Carlos Camps Herrero
University of Valencia
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Featured researches published by Carlos Camps Herrero.
Clinical & Translational Oncology | 2010
Yolanda Escobar Álvarez; César A. Rodríguez Sánchez; Fernando Martínez; Virginia Recuero Cuervo; Carlos Camps Herrero
Cancer pain is still not treated adequately. The barriers impeding its appropriate treatment include lack of knowledge, erroneous beliefs and inappropriate attitudes with regard to pain, which are sustained by some or all of those involved in the problem. The present study shows the results of an exploratory survey using a large sample of specialists in clinical oncology. Its main objective is to evaluate daily analgesic practices and compliance with clinical guidelines in order to identify areas that should be improved in this particular therapeutic fi eld. Information collection from the responders was in the form of a self-administered written questionnaire, structured in three thematic areas: clinical patterns and resources used in pain treatment in clinical practice, pain and pain-relief therapy, and theoretical knowledge and decision-making in clinical practice. The study identifi ed those skills that most need improvement in the treatment of pain (scientifi c and technical knowledge and clinical decision-making capacity of professionals) in order to reduce the unjustifi ed variability in current clinical practice.
Clinical & Translational Oncology | 2005
Carlos Camps Herrero; Joaquín Gavilá Gregori; Javier Garde Noguera; Cristina Caballero Díaz; Vega Iranzo González-Cruz; Asunción Juárez Marroquí; Ma José Safont Aguilera; Ana Blasco Cordellat; Alfonso Berrocal Jaime; Ma Godes Sanz de Bremond
ResumenLa evolución de los enfermos con cáncer conduce en muchas ocasiones a fases de la enfermedad en las que no existen tratamientos específicos y éstos debemos aplicarlos en la consecución del máximo confort a través de un adecuado control sintomático, en esa etapa es fundamental el respeto de la autonomía personal y la posibilidad del rechazo de tratamientos fútiles. Con el adecuado control de síntomas es posible lograr que la mayoría de los enfermos no padezcan sufrimientos. Los cuidados continuos en el paciente oncológico son los responsables de ayudarnos a resolver estas situaciones. En medicina paliativa existe un procedimiento altamente eficaz en la ayuda en las últimas horas, la sedación, aplicable cuando sea imposible el control sintomático con otros medios. Con una cobertura adecuada de cuidados no debería ser necesario introducir leyes de suicidio asistido y/o eutanasia activa voluntaria, ni por la magnitud de la demanda, ni por las dificultades en el adecuado control sintomático.AbstractDuring the clinical evolution of patients with cancer there are many occasions, or phases of the disease, when there are no specific treatments and, as such, we need to provide maximum comfort following appropriate symptom control; in this stage it is fundamental to respect personal autonomy together with the option to reject futile treatment. With appropriate control of symptoms it is possible to reach the stage where the majority of the patients do not continue to suffer. Continuous-care providers for cancer patients are those who are responsible for providing help to resolve these situations. In palliative medicine there are highly-efficacious procedures to the help in these last hours. Sedation is applied when it is impossible to control symptoms by other means. With appropriate Carer cover, it is not necessary to introduce laws on assisted suicide and/or active voluntary euthanasia, neither because of the magnitude of demand, nor because of the difficulties in achieving appropriate control of symptoms.During the clinical evolution of patients with cancer there are many occasions, or phases of the disease, when there are no specific treatments and, as such, we need to provide maximum comfort following appropriate symptom control; in this stage it is fundamental to respect personal autonomy together with the option to reject futile treatment. With appropriate control of symptoms it is possible to reach the stage where the majority of the patients do not continue to suffer. Continuous-care providers for cancer patients are those who are responsible for providing help to resolve these situations. In palliative medicine there are highly-efficacious procedures to the help in these last hours. Sedation is applied when it is impossible to control symptoms by other means. With appropriate Carer cover, it is not necessary to introduce laws on assisted suicide and/or active voluntary euthanasia, neither because of the magnitude of demand, nor because of the difficulties in achieving appropriate control of symptoms.
Molecular and Clinical Oncology | 2017
Javier Garde Noguera; Eloisa Jantus‑Lewintre; Mireia Gil‑Raga; Elena Evgenyeva; Sonia Maciá Escalante; Antonio Llombart Cussac; Carlos Camps Herrero
The role of Kirsten rat sarcoma viral oncogene homolog (KRAS) and neuroblastoma RAS viral oncogene homolog (NRAS) mutations as negative predictors for anti-epidermal growth factor receptor (EGFR) therapies in metastatic colorectal cancer (CRC) has been firmly established. However, whether the RAS mutation status plays a role as a biomarker for anti-vascular endothelial growth factor (VEGF) treatment remains controversial. Data from 93 CRC patients who received first-line cytotoxic chemotherapy with fluoropyrimidines and oxaliplatin, with or without bevacizumab, were analyzed. We investigated the association between the RAS mutation status and clinical outcomes in terms of response rate, progression-free survival (PFS) and overall survival (OS). Mutations in RAS genes were observed in 47 (52.6%) patients (45 KRAS and 2 NRAS mutations). Patients with tumours harbouring RAS mutations were less suitable for primary tumour resection, were more likely to develop lung metastases, and received bevacizumab treatment for a shorter time period compared with those with wild-type tumours. The response rate to chemotherapy did not differ according to the RAS mutation status, and there were no significant differences in PFS [RAS mutation: 12 months, 95% confidence interval (CI): 8.7-15.2 vs. RAS wild-type: 12 months, 95% CI: 9.67-14.32; P=0.857] or OS (RAS mutation: 20 months, 95% CI: 14.3-25.6 vs. RAS wild-type: 24 months, 95% CI: 18.7-29.2; P=0.631). Patients with RAS mutation vs. those with RAS wild-type exhibited a favourable trend in PFS when treated with bevacizumab (13 months, 95% CI: 6.5-19.4 vs. 10 months, 95% CI: 4.2-15.7, respectively; P=0.07) and OS (27 months, 95% CI: 18.5-35.4 vs. 15 months, 95% CI: 12.4-17.5, respectively; P=0.22). In conclusion, RAS mutations are not a prognostic marker for PFS and OS in CRC patients receiving fluoropyrimidine-oxaliplatine treatment, with or without bevacizumab. RAS mutations are not predictive of the lack of efficacy of bevacizumab, and these patients appear to benefit from anti-angiogenic treatment.
Journal of Analytical Oncology | 2013
Javier Garde Noguera; Elena Evgenyeva; Mireia Gil‑Raga; Asunción Juárez Marroquí; Juan Manuel Gasent Blesa; Juan Laforga; Laia Bernet; Mónica Clemente Císcar; Carlos Camps Herrero; Antonio Llombart Cussac
Purpose : To analyze the impact of primary tumour resection on treatment outcomes in patients with advanced colorectal cancer (CRC) and inoperable metastases at diagnosis in combination with optimal systemic therapy. Methods : A retrospective study was carried out in four hospitals in Valencia (Spain) including all consecutive patients diagnosed between 1/2009 and 12/2010 of advanced CRC with inoperable metastasis and treated with a fluoropyrimidine and oxaliplatin combination chemotherapy regimens with or without bevacizumab (B). Treatment outcomes were compared between patients undergoing or not primary tumour resection. Results : A total of 112 patients met inclusion criteria: 62 patients underwent resection of the primary tumour (Group 1) and 50 were treated with exclusive chemotherapy (Group 2). Globally, patients in group 2 presented more disfavorable characteristics. Forty-five (72%) and 31 (62%) patients received chemotherapy with bevacizumab respectively. Overall response rate (ORR) were 67% in Group 1 and 56% in Group 2. There were no statistically significant differences between the two groups in progression free survival (PFS) (12 vs. 10 months; p =0.11) and overall survival (OS) (27 vs. 22 months; p 0.1). B regimens increased ORR (73% vs. 42%; p = 0.003) and PFS (12 vs. 11 months; p = 0.019) but not OS. Complications were higher in the group of patients without primary tumour resection, particularly when associated to B regimens. Conclusions : Primary tumour resection offers no survival gain for patients with advanced CRC and inoperable metastases. Benefits of adding Bevacizumab to standard chemotherapy were similar in both groups, but it increases the risk of complications in non-resected patients.
Supportive Care in Cancer | 2016
Ramón De las Peñas; Santiago Ponce; Fernando Henao; Carlos Camps Herrero; Enric Carcereny; Yolanda Escobar Álvarez; César A. Rodríguez; Juan Antonio Virizuela; Rafael López López
Clinical & Translational Oncology | 2009
Vicente Alberola Candel; Alfredo Carrato Mena; Eduardo Díaz Rubio García; Pere Gascón Vilaplana; Manuel González Barón; Miguel Martín Jiménez; Emilio Alba Conejo; Javier Cassinello Espinosa; Ramon Colomer; Juan Jesús Cruz Hernández; Agustí Barnadas‑Molins; Carlos Camps Herrero; Ana M. Casas Fernández de Tejerina; Joan Carulla Torrent; Manuel Constenla Figueiras; Joaquín Gavilá Gregori; Ma. Dolores Isla Casado; Bartomeu Massuti Sureda; Mariano Provencio Pulla; César A. Rodríguez Sánchez; Jaime Sanz Ortiz
Molecular and Clinical Oncology | 2015
Javier de Castro Carpeño; Pere Gascón-Vilaplana; Ana Maria Casas‑Fernández‑de Tejerina; Antonio Antón Torres; Rafael López López; Agustí Barnadas‑Molins; Juan Jesús Cruz Hernández; Bartomeu Massuti Sureda; Carlos Camps Herrero; E. Aguilar; Francisco José Rebollo Laserna
Cuadernos Monográficos de Psicobioquímica | 2013
Ana Blasco Cordellat; Cristina Caballero Díaz; Carlos Camps Herrero
REME | 2008
Pedro T. Sánchez; Rafael Sirera Pérez; Gema Peiró; Julia M. Sánchez; Francisco Palmero; Ana Blasco Cordellat; Carlos Camps Herrero; Pilar Blasco
REME | 2008
Pedro T. Sánchez; Gema Peiró; Miguel de Lamo; Nieves del Pozo Alonso; Francisco Palmero; Ana Blasco Cordellat; Carlos Camps Herrero