Ipilimumab for the treatment of advanced melanoma in six kidney transplant patients

被引:39
|
作者
Zehou, Ouidad [1 ]
Leibler, Claire [2 ]
Arnault, Jean-Philippe [3 ]
Sayegh, Johnny [4 ]
Montaudie, Henri [5 ,6 ]
Remy, Philippe [2 ]
Glotz, Denis [7 ]
Cordonnier, Carole [8 ]
Martin, Ludovic [9 ]
Lebbe, Celeste [10 ]
机构
[1] Henri Mondor Hosp, AP HP, Dept Dermatol, Creteil, France
[2] Henri Mondor Hosp, AP HP, Dept Nephrol & Transplantat, Creteil, France
[3] CHU Amiens Picardie, Dept Dermatol, Amiens, France
[4] CHU Angers, Dept Nephrol Dialysis & Transplantat, Angers, France
[5] Hop Archet 2, Dept Dermatol, Nice, France
[6] INSERM, Ctr Mediterraneen Med Mol, U1065, Nice, France
[7] St Louis Hosp, AP HP, Dept Nephrol & Transplantat, Paris, France
[8] CHU Amiens Picardie, Dept Pathol, Amiens, France
[9] CHU Angers, Dept Dermatol, Angers, France
[10] Univ Paris Diderot, St Louis Hosp, AP HP, Dermatol Dept,INSERM,U976, Paris, France
关键词
cancer/malignancy/neoplasia: melanoma; cancer/malignancy/neoplasia: metastatic disease; clinical research/practice; complication: malignant; dermatology; drug toxicity; hematology/oncology; immunosuppression/immune modulation; lymphocyte biology; PD-1 PATHWAY INHIBITOR; IMMUNE CHECKPOINT INHIBITORS; ALLOGRAFT-REJECTION; LIVER-TRANSPLANT; METASTATIC MELANOMA; THERAPY; ANTI-PD-1; FAILURE; RECIPIENTS; NIVOLUMAB;
D O I
10.1111/ajt.15071
中图分类号
R61 [外科手术学];
学科分类号
摘要
Immune checkpoint inhibitors are new therapeutic options for metastatic melanoma, but few data are available in organ transplant recipient populations. Six French patients, three men and three women, mean age 66 years (range 44-74), all kidney transplant recipients, received ipilimumab (CTLA-4 inhibitor) for metastatic melanoma. At diagnosis of advanced melanoma, immunosuppressive therapy had been minimized in all but one. Adverse effects included one case of grade 1 diarrhea and one of grade 1 pruritus. One patient had acute T cell-mediated rejection confirmed by histology after the first injection of ipilimumab. After a median follow-up of 4.5 (3-20) months, one patient achieved partial response, one had stable disease, and four had disease progression. All the patients died, five from melanoma, one from another cause. In this series and in the literature, ipilimumab proved to be safe and possibly active. The acute rejection we encountered was probably related to both a rapid, drastic reduction of immunosuppression and the use of ipilimumab. Our safety data on ipilimumab contrast with the organ transplant rejections already reported with PD-1 inhibitors. We consider that immunosuppression should not be minimized, as the impact on metastatic disease control is probably small.
引用
收藏
页码:3065 / 3071
页数:7
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