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   Table of Contents      
ORIGINAL ARTICLE
Year : 2015  |  Volume : 63  |  Issue : 4  |  Page : 331-334

Intra-arterial chemotherapy for retinoblastoma: First Indian report


1 Shri Bhagwan Mahavir Vitreoretinal Services, Sankara Nethralya, Chennai, Tamil Nadu, India
2 Apollo Hospitals Interventional Radiology Unit, Division of Interventional Neuroradiology, Institute of Neurosciences, Apollo Hospital, Chennai, Tamil Nadu, India

Date of Submission13-Jan-2015
Date of Acceptance03-Apr-2015
Date of Web Publication3-Jun-2015

Correspondence Address:
Dr. Pukhraj Rishi
Shri Bhagwan Mahavir Vitreoretinal Services, Sankara Nethralaya, 18 College Road, Chennai - 600 006, Tamil Nadu
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0301-4738.158076

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  Abstract 

Aim: To describe treatment outcomes and complications of selective intra-arterial chemotherapy (IAC) for retinoblastoma (RB) in Indian eyes. Materials and Methods: Single center, retrospective interventional case series of 6 eyes with RB who underwent IAC using Melphalan (3 mg/5 mg/7.5 mg) and topetecan (1 mg) (n = 4) or melphalan (3 mg/5 mg/7.5 mg) alone (n = 2) between December 2013 and June 2014. In all, 17 IAC procedures were performed using selective ophthalmic artery cannulation. Treatment outcomes were evaluated in terms of tumor control, vitreous and subretinal seeds control and globe salvage rates. Results: IAC was employed as primary (n = 1) or secondary (n = 5) modality of treatment. Each eye received mean 3 IAC sessions (median: 3; range: 1-4 sessions). Eyes were classified according to international classification of RB as Group B (n = 1), C (n = 1), D (n = 2) and E (n = 2). Following IAC, complete regression of the main tumor was seen in 3 cases (50%), partial regression in 2 (33%), while 1 case (15%) showed no response. Of 4 eyes with subretinal seeds, 1 (25%) eye had complete regression while 3 (75%) eyes had partial regression. Of 5 eyes with vitreous seeds, 2 (40%) eyes had complete regression while 3 (60%) eyes had a partial response. Globe salvage was achieved in 5 of 6 eyes (83%). Diffuse choroidal atrophy and vitreous hemorrhage were observed in 1 (17%) eye, each. No hematologic toxicity or cerebro-vascular events were observed. Mean follow-up period was 5.5 months (median: 6 months, range: 1-6 months). Conclusion: IAC is an effective therapy for globe preservation in eyes with RB. Larger studies with longer follow-up are required to validate these results.

Keywords: Eye, intra-arterial chemotherapy, retinoblastoma, tumor


How to cite this article:
Rishi P, Sharma T, Koundanya V, Bansal N, Saravanan M, Ravikumar R, Ramamurthy S. Intra-arterial chemotherapy for retinoblastoma: First Indian report. Indian J Ophthalmol 2015;63:331-4

How to cite this URL:
Rishi P, Sharma T, Koundanya V, Bansal N, Saravanan M, Ravikumar R, Ramamurthy S. Intra-arterial chemotherapy for retinoblastoma: First Indian report. Indian J Ophthalmol [serial online] 2015 [cited 2018 Jun 19];63:331-4. Available from: http://www.ijo.in/text.asp?2015/63/4/331/158076

Intra-arterial chemotherapy (IAC) for retinoblastoma (RB) came into existence when in 1958, Reese et al. first explored chemotherapy delivery into the carotid artery. They employed X-ray together with one injection of triethylenemelamine in the carotid artery with successful regression of the tumor. [1] Several years later in 1966, Kiribuchi from Japan injected 5-fluorouracil into the frontal or supraorbital artery of children with RB and obtained favorable results. [2] In 1980s, Inomata and Kaneko, compared 12 anti-cancer drugs and found that the long-used, potent chemotherapy drug, melphalan, was the most effective agent against RB. With melphalan, 13 out of 14 plates growing primary RB cells showed a decrease in the colony formation of more than 70% [3] Kaneko et al. treated 6 patients with recurrent RB using 40 mg of intracarotid artery melphalan plus hyperthermia and cured 2 patients of the malignancy but with high systemic toxicity, mainly bone marrow suppression and hair loss. [4] Between 1989 and 1999, they attempted a more focal delivery system comprising of balloon occlusion of the distal internal carotid artery with delivery of a lower melphalan dose of 5-10 mg/m 2 to minimize systemic toxicity. [5] They performed 563 infusions in 187 patients, with the technical success rate of 97.51%. In their report in 2004, they pointed out that although the rates of complications were low; the infusions were not truly selective, because intracranial vascular territories also received high concentrations of chemotherapy through the cavernous branches of the internal carotid. [6]

In 2008, Abramson et al. used a similar but slightly more direct technique to cannulate specifically into the ophthalmic artery for chemotherapy infusion without the need for distal balloon occlusion of the internal carotid artery. [7] In 2011, Gobin et al. reported their results with selective catheterization of the ophthalmic artery and injection of melphalan in 95 eyes with unilateral RB. The Kaplan-Meier estimates of ocular event-free survival rates at 2 years in their study were 70.0% (95% confidence interval = 57.9-82.2%) for all eyes. They concluded by saying that IAC is safe and effective in the treatment of advanced intraocular RB. [8] More recently, Shields et al. reported their outcomes of IAC for RB in 70 eyes. [9] In their study, globe salvage was achieved in 72% of primary-treated cases and in 62% of secondary-treated cases. Specifically, primary therapy achieved globe salvage for Group B (100%), Group C (100%), Group D (94%), and Group E (36%).


  Materials and Methods Top


This study was a retrospective, nonrandomized, interventional case series. The medical records of all patients with RB treated with IAC at the Oncology Service between December 2013 and June 2014 were reviewed. Six eyes of 6 patients with RB who underwent IAC using melphalan (3 mg/5 mg/7.5 mg) plus topotecan (1 mg) (n = 4) or melphalan (3 mg/5 mg/7.5 mg) alone (n = 2) were included. The IAC catheterization procedure was performed by the interventional radiologist in the operating room under general anesthesia. Institutional review board approval was sought for this study.

The patient data were reviewed for the demographic association, clinical findings, management, complications, and outcomes. All prior treatments to the eye and prior systemic or local chemotherapy were recorded. A comprehensive ocular examination under anesthesia was performed with assessment for laterality, tumor growth pattern, total number of tumors per eye, international classification of RB, Reese-Ellsworth classification, intraocular pressure (Schiotz tonometer), and status of anterior and posterior chamber involvement with RB or associated features. All patients had magnetic resonance imaging imaging (MRI) scan done at 6 months interval during the course of treatment. Complete blood counts and basic coagulation tests were done at baseline and blood counts repeated 2 weeks after every IAC.

Each tumor was measured for greatest basal diameter and thickness, proximity to the Optic nerve and foveola (mm), associated retinal detachment (percent, 0-100%), subretinal tumor seeds (absent/present) and vitreous tumor seeds (absent/present). Intra-operative examinations were documented with fundus drawing, fundus photography with RetCam camera (Massey Industries, Dublin, CA, USA) and ultrasonography. Pros and cons of IAC were discussed with the family, and a signed informed consent was obtained.

After the parent or legal guardian had consented, the IAC catheterization procedure was performed by the interventional radiologist in the operating room under general anesthesia. Intravenous heparin (75 IU/kg) was used for anticoagulation. The groin area was prepared, draped and a 4-French arterial sheath was placed into the femoral artery region. Under fluoroscopic guidance, the French (1.3-mm-diameter) catheter was guided into the ipsilateral internal carotid artery. Serial arteriograms helped visualize the eye and cerebral vasculature so as to select the best approach, showing the path of the ophthalmic artery from the internal carotid artery. The ipsilateral proximal portion of the ophthalmic artery was catheterized with a 450-μm microcatheter using fluoroscopy and road mapping, and a confirmatory angiogram was taken. Chemotherapeutic agents were diluted in 30 mL of saline and delivered using a pulsatile, nonlaminated technique over 30 min to maximize homogeneous drug delivery. Chemotherapeutic agents used were melphalan (3 mg/5 mg/7.5 mg) and topotecan (1 mg). The choice of drugs was influenced by patient age, size of tumor and presence of vitreous seeds (VS). As a protocol, we plan 3 cycles of melphalan in all cases. A dose of 3 mg is considered for tumors of Group B, C, or small D. A dose of 5 mg is used for most Group D and E eyes. A dose of 7.5 mg is used if tumor activity persists following treatment with 5 mg melphalan. Topotecan 1 mg is used in cases with extensive VS or if there isn't a good response with melphalan alone. At conclusion of the infusion, the catheters were withdrawn, the femoral sheath was removed, and hemostasis of the femoral artery was achieved by manual compression. The child was observed for 6 hours and discharged the same day. A sterile dressing over the cannulation wound was maintained for 2 days and treated with topical antibiotic ointment.

The same standard technique was followed throughout the study period. Patients were followed-up at 1 monthly intervals and IAC repeated as necessary. The globe was assessed for patency of vascular flow to the eye including the central carotid artery, internal carotid artery, ophthalmic artery, central retinal artery, branch retinal artery, retinal veinous drainage and choroidal vascular bed. The fundus was evaluated for the status of the retina, retinal pigment epithelium and optic nerve. New or preexisting neovascularization of the iris with/without neovascular glaucoma was recorded. Treatment outcomes were evaluated in terms of tumor control, vitreous and subretinal seeds control and globe salvage rates. Treatment complications were noted.


  Results Top


The average age at treatment was 25 months (median: 20, range: 12-44 months). The condition was bilateral in 5 cases [Figure 1]. There were 4 male and 2 female patients. One patient had familial RB while the other 5 had sporadic occurrence of RB. Patient demographics, disease characteristics at baseline, and prior treatment details are provided in [Table 1]. Patients presented with leukocoria (n = 4), strabismus (n = 2) or eye redness (n = 1). Average duration of symptoms at presentation was 17 weeks (median: 1, range: 1-48 weeks). Eyes with RB were classified according to the international classification of RB as Group B (n = 1), C (n = 1), D (n = 2) and E (n = 2). According to Reese-Ellsworth classification, eyes were classified as 4a (n = 1) and 5b (n = 5). The mean tumor base was 12.8 mm (median: 12.8, range: 6-18 mm) and the mean tumor thickness was 6.4 mm (median: 5.5, range: 2.6-14 mm). VS were present in 5 eyes involving two quadrants (n = 1), three quadrants (n = 2) or all four quadrants (n = 2). Subretinal seeds (SRS) were present in 4 eyes involving two quadrants (n = 2), three quadrants (n = 1) or all four quadrants (n = 1). Optic nerve was visible in 3 eyes, and obscured by tumor overhang in the other three eyes. Secondary retinal detachment was present in 1 eye. The number of tumors per eye ranged from 1 (n = 3), 2 (n = 1), 4 (n = 1) or 5 (n = 1). Mean proximity of tumor to optic disc was 1 mm (median: 1, range: 0-3 mm). Mean proximity of the tumor to foveola was 1 mm (median: 1, range: 0-4 mm). All eyes had tumors that were predominantly endophytic.
Figure 1: Magnetic resonance imaging axial scan T1 images without (a) and with contrast (b) reveal enhancing tumor in both eyes. RetCam photo of left eye shows Group D tumor with vitreous seeds (c) RetCam photo of left eye reveals main tumor overhanging disc, submacular hemorrhage and a second tumor in temporal periphery (d) Cerebral angiogram reveals microcatheter within internal carotid artery, placed at ostium of ophthalmic artery (arrow, e). Confirmatory angiography reveals orbitovascular anatomy and accurate localization of microcatheter tip (arrow, f)

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Table 1: IAC for RB: Patient demographics, disease characteristics and prior treatment details at baseline


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Intra-arterial chemotherapy was employed as primary (n = 1) or secondary (n = 5) modality of systemic treatment. Patient selection was influenced by the progression of disease despite earlier treatment and status of fellow eye. Totally, 5 of 6 patients had bilateral RB-fellow eye of 4 patients was enucleated for Group E tumor, and 1 patient had Group A tumor in fellow eye that regressed with focal treatment [Table 1]. One case had unilateral RB that progressed despite treatment. So, the progression of disease despite treatment led to considering IAC for globe salvage in 5 of 6 eyes. One patient opted for IAC as "primary" therapy (case 6), where fellow eye was enucleated for Group E tumor. Of the 5 patients that had secondary IAC, prior systemic treatments included conventional intravenous chemotherapy alone (n = 4) or in combination with external radiation therapy (n = 1). Likewise, ocular treatments included cryotherapy (n = 5) and transpupillary thermotherapy (n = 3). Each eye received a mean of 3 IAC sessions per eye (median: 3; range: 1-4 sessions).

Treatment details, complications and outcomes are summarized in [Table 2]. Following IAC, complete regression of the main tumor was seen in 3 cases (50%) [Figure 2], partial regression was seen in 2 (33%) while 1 case (15%) showed no response to therapy. Globe salvage was possible in 5 of 6 (83%) eyes and one eye underwent enucleation due to dense vitreous hemorrhage during the course of treatment (case 1). Histopathologic examination revealed poorly differentiated RB with choroidal invasion more than 3 mm. This constituted a metastatic risk factor, and the child underwent 6 cycles of adjuvant chemotherapy. Of 4 eyes with SRS, 1 (25%) eye had complete regression while 3 (75%) eyes had partial regression. Of 5 eyes with VS, 2 (40%) eyes had complete regression while 3 (60%) eyes had a partial response. Globe salvage was achieved in 5 of 6 eyes (83%). Diffuse choroidal atrophy and vitreous hemorrhage was observed in 1 eye, each. No vascular occlusion or hypotony was noted in any eye. No hematologic toxicity, cerebro-vascular events, systemic metastasis or death were observed. Mean follow-up period was 5.5 months (median: 6 months, range: 1-6 months).
Figure 2: RetCam photograph of left eye 1-month after first cycle of intra-arterial chemotherapy (IAC) reveals remarkable tumor regression with extensive vitreous seeds (a). Optic disc is still obscured by tumor overhang. RetCam photograph after second cycle of IAC reveals further tumor regression with optic disc partially seen (b). RetCam photograph after third cycle of IAC reveals complete tumor regression (c). Optic disc and macula are clearly seen. Second tumor in the temporal periphery is also regressed (d)

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Table 2: IAC for RB: Treatment details, complications, and outcomes


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  Discussion Top


The principles in the management of RB include protection of life, preservation of globe and if possible, salvage vision. Current treatment strategies for the management of intraocular RB include chemotherapy and/or radiotherapy coupled with focal tumor-reduction treatments like cryotherapy, thermotherapy, and laser photocoagulation. Chemotherapy can be delivered by intravenous, intra-arterial, sub-tenon's and intravitreous routes. [10]

In our series, 4 of 6 cases (Group D = 2, Group E = 2) were advanced RB. The success rate for regression of Group E tumors with IAC has been reported to be 36%. [11] The staging of tumor at baseline has a significant bearing on the overall outcomes. In our series, most (5 of 6) cases had IAC as a salvage treatment following failed conventional chemotherapy. It has been previously observed that primary IAC has far better outcomes in term of globe salvage, tumor control and functional outcomes as compared to secondary IAC. [9] The only case that had primary IAC for Group D RB had complete regression of the tumor with 3 cycles of IAC. This is an important factor determining the outcomes in such eyes. Probably with a greater risk-acceptance of IAC among parents and better affordability of the procedure, a larger cohort of eyes with "primary IAC" and a longer follow-up could show better results in the future.

The limitations of this study include the small cohort of 6 treated eyes and relatively short follow-up of mean 6 months. We anticipate that longer follow-up will provide more information regarding lasting tumor response. However, at least in the short-term, this technique appears favorable for Group B, C and D eyes.

Even though IAC for RB is technically challenging, skill-intensive and a costly procedure, it is a precise and effective technique that helps in reducing the dosage of chemotherapeutic agents required for regression of RB and is an effective therapy for globe preservation.

In summary, we describe the short-term results of IAC for RB for the 1 st time in India. We hope to have a better understanding about the choice and dose of drugs as we gain experience with this technique amongst Indian children. Although the ideal dose and number of cycles have not yet been determined, we have found 2-3 cycles satisfactory for most tumors. Case selection is important; Groups B, C and D show more favorable results. Literature review suggests that "primary" IAC is more effective than "secondary" IAC. After the advent of intravitreal chemotherapy, we are probably better equipped in dealing with the issue of VS. Indeed, the two techniques of drug delivery, IAC, and intravitreal chemotherapy are now employed complementarily to one another. [11],[12] Having witnessed the requirements of logistic support, we believe this technique should be limited to select, experienced centers until the full value and limits of this approach are realized. We continue to use this technique with caution. [13]


  Acknowledgments Top


Carol L Shields, MD for her invaluable inputs and guidance.

 
  References Top

1.
Reese AB, Hyman GA, Tapley ND, Forrest AW. The treatment of retinoblastoma by x-ray and triethylene melamine. AMA Arch Ophthalmol 1958;60:897-906.  Back to cited text no. 1
    
2.
Kiribuchi M. Retrograde infusion of anti-cancer drugs to ophthalmic artery for intraocular malignant tumors. Nihon Ganka Gakkai Zasshi 1966;70:1829-33.  Back to cited text no. 2
    
3.
Inomata M, Kaneko A. Chemosensitivity profiles of primary and cultured human retinoblastoma cells in a human tumor clonogenic assay. Jpn J Cancer Res 1987;78:858-68.  Back to cited text no. 3
    
4.
Kaneko A, Ise T, Oohira M. Chemothermotherapy was successful in two cases of recurrence of intraocular retinoblastoma after irradiation. Jpn J Ophthalmol Clin Ophthalmol 1990;44:289-92.  Back to cited text no. 4
    
5.
Yamane T, Kaneko A, Mohri M. The technique of ophthalmic arterial infusion therapy for patients with intraocular retinoblastoma. Int J Clin Oncol 2004;9:69-73.  Back to cited text no. 5
    
6.
Suzuki S, Kaneko A. Management of intraocular retinoblastoma and ocular prognosis. Int J Clin Oncol 2004;9:1-6.  Back to cited text no. 6
    
7.
Abramson DH, Dunkel IJ, Brodie SE, Kim JW, Gobin YP. A phase I/II study of direct intraarterial (ophthalmic artery) chemotherapy with melphalan for intraocular retinoblastoma initial results. Ophthalmology 2008;115:1398-404, 14041.  Back to cited text no. 7
    
8.
Gobin YP, Dunkel IJ, Marr BP, Brodie SE, Abramson DH. Intra-arterial chemotherapy for the management of retinoblastoma: Four-year experience. Arch Ophthalmol 2011;129:732-7.  Back to cited text no. 8
    
9.
Shields CL, Manjandavida FP, Lally SE, Pieretti G, Arepalli SA, Caywood EH, et al. Intra-arterial chemotherapy for retinoblastoma in 70 eyes: Outcomes based on the international classification of retinoblastoma. Ophthalmology 2014;121:1453-60.  Back to cited text no. 9
    
10.
Shields CL, Fulco EM, Arias JD, Alarcon C, Pellegrini M, Rishi P, et al. Retinoblastoma frontiers with intravenous, intra-arterial, periocular, and intravitreal chemotherapy. Eye (Lond) 2013;27:253-64.  Back to cited text no. 10
    
11.
Shields CL, Manjandavida FP, Arepalli S, Kaliki S, Lally SE, Shields JA. Intravitreal melphalan for persistent or recurrent retinoblastoma vitreous seeds: Preliminary results. JAMA Ophthalmol 2014;132:319-25.  Back to cited text no. 11
    
12.
Ghassemi F, Shields CL. Intravitreal melphalan for refractory or recurrent vitreous seeding from retinoblastoma. Arch Ophthalmol 2012;130:1268-71.  Back to cited text no. 12
    
13.
De Francesco S, Pichi F, Lembo A, Mastrangelo D, Paradiso A, De Luca M, et al. Massive anterior chamber involvement after intra-arterial chemotherapy for retinoblastoma: Ultrasound biomicroscopy and histopathology. Int Ophthalmol 2014;34:967-70.  Back to cited text no. 13
    


    Figures

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