Family History of Cancer as Surrogate Predictor for Immunotherapy with Anti-Pd1/Pd-L1 Agents: Preliminary Report of the Fami-L1 Study
Author(s) -
Alessio Cortellini,
Melissa Bersanelli,
Sebastiano Buti,
Elisabetta Gambale,
Francesco Atzori,
Federica Zoratto,
Alessandro Parisi,
Davide Brocco,
Annagrazia Pireddu,
Katia Cannita,
Daniela Iacono,
Maria Rita Migliorino,
Teresa Gamucci,
Michele De Tursi,
Tina Sidoni,
Marcello Tiseo,
Maria Michiara,
Anselmo Papa,
Gesuino Angius,
Federica Tomao,
Maria Concetta Fargnoli,
Clara Natoli,
Corrado Ficorella
Publication year - 2018
Publication title -
immunotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.127
H-Index - 48
eISSN - 1750-7448
pISSN - 1750-743X
DOI - 10.2217/imt-2017-0167
Subject(s) - medicine , cancer , colorectal cancer , oncology , family history , immunotherapy , clinical trial , lung cancer , disease , surrogate endpoint
Aim: Tumors related to hereditary susceptibility seem to have an immunosensitive phenotype. Materials & methods: We conducted a multicenter retrospective study, to investigate if family history of cancer, multiple neoplasms and early onset of cancer could be related to clinical outcomes of anti-PD-1/PD-L1 therapy. Activity and efficacy data of 211 advanced cancer patients (kidney, non-small-cell lung cancer, melanoma, urothelium, colorectal and HeN), treated at seven Italian centers with anti-PD-1/PD-L1 agents, were analyzed. Results: In this preliminary report at multivariate analyses, positive family history of cancer showed a statistically significant relationship with a better objective response rate (p = 0.0024), disease control rate (p = 0.0161), median time to treatment failure (p = 0.0203) and median overall survival (p = 0.0221). Diagnosis of multiple neoplasms significantly correlates only to a better disease control rate, while interestingly non-early onset of cancer and sex (in favor of female patients) showed significant correlation with a better median overall survival (p = 0.0268 and p = 0.0272, respectively). Conclusion: This pilot study seems to individuate easily available patient's features as possible predictive surrogates of clinical benefit for anti-PD-1/PD-L1 treatments. These preliminary results need to be confirmed with a greater sample size, in prospective trials with immunotherapy.
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