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Abstract Number: 847

Safety of TNF Inhibitor Therapy in Patients Who Have Had a Prior Malignancy

Seung-Hyeon Bae, Doo-Ho Lim, Soo Min Ahn, Seokchan Hong, Yong-Gil Kim, Chang-Keun Lee and Bin Yoo, Division of Rheumatology, Department of Internal Medicine, University of Ulsan College of Medicine, Asan Medical Center, Seoul, South Korea

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Anti-TNF therapy and cancer

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Session Information

Title: Rheumatoid Arthritis - Small Molecules, Biologics and Gene Therapy I: Safety of Biologics and Small Molecules in Rheumatoid Arthritis - Malignancy and Infection

Session Type: Abstract Submissions (ACR)

Background/Purpose

A few is known about the effects of biologic therapy in patients with a history of a solid cancer. According to the 2012 updated American College of Rheumatology Recommendations, it is possible to start or resume any biologic agent in patients who have been treated for solid tumor (level of evidence C). But, there is no evidence in patients with history of a solid cancer within the past 5 years because of the lack of studies examining the risk of recurrent cancer in this subgroup. The purpose of this study was to explore the influence of TNF inhibitor (TNFi) therapy in patients with prior cancer treatment within the past 5 years.

Methods

The medical records of all patients (n=859) that received TNFi therapy at a single rheumatology clinic between June 2005 and May 2014 were retrospectively reviewed. Among them, data from patients who had a history of solid cancer treatment before TNFi therapy were collected and patient outcomes were evaluated especially for those who have been treated cancer within the last 5 years.

Results

Of 859 patients who underwent TNFi therapy, 22 patients (1 on infliximab, 11 on etanercept, 7 on adlimumab and 3 on golimumab) had a history of malignancy before initiating TNFi therapy for ankylosing spondylitis (AS) and rheumatoid arthritis (RA) (Table 1). The median AS, RA disease duration was 8 (3.75-12.25) years and median time to TNFi therapy after prior cancer treatment was 62.5 (21.25-140.25) months. Most common site of prior cancer is stomach (36.4%) and followed by thyroid, colorectum, liver, kidney, and breast. There was no recurrence of previous cancer during 40 (7.0-50.75) months of TNFi therapy. Especially, 10 patients started TNFi therapy before 5 years prior cancer treatment (Table 2). All of our 10 cases were limited in an early stage without distant metastasis. When they have been followed for 36 months, recurrence of cancer was not found.

Conclusion

Our results suggest that starting TNFi therapy in patients with history of solid cancer in locally limited stage is safe even less than 5 years after prior cancer treatment.

Table 1. Clinical characteristics of patients with prior cancer history when starting TNFi

characteristics

patients(n=22)

Age, mean(range), years

63 (41-81)

Sex, female, n (%)

15 (68.2)

Diagnosis, n (%)

AS

8 (36.4)

RA

14 (63.6)

Disease duration of AS and RA, median(IQR), years

8 (3.75-12.25)

Time to TNFi therapy after prior cancer treatment , median(IQR), month 

62.5 (21.25-140.25)

TNFi, n (%)

infliximab

1 (4.5)

etanercept

11 (50)

adalimumab

7 (31.8)

golimumab

3 (13.6)

Site of prior cancer, n (%)

stomach

8 (36.4)

colon,rectum

2 (9.1)

gallblader

1 (4.5)

liver

2 (9.1)

kidney

2 (9.1)

breast

2 (9.1)

skin (non melanoma)

1 (4.5)

cervix

1 (4.5)

thyroid

3 (13.6)

Duration of TNFi use, median(IQR), month

40.0 (7.0-50.75)

Incidence of cancer recur, n (%)

0 (0)

AS: ankylosing  spondylitis, RA: rheumatoid arthritis, IQR: interquartile range, TNFi: TNF inhibitor

Table 2. clinical characteristics of 10 patients  who starting TNFi less than 5 years after prior cancer treatment

Age,years
/sex

diagnosis

site of
prior cancer

type/
staging

treatment

time to TNFi therapy
after prior cancer
treatment, month

TNF inhibitor

duration of
TNFi use, month

cancer recur

60/F

RA

liver

HCC
T1N0M0

surgical resection

1

A

75

No

41/F

RA

stomach

MALToma
low grade

H.pyrori
eradication

42

A

64

No

73/F

RA

thyroid

PTC
T3N0M0

surgical resection,
RAI

8

G

7

No

78/F

RA

skin

BCC

surgical resection

2

E

45

No

44/M

AS

stomach

AGC
T2N0M0

surgical resection,
adjuvant chemo

22

E

213

No

62/F

AS

kidney

RCC
T1N0M0

surgical resection

47

E

56

No

72/M

RA

stomach

AGC

(?)

surgical resection

47

E

7

No

51/M

AS

stomach

AGC
T2N1M0

surgical resection

19

A

27

No

67/F

RA

thyroid

PTC
T1N0M0

surgical resection,
RAI

18

I

7

No

63/F

AS

colon

colon cancer
T2N1M0

surgical resection,
adjuvant chemo

36

G

6

No

TNFi: TNF inhibitor, RA: rheumatoid arthritis, AS: ankylosing spondylitis, HCC: hepatocelluar carcinoma

MALToma: extranodal marginal zone B cell lymphoma, PTC: papillary thyroid cancer, BCC: basal cell carcinoma

AGC: andvanced gastric cancer, RCC: renal cell carcinoma, RAI: radioactive iodine, chemo: chemotherapy

A: adalimumab, E: etanercept, G: golimumab, I: infliximab                                                                    



Disclosure:

S. H. Bae,
None;

D. H. Lim,
None;

S. M. Ahn,
None;

S. Hong,
None;

Y. G. Kim,
None;

C. K. Lee,
None;

B. Yoo,
None.

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