Clinical Analysis of 16 Distant Metastatic Retinoblastoma Cases with Event-Free Survival.

AIM: This study aimed to summarize the clinical characteristics, treatment, and outcomes of distant metastatic retinoblastoma with event-free survival.
DESIGN: Retrospective interventional case series.
METHODS: We screened patients with retinoblastoma who survived without events after the comprehensive treatment of distant metastases from June 2015 to February 2021 and collected information regarding their basic characteristics, diagnosis, and treatment. All patients received systemic intravenous chemotherapy. Other treatments included surgical treatment, radiotherapy, intrathecal chemotherapy, and autologous stem cell transplantation.
RESULTS: Among 780 hospitalized patients with retinoblastoma in the pediatric ward, a total of 94 patients with retinoblastoma were diagnosed with distant metastases, and 16 patients with distant metastatic retinoblastoma who survived more than 6 months without events were screened, including eight male and eight female patients. The median age of onset was 29 (range, 11-120) months. Among the 16 patients, central nervous system metastasis (8/16), bone metastasis (8/16), bone marrow infiltration (4/16), lymph node metastasis (4/16), and parotid gland metastasis (3/16) were presented. All patients received treatment for more than 6 months, completed their regimen by February 2021, and survived without events. The median survival time after the onset of retinoblastoma was 50.5 (range, 23-102) months, the median survival time after metastasis was 43.5 (range, 16-71) months, and the median event-free survival was 29.0 (range, 6-59) months.
CONCLUSION: Metastatic retinoblastoma may benefit from comprehensive treatments including systemic intravenous chemotherapy and hematopoietic stem cell transplantation. However, recurrence after treatment still needs attention, and patients in complete remission still need long-term follow-up.

Introduction

Retinoblastoma (RB) is a malignant tumor of the eye occurring in childhood. The incidence is 1 in 16,000 to 18,000 live births, accounting for approximately 11% of cancers diagnosed in the first year of life.1–3 The goals of treatment for RB include life, globe, and vision salvage.4 RB is considered curable, and improved medical conditions and modern technology have decreased the RB-associated mortality rates in Europe and the US to about 5% and 3%, respectively.5 However, extraocular dissemination and distant metastasis are important factors leading to poor prognosis of patients with RB, and there are few previous reports of cured cases. Effective treatment of metastatic RB is still a difficult problem in current RB treatment. More effective and standardized treatment methods and clinical guidelines are needed. We summarized the clinical data of 16 patients with metastatic RB who survived without events in Beijing Tongren Hospital, to share our experiences.

Methods

The data of patients with RB admitted to the Pediatrics Department of Beijing Tongren Hospital June 2015 to February 2021 were collected. Beijing Tongren Hospital is one of the largest retinoblastoma diagnosis and treatment centers in China. The pediatric department of our hospital admitted patients with advanced RB from all over China. Among 780 hospitalized patients with retinoblastoma in the pediatric ward, a total of 94 patients with retinoblastoma were diagnosed with distant metastases. The inclusion criteria were as follows: 1) patients diagnosed with RB in our hospital with confirmed involvement of tissues other than the eyeball and orbit; 2) after comprehensive treatment in our hospital, the primary and metastatic tumors of the patients achieved complete remission and all patients survived events free more than 6 months by August 2021; and 3) all guardians of participating patients provided written informed consent for treatment. This study complies with the Declaration of Helsinki and this study protocol was approved by the Ethics Committee of Beijing Tongren Hospital, Capital Medical University [TRECKY2021-096].

The exclusion criteria were as follows: 1) irregular treatment after metastasis; 2) treatment had not ended or an event-free survival of less than 6 months; 3) during the treatment of RB, metastasis occurred due to disease progression; and 4) patients with trilateral RB.

Diagnosis of RB

All patients completed ocular ultrasound, orbital CT, ocular MRI, fundus examination, and/or pathological examination and were diagnosed as RB. According to the AJCC RB TNM staging system, all patients were in stage cM1a or cM1b.

Diagnosis of RB Metastasis

Patients completed systemic examinations, including serum neuron-specific enolase (NSE) analysis, bone puncture, lumbar puncture, lymph node ultrasound, cranial MRI, bone scan, PET/CT, or pathological examination. The involvement of tissues other than the eyeball and orbit was confirmed.

Intravenous Chemotherapy (IVC)

All patients with metastasis RB underwent systemic IVC. Commonly used chemotherapy drugs included vincristine (V), etoposide (E), carboplatin (C), cisplatin (P), cyclophosphamide (C), ifosfamide (I), and topotecan (T). Commonly used regimens included carboplatin, etoposide, vincristine (CEV)/ cisplatin, cyclophosphamide, etoposide, vincristine (PCEV)/ cyclophosphamide, carboplatin, etoposide, vincristine (CCEV), and individualized chemotherapy regimens were applied for children with poor treatment effects.

Surgical Treatment

Eyeball enucleation was performed for late-stage RB eye disease or failed eye-protecting treatment. Orbital exenteration was performed for children with extraocular orbital involvement to save lives.

Radiotherapy

For cases of central nervous system (CNS) metastasis or localized soft tissue/bone metastasis with poor therapeutic effects, radiotherapy was combined with other treatments. Generally, patients who receive radiotherapy are older than 3 years; and the age limit can be relaxed to 2 years old if necessary. The treatment is carried out in the form of fractionated radiotherapy, and the total dose of radiotherapy is generally 36–45 Gy.

Hematopoietic Stem Cell Transplantation

If the tumor did not reach complete remission (CR) after 4–6 cycles of IVC or combined treatment, autologous stem cell transplantation (ASCT) should be considered. Before treatment, consent shall be obtained from the patient’s family, and the tolerance of children’s physical condition to treatment needs to be evaluated.

Intrathecal Chemotherapy

All patients with CNS metastases or lesions close to the brain were given monthly lumbar punctures and intrathecal chemotherapy (dexamethasone, cytarabine, and methotrexate).

Follow-Up

All patients were followed up to August 2021 through outpatient review or telephone follow-up. The median follow-up time was 50.5 (range, 23–102) months, The RB overall survival (OS) refers to the diagnosis of retinoblastoma to the end of follow-up; Event-free survival (EFS) after metastasis refers to the time from the diagnosis of RB metastasis and the start of treatment to the occurrence of any events, including death, disease progression, and disease recurrence. EFS after treatment refers to the time from the end of all treatments to the occurrence of any events in patients with metastatic RB, including death, disease progression, and disease recurrence.

Results

Among 94 patients with retinoblastoma who were diagnosed with distant metastases, a total of 16 patients with RB met the above enrollment criteria up to August 2021, including eight cases with CNS metastasis and eight cases without CNS metastasis. Among them, eight were male, and eight were female. The median age of onset was 29 (range, 11–120) months. No children had a family history of RB. Two cases had binocular disease, 14 cases had monocular disease, and there were 18 diseased eyes. Seven patients had metastatic RB at diagnosis, and the remaining cases had metastatic disease after recurrence. The nine recurrent patients were treated before recurrence by enucleation (7/9), systemic IVC (2/13), and other methods, including laser therapy, intra-arterial chemotherapy, vitrectomy. One patient who was misdiagnosed as Coats disease received subretinal fluid drainage combined with intravitreal injection of anti-vascular endothelial growth factor.

The most common sign was leukocoria (9/16), and other manifestations included decreased vision, conjunctival hyperemia, strabismus, and exophthalmos (Table 1). After excluding two patients whose pathological report was lost, the pathological risk factors of other patients were optic nerve invasion (7/14), large choroidal invasion (3/14), and others, including anterior segment, lamina, sclera, and extraocular invasion (Table 1). Among the 16 patients, CNS metastasis (8/16), bone metastasis (8/16), bone marrow infiltration (4/16), lymph node metastasis (4/16), parotid gland metastasis (3/16) (Figure 1), and orbital involvement (including the optic nerve, 13/16) were presented. Nine patients had a significant increase in the serum NSE level at the time of metastasis. However, the increase in serum NSE was not significant in children with simple bone metastasis and simple optic nerve intracranial invasion.

Table 1

Characteristics of Included Patients

Characteristic	Number (n, %)
Age (years), < 3/≥3	9(56.2)/7(43.8)
Gender, M/F	8(50.0)/8(50.0)
Eye affected, Mon/Bin	14(87.5)/2(12.5)
Presenting signs
Leukocoria	9(56.2)
Vision loss	6(37.5)
Conjunctival hyperemia	5(31.3)
Squint	3(18.8)
Proptosis	3(18.8)
Metastasis sites
Bone metastasis	8(50.0)
CNS metastasis	8(50.0)
Lymph node metastasis	4(25.0)
Bone marrow infiltration	4(25.0)
Parotid gland metastasis	3(18.8)
Pathologically high-risk site of invasion
Optic nerve invasion	7(43.8)
Extensive choroidal invasion	3(18.8)
Anterior quarter	2(12.5)
Sieve plate	3(18.8)
Sclera	1(6.25)
Extraocular involvement	2(12.5)

Abbreviations: M, male; F, female; Mon, monocular; Bin, binocular; CNS, central nervous system.

Figure 1

RB case with metastasis to parotid gland. (A-1) T1WI+C FS Status after vitrectomy (misdiagnosed at onset) in the right eye. Irregular equal T1 signals can be seen around the eyeball, locally protruding outside the orbit, and the enhanced scan is slightly enhanced, involving the lacrimal sac area and extraocular muscles. (A-2) T1WI+C FS Abnormal signal in the right parotid area with swollen lymph nodes, and the enhanced scan showed uneven enhancement. (B-1) T1WI+C FS Postoperative state of the right eye, with mild and uneven enhancement of the orbital fat body; (B-2) T1WI+C FS The original parotid gland area and lymph node enlargement subsided.

All patients received systemic IVC after metastasis (Table 2). The chemotherapy cycles after metastasis depended on the condition (metastatic site, tumor load and response to treatment), with a median of 12.5 (range, 8–19) cycles. Common side effects in patients during chemotherapy included bone marrow suppression, liver damage, electrolyte disturbances, and gastrointestinal reactions. Other treatments included surgery, radiation therapy, and autologous stem cell transplantation. Among the 10 patients who underwent surgery, 11 diseased eyes in nine patients underwent eyeball enucleation, and one patient who had eye enucleation before recurrence underwent orbital exenteration. In addition, one patient underwent eyeball enucleation and cranioorbital metastasis resection. After treatment, only one eye with stage C remained in the 18 diseased eyes, and the eye preservation rate was 5.7%. Seven patients with CNS metastases and one patient with craniofacial bone and sinus metastases received fractionated radiotherapy. The median radiotherapy dose was 45 (range, 36–50) Gy. One recurrent RB patient with bone, lymph node, and bone marrow metastases underwent ASCT and achieved CR. By the end of the follow-up period, the EFS after metastasis was 33 months. Lumbar puncture and intrathecal chemotherapy (range, 6–14 times) were given monthly for all patients with CNS metastasis or lesions close to the brain; other patients undergo intermittent lumbar punctures to assess whether the CNS was involved.

Table 2

Diagnosis and Treatment of Patients with Metastasis

	Age (Mon)	Stage		Metastasis Site		Treatment after RB Metastasis					EFS (Mon)
			Time to Metastasis	Evidence	Metastatic Sites	IVC Cycles	RT (Gy)	Surgery	Intrathecal Chemotherapy (Cycles)	Other Treatments
1	22	cM1a	Recurrence	PET/CT,BM cytology	Bone, lymph nodes, bone marrow	8		—		ASCT	33
2	27	cM1a	Recurrence	PET/CT,BM cytology	Bone, lymph nodes, bone marrow	9		—			28
3	28	cM1a	Recurrence	Bone scan, MRI	Bone, sinuses (near intracranial)	14	43.2	—	14		37
4	53	pM1a	Recurrence	Pathology, MRI	Orbit, lymph node, parotid gland	11		Enucleation			42
5	23	cM1a	Recurrence	MRI, bone scan	Bone, orbit	9		Orbital exenteration			71
6	44	cM1a	Onset	Bone scan	Bone, Intraorbital segment of optic nerve	9		Enucleation	6		64
7	38	cM1a	Onset	Bone scan	Bone, Intraorbital segment of optic nerve	12		Enucleation	11		45
8	17	pM1a	Recurrence	MRI,BM immunocytology	Bone marrow, orbit, parotid gland	12		Enucleation	6		16
9	27	cM1b	Recurrence	MRI	Anterior and middle cranial fossa, frontotemporal lobe, orbit, bone marrow, bone, lymph nodes, sinuses	19	46	—	13		65
10	25	cM1b	Recurrence	MRI	Temple lobe, orbits, bones, sinuses, parotid gland	17	45	—	11		68
11	120	cM1b	Onset	MRI	Optic nerve/Optic chiasm	9	45	Enucleation	9		47
12	56	cM1b	Onset	MRI	Intracranial optic nerve	14	—	Enucleation+cranioorbital communication mass resection	9		69
13	11	cM1b	Recurrence	MRI, BM cytology	Optic nerve/Optic chiasm	15	36		9		46
14	37	cM1b	Onset	MRI	Optic nerve/Optic chiasm	15	45	Enucleation	14		22
15	82	cM1b	Onset	MRI	Optic nerve/Optic chiasm	16	43.2	Enucleation	14		35
16	30	cM1b	Onset	MRI	Intracranial optic nerve	13	50.4	Enucleation	9		33

Abbreviations: IVC, intravenous chemotherapy; EFS, event-free survival after metastasis; BM, bone marrow; ASCT, autologous stem cell transplantation; RT, radiation Therapy.

All patients had completed treatment by February 2021, and survived without events. By the end of treatment, the serum NSE levels of all patients were within 10.6–27.3ng/mL. The median OS of RB was 50.5 (range, 23–102) months, the median EFS after metastasis was 43.5 (range, 16–71) months, the median EFS after treatment was 29 (range, 6–59) months (Figure 2), six patients (6/16) achieved an EFS of more than 3 years after all treatments ended. Among all 94 patients with metastatic RB, 65 patients died, including eight patients who died of tumor recurrence after CR; two patients were lost to follow-up; 27 patients survived (four patients were under treatment, and seven patients achieved CR but did not meet the above inclusion criteria). The overall survival rate of 94 patients with metastatic RB was 28.7% (Figure 3). Of the 90 patients who ended the treatment, 31 patients achieved CR, and eight patients died after recurrence, including one patients who received ASCT. The recurrence rate after CR was 25.8%.

Figure 2

Survival curve of the 16 patients with RB with metastasis. Kaplan-Meier survival curve of the 16 included patients, the median OS of RB was 50.5 (range, 23–102) months, the median EFS after metastasis was 43.5 (range, 16–71) months, the median EFS after treatment was 29 (range, 6–59) months.

Figure 3

RB case with metastasis. Among all 94 patients with metastatic RB, 65 patients died, including eight patients who died of tumor recurrence after CR; two patients were lost to follow-up; 27 patients survived (four patients were under treatment, and seven patients achieved CR but did not meet the above inclusion criteria). The overall survival rate of 94 patients with metastatic RB was 28.7%.

Discussion

China is the most populous country globally and documents approximately 1000 new cases of RB every year, accounting for 1/8 of all cases worldwide.6 An increased number of cases diagnosed in middle and late stages and limited medical resources have resulted in lower eye protection rates and survival rates of RB patients in China compared with those in developed countries. The prognosis remains relatively poor for patients whose disease disseminates into the CNS and those with distant metastatic disease.7 The most common metastatic site of RB is the intracranial area, accounting for approximately 50% of cases.8 Bone is the second most common site. In addition, studies have confirmed that RB metastasizes to the parotid glands and submandibular lymph nodes through lymphatic vessels, but there are few previous case reports.9

Patients with metastatic RB should undergo a whole-body examination to assess their condition, including a fundus examination, lumbar puncture, bone puncture, MRI of the eye and head, bone scan, and imaging of lymph nodes, lungs, and abdomen (or PET-CT examination). Serum NSE levels can be elevated in some RB patients with metastases and are used as a blood indicator for monitoring. However, they are not sensitive enough in patients with metastases, especially in those with simple bone and optic nerve metastases. During the follow-up period in this study, the serum NSE level of all patients was maintained within 10.6–27.3ng/mL at the end of treatment, indicating that the serum NSE level may have biomarker value in the diagnosis and treatment of RB.

Patients with RB metastasis have a low survival rate and poor prognosis. RB metastasis is an important cause of death in RB patients. Previously, there have been some reports of successful RB treatment in the metastatic stage. Wang et al.,9 Purkayastha et al10 have reported the successful treatment of RB patients with parotid gland and soft tissue metastasis by systemic IVC combined with local radiotherapy. Wang et al.,11 Vempuluru et al,12 and others reported the use of systemic IVC combined with external radiotherapy for the treatment of RB patients with bone metastasis and CNS metastasis. In a study by Palma et al,13 11 patients with RB metastasis were reported to have undergone high-dose chemotherapy (HDC) combined with ASCT, and two children received post-ASCT CNS radiotherapy. Seven children showed disease-free survival, including those with bone metastasis, bone marrow metastasis, optic chiasm masses, and cerebrospinal fluid metastasis. Consequently, they proposed that HDC-ASCT is a feasible and effective treatment for children with metastatic RB.13 In our study, we reported 16 patients with metastatic RB, including eight children with CNS metastasis (two cases of brain parenchyma metastasis and six cases of optic nerve and chiasm metastasis) and eight patients with metastases in other tissues (bone, parotid glands, lymph nodes, and bone marrow). All patients achieved CR after treatment and survived event-free during the follow-up period. The overall survival rate of 94 children with RB metastasis was 28.7%; those with event-free survival of more than 6 months who met the enrollment criteria accounted for 17.0%. In summary, although the prognosis is particularly poor, a reasonable selection of comprehensive treatment methods may provide effective treatment for patients with metastatic RB. However, since the recurrence rate of children with RB who achieved CR after treatment was as high as 25.8%, long-term follow-up is mandatory in all metastatic RB survivors, and it is necessary to be alert to the recurrence of RB, even in patients with CR after ASCT.

On the basis of our experience, systemic IVC is effective for the treatment of metastatic RB. The chemotherapy regimen for the treatment of IVC should be improved on the basis of the traditional CEV regimen. The chemotherapy cycle and regimen should be adjusted based on the patient’s condition; patients with CNS metastasis or systemic dissemination, high tumor load, or patients with poor response to treatment usually require more chemotherapy cycles; individualized treatment can be considered for complex cases. For patients with intracranial metastases or lesions close to the brain, combined fractionated radiotherapy (recommended total radiation dose of 45 Gy) and intrathecal chemotherapy (recommended 9–12 cycles of intrathecal chemotherapy) are required. Among cases with CNS metastasis, simple intracranial optic nerve infiltration may be the subtype with the best prognosis. For patients with late-stage metastatic RB, eyeball enucleation should be performed as appropriate. For intra-orbital metastases, orbital exenteration can be performed; the lesions should be removed as much as possible, and the eyeballs should not be preserved blindly. For large tumors or extensive lesions, systemic chemotherapy can be administered first for tumor reduction, and then other treatment options may be combined. Autologous stem cell transplantation may be effective for metastatic RB.

At present, the main chemotherapeutic strategy for RB is the CEV regimen. Although this chemotherapy regimen has been proven effective in the treatment of non-metastatic RB patients, it is insufficient in the treatment of advanced RB. In recent years, individualized treatment has been increasingly recognized, and we have administered individualized treatment for complex cases. However, new chemotherapeutic drugs and chemotherapy regimens require further research and clinical observation of their efficacy. Molecular targeted drugs have recently been suggested to be more effective and less toxic than traditional treatments, and local administration enhances the effect of drugs,14 but there is no effective clinical application. Published literature indicates that HDC-ASCT is an option for the treatment of metastatic and extraocular RB. Long-term survival rates are reported to be 50% to 75%, but there are still some limitations, such as recurrence after transplantation and the small sample size of existing studies.15,16 Furthermore, hematopoietic stem cell transplantation for the treatment of metastatic RB still needs additional clinical research and exploration.

The prognosis of early stage RB cases is good, but the prognosis of metastatic cases is very poor. The high survival rate of Rb patients in developed countries benefits from the early identification and standardized management of diseases. At present, Rb has been included in the “national catalogue of rare diseases” in China. As a developing country, the distribution of medical resources in China is unbalanced; ophthalmologists in primary medical institutions should improve the ability to recognize RB disease, and refer patients to regional medical centers for early and standardized treatment as soon as possible. In addition, families with genetic risk of RB need to seek for genetic counseling and early screening of RB disease. Under the current medical situation, early identification of retinoblastoma, standardized treatment and long-term follow-up management are very important to improve the prognosis of Rb.

Conclusion

The prognosis of distant metastatic RB is particularly poor. Systemic IVC combined with surgery, intrathecal chemotherapy, radiotherapy, hematopoietic stem cell transplantation, and other treatments may be effective in the treatment of metastatic RB. However, distant metastasis of RB is difficult to treatment, and the survival rate is low, recurrence after treatment is also worrying, even ASCT cannot completely avoid RB recurrence. Thus, it remains the main cause of death in children with RB, and patients in complete remission still need long-term follow-up. A larger sample for clinical research and the exploration of new treatment methods are needed.

Synopsis

We report 16 cases of metastatic retinoblastoma who survived event-free through chemotherapy-based comprehensive treatment. Comprehensive treatment may improve the prognosis of patients with metastatic retinoblastoma.