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Immunotherapy With Programmed Cell Death 1 Inhibitors for 5 Patients With Conjunctival Melanoma.

Publication ,  Journal Article
Sagiv, O; Thakar, SD; Kandl, TJ; Ford, J; Sniegowski, MC; Hwu, W-J; Esmaeli, B
Published in: JAMA Ophthalmol
November 1, 2018

IMPORTANCE: Conjunctival melanoma has the potential for regional lymphatic and distant metastasis. There is an urgent need for effective treatment for patients with metastatic or locally advanced conjunctival melanoma. OBJECTIVE: To describe the use of immune checkpoint inhibitors for the treatment of conjunctival melanoma in 5 adult patients. DESIGN, SETTING, AND PARTICIPANTS: A retrospective review was conducted of the medical records of 5 patients with conjunctival melanoma who were treated with immune checkpoint inhibitors from March 6, 2013, to July 7, 2017. MAIN OUTCOMES AND MEASURES: Response to treatment and disease-free survival. RESULTS: Of the 5 patients (4 women and 1 man) with metastatic conjunctival melanoma, 4 were treated with a programmed cell death 1 (PD-1) inhibitor, nivolumab, and had a complete response to treatment with no evidence of disease at 1, 7, 9, and 36 months after completing treatment. One patient with metastatic conjunctival melanoma was treated with another PD-1 inhibitor, pembrolizumab, and had stable metastases during the first 6 months of treatment. Later disease progression resulted in treatment cessation after 11 months and switching to another therapy. Two patients treated with nivolumab developed autoimmune colitis that necessitated stopping the immunotherapy; these patients subsequently were managed with systemic corticosteroids or infliximab. CONCLUSIONS AND RELEVANCE: This case series report suggests that anti-PD-1 therapy can be used to treat metastatic conjunctival melanoma. Longer follow-up is needed to determine the long-term disease-free survival. Future studies might assess the potential for immune checkpoint inhibitors to obviate the need for orbital exenteration in selected patients with locally advanced disease.

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Published In

JAMA Ophthalmol

DOI

EISSN

2168-6173

Publication Date

November 1, 2018

Volume

136

Issue

11

Start / End Page

1236 / 1241

Location

United States

Related Subject Headings

  • Skin Neoplasms
  • Retrospective Studies
  • Programmed Cell Death 1 Receptor
  • Ophthalmology & Optometry
  • Nivolumab
  • Middle Aged
  • Melanoma
  • Male
  • Immunotherapy
  • Humans
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Sagiv, O., Thakar, S. D., Kandl, T. J., Ford, J., Sniegowski, M. C., Hwu, W.-J., & Esmaeli, B. (2018). Immunotherapy With Programmed Cell Death 1 Inhibitors for 5 Patients With Conjunctival Melanoma. JAMA Ophthalmol, 136(11), 1236–1241. https://doi.org/10.1001/jamaophthalmol.2018.3488
Sagiv, Oded, Sudip D. Thakar, Thomas J. Kandl, Joshua Ford, Matthew C. Sniegowski, Wen-Jen Hwu, and Bita Esmaeli. “Immunotherapy With Programmed Cell Death 1 Inhibitors for 5 Patients With Conjunctival Melanoma.JAMA Ophthalmol 136, no. 11 (November 1, 2018): 1236–41. https://doi.org/10.1001/jamaophthalmol.2018.3488.
Sagiv O, Thakar SD, Kandl TJ, Ford J, Sniegowski MC, Hwu W-J, et al. Immunotherapy With Programmed Cell Death 1 Inhibitors for 5 Patients With Conjunctival Melanoma. JAMA Ophthalmol. 2018 Nov 1;136(11):1236–41.
Sagiv, Oded, et al. “Immunotherapy With Programmed Cell Death 1 Inhibitors for 5 Patients With Conjunctival Melanoma.JAMA Ophthalmol, vol. 136, no. 11, Nov. 2018, pp. 1236–41. Pubmed, doi:10.1001/jamaophthalmol.2018.3488.
Sagiv O, Thakar SD, Kandl TJ, Ford J, Sniegowski MC, Hwu W-J, Esmaeli B. Immunotherapy With Programmed Cell Death 1 Inhibitors for 5 Patients With Conjunctival Melanoma. JAMA Ophthalmol. 2018 Nov 1;136(11):1236–1241.

Published In

JAMA Ophthalmol

DOI

EISSN

2168-6173

Publication Date

November 1, 2018

Volume

136

Issue

11

Start / End Page

1236 / 1241

Location

United States

Related Subject Headings

  • Skin Neoplasms
  • Retrospective Studies
  • Programmed Cell Death 1 Receptor
  • Ophthalmology & Optometry
  • Nivolumab
  • Middle Aged
  • Melanoma
  • Male
  • Immunotherapy
  • Humans