, St Leonards, NSW 2065, Australia.
Northern Clinical School, University of Sydney, St Leonards, NSW 2065, Australia.

Bob T Li (BT)

Memorial Sloan Kettering Cancer Centre, Weill Cornell Medical College, New York, NY 10065, USA.

Nick Pavlakis (N)

Royal North Shore Hospital, St Leonards, NSW 2065, Australia.
Northern Clinical School, University of Sydney, St Leonards, NSW 2065, Australia.

David L Chan (DL)

Royal North Shore Hospital, St Leonards, NSW 2065, Australia.
Northern Clinical School, University of Sydney, St Leonards, NSW 2065, Australia.

Stephen J Clarke (SJ)

Royal North Shore Hospital, St Leonards, NSW 2065, Australia.
Northern Clinical School, University of Sydney, St Leonards, NSW 2065, Australia.

Classifications MeSH