Alessio Cortellini1,2, Melissa Bersanelli3, Sebastiano Buti3, Elisabetta Gambale4,5, Francesco Atzori6, Federica Zoratto7, Alessandro Parisi1,2, Davide Brocco4,5, Annagrazia Pireddu6, Katia Cannita1, Daniela Iacono8, Maria R Migliorino8, Teresa Gamucci7, Michele De Tursi4,5, Tina Sidoni1, Marcello Tiseo3, Maria Michiara3, Anselmo Papa9, Gesuino Angius9, Silverio Tomao10, Maria C Fargnoli11, Clara Natoli4,12, Corrado Ficorella1,2. 1. Medical Oncology Unit, St Salvatore Hospital, Department of Biotechnological & Applied Clinical Sciences, University of L'Aquila, Via Vetoio, 67100, L'Aquila, Italy. 2. Department of Biotechnological & Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy. 3. Medical Oncology Unit, University Hospital of Parma, Parma, Italy. 4. Medical Oncology Unit, SS Annunziata Hospita, Chieti, Italy. 5. Department of Medical, Oral & Biotechnological Sciences University G. D'Annunzio, Chieti-Pescara, Italy. 6. Medical Oncology Unit, University Hospital of Cagliari, Cagliari, Italy. 7. Medical Oncology Unit, F. Spaziani Hospital, Frosinone, Italy. 8. Pulmonary Oncology Unit, St. Camillo Forlanini Hospital, Rome, Italy. 9. Department of Medico-Surgical Sciences & Biotechnologies, University of Rome 'Sapienza', Latina, Italy. 10. Oncology Unit, Department of Radiological Sciences, Oncology & Pathology, University of Rome 'Sapienza', Latina, Italy. 11. Oncological Dermatology Unit, San Salvatore Hospital, University of L'Aquila, L'Aquila, Italy. 12. Department of Medical, Oral & Biotechnological Sciences & CeSI-MeT, University of Chieti-Pescara, Chieti and Pescara, Italy.
Abstract
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.
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 cancerpatients (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.
Entities:
Keywords:
family history of cancer; immunotherapy; multiple neoplasms
Authors: B Pellegrino; A Musolino; A Llop-Guevara; V Serra; P De Silva; Z Hlavata; D Sangiolo; K Willard-Gallo; C Solinas Journal: Transl Oncol Date: 2020-01-02 Impact factor: 4.243
Authors: Qian Qin; Tomi Jun; Bo Wang; Vaibhav G Patel; George Mellgard; Xiaobo Zhong; Mahalya Gogerly-Moragoda; Anish B Parikh; Amanda Leiter; Emily J Gallagher; Parissa Alerasool; Philip Garcia; Himanshu Joshi; Matthew Galsky; William K Oh; Che-Kai Tsao Journal: Discov Oncol Date: 2022-08-12