Author:
Metzenmacher Martin,Griesinger Frank,Hummel Horst-Dieter,Elender Corinna,Schäfer Harald,de Wit Maike,Kaiser Ulrich,Kern Jens,Jänicke Martina,Spring Lisa,Zacharias Stefan,Kaiser-Osterhues Anja,Groth Annika,Hipper Annette,Zaun Gregor,Dörfel Steffen,Güldenzoph Björn,Müller Lothar,Uhlig Jens,Thomas Michael,Sebastian Martin,Eberhardt Wilfried E.E.
Abstract
IntroductionUnderstanding prognosis, especially long-term outcome, in advanced nonsmall cell lung cancer (NSCLC) is crucial to inform patients, guide treatment and plan supportive and palliative care.MethodsPrognostic factors influencing overall survival (OS) and progression-free survival (PFS) in 2082 patients with wild-type (WT)-NSCLC (629 M1a, 249 M1b, 1204 M1c) are reported. Patients were included in the prospective German CRISP registry recruiting in >150 centres. Analysis for pre-therapeutic factors was based on results from Cox proportional hazard models.ResultsCurrent M-descriptors of the Union for International Cancer Control-8 staging system were validated: M1a and M1b patients had significantly longer median time to events compared to M1c (OS/PFS 16.4/7.2 months, 17.8/6.7 months and 10.9/5.4 months, respectively). OS and PFS were influenced by number and location of metastatic organ systems. M1c and four or more metastatic organs involved had shorter OS and PFS than M1c with one to three organs (OS hazard ratio (HR) 1.69, p<0.001; PFS HR 1.81, p<0.001). M1b-liver metastases had shorter OS/PFS than M1b involving other organs (OS HR 2.70, p=0.006; PFS HR 2.48, p=0.007). Based on number of involved organs (orgsys) and liver metastases, two risk groups (low-risk: M1a, M1b-non-liver, M1c-1-3-orgsys-non-liver; high-risk: M1c-liver, M1b-liver, M1c-4+-orgsys) with significantly different prognoses could be amalgamated (median OS/PFS 14.3/6.5 months and 7.7/4.1 months, respectively). Other favourable factors were female gender and Eastern Cooperative Oncology Group stage 0, with age showing no impact. Those with T1- or N0-status were associated with longer OS than T2–4 or N2–3.ConclusionIn this large observational dataset, we further defined factors for outcome in WT-NSCLC, including increased number of involved metastatic organ systems and liver metastases, as those with overall poorer prognosis and reduced survival chance.
Funder
Novartis
Takeda Pharmaceutical Company
Bristol-Myers Squibb
Boehringer Ingelheim
Merck Sharp and Dohme
Roche
Janssen-Cilag
AstraZeneca
Eli Lilly and Company
Pfizer
Amgen
Celgene
Publisher
European Respiratory Society (ERS)
Subject
Pulmonary and Respiratory Medicine