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Dive into the research topics where Yacine Merrouche is active.

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Featured researches published by Yacine Merrouche.


European Journal of Cancer | 2014

Feasibility of radiation therapy in patients 90 years of age and older: A French multicentre analysis

Cyrus Chargari; Guillaume Moriceau; Pierre Auberdiac; Jean-Baptiste Guy; Avi Assouline; Fabien Tinquaut; Alexander Tuan Falk; Houda Eddekkaoui; Aurélie Bourmaud; Yvan Coscas; Pierre Annede; Romain Rivoirard; Benoîte Méry; Jane-Chloé Trone; Yves Otmezguine; Cécile Pacaut; O. Bauduceau; Lionel Védrine; Yacine Merrouche; Nicolas Magné

BACKGROUNDnThere are only scarce data on the management of patients aged 90years or older with cancer, and more particularly on the place of radiation therapy (RT). We report the first large study on patients (pts) aged 90years or older receiving RT.nnnMETHODS AND MATERIALSnRecords from RT departments from five institutions were reviewed to identify pts 90years of age and older who underwent RT for various malignant tumours treated between 2003 and 2012. Tumours characteristics were examined, as well as treatment specificities and treatment intent.nnnRESULTSn308 pts receiving 318 RT courses were identified, mean age was 93.2years (standard deviation 2.8). Treatment was given with curative and palliative intent in 44% and 56%, respectively. Factors associated with a curative treatment were performance status (PS), place of life, previous surgery and tumour stage. Median total prescribed dose was 36Gy (4-76Gy). Hypofractionation and split course were used in 88% and 7.3%, respectively. Most toxicities were mild to moderate. RT could not be completed in 23 pts (7.5%). No long-term toxicity was reported. Median overall survival was 22.9months (95CI: 15.5-42.7months). Cancer was the cause of death in 8.7% and 46% of pts treated with curative and palliative intent, respectively.nnnCONCLUSIONnThis study shows that RT is feasible for patients aged 90years or more. PS, place of life and tumour stage were factors of the therapeutic decision. There is no reason to withdraw pts with good general health condition from potentially curative RT, provided that careful attention is paid to factors of toxicity and to geriatric vulnerabilities.


American Journal of Clinical Oncology | 2015

Uterine and ovary carcinosarcomas: outcome, prognosis factors, and adjuvant therapy.

Cécile Pacaut; Aurélie Bourmaud; Romain Rivoirard; Guillaume Moriceau; Jean-Baptiste Guy; Olivier Collard; Claire Bosacki; Jean-Philippe Jacquin; Antonin Levy; Céline Chauleur; Nicolas Magné; Yacine Merrouche

Objectives:The aim of this study was to assess the outcome and the prognosis factors of uterine and ovarian carcinosarcomas. Methods:From January 1993 to January 2010, data from 68 consecutively treated patients with uterine (n=59) and ovarian (n=9) carcinosarcomas were retrospectively analyzed in a single French comprehensive cancer center. Results:The median follow-up was 24.2 months (interquartile range [IQR]: 13.5 to 54.6). The median age was 69 years (IQR: 63 to 77). Patients were classified as FIGO stage I (n=28; 41%) and FIGO stage II to IV (n=40; 59%), respectively. There were 33 (49%) and 29 (43%) homologous and heterologous type, respectively. The median disease-free survival and overall survival were 21.9 months (IQR: 7.9 to 22.3) and 27.1 months (IQR: 14.5 to 72), respectively. No statistical differences of survival were reported concerning the initial location of the carcinosarcoma (uterine vs. ovarian). Radiation therapy (hazards ratio [HR]=0.3; 95% confidence interval [CI], 0.16-0.67) and FIGO stage I (HR=0.4; 95% CI, 0.17-0.9) were associated with an increased disease-free survival. Homologous type (HR=3; 95% CI, 1.4-6.3) and FIGO stage II to IV (HR=2.64; 95% CI, 1.3-5.4) were associated with a decreased overall survival. There was no survival improvement for the 12% of patients receiving a multimodal adjuvant therapy. Conclusions:Uterine and ovary carcinosarcomas present a worse prognosis. On the basis of the present study data, although it should be prospectively confirmed, a sequential or multimodal adjuvant therapy should be proposed to patients with early-stage uterine and ovary carcinosarcomas.


The Breast | 2014

Portrait, treatment choices and management of breast cancer in nonagenarians: An ongoing challenge

Benoîte Méry; Avi Assouline; Romain Rivoirard; Claire Bosacki; Pierre Auberdiac; Alexander Tuan Falk; Jane-Chloé Trone; Jean-Baptiste Guy; Jean-Philippe Jacquin; Yacine Merrouche; Cyrus Chargari; Nicolas Magné

There are only scarce data on the management of nonagenarians with breast cancer, and more particularly on the place of radiation therapy (RT). We report a retrospective study on patients aged 90 years old or older, with breast cancer, receiving RT. Records from RT departments from five institutions were reviewed to identify patients 90 years old of age and older undergoing RT over past decade for breast cancer. Tumors characteristics were examined, as well treatment specificities and treatment intent. 44 patients receiving RT courses were identified, mean age 92 years. Treatment was given with curative and palliative intent in 72.7% and 27.3% respectively. Factors associated with a curative treatment were performance status (PS), place of life, previous surgery, and tumor stage. Median total prescribed dose was 40xa0Gy (23-66). Hypo fractionation was used in 77%. Most toxicities were mild to moderate. RT could not be completed in 1 patient (2.3%). No long-term toxicity was reported. Among 31 patients analyzable for effectiveness, 24 patients (77.4%) had their diseased controlled until last follow-up, including 17 patients (54.8%) experiencing complete response. At last follow-up, 4 patients (12.9%) were deceased, cancer being cause of death for two of them. The study shows that breast/chest RT is feasible in nonagenarians. Although the definitive benefit of RT could not be addressed here, hypofractionated therapy allowed a good local control with acceptable side effects.


Chemotherapy | 2016

Chemotherapy Regimen in Nonagenarian Cancer Patients: A Bi-Institutional Experience

Romain Rivoirard; Cyrus Chargari; Sharif Kullab; Jane-Chloé Trone; Julien Langrand-Escure; Guillaume Moriceau; Jean-Baptiste Guy; Pierre Annede; Benoîte Méry; Coralie Moncharmont; Alexander Tuan Falk; Lionel Védrine; Yacine Merrouche; Pierre Fournel; Nicolas Magné

Background: The elderly population in Western countries is growing and constitutes a public health issue. Concomitantly, age-related diseases such as cancer increase. There are few data on the efficacy, tolerability and toxicity of specific anticancer therapy in the very elderly patients; therefore, their management is not standardized. Methods: In this bi-institutional study, we reviewed medical records of patients who received or continued specific anticancer therapy beyond the age of 90 years. Geriatric assessment was not reported for our patients. Twelve patients were enrolled. Their general health condition was good, and half of them were living in elderly institutions. Ten patients had a solid tumor and 2 were treated for hematological malignancies. Most were diagnosed with a locally advanced or metastatic disease, and the goal of treatment was curative for only 1 patient. Six patients received chemotherapy as first-line treatment, 4 patients received targeted therapy and 2 received concomitant chemoradiation. Four patients received a second-line treatment. Results: Despite a significant reduction in treatment posology in half of the patients, 8 acute grade 3/4 toxicities were reported and 2 patients died of treatment-related septic shock. Median duration of first-line treatment was 3.2 months, and progression-free survival ranged from 18 to 311 days. Overall survival ranged from 18 days to 11 years. Conclusion: Aging is a heterogeneous process, and management of elderly patients is a multidisciplinary approach. Geriatric assessment helps to identify older patients with a higher risk of morbidity/mortality and allows to assess the risks and benefits of specific anticancer therapy. The choice of treatment should be based primarily on the expected symptomatic benefit, and treatment should not compromise the quality of life.


European Archives of Oto-rhino-laryngology | 2015

Radiotherapy for head and neck cancer in nonagenarian patients: a possible cornerstone?

Romain Rivoirard; Coralie Moncharmont; Avi Assouline; Pierre Auberdiac; Benoîte Méry; Alexander Tuan Falk; Pierre Annede; Jane-Chloé Trone; Jean-Baptiste Guy; N. Vial; Pierre Fournel; Yacine Merrouche; Cyrus Chargari; Nicolas Magné

In the field of radiotherapy, there is very little scientific data on the management of nonagenarians, especially in patients aged 90xa0years or more and with head and neck cancer (HNC). We made one of the first retrospective study of the feasibility and safety of radiotherapy in this population with HNC. Records of radiotherapy coming from four health facilities were studied to include all nonagenarian patients with HNC in the last 10xa0years and who received radiation therapy. We analyzed patient characteristics and primary cancers, as well as objective of the treatment (curative or palliative), efficacy and toxicity. Twenty patients receiving radiotherapy were identified; mean age was 93.2xa0years (standard deviation 2.8). Treatment was given with curative and palliative intent in 40 and 60xa0% of cases, respectively. The most common primary tumors were tumors of the salivary glands (30xa0% of cases), oral cavity tumors (25xa0% of cases) and thyroid tumors (15xa0% of cases). Median total prescribed dose was 47.5xa0Gy (12–70xa0Gy). Median number of delivered fractions was 18.5 (2–35 fractions). All patients received intensive supportive care during radiotherapy. Toxicities were mild to moderate. Radiotherapy could not be completed for four patients (20xa0% of cases). One patient developed grade 1–2 delayed toxicities. At the last follow-up, only four patients (20xa0% of cases) were alive. Cancer was cause of death in most cases. Radiotherapy may be performed for the nonagenarians with HNC. The total dose and fractionation must be adjusted to optimize the tolerance. However, the prognosis remains very poor, cancer being the main cause of death. Research of geriatric vulnerabilities prior to any treatment, in the context of a comprehensive geriatric assessment, is still recommended to select patients for radiotherapy.


Bulletin Du Cancer | 2017

Hépatite B : dépistage et traitement en oncologie

Anaïs Jaillais; Anne Herber-Mayne; Louis D’Alteroche; Alain Landau; Yacine Merrouche; Stéphane Vignot

Patients with chronic hepatitis B infection are at risk of viral reactivation when treated by immuno- or chemotherapy, with potentially serious or even fatal consequences. This article proposes an overview on screening strategies and antiviral treatment recommendations for oncology patients. We have learned in hematology that reactivations are commun with rituximab and prophylactic treatment is recommanded for any patient who has been in contact with the virus. The risk appears to be lower with cytotoxics but has been far less studied. The recommandations are not formally consensual and upcoming studies will help to establish clearer practice guidelines.


Oncology Nursing Forum | 2016

Improving Adherence to Adjuvant Endocrine Therapy in Breast Cancer Through a Therapeutic Educational Approach: A Feasibility Study

Aurélie Bourmaud; Vanessa Rousset; Véronique Regnier-Denois; Olivier Collard; Jean-Philippe Jacquin; Yacine Merrouche; Joelle Lapoirie; Fabien Tinquaut; Laurence Lataillade; Franck Chauvin

PURPOSE/OBJECTIVESnTo develop and test the feasibility of a tailored therapeutic educational program, with the aim of improving adherence to oral endocrine adjuvant chemotherapy in women with breast cancer. u2029.nnnDESIGNnA qualitative study to identify educational needs and a feasibility study assessing the efficacy of the program.u2029.nnnSETTINGnA comprehensive cancer center, the Lucien Neuwirth Cancer Institute in Saint-Priest-en-Jarez, France.u2029.nnnSAMPLEnTwo consecutive samples (N = 11, N = 6) of women taking adjuvant oral endocrine chemotherapy for breast cancer. u2029.nnnMETHODSnA mixed qualitative and quantitative method was used. The participants representations of disease and treatment were explored through one-on-one interviews and then translated into educational needs, which were used to develop a tailored therapeutic education program. The pilot study evaluated the reach and efficacy using before-and-after comparisons. u2029.nnnMAIN RESEARCH VARIABLESnEducational objectives, knowledge, trust in the treatment, and anxiety.u2029.nnnFINDINGSnFive educational objectives (acquiring knowledge, improving communication skills, managing anxiety, managing side effects, and improving adherence) were identified through 11 interviews. A three-session program was developed. Eight of the 23 patients invited to participate in a pilot study accepted, and six completed the intervention. Knowledge improved from 38.9 of 100 preintervention to 69.4 of 100 postintervention (p = 0.045). Trust in treatment showed a trend to improvement from 5.5 of 10 to 8 of 10 (p = 0.14), but anxiety did not change significantly; anxiety went from 6 to 7 (p = 0.88).u2029.nnnCONCLUSIONSnResults from the feasibility study showed promising efficacy for the educational objectives and provided information about how the program could be improved. u2029.nnnIMPLICATIONS FOR NURSINGnTailored educational programs conducted by trained nurses may help patients to adhere to and live with the effects of endocrine therapy.


Chemotherapy | 2016

Translating Clinical Evidence-Based Medicine into the Real World: Single-Center Experience with Cabazitaxel in Metastatic Prostate Cancer Patients

Guillaume Moriceau; Aline Guillot; Cécile Pacaut; Benoîte Méry; Alexander Tuan Falk; Jane-Chloé Trone; Olivier Collard; Guy de Laroche; Pierre Fournel; Yacine Merrouche; Nicolas Magné

Background: We studied the efficacy and safety of cabazitaxel in unselected real-life patients. Patients and Methods: We retrospectively investigated all patients with metastatic prostate cancer (mPC) treated with cabazitaxel 25 mg/m2 i.v. every 3 weeks combined with oral prednisolone (10 mg once daily) after first-line docetaxel chemotherapy. Study issues were to report patient characteristics and cabazitaxel data in terms of tolerance and efficacy. Overall survival (OS) and progression-free survival (PFS) were evaluated using the Kaplan-Meier method. All data were compared with TROPIC results. Results: From 2011 to 2014, 41 patients received cabazitaxel; 15 patients (37%) had a performance status (PS) ≥2 versus 7% (p < 0.0001) in TROPIC, and 38 patients (93%) presented a Gleason score ≥7 at baseline (vs. 60%; p < 0.0001). All patients had metastatic disease at baseline. Previous therapies were radiotherapy in 17 patients (41 vs. 61%; p = 0.01) and surgery in 24 patients (59 vs. 52%; p = 0.4). The median number of cabazitaxel cycles was 5 (1-10) versus 6 (3-10) in TROPIC. Five patients completed 10 cycles of cabazitaxel (12%) versus 28% in TROPIC (p = 0.03). Toxicities were anemia (12 patients, 29%), diarrhea (9 patients, 22%), nausea (7 patients, 17%), pain (6 patients, 15%), sepsis (4 patients, 10%), neutropenia (3 patients, 7%) and urinary tract infection (1 patient, 2%). The tumor response rate was 19.5 versus 14.4% in TROPIC (nonsignificant). PFS was 4.5 months (95% CI 3.3-6.4) in our analysis and 2.8 months (95% CI 2.4-3.0) in TROPIC. OS was 12.1 months (95% CI 9.2 to not reached) and 15.1 months (95% CI 14.1-16.3), respectively. Conclusion: In our unselected mPC patients with poorer baseline clinical conditions and aggressive disease, cabazitaxel seems efficient and not more toxic than in the TROPIC study.


Bulletin Du Cancer | 2014

Évaluation du dépistage des cancers de la femme et du dépistage après 75 ans dans le département de la Loire

Aurélie Swalduz; Cyril Guibert; Jane-Chloé Trone; Jean-Baptiste Guichard; Romain Rivoirard; Cécile Pacaut; Benoîte Méry; Jean-Baptiste Guy; Houda Eddekkaoui; Pierre Fournel; Guy de Laroche; Yacine Merrouche; Nicolas Magné

In France, there is an important interregional disparity concerning participation to cancer screening programs. The aim of this study was to assess oncologic screening practices in Loire, a French rural department, in women and in the elderly (over age 74 years). For this, two surveys were conducted. The first one was regarding screening for breast, cervical and colorectal cancer in women over age 18 years living in Loire. The second survey was regarding onco-geriatric screening through two questionnairesxa0: one for the elderly and the other for general practitioner (GP) of the department, evaluating screening for breast, colorectal, prostate, cervical and lung cancer. One hundred sixty six women were included in the first investigation mean age of 47.6 years. Ninety three point six per cent were screening for breast cancer, 19% received Human Papilloma virus vaccine, 83.1% were screening by Papanicolau smear for cervical cancer and finally, 51.7% were screening for colorectal cancer, among the one entering screening program criteria. In the second survey, 44 patients and 28 GP were included. Thirty-eight point six per cent of patients over 74 years continue screening. Only 11.4% were reluctant to screening and in 80% because of anxiety du to the results. Among GP, 50xa0% continued screening on two major criteriaxa0: life expectancy and performans status. The present study shows heterogeneity of screening in this department both rural and working class and gives us a societo-medical photography.


Bulletin Du Cancer | 2017

Obésité et cancer

Hélène Salaün; Juliette Thariat; Marina Vignot; Yacine Merrouche; Stéphane Vignot

The proportion of people affected by obesity is increasing and this finding emphasizes several issues in oncology: obesity as a risk factor for cancer, prognostic value of obesity in cancer patients, nutritional assessment in overweight patients and impact of obesity on treatment management. It is important to remember the common underevaluation of malnutrition in overweight or obese patients. Every caregiver must be especially careful about the management of comorbidities in these patients.

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Benoîte Méry

Centre national de la recherche scientifique

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A. Levy

University of Paris-Sud

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Anaïs Jaillais

François Rabelais University

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