Josep Caminal

Dr. Josep Caminal

orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 July 2008 in British Journal of Ophthalmology
Verified
Journal Article
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LALUIS ARIAS
LUIS ARIAS
NPN Planas
N Planas
SPS Prades
S Prades
JCJosep Caminal
Josep Caminal
MRM Rubio
M Rubio
GRG Roca
G Roca
Background: To determine the efficacy and safety of intravitreal Avastin (bevacizumab) in the treatment of choroidal neovascularisation (CNV) secondary to pathological myopia (PM). Methods: This paper reports on a consecutive prospective study of patients with CNV secondary to PM who were treated with intravitreal bevacizumab (1.25 mg/0.05 ml). Patients underwent complete ophthalmic evaluation, which included best-corrected visual acuity testing measured with Early Treatment Diabetic Retinopathy Study charts, optical coherence tomography (OCT), and fluorescein angiography. Results: There were 17 eyes of 17 patients, and the mean age was 55.4 (SD 10.0) years. At the 6-month follow-up, the mean visual acuity improved by 8.4 letters (p = 0.04). Forty-one per cent of patients increased at least one line, and 17% increased more than six lines. There were no cases of moderate vision loss (⩾3 lines) or severe vision loss (⩾6 lines). The mean OCT foveal thickness decreased by 79.6 μm (p = 0.002). Favourable outcomes were obtained in all subgroups. Patients received an average of one injection. As a complication, there was a tear of the retinal pigment epithelium. No other ocular or systemic side effects were observed. Conclusion: In our study, intravitreal bevacizumab appeared to be safe and efficacious in eyes with CNV secondary to PM.

17 June 2019 in Cancers
Verified
Journal Article
Open access
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FCFlorian Castet
Florian Castet
SGSandra García-Mulero
Sandra García-Mulero
RSRebeca Sanz-Pamplona
Rebeca Sanz-Pamplona
ACAndres Cuellar
Andres Cuellar
OCOriol Casanovas
Oriol Casanovas
JPJosep M. Piulats
Josep M. Piulats
Uveal melanoma is considered a rare disease but it is the most common intraocular malignancy in adults. Local treatments are effective, but the systemic recurrence rate is unacceptably high. Moreover, once metastasis have developed the prognosis is poor, with a 5-year survival rate of less than 5%, and systemic therapies, including immunotherapy, have rendered poor results. The tumour biology is complex, but angiogenesis is a highly important pathway in these tumours. Vasculogenic mimicry, the ability of melanomas to generate vascular channels independently of endothelial cells, could play an important role, but no effective therapy targeting this process has been developed so far. Angiogenesis modulates the tumour microenvironment of melanomas, and a close interplay is established between them. Therefore, combining immune strategies with drugs targeting angiogenesis offers a new therapeutic paradigm. In preclinical studies, these approaches effectively target these tumours, and a phase I clinical study has shown encouraging results in cutaneous melanomas. In this review, we will discuss the importance of angiogenesis in uveal melanoma, with a special focus on vasculogenic mimicry, and describe the interplay between angiogenesis and the tumour microenvironment. In addition, we will suggest future therapeutic approaches based on these observations and mention ways in which to potentially enhance current treatments.

9 September 2008 in British Journal of Ophthalmology
Verified
Journal Article
Closed access
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LALUIS ARIAS
LUIS ARIAS
JCJosep Caminal
Josep Caminal
LCL Casas
L Casas
CMC Masuet
C Masuet
MBM B Badia
M B Badia
JAJ Arruga
J Arruga
Aims: The aim of this study was to compare two treatment options for choroidal neovascularisation (CNV) secondary to age-related macular degeneration (AMD): (1) bevacizumab administered once a month for 3 months and thereafter as needed (loading dose (LD)); and (2) bevacizumab administered as needed, after the first injection (pro re nata (as needed) (PRN)). Methods: Fifty consecutive patients were enrolled in this prospective study. The first 25 patients were included in the LD group and the last 25 patients in the PRN group. In both groups, the need for re-treatment was based on the presence of persistent or recurrent macular oedema, subretinal fluid or pigment epithelial detachment on optical coherence tomography scans. Results: At the 6-month follow-up, mean visual acuity improved by 13.7 letters (p<0.001) in the LD group and 4.6 in the PRN group (p<0.001). Thirty-six per cent of patients in the LD group compared with 12% in the PRN group gained 15 or more letters (p = 0.04). Mean foveal thickness decreased by 91.3 µm (p<0.001) in the LD group and 48.2 µm in the PRN group (p<0.001). No ocular or systemic side effects were observed. Conclusion: Patients with CNV secondary to AMD treated with a LD protocol had better results than patients treated with a PRN protocol with intravitreal bevacizumab.

1 April 2006 in Archives of Ophthalmology (1950)
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Journal Article
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JCJosep Caminal
Josep Caminal
SSSilvia Sanz
Silvia Sanz
MCMarta Carreras
Marta Carreras
ICIsabel Català
Isabel Català
JAJorge Arruga
Jorge Arruga
GRGuillermo Roca
Guillermo Roca
Case Report from JAMA Ophthalmology — Epibulbar Seeding at the Site of a Transvitreal Fine-Needle Aspiration Biopsy

1 July 2013 in Clinical Ophthalmology
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Journal Article
Open access
ECE Cobos
E Cobos
LAL Arias
L Arias
JRJm Ruiz-Moreno
Jm Ruiz-Moreno
MRMj Rubio
Mj Rubio
PGP Garcia-Bru
P Garcia-Bru
JAJ Arruga
J Arruga
Peer reviewed article authored by (Cobos E, Arias L, Ruiz-Moreno JM, Rubio MJ, Garcia-Bru P, Caminal JM, Catala-Mora J, Arruga J). Read article or submit your manuscript for publishing.

1 August 2013 in American Journal of Ophthalmology
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Journal Article
Closed access
JCJosep Caminal
Josep Caminal
KMKarol Mejia
Karol Mejia
CMCristina Masuet-Aumatell
Cristina Masuet-Aumatell
LALluis Arias
Lluis Arias
JPJosep M. Piulats
Josep M. Piulats
JAJordi Arruga
Jordi Arruga