Toxicity management and efficacy of carboplatin desensitization therapy for recurrent epithelial ovarian carcinoma: A real-world study.

Epithelial Ovarian cancer (EOC) is the most lethal gynecologic cancer worldwide. Carboplatin (CP) is the main chemotherapeutic agent in the treatment of ovarian cancer. However, the development of a hypersensitivity reaction (HSR) in 10% to 15% of patients with EOC is an important limiting factor for the clinical use of CP. Herein, we aimed to investigate the efficacy and safety of CP-desensitization (CP-D) therapy in the treatment of recurrent patients with EOC. Forty-seven ovarian cancer cases treated with CP-desensitization at the Istanbul University Oncology Institute were retrospectively analyzed between 01.01.2017 and 01.01.2022. The decision for CP-D was based on the patients' history of HSR and/or a positive skin test. For all patients, a 6-hour 12-step rapid drug desensitization protocol with a 30-minutes premedication regimen was used. Forty-seven patients were included in this study, and the median age at diagnosis was 53 years (range; 27-80). Twenty-one (43.7%) patients had 1 or more comorbid diseases, and 12.7% had a previous history of drug allergy. On average, HSR due to carboplatin was identified after 9 (7-16) cycles, and carboplatin was administered n = 11 (range, 3-36) times to patients. The overall survival from the first desensitization procedure (0S2) was 42.2 months (range: 25.3-59.1), and the 1-, 2-, and 5-years survival rates were 92.6%, 75.6%, and 47.2%, respectively. The objective response rate (ORR) was 78.5%. Cumulatively, 496 CP-D procedures were performed, of which 478 (96.3%) were successfully completed. None of the patients included in this study developed severe (grade 3-4) HSR during CP administration (no adrenaline was used, no need for intensive care). No deaths due to CP-D were noted. CP-D is a beneficial and safe method in treating platinum-sensitive recurrent EOC patients with CP-induced HSR.

[1]  Rieko Kawase,et al.  Efficacy and Adverse Events of Carboplatin Desensitisation Therapy for Gynaecological Cancer: A Retrospective Study , 2022, Medicines.

[2]  S. Morita,et al.  4-step, 2-h carboplatin desensitization in Japanese patients with ovarian cancer: a prospective study , 2021, International Journal of Clinical Oncology.

[3]  D. Matei,et al.  Ovarian Cancer, Version 2.2020, NCCN Clinical Practice Guidelines in Oncology. , 2021, Journal of the National Comprehensive Cancer Network : JNCCN.

[4]  B. Monk,et al.  Ovarian cancer: new strategies and emerging targets for the treatment of patients with advanced disease , 2021, Cancer biology & therapy.

[5]  D. Hong,et al.  Does Carboplatin Rapid Desensitization Change Its Adverse Drug Reactions Other than Hypersensitivity and Efficacy in Patients With Ovarian Cancer? , 2020, Allergy, asthma & immunology research.

[6]  B. Monk,et al.  Treatment of patients with recurrent epithelial ovarian cancer for whom platinum is still an option. , 2019, Annals of oncology : official journal of the European Society for Medical Oncology.

[7]  Gloria S. Huang,et al.  Impact of carboplatin hypersensitivity and desensitization on patients with recurrent ovarian cancer , 2018, Journal of Cancer Research and Clinical Oncology.

[8]  D. Cohn,et al.  Outpatient desensitization in selected patients with platinum hypersensitivity reactions. , 2017, Gynecologic oncology.

[9]  E. Phillips,et al.  Carboplatin-allergic patients undergoing desensitization: prevalence and impact of the BRCA 1/2 mutation. , 2017, The journal of allergy and clinical immunology. In practice.

[10]  Henry C Kitchener,et al.  Ovarian cancer , 2014, The Lancet.

[11]  C. Sessa,et al.  Newly diagnosed and relapsed epithelial ovarian carcinoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. , 2018, Annals of oncology : official journal of the European Society for Medical Oncology.

[12]  P. Harter,et al.  Carboplatin Hypersensitivity: Does Introduction of Skin Test and Desensitization Reliably Predict and Avoid the Problem? A Prospective Single-Center Study , 2009, International Journal of Gynecologic Cancer.

[13]  E. Oren,et al.  Risk stratification for desensitization of patients with carboplatin hypersensitivity: clinical presentation and management. , 2009, The Journal of allergy and clinical immunology.

[14]  Jubilee Brown,et al.  Evaluation of the incidence of carboplatin hypersensitivity reactions in cancer patients. , 2006, Gynecologic oncology.

[15]  U. Matulonis,et al.  Carboplatin hypersensitivity: a 6-h 12-step protocol effective in 35 desensitizations in patients with gynecological malignancies and mast cell/IgE-mediated reactions. , 2004, Gynecologic oncology.

[16]  S. Sliesoraitis,et al.  Carboplatin hypersensitivity , 2004, International Journal of Gynecologic Cancer.

[17]  T. Bauknecht,et al.  A randomized clinical trial of cisplatin/paclitaxel versus carboplatin/paclitaxel as first-line treatment of ovarian cancer. , 2003, Journal of the National Cancer Institute.

[18]  Robert S Mannel,et al.  Phase III trial of carboplatin and paclitaxel compared with cisplatin and paclitaxel in patients with optimally resected stage III ovarian cancer: a Gynecologic Oncology Group study. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[19]  L. Rybicki,et al.  Carboplatin skin testing: a skin-testing protocol for predicting hypersensitivity to carboplatin chemotherapy. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[20]  P. Elson,et al.  Clinical features of hypersensitivity reactions to carboplatin. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[21]  E. Ratner,et al.  Platinum desensitization in patients with carboplatin hypersensitivity: A single-institution retrospective study. , 2017, Gynecologic oncology.