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Abstract Number: 363

Immune-Related Adverse Events in Cancer Immunotherapy: How Often Do We See Them?

Valeria Scaglioni1, Marina Scolnik1, Jose Maria Lastiri2, Lorena Lupinacci2 and Enrique R Soriano1, 1Rheumatology Unit, Internal Medicine Service. Hospital Italiano Buenos Aires. Argentina, Buenos Aires, Argentina, 2Oncology Service. Hospital Italiano Buenos Aires. Argentina, Buenos Aires, Argentina

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: Immune regulation, Immunotherapy and rheumatic disease

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Session Information

Date: Sunday, October 21, 2018

Title: Miscellaneous Rheumatic and Inflammatory Diseases Poster I: Checkpoint Inhibitors, Retroperitoneal Fibrosis

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: Over the years there has been a huge effort to change the traditional way to treat cancer, that was previously based on chemotherapy and/or radiotherapy. Enhancing the immune system with immunotherapy, instead of suppressing it, has achieved impressive results in some tumors, mainly metastatic melanoma, and nowadays several other tumors are been treated with it. Along with better results regarding tumor control, several immune-mediated adverse events have emerged

Methods: We included retrospectively all patients diagnosed with cancer that received immunotherapy (check point inhibitors) as part of their treatment between January 2014 and June 2018. Immunotherapy includes: monoclonal antibody to CTLA4 ipilimumab, IgG4 programmed death 1 (PD-1) inhibitor antibody nivolumab and pembrolizumab. There were no patients receiving IgG4 programmed death 1 ligand (PDL-1) inhibitor antibody atezolizumab, avelumab or durvalumab. We reported all immune-mediated adverse event (IMAE), time to first IMAE, treatment received, response to treatment, discontinuation of immunotherapy and deaths.

Results: Results: A total of 27 patients, (54.5% males) were included. Type of tumor, name of check point inhibitor received, type of IMAE, time to first IMAE, treatment and response are summarized in table 1. We observed a total of 11 (40.7%, CI 95% 23.2-60.9) IMAE. Incidence density rate was 120.9 (100 person-year). The most frequents were hematologic and dermatologic adverse events. Most of the IMAE were mild to moderate, 27.3% required treatment, with 66% of response. Among the rheumatologic related IMAE, there were only arthritis and Sicca syndrome, the last one been the most frequent and generally mild, with no need for treatment. 2 patients presented with arthritis, one of them required methotrexate because of persistent arthritis. No specific autoantibodies were found. Only 1 out of 5 patients with rheumatic IMAE was sent to a rheumatologist for treatment, all others were managed by oncologists. No patients were evaluated by a rheumatologist before started immunotherapy.

Conclusion: immune-mediated adverse events related to check point’s inhibitors are a new entity and oncologist and rheumatologist must be aware of them. Rheumatic IMAE had a frequency of 27.3%, with Sicca syndrome and seronegative arthritis as the only manifestations in our cohort.

TABLE 1. General Characteristics

IMAE

Age, mean (SD)

65.8 (10.66)

Male, n (%)

6 (54.5)

Type of tumor, n (%)

– Melanoma

– Lung

– Larynx

– Kidney

– NHL (non-Hodgkin lymphoma)

.

4 (14.8)

20 (74.1)

1 (3.7)

1 (3.7)

1 (3.7)

Check Point Inhibitor, n (%)

– Ipilimumab

– Nivolumab

– Ipilimumab + Nivolumab

– Pembrolizumab

.

1 (3.7)

14 (51.8)

6 (22.2)

6 (22.2)

Type of IMAE, n (%)

– Thyroiditis

– Pneumonitis

– Hematologic

– Dermatologic

– Arthritis

– Sicca Syndrome

– Pancreatitis

– Hepatitis

.

1 (9.1)

1 (9.1)

4 (36.4)

5 (45.4)

2 (18.2)

3 (27.3)

1 (9.1)

1 (9.1)

Time to onset to the 1st IMAE (years)

0.17

Incidence density rate, 100 person-year

120.9 (CI 95% 69.2-180.2)

% discontinuation of immunotherapy

27.3

Treatment required, n (%)

3 (27.3)

Response to treatment, n (%)

2 (66.7)

Deaths, n (%)

3 (27.3)

TABLE 2. Rheumatologic IMAE

N (%)

Pre-existent autoimmune disease

Fulfill criteria for specific rheumatic disease

Evaluation by rheumatologist n (%)

Use of steroids

n (%)

Use of synthetic DMARD n (%)

Use of biologic DMARD n (%)

Arthritis/arthralgia

2 (40)

0

0

1 (50)

1 (50)

1 (50)

0

Sicca Syndrome

3 (60)

0

0

0

0

0

0


Disclosure: V. Scaglioni, None; M. Scolnik, None; J. M. Lastiri, None; L. Lupinacci, None; E. R. Soriano, AbbVie, Bristol-Myers Squibb, GSK, Janssen, Novartis, Pfizer Inc, Roche, UCB, 2,AbbVie, Bristol-Myers Squibb, Eli Lilly, GSK, Janssen, Novartis, Pfizer Inc, Roche, Sanofi, UCB, 5,AbbVie, Bristol-Myers Squibb, Eli Lilly, Janssen, Novartis, Pfizer Inc, Roche, Sandoz, UCB, 8.

To cite this abstract in AMA style:

Scaglioni V, Scolnik M, Lastiri JM, Lupinacci L, Soriano ER. Immune-Related Adverse Events in Cancer Immunotherapy: How Often Do We See Them? [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/immune-related-adverse-events-in-cancer-immunotherapy-how-often-do-we-see-them/. Accessed .
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