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DOI 10.1200/jco.23.02233

Медицинская библиотека · Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024

Final Results From a Phase I Trial and Expansion Cohorts of Cabozantinib and Nivolumab Alone or With Ipilimumab for Advanced/Metastatic Genitourinary Tumors.

Apolo Andrea B, Girardi Daniel M, Niglio Scot A, Nadal Rosa, Kydd Andre R, Simon Nicholas, Ley Lisa, Cordes Lisa M, Chandran Elias, Steinberg Seth M, Lee Sunmin, Lee Min-Jung, Rastogi Shraddha, Sato Nahoko, Cao Liang, Banday A Rouf, Boudjadi Salah, Merino Maria J, Toubaji Antoun, Akbulut Dilara, Redd Bernadette, Bagheri Hadi, Costello Rene, Gurram Sandeep, Agarwal Piyush K, Chalfin Heather J, Valera Vladimir, Streicher Howard, Wright John Joseph, Sharon Elad, Figg William D, Parnes Howard L, Gulley James L, Saraiya Biren, Pal Sumanta K, Quinn David, Stein Mark N, Lara Primo N, Bottaro Donald P, Mortazavi Amir

СтатьяКлиническое исследование I фазыМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

PURPOSE: Cabozantinib and nivolumab (CaboNivo) alone or with ipilimumab (CaboNivoIpi) have shown promising efficacy and safety in patients with metastatic urothelial carcinoma (mUC), metastatic renal cell carcinoma (mRCC), and rare genitourinary (GU) tumors in a dose-escalation phase I study. We report the final data analysis of the safety, overall response rate (ORR), progression-free survival (PFS), and overall survival (OS) of the phase I patients and seven expansion cohorts.

METHODS

This is an investigator-initiated, multicenter, phase I trial. CaboNivo doublet expansion cohorts included (1) mUC, (2) mRCC, and (3) adenocarcinoma of the bladder/urachal; CaboNivoIpi triplet expansion cohorts included (1) mUC, (2) mRCC, (3) penile cancer, and (4) squamous cell carcinoma of the bladder and other rare GU tumors (ClinicalTrials.gov identifier: NCT02496208).

RESULTS

The study enrolled 120 patients treated with CaboNivo (n = 64) or CaboNivoIpi (n = 56), with a median follow-up of 49.2 months. In 108 evaluable patients (CaboNivo n = 59; CaboNivoIpi n = 49), the ORR was 38% (complete response rate 11%) and the median duration of response was 20 months. The ORR was 42.4% for mUC, 62.5% for mRCC (n = 16), 85.7% for squamous cell carcinoma of the bladder (n = 7), 44.4% for penile cancer (n = 9), and 50.0% for renal medullary carcinoma (n = 2). Grade ≥ 3 treatment-related adverse events occurred in 84% of CaboNivo patients and 80% of CaboNivoIpi patients.

CONCLUSION

CaboNivo and CaboNivoIpi demonstrated clinical activity and safety in patients with multiple GU malignancies, especially clear cell RCC, urothelial carcinoma, and rare GU tumors such as squamous cell carcinoma of the bladder, small cell carcinoma of the bladder, adenocarcinoma of the bladder, renal medullary carcinoma, and penile cancer.

Для цитирования: Apolo Andrea B, Girardi Daniel M, Niglio Scot A, Nadal Rosa, Kydd Andre R, Simon Nicholas, Ley Lisa, Cordes Lisa M, Chandran Elias, Steinberg Seth M, Lee Sunmin, Lee Min-Jung, Rastogi Shraddha, Sato Nahoko, Cao Liang, Banday A Rouf, Boudjadi Salah, Merino Maria J, Toubaji Antoun, Akbulut Dilara, Redd Bernadette, Bagheri Hadi, Costello Rene, Gurram Sandeep, Agarwal Piyush K, Chalfin Heather J, Valera Vladimir, Streicher Howard, Wright John Joseph, Sharon Elad, Figg William D, Parnes Howard L, Gulley James L, Saraiya Biren, Pal Sumanta K, Quinn David, Stein Mark N, Lara Primo N, Bottaro Donald P, Mortazavi Amir. Final Results From a Phase I Trial and Expansion Cohorts of Cabozantinib and Nivolumab Alone or With Ipilimumab for Advanced/Metastatic Genitourinary Tumors.. Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 2024. DOI: 10.1200/jco.23.02233.

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