Topical Chemotherapy for Treating Ocular Surface Squamous Neoplasia with a Combination of Interferon α-2b and 5-Fluorouracil.

INTRODUCTION: This study evaluated the efficacy of combined interferon α-2b (IFNα2b) and 5-fluorouracil (5-FU) as primary treatment for ocular surface squamous neoplasia (OSSN).
METHODS: In this retrospective study, 27 eyes with OSSN followed by topical application of combined IFNα2b and 5-FU were examined. Reported outcome measures were tumor response, visual acuity, time to complete resolution, recurrence and treatment complications.
RESULTS: Twenty-six patients (17 male, 9 female) had a mean age of 63.9 (median, 67; range 22-83) years. Complete tumor response was observed in 24 eyes (88.9%). Three eyes (11.1%) showed partial response to the chemotherapy agents and later underwent surgical tumor removal. The median time to complete resolution was 6 (mean, 6.1; range, 3-11) weeks. Of these, the patients received between one to three cycles of 5-FU therapy (median, 2; mean, 1.8). Complications noted were transient irritation at 5-FU cycle (11 eyes, 40.7%). There was no tumor recurrence at mean follow-up of 16.1 (median, 12; range 6-38) months.
CONCLUSIONS: Combination therapy of IFNα2b and 5-FU was a safe and effective treatment, inducing a short duration of administration and low recurrence rate for OSSN. TRIAL REGISTRATION: Retrospectively registered, UHCT22048.

Key Summary Points

Introduction

Ocular surface squamous neoplasia (OSSN) is the most common malignancy of the ocular surface, with a worldwide incidence 0.13 to 1.9 per 100,000 individuals [1, 2]. Many factors contribute to the development of OSSN such as ultraviolet radiation, human immunodeficiency virus infection, human papillomavirus infection, vitamin A deficiency, xeroderma pigmentosum, allergic conjunctivitis, smoking, chemical exposure and immunosuppression caused by medications after organ transplantation [3-7]. Although surgical removal has been considered the standard care for OSSN [8-10], local chemotherapy has increased in popularity over the past 20 years [9, 11–13]. Topical chemotherapeutic agents used today are mainly mitomycin-C (MMC), 5-fluorouracil (5-FU) and interferon α-2b (IFNα2b) [14-16].

Mitomycin C is a potent antimetabolite resulting in DNA alkylation in all phases of the cell cycle [17]. It has frequent side effects that include pain in most patients and epitheliopathy [12, 18], which has limited its usage.

5-Fluorouracil is structurally similar to thymidine and uracil and inhibits DNA formation [19]. It has been used to treat many epithelial cancers because of its actions on rapidly multiplying tumor cells [20]. Treatment with 5-FU is generally well tolerated especially when administered four times daily for 1 week, followed by a drug holiday for 3 weeks [15].

IFNα2b is a recombinant glycoprotein that activates effector proteins by binding to the cell surface of their targets [21]. Its role as antineoplastic agent is due to a combination of antiproliferative, antiangiogenic and cytotoxic effects, as well as through a possible enhancement of the host antitumor surveillance mechanism [22]. IFNα2b maintains comparable rates of resolution and recurrence to the aforementioned drugs [12]. The fact that the topical form is extremely well tolerated makes it most popular nowadays [12].

Nevertheless, the resolution time is as long as 11 weeks to 6.6 months for 5-FU and 2.3–6 months for IFNα2b in the literature from 2003 to 2022 including > 20 cases (Table 1). We speculated the combined use of IFNα2b and 5-FU enhances the effectiveness by shortening the resolution time and reducing the 5-FU cycle. Herein, we share our experiences and insights from the combined application of IFNα2b and 5-FU in the treatment of OSSN.

Table 1

Tumor response, recurrence rate and side effects of topical chemotherapy for OSSN

Modality	Author	Years of publication	Eyes (n)	Treatment duration	Complete resolution rate	Time to resolution (months)	Follow-up (months)	Recurrence rate	Side effects
IFNα2b	Kusumesh et al. [16]	2015	24	3.25 months (mean)	91.6%	3.25 (mean)	18.81	0	Conjunctival congestion (4.2%), intratumoral bleeding (8.3%), foreign body sensation (4.2%)
	Nanji et al. [51]	2014	49	3.9 months (median)	100%	2.3 (median)	21	3%	Pain (27%), irritation (53%), itching (12%), conjunctival redness (29%)
	Kusumesh et al. [52]	2017	26	N/A	89%	3.1 (median)	22.2	3.85%	Conjunctival hyperemia (8%), burning sensation (4%)
	Venkateswaran et al. [42]	2019	48	4.2 months (mean)	81.3%	5.5 (mean)	N/A	5.1%	Pain (19.6%), redness (13.0%), blurred vision (13.0%), tearing (4.3%)
	Kaliki et al. [53]	2019	91	6 months (mean)	79%	6 (mean)	14	3%	Transient flu-like symptoms (16%)
5-FU	Joag et al. [15]	2016	44	3.8 cycle (mean)	82%	N/A	10 (median)	11.1%	Pain (39%), tearing (23%), photophobia (14%), itching (9%), swelling (5%), infection (2%)
	Venkateswaran et al. [42]	2019	54	4.2 cycle (mean)	96.3%	6.6 (mean)	N/A	11.5%	Pain (22.2%), tearing (22.2%), redness (20.4%), eyelid edema (9.3%), keratopathy (7.4%)
	Parrozzani et al.a [32]	2017	41	1.5 coursesb (mean)	83%	11 weeks (mean)	105	10%	Pain (36%), photophobia(51%), irritation(43%), punctate keratitis(28%), hyperemia(48%), eyelid swelling/erythema(8%)

IFNα2b, interferon α-2b; N/A, not assessed

aTopical 5-FU, four times/daily for 4 weeks

bOne course was defined as 4 continuous weeks of topical chemotherapy

Methods

Study Population

This retrospective study was approved (UHCT22048) by the Ethics Committee of Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, according to the tenets of the Declaration of Helsinki. Twenty-six consecutive patients (27 eyes) with a clinical diagnosis of OSSN by two cornea specialists using slit-lamp biomicroscopy between July 1, 2016, and July 1, 2021, were recorded.

Data Extracted

Patient records were reviewed for demographic information (age, sex), best corrected visual acuity (BCVA), OSSN risk factors (human immunodeficiency virus, smoking, history of OSSN, chronic systemic immunosuppression) and other diagnoses. Specific characteristics of each tumor were documented including the involved eye, unifocal versus multifocal status, number of involved limbal clock hours and morphological findings (leukoplakic, gelatinous, papillomatous, or flat) based on descriptions and photographs.

Topical IFNα2b Chemotherapy Combined with 5-FU

Topical IFNα2b (1 million IU per milliliter, MIU/ml) was compounded by adding 4 ml of distilled sterile water to 1 ml 5 MIU/ml IFNα2b (Anfulong, Tianjing Sinobioway Biomedicine, China) and preserved in a refrigerator at 4 °C. The drops were administered as one drop four times daily and continued until clinical resolution. To prevent tumor recurrence, an additional 4-week treatment was used after the tumor had completely resolved. Topical 5-FU was used at a concentration of 1%, administered as one drop four times daily for 1 week, followed by a drug holiday for 3 weeks. This monthly cycle was continued until complete clinical resolution, after which the drops were discontinued. For some patients who were sensitive to side effects, preservative-free artificial tears were added four times daily. All patients were followed up weekly until complete resolution and then at different intervals.

Outcome Measures

The main outcome measures were tumor response, time to tumor complete resolution, total duration of IFNα2b, 5-FU cycle, tumor recurrence, new tumor appearance, visual acuity and treatment-related complications.

Tumor response was recorded as the time to complete resolution (clinically defined on slit-lamp examination). Partial response to chemotherapy was defined as initial effectiveness followed by 2 consecutive weeks of no significant change in tumor. No response was defined as no significant change for 4 consecutive weeks from the start of treatment. Recurrence was defined as reappearance at a similar location as the original tumor (after complete resolution of original tumor). New tumors were defined as those appearing at a different location from that of original tumor (after complete resolution of original tumor). Follow-up duration was defined from the time of resolution of lesion until the last visit. Complication surveys included irritation (pain, redness, tearing and photophobia), limbal stem cell deficiency and infection.

Statistical Analyses

Statistical analyses were performed using Microsoft Excel (Microsoft, Redmont, WA). Frequencies of demographic and clinical variables were calculated. The data were expressed as means ± SD, median and range for quantitative parameters.

Results

Pretreatment Characteristics

Demographics of the study population are presented in Table 2. Seventeen males (65.4%) and nine females (34.6%) were included in this study. The average age was 63.9 (range, 22 to 83) years. Of the risk factors associated with OSSN, 1 (3.8%) patient had a history of HIV, 16 (61.5.%) were current smokers, 4 (15.4%) had a prior history of OSSN, and 1 (3.8%) patient with thrombocytopenia, a chronic systemic immune disorder, was being treated with oral steroids. Other ocular diagnoses of patients included 14 (53.8%) cataracts, 1 (3.8%) chronic dacryocystitis, 1 (3.8%) intraocular lens eye and 1 (3.8%) myopia.

Table 2

Demographic and clinical features of patients with OSSN treated by the combined application of topical IFNα2b and 5FU: pretreatment

Demographic and clinical features	Data
Age (years)
Median	67
Mean (SD)	63.9 (17.5)
Range	22–83
Male gender	17 (65.4)
Current smoker	16 (61.5)
Chronic systemic immunosuppression	2 (7.7)
Involved right eye	16 (59.3)
History of OSSN	4 (15.4)
Limbal clock hours involvement
Median	4
Mean (SD)	4.3 (2.9)
Range	0–9
Morphologic appearance
Papillomatous	19 (70.1)
Gelatinous	2 (7.4)
Leukoplakia	2 (7.4)
Flat	4 (14.8)
Multifocal tumor	4 (14.8)
Other diagnosis
Cataract	14 (53.8)
IOL	1 (3.8)
Myopia	1 (3.8)
Chronic dacryocystitis	1 (3.8)
HIV	1 (3.8)
Thrombocytopenia	1 (3.8)

OSSN, ocular surface squamous neoplasia; HPV, human papillomavirus; HIV, human immunodeficiency virus

The 27 eyes included 16 (59.3%) right eyes and 11 (40.7%) left eyes (one patient with bilateral onset). The mean number of limbal clock hours involved was 4.3 (median, 4; range, 0–9). The tumor appearances were 19 (70.1%) papillomatous (Fig. 1A), 2 (7.4%) gelatinous (Fig. 1B, white arrows), 2 (7.4%) leukoplakic (Fig. 1C) and 4 (14.8%) flat (Fig. 1D, E white arrows). Four (14.8%) papillomatous eyes developed multifocal tumors (Fig. 1F).

Fig. 1

Appearance of OSSN. A papillomatous, B gelatinous, C leukoplakic, D, E flat, F papillomatous eyes developed multifocal tumors. Tumor boundaries are marked with white arrows

Tumor Response

Tumors of all patients responded to IFNα2b combined with 5-FU therapy (Table 3). Twenty-four (88.9%) lesions resolved completely. Among the 24 eyes, the median time to complete resolution was 6 (mean, 6.1; range, 3–11) weeks. Patients received one to three cycles (median, 2; mean, 1.8) of 5-FU therapy. The total duration of IFNα2b ranged from 8–15 (median, 10; mean, 10.25) weeks.

Table 3

Primary treatment of OSSN with combined application of topical IFNα2b and 5FU: outcomes

Outcomes	Data
Tumor response
Complete	24 (88.9)
Partial	3 (11.1)
No	0 (0)
Time to complete resolution (weeks)a
Median	6
Mean (SD)	6.1 (8.4)
Range	3–11
5-Fu cyclea
Median	2
Mean (SD)	1.8 (2.4)
Range	1–3
Total duration of IFNα2b (weeks)a
Median	10
Mean (SD)	10.25 (12.6)
Range	8–15
Tumor recurrence	0 (0)
Visual acuitya
Improved	9 (37.5)
Unchanged	15 (62.5)
Decreased	0 (0)
Side effects and complications
Irritation at 5-FU cycle	11 (40.7)
Limbal stem cell deficiency	0 (0)
Persistent epithelial defect	0 (0)
Follow-up (months)
Median	12
Mean (SD)	16.1 (24.3)
Range	6–38

5-FU, 5-fluorouracil

aEyes with complete tumor response were analyzed for this index

Two patients (3 eyes) showed partial response to the chemotherapy. The number and size of the masses decreased during the first 4 to 5 weeks. However, over the next 2 weeks, the tumor changes stalled. Eventually, one patient underwent surgery at week 7 and the other at week 8. Postoperatively, both were then treated with adjuvant IFNα2b for 4 weeks and one cycle of 5-FU.

Visual Acuity

The causes of low visual acuity at presentation included preexisting cataract (n = 14), myopia (n = 1) and tumor-induced occlusion of the pupillary area (n = 9). No loss of vision was associated with the treatment. At the last follow-up, 9 (37.5%) patients showed improvement of visual acuity; 15 (62.5%) patients still had their pretreatment visual acuity (Table 3).

Side Effects and Complications

Eleven (40.7%) patients experienced medication-related side effects which were tolerated. All of them experienced redness, pain, tearing, photophobia and swelling during 5-FU use, which disappeared within 1 to 2 weeks after 5-FU was discontinued. All patients completed the course of 5-FU therapy. No signs of partial or total limbal stem cell deficiency or persistent epithelial defect were noted (Table 3).

Follow-up and Tumor Recurrence

With longer follow-up (median, 12 months; mean 16.1 months; range, 6–38 months), there was no evidence of recurrence in all patients (Table 3).

Representative Case Reports

Case 8: Papillomatous Tumor

An 80-year-old man complained of redness and loss of vision in his right eye for 10 months. He had undergone excisional biopsy 1 year ago in another hospital because of a history of OSSN. The pathology confirmed atypical hyperplasia without specific description of the margin. The papillomatous tumor involved 8 clock hours of limbus (Fig. 2A1). His visual acuity had deteriorated to finger counting/50 cm because of the occlusion of the pupillary area (Fig. 2A1, A2). After topical chemotherapy, the tumor displayed complete regression at the 3-week visit (Fig. 2B1) although an uneven corneal surface was noted (Fig. 2B2). He received 8 weeks of chemotherapy including two cycles of 5-FU. No tumor recurrence was observed (Fig. 2C1) and the ocular surface was stable (Fig. 2C2) at 38-month follow-up.

Fig. 2

Case 8: Slit-lamp photographs of an 80-year-old man with OSSN. A1 Papillomatous tumor in the right eye involving 8 clock hours of limbus, cornea and conjunctiva. B1 After topical chemotherapy, the tumor displayed complete regression at 3-week visit (B2) although an uneven corneal surface was noted. C1 No tumor recurrence was observed and (C2) the ocular surface was stable at 38-month follow-up

Case 21: Gelatinous Tumor

A 43-year-old female complained of redness, foreign body sensation and the presence of a reddish mass in her left eye for 6 months. She had a medical history of chronic dacryocystitis without any treatment. The gelatinous tumor involved 2.5 clock hours of limbus (Fig. 3A). It displayed complete tumor regression after 4 weeks of topical IFNα2b and one cycle of 5-FU without corneal epithelial defect (Fig. 3C). She received another 4 weeks of topical IFNα2b after complete resolution to prevent tumor recurrence. The ocular surface was stable without any inflammation or recurrence for 18 months of follow-up (Fig. 3D).

Fig. 3

Case 21: Slit-lamp photographs of a 43-year-old female with diagnosis of OSSN and chronic dacryocystitis. A The gelatinous tumor in the right eye involving 2.5 clock hours of limbus. B It displayed complete tumor regression with 2 weeks of topical IFNα2b and one cycle of topical 5-FU and showed typical symptoms of redness and irritation during the 5-FU treatment, (C) without corneal epithelial defect. D No tumor recurrence was observed at 18-month follow-up

Case 26: Flat Tumor

A 71-year-old female was referred to our clinic with foreign body sensation and blurred vision for 9 months. Slit-lamp biomicroscopy showed an elevated diffuse epitheliopathy (Fig. 4A1, white arrows) with a central ulcer (Fig. 4A2, black arrow). Under the clinical diagnosis of OSSN, topical IFNα2b and 5-FU chemotherapy was administrated. The tumor had shrunk (Fig. 4B1, B2, white arrows) and ulcer healed at the 4-week visit (Fig. 4B2). Complete regression was observed after 5-week treatment including two cycles of 5-FU (Fig. 4C1, C2). She was followed up for 6 months without recurrence.

Fig. 4

Case 26: Slit-lamp photographs of a 71-year-old female with flat OSSN. A1 Slit-lamp biomicroscopy showed an elevated diffuse epitheliopathy (white arrows) with a central ulcer (A2, black arrow). B1, B2 The tumor had shrunk (white arrows) and ulcer healed at the 4- week visit after topical IFNα2b and 5-FU chemotherapy. C1, C2 Complete regression was observed after 5 weeks of treatment

Case 22: Mutifocal Tumor Partial Response to Chemotherapy

A 34-year-old male presented with a recurrent OSSN in both eyes for 12 months. He had undergone surgical resection 18 months before in another hospital (pathological diagnosis was atypical hyperplasia). The multiple papillomatous tumors in the right eye involved upper and lower palpebral and fornix conjunctiva (Fig. 5A). The tumors shrank after 8 weeks of IFNα2b and two cycles of 5-FU (Fig. 5B). Partial response was judged when tumors had not shrunk further according to comparison of the slit-lamp photos from week 6 and week 8. The patient received bilateral surgery to remove the masses at week 8. Postoperatively, adjuvant IFNα2b for an additional 4 weeks combined with one cycle of 5-FU was administered. No tumor recurrence was observed at 11-month follow-up (Fig. 5C).

Fig. 5

Case 22: Slit-lamp photographs of a 34-year-old male with multiple papillomatous tumors in both eyes. A Papillomatous multiple tumors in the right eye involving upper and lower fornix palpebral conjunctiva. B The tumors shrank after 8 weeks of IFNα2b and two cycles of 5-FU. The patient received bilateral surgery to remove the masses at week 8. C No tumor recurrence was observed at 11-month follow-up

Discussion

Surgical removal of OSSN has the advantage of serving as both a diagnostic and therapeutic procedure, providing both an accurate histological diagnosis and rapid tumor resolution. Studies have shown that no difference in the recurrence rate of OSSN was found between surgical versus IFNα2b therapy [23]. However, surgery often leads to serious complications including limbal stem cell deficiency and conjunctival scarring [24]. Over the past 20 years, there has been a shift in the treatment of OSSN from surgical treatment alone to the use of local chemotherapeutic agents or surgery in combination with chemotherapeutic agents. Topical chemotherapy minimizes complications, and the medication acts on the entire ocular surface, offering significant advantages in the treatment of diffuse lesions, microscopic lesions and surgical residual tumors [14, 23, 25]. However, local chemotherapeutic agents like IFNα2b and 5-FU have long duration of use and cause irritation symptoms and pain, which often lead to poor patient compliance. Therefore, we strove to achieve the goal of rapid regression of OSSN by combining IFNα2b and 5-FU.

Since use of IFN and 5-FU for ocular surface lesions was reported in the nineteenth century, several studies have confirmed their effectiveness in the treatment of OSSN [26-29]. For IFN treatment, the overall response frequency ranged from 75 to 100% [16, 30, 31]; for 5-FU, it ranged from 82–100% [15, 32, 33]. In our current study, all the tumors were in remission, although 12.5% showed partial response. There was no one case of primary tumor recurrence, new tumor or metastasis. In the two cases of partial response, one patient was HIV infected and the other had a history of OSSN and had undergone excisional surgery as the primary treatment in both eyes 18 months ago; both were identified as recurrent patients. Both patients had multiple masses. These factors may reduce the sensitivity of tumors to chemotherapeutic agents. OSSN often presents a variety of appearances [34]. A patient with OSSN masquerading as a recalcitrant epithelial keratitis recovered after four cycles of topical chemotherapy with 5-FU [35]. Flat tumor with epithelial defect (case 26) tends to be misdiagnosed as keratitis, and doctors should pay more attention to it.

Wadler et al. [36] first reported that IFNα2b combined with 5-FU has achieved certain effects on the treatment of colon cancer. This combination therapy was also applied to esophageal cancer [37] and gastric cancer [38] and achieved satisfactory results. The combination of IFNα2b and 5-FU reduced the dosage of chemotherapy agents and the toxic and side effects on normal tissue cells. Several investigations suggest that alpha-IFN could play a positive role in immuno-chemotherapy of cancer through multiple mechanisms not entirely related to direct antitumor effects of the agent [39, 40]. Alpha-IFN might elevate the levels of the active 5-FU metabolite 5-fluoro-2’-deoxyuridine-5’- monophosphate in the cell, possibly leading to increased inhibition of the target enzyme thymidylate synthase, which might enhance DNA damage [41]. Compared with monotherapy in the most recently published analysis (Table 1), our study confirmed that combination therapy could reduce the frequency of 5-FU use (median, 2; mean, 1.8; range, 1–3) and shorten the duration of IFNα2b treatment (median, 10 weeks; mean, 10.25; range, 8–15;) for OSSN. Joag et al. [15] reported that among the 44 eyes, 36 lesions (82%) resolved completely with 5-FU therapy; the median number of cycles was 4 (range, 2–9; mean, 3.8). In Venkateswaran’s study [42], the number of 5-FU cycles was 4 (range, 2–12; mean, 4.2), and she also reported that in the 48 eyes treated with IFNα2b therapy, 81.3% of lesions (n = 39) completely resolved (median number of months treated 4, range 2–8, mean 4.2). In most studies, the duration of IFNα2b was a few (range 2–6) months [30, 43, 44]. However, the mechanism of the combination treatment in OSSN needs to be further studied.

In this study, pathological biopsies were not performed on all patients. Instead, two experienced cornea specialists independently made the diagnosis of OSSN. Biopsy, on the other hand, increases the risk of seed transfer and additional invasive procedures for patients. It may not make sense to remove part of the tumor to confirm the pathological diagnosis while treating the rest with chemotherapy. Hence, we chose to avoid biopsy as this is consistent with how most clinicians currently approach clinically evident OSSN, especially when starting topical therapy. This view was recently supported by Shields [45]. Nowadays, as a non-contact, non-invasive examination, ultra-high-resolution anterior segment optical coherence tomography (HR-OCT) has emerged as a useful methods to aid in the diagnosis and management of OSSN [46]. It is particularly useful at detecting epithelial thickening and differentiating epithelial lesions from subepithelial lesions of the conjunctiva and cornea, assisting in the differentiation of OSSN, pterygia, pinguecula, lymphoma and melanocytic lesions [47, 48]. Some researchers also believed that the tumor response defined by a detailed slit-lamp examination would result in a premature termination and reduction time of treatment in some patients with subclinical disease that can be detected with HR-OCT [15, 49]. Although definitive imaging and pathology were lacking to exclude subclinical lesions, no tumor recurrence was found at mean follow-up time of 16.1 months; there was no premature discontinuation of chemotherapy in our study.

The costs of treatment are also an important factor influencing the treatment options. Of the therapeutic agents, interferon has fewer side effects but is much more expensive (approximately $600 for a month's supply in the USA) and requires refrigeration for storage [34, 50]. 5-Fluorouracil is relatively inexpensive and stable at room temperature. A 1-month treatment of 5-FU costs approximately $38 in the US [34, 42]. Fortunately, in China, both IFNα2b and 5-FU are cheap and readily available. For patients in our study, the cost of IFNα2b drops was $16 for a 4-week supply and $8 for one cycle of 5-FU, which is much lower than that of surgical treatment in our hospital. Combination chemotherapy has been proposed as a promising therapeutic strategy to overcome drug resistance and improve efficacy of monotherapy regimens in cancer. Since we proposed this combination of IFNα2b and 5-FU based on clinical observations, more cellular and molecular experimenta will be performed in our next study to demonstrate the advantages of this therapy.

In our current study, few patients experienced discomfort during IFNα2b treatment. Side effects were more likely observed during 5-FU use. One limitation of our study was a non-standardized method for evaluating side effects and treatment. In this retrospective, we classified redness, pain, tearing, photophobia, swelling and itching as 5-FU irritation, which resulted in a much higher side effect index (40.7%) than previously reported [15, 42]. Encouragingly, all side effects abated when the chemotherapeutic agents were discontinued. A confocal microscopy study showed no long-term differences between the treated and control (fellow) eyes after treatment with 5-FU [33]. Other limitations were due to the nature of retrospective studies. Ultimately, a prospective study with a larger sample size on IFNα2b combined with 5-FU will be needed to further validate our results.

Conclusion

Our study with a cohort of 26 patients showed the efficacy of IFNα2b combined with 5-FU in the treatment of OSSN. This regimen reduced the duration of IFNα2b use and the frequency of 5-FU cycles with an increased tumor resolution and low recurrence rate.

Ocular surface squamous neoplasia (OSSN) is the most common malignancy of the ocular surface. Surgical removal for OSSN has a high recurrence and complication rate, including limbal stem cell deficiency and conjunctival scarring.

There has been a shift in the treatment of OSSN from surgical treatment alone to the use of local chemotherapeutic agents alone or surgery in combination with chemotherapeutic agents, but chemotherapeutic agents like IFNα2b, MMC and 5-FU also have side effects.

We hypothesized that IFNα2b combined with 5-FU could be more effective and rapid in treating OSSN than monotherapy.

Combination therapy of IFNα2b and 5-FU was a safe and effective treatment for OSSN. This regimen reduced the duration of IFNα2b use and the frequency of 5-FU cycle with a high frequency of tumor resolution and low recurrence rates. It provides a new method for the treatment of OSSN.