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1.
Eur Rev Med Pharmacol Sci ; 28(4): 1575-1584, 2024 Feb.
Article in English | MEDLINE | ID: mdl-38436190

ABSTRACT

OBJECTIVE: Sarcopenia is a frequent disorder among cancer patients. It commonly leads to muscle mass wasting and poor clinical outcomes, even though it is rarely recognized and often undertreated. The relationship between skeletal muscle depletion and chemotherapy toxicity or postoperative complications is well known. The aim of the present study was to analyze the impact of sarcopenia on clinical outcomes of pretreated metastatic gastric cancer (GC) patients. PATIENTS AND METHODS: 88 pretreated GC patients were retrospectively analyzed. Patients were divided into two groups according to their skeletal mass index (SMI): sarcopenic patients with low SMI (≤39 cm2/m2 for women and ≤55 cm2/m2 for men) and non-sarcopenic patients with normal/high SMI value. The two groups were compared according to outcomes and adverse events. RESULTS: Progression-free survival (PFS) was significantly higher in patients with normal/high SMI than in those with low SMI (6 vs. 3.5 months, respectively; HR 0.52). Similarly, the overall response rate (ORR) was higher in the subgroup with normal/high SMI (41% vs. 20%; p=0.02). Overall survival (OS) was not significantly different, but multivariate analysis demonstrated that both SMI and performance status were associated with OS. In the sarcopenic group, the patients treated in the second line with paclitaxel and ramucirumab regimen showed a better outcome profile. Overall, adverse events (AEs) were more frequent in the group of patients with low SMI (p<0.0001). CONCLUSIONS: Early recognition of sarcopenia may contribute to personalizing second or further lines of treatment in advanced GC and to weigh up the potential risk of serious toxicities.


Subject(s)
Sarcopenia , Stomach Neoplasms , Male , Humans , Female , Stomach Neoplasms/drug therapy , Retrospective Studies , Muscular Atrophy , Muscle, Skeletal
2.
Strahlenther Onkol ; 193(11): 971-981, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28884310

ABSTRACT

PURPOSE: Acute toxicity in head and neck (H&N) cancer patients treated with definitive radiotherapy (RT) has a crucial role in compliance to treatments. The aim of this study was to correlate doses to swallowing-associated structures and acute dysphagia. METHODS: We prospectively analyzed 42 H&N cancer patients treated with RT. Dysphagia (grade ≥ 3) and indication for percutaneous endoscopic gastrostomy (PEG) insertion were classified as acute toxicity. Ten swallowing-related structures were considered for the dosimetric analysis. The correlation between clinical information and the dose absorbed by the contoured structures was analyzed. Multivariate logistic regression method using resampling methods (bootstrapping) was applied to select model order and parameters for normal tissue complication probability (NTCP) modelling. RESULTS: A strong multiple correlation between dosimetric parameters was found. A two-variable model was suggested as the optimal order by bootstrap method. The optimal model (Rs = 0.452, p < 0.001) includes V45 of the cervical esophagus (odds ratio [OR] = 1.016) and Dmean of the cricopharyngeal muscle (OR = 1.057). The model area under the curve was 0.82 (95% confidence interval 0.69-0.95). CONCLUSION: Our results suggested that the absorbed dose to the cricopharyngeal muscle and cervical esophagus might play a relevant role in the development of acute RT-related dysphagia.


Subject(s)
Carcinoma, Squamous Cell/radiotherapy , Deglutition Disorders/etiology , Deglutition/radiation effects , Otorhinolaryngologic Neoplasms/radiotherapy , Radiation Injuries/etiology , Adult , Aged , Deglutition Disorders/therapy , Enteral Nutrition , Esophagus/radiation effects , Female , Gastrostomy , Humans , Male , Middle Aged , Pharyngeal Muscles/radiation effects , Prospective Studies , Radiation Injuries/therapy , Radiotherapy Dosage , Statistics as Topic
3.
Clin. transl. oncol. (Print) ; 18(10): 988-995, oct. 2016. tab, graf
Article in English | IBECS | ID: ibc-155961

ABSTRACT

Purpose: hENT1 is a transmembrane protein which acts as a nucleoside transporter and is the main mediator of Gemcitabine (GEM) uptake into human cells. In this retrospective study we compared GEM versus FOLFIRINOX in patients with metastatic pancreatic cancer in which hENT1 evaluation was available. Methods: 149 patients affected by unresectable metastatic pancreatic cancer, treated in our institution from 2009 to 2013, have been screened for inclusion in this retrospective study. Seventy patients, treated with GEM or FOLFIRINOX in first-line therapy, fulfilled clinical inclusion criteria for survival analysis. Thirty-one patients were available and contained sufficient quality/quantity RNA for evaluation of hENT1 expression by RT-PCR. The primary endpoint was OS and the secondary endpoint was PFS. Results: The survival analysis, carried out on 70 patients regardless of hENT1 expression, showed a statistically longer OSandPFS in the group treated with FOLFIRINOX compared to GEM. Within the exploratory analysis, which included 31 patients, no differences were found in hENT1 positive patients treated with FOLFIRINOX compared to GEM in terms of OS (8.5 vs 7 months, HR: 0.89; 95 % CI 0.3-2.5; p = 0.8) and PFS (5.5 vs 5 months, HR: 0.8, 95 % CI 0.2-2.2; p = 0.61). GEM-treated hENT1 positive patients showed a statistically significant improvement both of OS (8 vs 2 months; p = 0.0012) and PFS (5 vs 1 months; p = 0.0004) in comparison to GEM-treated hENT1 negative patients. Conclusions: In our exploratory analysis GEM seems as effective as FOLFIRINOX in terms of survival with a better safety profile in hENT1 positive metastatic pancreatic cancer (AU)


No disponible


Subject(s)
Humans , Pancreatic Neoplasms/drug therapy , Neoplasm Metastasis/drug therapy , Antineoplastic Agents/pharmacokinetics , Equilibrative Nucleoside Transporter 1/analysis , Antineoplastic Combined Chemotherapy Protocols/pharmacokinetics , Antigens, CD/analysis , Receptors, Tumor Necrosis Factor/analysis , Nucleoside Transport Proteins/physiology
4.
Clin Transl Oncol ; 18(10): 988-95, 2016 Oct.
Article in English | MEDLINE | ID: mdl-26742940

ABSTRACT

PURPOSE: hENT1 is a transmembrane protein which acts as a nucleoside transporter and is the main mediator of Gemcitabine (GEM) uptake into human cells. In this retrospective study we compared GEM versus FOLFIRINOX in patients with metastatic pancreatic cancer in which hENT1 evaluation was available. METHODS: 149 patients affected by unresectable metastatic pancreatic cancer, treated in our institution from 2009 to 2013, have been screened for inclusion in this retrospective study. Seventy patients, treated with GEM or FOLFIRINOX in first-line therapy, fulfilled clinical inclusion criteria for survival analysis. Thirty-one patients were available and contained sufficient quality/quantity RNA for evaluation of hENT1 expression by RT-PCR. The primary endpoint was OS and the secondary endpoint was PFS. RESULTS: The survival analysis, carried out on 70 patients regardless of hENT1 expression, showed a statistically longer OS and PFS in the group treated with FOLFIRINOX compared to GEM. Within the exploratory analysis, which included 31 patients, no differences were found in hENT1 positive patients treated with FOLFIRINOX compared to GEM in terms of OS (8.5 vs 7 months, HR: 0.89; 95 % CI 0.3-2.5; p = 0.8) and PFS (5.5 vs 5 months, HR: 0.8, 95 % CI 0.2-2.2; p = 0.61). GEM-treated hENT1 positive patients showed a statistically significant improvement both of OS (8 vs 2 months; p = 0.0012) and PFS (5 vs 1 months; p = 0.0004) in comparison to GEM-treated hENT1 negative patients. CONCLUSIONS: In our exploratory analysis GEM seems as effective as FOLFIRINOX in terms of survival with a better safety profile in hENT1 positive metastatic pancreatic cancer.


Subject(s)
Adenocarcinoma/drug therapy , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Pancreatic Neoplasms/drug therapy , Adenocarcinoma/metabolism , Adenocarcinoma/secondary , Adult , Aged , Aged, 80 and over , Camptothecin/administration & dosage , Camptothecin/analogs & derivatives , Capecitabine/administration & dosage , Deoxycytidine/administration & dosage , Deoxycytidine/analogs & derivatives , Equilibrative Nucleoside Transporter 1 , Female , Fluorouracil/administration & dosage , Follow-Up Studies , Humans , Irinotecan , Leucovorin/administration & dosage , Lymphatic Metastasis , Male , Middle Aged , Neoplasm Staging , Organoplatinum Compounds/administration & dosage , Oxaliplatin , Pancreatic Neoplasms/metabolism , Pancreatic Neoplasms/pathology , Prognosis , Retrospective Studies , Survival Rate , Gemcitabine , Pancreatic Neoplasms
5.
Minerva Gastroenterol Dietol ; 43(3): 143-8, 1997 Sep.
Article in Italian | MEDLINE | ID: mdl-16501483

ABSTRACT

Bioimpedance analysis (BI) of body composition has been carried out in 116 women: 22 patients with anorexia nervosa (AN) and IMC between 16 and 18.5 kg/m2 (MPE-I: weight 45.3+/-3.1 kg; BMI 17.0+/-0.7 kg/m2); 39 AN patients with BMI< 16 kg/m2 (MPE-II: weight 37.2+/-3.8 kg; BMI 14.5+/-1.0 kg/ m2; 55 healthy women (control= CTR: weight 60.5+/-9.0 kg; BMI 22.8+/-3.1 kg/m2). BI was determined for the whole body and for body segments (arms, legs and trunk): phase angle (AF) of 50 kHz and impedance (Z) of 100, 50 and 5 kHz. Body water was estimated from Z to 50 kHz according to Kushner et al. (AJCN 1993). AF and Z100/Z5 (multifrequency BI) were considered as related to the ratio between extracellular water and intracellular water. Total body water was significantly different between the three groups: 26.5+/-2.9 L in the MPE-II group, 23.6+/-2.9 L in the MPE-I group; 30.3+/-3.7 L in the CTR women. In comparison with the CTR group whole-body AF and leg-AF was lower (p<0.01) in the MPE-II patients while both the MPE groups differed from the CTR group with respect to arm-AF. Multifrequency BI showed differences (p<0.01) between all the groups for the whole-body and segmental measures. Significant correlations for AF and Z100/Z5 vs BMI and % BF were apparent only in the MPE-II group. In conclusion, in the AN the marked modifications of BI parameters indicated a relative increase of extracellular water and were related to BMI and % BF in the very undernourished patients.

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