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Case Reports
. 2018 Nov 19;6(1):122.
doi: 10.1186/s40425-018-0437-4.

Kaposi's varicelliform eruption in a patient with metastatic melanoma and primary cutaneous anaplastic large cell lymphoma treated with talimogene laherparepvec and nivolumab

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Case Reports

Kaposi's varicelliform eruption in a patient with metastatic melanoma and primary cutaneous anaplastic large cell lymphoma treated with talimogene laherparepvec and nivolumab

David M Miller et al. J Immunother Cancer. .

Abstract

Background: Immune-directed therapies have become front-line therapy for melanoma and are transforming the management of advanced disease. In refractory cases, multi-modal immunoncology (IO) approaches are being utilized, including combining immune checkpoint blockade (ICB) with oncolytic herpes viruses. Talimogene laherparepvec (T-VEC) is the first genetically modified oncolytic viral therapy (OVT) approved for the treatment of recurrent and unresectable melanoma. The use of IO in patients with concomitant malignancies and/or compromised immune systems is limited due to systematic exclusion from clinical trials. For example, a single case report of a solid organ transplant patient successfully treated with T-VEC for metastatic melanoma has been reported. Furthermore, the use of ICB in T-cell malignancies is limited and paradoxical worsening has been described. To our knowledge, this is the first report of dual ICB/T-VEC being administered to a patient with concurrent primary cutaneous anaplastic large cell lymphoma (pcALCL) and melanoma.

Case presentation: Here we present the case of a patient with concomitant primary cutaneous ALCL and metastatic melanoma, progressing on anti-programmed death (PD)-1 therapy, who developed Kaposi's varicelliform eruption after receiving the first dose of Talimogene laherparepvec.

Conclusion: This case highlights the complexities of care of patients with coexistent cancers, demonstrates rapid progression of primary cutaneous ALCL on nivolumab and introduces a novel adverse effect of Talimogene laherparepvec.

Keywords: Anaplastic large cell lymphoma; Immunocompromised; Kaposi varicelliform eruption; Melanoma; Talimogene laherparepvec; eczema TVECium.

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Conflict of interest statement

Ethics approval and consent to participate

Patient described in this case signed a case report informed consent form, which is available for review.

Consent for publication

Patient consented to publication of the case report.

Competing interests

The authors declare that they have no competing interests.

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Figures

Fig. 1
Fig. 1
Timeline of the patient’s clinical course. A time reference has been included, with Day 0 referring to the day of the diagnosis of pcALCL. C1D1, cycle 1 day 1; c/f, concerning for; Dx:, diagnosis; Gy, gray; Hosp adm, hospital admission; KVE, kaposi’s varicelliform eruption; pcALCL, primary cutaneous anaplastic large cell lymphoma; R-Benda, rituximab-bendamustine; T-VEC, Talimogene laherparepvec; WBC, white blood cell count; WLE, wide-local excision; XRT, radiotherapy
Fig. 2
Fig. 2
Progression of the patient’s primary cutaneous anaplastic large cell lymphoma. The patient’s lesions prior to nivolumab treatment (a-c); on treatment (d-h), with corresponding cycle days denoted in the white box on the bottom of each insert
Fig. 3
Fig. 3
Kaposi’s varicelliform eruption. Scattered 2–3 mm eroded and crusted papules on the bilateral upper arms and trunk. Lesions are concentrated on the right upper arm and trunk
Fig. 4
Fig. 4
Tzanck smear from a vesicle on the right arm. Under medium power, multinucleated giant cells with viral cytopathic effects, including nuclear molding, are seen

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References

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