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Comparison of clinical outcomes of conbercept versus ranibizumab treatment for retinopathy of prematurity: a multicentral prospective randomised controlled trial
  1. Zhenquan Wu1,
  2. Jinfeng Zhao1,
  3. Waiching Lam2,
  4. Mingmin Yang1,
  5. Lu Chen1,
  6. Xuelin Huang3,
  7. Meirong Wei4,
  8. Hui Yang5,
  9. Fan Lv6,
  10. Fuyan Zhang7,
  11. Jian Zeng1,
  12. Guo-Ming Zhang1
  1. 1Ophthalmology, Shenzhen Eye Hospital, Shenzhen Key Laboratory of Ophthalmology, Shenzhen University School of Medicine, Shenzhen, Guangdong, China, Shenzhen, Guangdong, China
  2. 2Ophthalmology, The University of Hong Kong, Grantham Hospital, Hong Kong, China
  3. 3Ophthalmology, Guangdong Provincial Maternity and Children’s Hospital, Guangzhou, Guangdong, China
  4. 4Ophthalmology, Liuzhou Maternity and Children’s Hospital, Liuzhou, China
  5. 5Ophthalmology, Xiamen Children’s Hospital, Xiamen, China
  6. 6Ophthalmology, Quanzhou Children’s Hospital, Quanzhou, China
  7. 7Ophthalmology, Guizhou Medical University, Guiyang, Guizhou, China
  1. Correspondence to Dr Guo-Ming Zhang, ophthalmology, Shenzhen Eye Hospital, Shenzhen 518040, Guangdong, China; 13823509060{at}


Purpose To compare the recurrence rate and surgical complications of retinopathy of prematurity (ROP) between patients treated with intravitreal injection of conbercept (IVC) and intravitreal injection of ranibizumab (IVR) within 6 months.

Methods A multicentral prospective, randomised controlled trial was applied from May 2017 to February 2019 for the infants diagnosed as aggressive posterior-ROP, zone I or posterior zone II treatment-requiring ROP by binocular indirect ophthalmoscope and RetCam3. These infants were assigned to randomly receive either intravitreal injection of 0.25 mg conbercept or 0.25 mg ranibizumab. The recurrence rate, fundus fluorescence angiography (FFA) and surgical complications were examined during the follow-up period of 6 months. Recurrent eyes were retreated by laser or another intravitreal injection within the 72 hours.

Results A total of 30 infant patients (60 eyes) underwent IVC and 30 patients (60 eyes) underwent IVR. A total of 10 eyes (16.67%) in the IVC group and 14 eyes (23.34%) in the IVR group developed recurrence. There was no significant statistical difference in the recurrence rate between the two groups (χ2=0.83, p=0.36). The postmenstrual age (PMA) at first injection was (34.60±3.47) weeks in IVC and (35.14±1.76) in IVR group. In recurrent cases, the mean PMA at second treatment were (43.31±3.85) and (43.43±3.89) weeks in the IVC and IVR group, respectively. The period between two treatments was (8.71±6.62) for the IVC and (8.29±2.56) weeks for the IVR group. All these results showed no significant statistical difference between these two groups. The fluorescein leakage were observed in the eyes of recurrent infants by FFA. There were no other complications in the two groups except for complicated cataract in three eyes.

Conclusion Both IVC and IVR are effective therapies for the treatment of ROP. Conbercept is a new option for treating ROP.

  • drugs
  • retina
  • treatment other

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Retinopathy of prematurity (ROP) is the major cause for childhood blindness worldwide.1 2 The vascular endothelial growth factor (VEGF) is regarded as a main factor leading to ROP.3 The dysregulation of VEGF associated with hypoxia is thought to play an significant role in its abnormal vasculogenesis and neovascularisation.4 The traditional standard treatment for ROP is laser photocoagulation (LP).5–7 But the side effect of LP should not be ignored including visual field loss and subsequent high myopia.4 In recent years, anti-VEGF treatment has become a new effective therapy for ROP.4 8 9 Compared with LP, anti-VEGF agents have the advantages including short operating time, no need of sedation or general anaesthesia and no ablation of peripheral retina.10–12

There have been some studies comparing the efficacy of different anti-VEGF agents in the treatment of ROP, such as conbercept and ranibizumab, ranibizumab and aflibercept, bevacizumab and ranibizumab.4 13–15 Some of these anti-VEGF agents have been used by experts in treating ROP for many years, while conbercept (KH902; Chengdu Kanghong Biotech, Sichuan, China), as a new anti-VEGF agent, has been used in China just in recent years. Conbercept was first approved by China Food and Drug Administration for intravitreal injection in treating age-related macular degeneration (AMD) in 2013. It is a recombinant fusion protein. And it has the characteristics of multiple targets, stronger affinity and the ability to inhibit neovascularisation. The safety and efficacy of injection of conbercept for AMD and ROP have been confirmed by retrospective studies.4 16

As we described above, the safety and efficacy of various anti-VEGF agents for ROP have been confirmed by many studies.4 13–15 The researches of these studies have shown that the anti-VEGF agents are effective for ROP. But most of these studies were retrospective. Prospective studies in this field to further investigate the efficacy of defferent anti-VEGF agents are particularly important. At present, few prospective studies have been reported in comparison of conbercept and ranibizumab in treating ROP.

This study aims to compare the recurrence rates and related outcomes between intravitreal injection of conbercept (IVC) and intravitreal injection of ranibizumab (IVR) in ROP treatment through a prospective randomised controlled trial (RCT), which might provide insights of ROP treatment for clinical ophthalmologists.


Examination and enrolment

A total of 60 infants of patients with ROP were consecutively enrolled in this study from various centres and hospitals nationwide during the period of May 2017 to February 2019. They included Shenzhen Eye Hospital, Guangdong Provincial Maternity and Children’s Hospital, Liuzhou Maternity and Children’s Hospital, Xiamen Children’s Hospital and Quanzhou Children’s Hospital. We employed a multicentral prospective RCT in this study. All the infants were examined via binocular indirect ophthalmoscope and fundus imaging by RetCam 3 (Clarity Medical System, Pleasanton, California, USA) at the first and each follow-up visit. Each infant was examined by two experienced retinal experts independently, and the eligibility was confirmed by both experienced retinal experts. The definition of stage and zone was based on the revised guidelines of the International Committee for the Classification of Retinopathy of Prematurity.17 The definition of treatment requiring ROP were based on the Early Treatment ROP.6 18 Inclusion criteria contain: (1) aggressive posterior ROP (AP-ROP); (2) Zone I or posterior zone II treatment-requiring ROP (any stage of ROP with plus disease or stage three without plus disease in zone I. Stages 2 and 3 with plus disease in zone II.); (3) agreement of parents to participate in the trial. Exclusion criteria include: (1) infants with other eye diseases; (2) infants with any previous treatment including intravitreal injection, LP, cryotherapy or other ocular surgery.

Study design

All eligible infants were randomly divided into two groups at a 1:1 proportion using a computer-generated randomisation schedule. Both eyes of each infant were then treated by either the IVC or IVR herapy. The primary observational indicators was the recurrence rate. Other observational indicators were retinal features of recurrence based on the fundus fluorescence angiography (FFA) and the complications after the treatment. The participants’ parents were informed about the severity of the disease, treatment options and complications. And this study obtained the informed consent of the parents before the study was performed.


All the included infants in the IVC group received an IVC (Conbercept; Chengdu Kanghong Biotech, China) with a dose of 0.25 mg/0.025 mL half of the adult dosage. For the IVR group, all the infants received an intravitreal injection of ranibizumab (Lucentis; Genentech and Novartis International AG) with the same dose of 0.25 mg/0.025 mL. Intravitreal injection was performed under topical anaesthesia in the standard ophthalmic operating room. This anti-VEGF agent was injected into the vitreous, pointing the needle toward the optic nerve in direction of the visual axis 1.0 mm posterior to the corneoscleral junction. An ophthalmic antibiotic eye-drop was prescribed for the treated eye four times a day for 1 week. Another intravitreal injection (IVI) or LP would be arranged as a secondary treatment when recurrence occurred. The application of anti-VEGF agents is suitable for the recurrent infants whose lesions are close to the posterior pole of retina, and LP is more appropriate for infants with lesions near the periphery. An indirect infrared diode laser (Iridis; Quantel-Medical, Cournon d'Auvergne Cedex, France) (810 nm) was used to apply photocoagulation through a 20-diopter condensing len under the state of sedation. The procedure of sedation was peformed by an experienced nurse in the neonatal intensive care unit using phenobarbital and diazepam intravenous injection. The sedative strategy was determined by neonatologists based on the weight of infants. Initial laser was set up at a power of 150 mW for 0.2 s. Confluent laser treatment was applied to the avascular retina between the fibrovascular ridge and the ora serrata. The laser treatment for peripheral retina was performed under scleral indentation. The antibiotic eye-drop was administrated for 1 week after laser treatment.


All infants were monitored by binocular indirect ophthalmoscope and RetCam 3 after the treatment following the timeline: 1, 2, 4, 6, 8, 10, 12, 18 and 24 weeks after the treatment. The follow-up occured at least 6 months. The main outcome measurements included the regression of plus disease, resolution of neovascularisation, disappearance of ridge, ROP recurrences and any complications. The recurrence was defined as any of the following: recurrent plus disease, recurrent neovascularisation or reformation of ridge despite treatment. Once the recurrence occurred, the secondary treatment was arranged for retreatment within 72 hours.19

Statistical analyses

Statistical analysis was performed by the SPSS software (V.23). Normally distributed variables were compared and constrasted by the t-test while the χ2 test was used to examine categorical variables . The p<0.05 was considered statistically significant in this study.


A total of 60 eyes of 30 infants were treated with IVC monotherapy, and 60 eyes of another 30 infants were treated with IVR monotherapy. These two groups of infants have completed the 6-month follow-up. Our results show that there was no statistically significant difference in gestational age (GA), birth weight (BW), sex ratio, the proportion of single or twin births, delivery methods and corrected GA at first treatment between two groups (table 1). And in the IVC group, the medians of BW, GA and postmenstrual age (PMA) were 1047.5 g (600–2500 g), 28.43 weeks (24–32.86 weeks) and 35 weeks (29.43–39.43 weeks), respectively. In the IVR group, the medians of BW, GA and PMA were 975 g(590–1930 g), 27 weeks (24–33.14 w) and 35.79 weeks (32–42 weeks), respectively.

Table 1

The characteristics of infants in the IVC and IVR groups

Main outcomes

After a single-dose injection, a total of 10 eyes of 5 infants (16.7%) developed ROP recurrence in the IVC group, and 14 eyes of 7 infants (23.34%) developed ROP recurrence in the IVR counterpart. There was no significant difference between the two groups (χ2=0.83, p=0.36). All of the recurrent infants in the IVC group and five recurrent infants in the IVR group were treated with the LP, and the remaining two recurrent infants in the IVR group were treated with the IVR. For the infants with and without recurrence, we selected a series of representative images to show the results of each examination. figure 1A–H shows the fundus images in the IVC and IVR group, respectively, which represented cases without recurrence. figure 2A–J shows the fundus images in the IVC and IVR group, respectively, which represented cases with recurrence.

Figure 1

Fundus images of no recurrence cases. (A–D) fundus images in the IVC group. (E–H) fundus images in the IVR group. (A,E) images before IVI shows plus disease and ridge. (B,F) regression of plus disease and ridge was observed at 1 week after treatment. (C,G) one month after treatment. (D,H) six months after treatment. No recurrence occurred during the 6 months follow-up. IVC, intravitreal injection of conbercept; IVI, intravitreal injection; IVR, intravitreal injection of ranibizumab.

Figure 2

Fundus images of recurrence cases. (A–E) fundus images in the IVC group. (F–J) fundus images in the IVR group. (A,F) Images before IVI shows plus disease and ridge. (B,G) Regression of plus disease and ridge was observed at 1 week after treatment. (C, H) aggravated plus disease and ridge was observed during follow-up. (D,I) FFA shows the retinal neovascularisation and fluorescence. (E,J) six months after IVI. No new recurrence was observed after secondary treatment. FFA, fundus fluorescence angiography; IVC, intravitreal injection of conbercept; IVR, intravitreal injection of ranibizumab.

For the recurrent infants, the PMA at first treatment reached 34.60±3.47 weeks in the IVC group and 35.14±1.7 weeks in the IVR counterpart. There was no statistically significant difference in both groups (t=−0.36, p=0.728). The PMA at second treatment in these two groups were 43.31±3.85 and 43.43±3.89 weeks. Likewise, there was no statistically significant difference in both groups (t=−0.05, p=0.961). The interval of these two treatments in the two groups was 8.71±6.62 and 8.29±2.56 weeks. Again, there was no statistically significant difference in both groups (t=−0.16, p=0.878). Details of the infants were given in the tables 1 and 2.

Table 2

The primary outcomes of IVC group and IVR group

We observed the total regression of plus disease and ridge in all recurrent infants after the secondary treatment, and there was no new recurrence occurred during the follow-up period (figure 2A–J).

Features of recurrence based on FFA

The FFA examination was performed in 5 recurrent infants (10 eyes) before the second treatment. Their vessels in the posterior pole are seen to be tortuous and dilated. There is a wide avascular area in the peripheral retina. The ROP ridge aggravated. The plexiform arteriovenous anastomosis occurred. The branches of peripheral vessels increased, presenting a ‘brush-like’ change. The vascular blunt, vascular loops and the neovascularisation were observed, accompanied by obvious fluorescence leakage, presenting a ‘popcorn-like’ change (figure 2D,I).


A total of three eyes (ie, two in the IVC and one in the IVR group) generated complicated cataracts after treatment. No anterior segment ischemia, pupillary membrane, retinal detachment, endophthalmitis, glaucoma, intraocular haemorrhage or systemic complications related to injection occurred during the follow-up period.


The LP is a conventional treatment for ROP.6 17 The mechanism of LP is known to suppress VEGF by ablating the avascular retina. However, LP shows several limitations, such as ametropia and defection of the visual field.19 Compared with LP, anti-VEGF therapy is more convenient to operate and shows no irreversible damage to the retina. It has been regarded as a primary monotherapy for zone I ROP and AP-ROP.10–12 Recently, anti-VEGF therapy has been increasingly applied in ROP treatment. The conbercept and ranibizumab have been reported and proved to be effective.4 Previous research has compared the curative effect of IVC and IVR in the treatment of ROP.4 But most of studies were retrospective, and the sample size is relatively small. This study is the multicentral prospective RCT of conbercept versus ranibizumab for ROP, which might provide insights from a new perspective for clinical ophthalmologists.

The results on the IVC recurrence rate showed great similarities in previous studies. For example, Bai et al16 enrolled 24 patients (48 eyes) who received 0.25 mg IVC treatment and a follow-up for more than 6 months. The authors showed that a total of 8 eyes (16.7%) required secondary treatment. In Jin’s retrospective study, the recurrence rate was 15% (3/20)in the IVC group but 53.6% (15/28) in the IVR counterpart.4 In our study, the recurrence rate of IVC is 16.7% (10/60). Recurrent ROP was treated by LP and obtained regression. This conclusion generally agrees with those in previous studies.

Conbercept, as a new anti-VEGF agent, is a fusion protein which combines the second Ig-like domain of VEGFR-1 and the third and fourth Ig-like domains of VEGFR-2 to the Fc portion of human IgG1. Thus, it has the characteristics of multiple targets, stronger affinity (such as VEGF-A, VEGF-B, VEGF-C and PIGF), and the ability to inhibit neovascularisation.20–24 Domain 4 of the conbercept can reduce positive charge, reduce adhesion of extracellular matrix, optimise pharmacokinetics and make it have stronger affinity and longer half-life.21 The use of conbercept for ROP has been reported.16 25 26 Cheng et al26 used a lower dose (0.15 mg/0.015 mL) of conbercept for ROP, and the recurrence rate was reported to be 15.8%. This suggested that a low dose of conbercept was also effective in ROP, which might reduce the potential systemic risks.

However, the IVR recurrence rate varied greatly from 0% to more than 80% in previous retrospective studies. Ranibizumab is a specific, recombinant, humanised monoclonal antibody with high binding affinity for VEGF-A, rendering the VEGF inactive. As for the different results of different studies, we consider that the different inclusion criteria with various researches, the subjectivity of different experts in diagnosis, recurrence definition, timing of operation and follow-up schedules may cause the diversity simultaneously. In this study, there is no significant statistical difference in the recurrence rate between the IVC and IVR groups. More importantly, this was a prospective RCT of conbercept vs ranibizumab with a relatively high level of evidence. Our inclusion criteria and intervention are more unified, and the evaluation of these two therapies is more objective and accurate.

For the timing of recurrence, previous research reported the time of 4–8 weeks after IVR or approximately 41–42 weeks’ PMA.27–29 In Lyu’s study, the recurrence of ROP occurred in 32 (64%) of 50 eyes at 7.9±2.7 weeks after IVR, and the major recurrence risk period was from 2.5 to 12.0 weeks after IVR, with its risk peak at 8 weeks. In our study, however, the interval of ROP in the IVC and IVR group reached 8.71±6.62 weeks and 8.29±2.56 weeks, respectively. A total of 91.67% (22/24) recurrence occurred within 12 weeks after IVC or IVR. Based on our study and previous reports, a close follow-up in the first 12 weeks after treatment is indispensable for timely identification of ROP recurrence. However, the one infant in the IVR group in this studiy had a long interval (20.28 weeks) between two treatments with an earlier GA and initial treatment time. As a result, a longer follow-up should be arranged for such infants with late recurrence in case of misdiagnosis. According to previous studies and the results of this study,30 a follow-up longer than 24 weeks after IVI would be better for management of ROP recurrence. The optimal follow-up time, if available, still needs to be further verified by long-term follow-ups with a larger sample size. In this study, half of the infants with recurrence were diagnosed with AP-ROP. This suggests that infants with severe disease are more likely to be recurrent. Although some cases of recurrence occurred, most of them were well controlled after the second treatment.16

The FFA, as an adjunct to indirect ophthalmoscope, is an important technique to identify the vascular changes of ROP.31 32 In this study, FFA was performed on certain infants with recurrence before secondary treatment, as this technology distinctly showed the vascular abnormalities, such as vascular blunt, loops and dilatation, and leakage. The leakage is a significant feature suggesting neovascularisation, which provides a convincing evidence for recurrence. Compared with direct observation, FFA is more sensitive for demarcation between vascular and avascular areas. After IVI treatment, we observed that retinal blood vessels could continue to develop to zone III, but not all infants' vessels could reach the ora serrata. The effects of the avascular areas remain unknown. How to deal with the avascular area after IVI treatment is still debatable, and thus long-tern observation and supplementing FFA are required. Owing to the limitation of equipment in certain centres, FFA was employed only in 5 infants (10 eyes) in this study.

Complicated cataract occurred in three eyes, characterised by a single localised punctate opacity on peripheral lens. This complication might be iatrogenic damage caused by the fact that the needle touched the lens during the surgery, indicating that sufficient topic anaesthesia should be undergone before the treatment. Surgical light and eyeball fixation should be ensured during the operation. The 1–1.5 mm posterior to the corneal limbus should be the entry point. The needle should be oriented towards the centre of the eyeball to reduce the risk of iatrogenic injury. For these infants who have developed cataracts, the opacity may not affect visual development because of the peripheral location, but more future observation is necessary.


First, the sample size (ie, 30 infants for IVC and 30 for VR) is relatively small and the follow-up (ie, 6 months) is not so long. More patients should be included to increase the conviction in further studies, and the follow-up duration should be prolonged too. Second, we did not evaluate the systematic effects of two medicines on infants. The comparison of preoperative and postoperative blood VEGF levels in infants is of great significance for the safety evaluation, which needs to be supplemented in further research.


In conclusion, there was no significant statistical difference in the recurrence rate between IVC and IVR for treating ROP within 6 months. Both of the IVC and IVR are effective treatments for ROP. Conbercept is a new option for ROP treatment.


The authors would like to thank all the patients who participated in this study.



  • Contributors ZW and JZ contributed equally to this work. JZ and ZW contributed to the conception of the study. JZ, ZW and G-MZ performed the data analyses and wrote the manuscript. WL, JZ and FZ helped perform the analysis with constructive discussions. MY and LC contributed significantly to analysis and manuscript preparation. XH, MW, HY and FL in the Shenzhen Screening for Retinopathy of Prematurity Cooperative Group provided multicentre cases.

  • Funding This work was supported by the Basic Discipline Layout Foundation of the Shenzhen Science and Innovation Commission. P.R. China (Grant No. JCYJ20170817112542555); Shenzhen-hong Kong Cofunded Projects (Category A): SGDX20190920110403741.

  • Competing interests None declared.

  • Patient consent for publication Not required.

  • Ethics approval This protocol was approved by the Institutional Review Board of Shenzhen Eye Hospital, which was conducted in accordance with the Declaration of Helsinki.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement Data are available in a public, open access repository. Data are available on reasonable request.

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