[Immunoglobulin for prevention of radiogenic mucositis]

Standard

[Immunoglobulin for prevention of radiogenic mucositis]. / Mose, S; Adamietz, I A; Thilmann, C; Saran, F; Heyd, R; Knecht, Rainald; Böttcher, H D.

in: HNO, Jahrgang 43, Nr. 7, 7, 1995, S. 421-426.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Mose, S, Adamietz, IA, Thilmann, C, Saran, F, Heyd, R, Knecht, R & Böttcher, HD 1995, '[Immunoglobulin for prevention of radiogenic mucositis]', HNO, Jg. 43, Nr. 7, 7, S. 421-426. <http://www.ncbi.nlm.nih.gov/pubmed/7672999?dopt=Citation>

APA

Mose, S., Adamietz, I. A., Thilmann, C., Saran, F., Heyd, R., Knecht, R., & Böttcher, H. D. (1995). [Immunoglobulin for prevention of radiogenic mucositis]. HNO, 43(7), 421-426. [7]. http://www.ncbi.nlm.nih.gov/pubmed/7672999?dopt=Citation

Vancouver

Mose S, Adamietz IA, Thilmann C, Saran F, Heyd R, Knecht R et al. [Immunoglobulin for prevention of radiogenic mucositis]. HNO. 1995;43(7):421-426. 7.

Bibtex

@article{e65fb32d581249a381541a0c47e78123,
title = "[Immunoglobulin for prevention of radiogenic mucositis]",
abstract = "Among various therapies administered during radiation-induced mucositis, treatment with immunoglobulin has proven clinically successful. In this study the efficacy of prophylactic applications of immunoglobulin was investigated from January 1992 through August 1993. Forty-two patients with histologically-proven head and neck cancer were given postoperative radiation treatment. In cases with macroscopic tumor residues or inoperability, combined radio-chemotherapy was given. This included 51.3 Gy at 1.9 Gy 5x/week, boosted to 10-26 Gy at 2 Gy 5x/week and carboplatin 60 mg/m2 at days 1-5 and 29-33. Panthenol (4x10 ml/day) and nystatin (4 x 1 ml/day) were given to 20 patients as prophylactic treatment for mucositis. Twenty-two subsequent patients also received intramuscular 800 mg (5 ml) human immunoglobulin (1x/week). According to the Seegenschmiedt/Sauer classification the extent of mucositis was determined 3x/week. Comparison of the distribution of maximal mucositis revealed a slightly more severe mucosal reaction in the control group (n.s.). Analysis of the mean degree of mucositis in both groups demonstrated statistically significant differences (p = 0.031) related to the whole collective and patients receiving concomitant chemotherapy while no effect of immunoglobulin was found in patients treated by radiation alone. In the immunoglobulin-treated-group, the time from the beginning of therapy to the first interruption was prolonged 5 days (37.5 +/- 13.1 vs. 42.7 +/- 13.3 days), but this difference was not significant. Although prophylactic application of immunoglobulin seemed to lower the degree of radiation-induced mucositis, this effect was less significant when compared to the immunoglobulin given in a therapeutic manner.",
author = "S Mose and Adamietz, {I A} and C Thilmann and F Saran and R Heyd and Rainald Knecht and B{\"o}ttcher, {H D}",
year = "1995",
language = "Deutsch",
volume = "43",
pages = "421--426",
journal = "HNO",
issn = "0017-6192",
publisher = "Springer",
number = "7",

}

RIS

TY - JOUR

T1 - [Immunoglobulin for prevention of radiogenic mucositis]

AU - Mose, S

AU - Adamietz, I A

AU - Thilmann, C

AU - Saran, F

AU - Heyd, R

AU - Knecht, Rainald

AU - Böttcher, H D

PY - 1995

Y1 - 1995

N2 - Among various therapies administered during radiation-induced mucositis, treatment with immunoglobulin has proven clinically successful. In this study the efficacy of prophylactic applications of immunoglobulin was investigated from January 1992 through August 1993. Forty-two patients with histologically-proven head and neck cancer were given postoperative radiation treatment. In cases with macroscopic tumor residues or inoperability, combined radio-chemotherapy was given. This included 51.3 Gy at 1.9 Gy 5x/week, boosted to 10-26 Gy at 2 Gy 5x/week and carboplatin 60 mg/m2 at days 1-5 and 29-33. Panthenol (4x10 ml/day) and nystatin (4 x 1 ml/day) were given to 20 patients as prophylactic treatment for mucositis. Twenty-two subsequent patients also received intramuscular 800 mg (5 ml) human immunoglobulin (1x/week). According to the Seegenschmiedt/Sauer classification the extent of mucositis was determined 3x/week. Comparison of the distribution of maximal mucositis revealed a slightly more severe mucosal reaction in the control group (n.s.). Analysis of the mean degree of mucositis in both groups demonstrated statistically significant differences (p = 0.031) related to the whole collective and patients receiving concomitant chemotherapy while no effect of immunoglobulin was found in patients treated by radiation alone. In the immunoglobulin-treated-group, the time from the beginning of therapy to the first interruption was prolonged 5 days (37.5 +/- 13.1 vs. 42.7 +/- 13.3 days), but this difference was not significant. Although prophylactic application of immunoglobulin seemed to lower the degree of radiation-induced mucositis, this effect was less significant when compared to the immunoglobulin given in a therapeutic manner.

AB - Among various therapies administered during radiation-induced mucositis, treatment with immunoglobulin has proven clinically successful. In this study the efficacy of prophylactic applications of immunoglobulin was investigated from January 1992 through August 1993. Forty-two patients with histologically-proven head and neck cancer were given postoperative radiation treatment. In cases with macroscopic tumor residues or inoperability, combined radio-chemotherapy was given. This included 51.3 Gy at 1.9 Gy 5x/week, boosted to 10-26 Gy at 2 Gy 5x/week and carboplatin 60 mg/m2 at days 1-5 and 29-33. Panthenol (4x10 ml/day) and nystatin (4 x 1 ml/day) were given to 20 patients as prophylactic treatment for mucositis. Twenty-two subsequent patients also received intramuscular 800 mg (5 ml) human immunoglobulin (1x/week). According to the Seegenschmiedt/Sauer classification the extent of mucositis was determined 3x/week. Comparison of the distribution of maximal mucositis revealed a slightly more severe mucosal reaction in the control group (n.s.). Analysis of the mean degree of mucositis in both groups demonstrated statistically significant differences (p = 0.031) related to the whole collective and patients receiving concomitant chemotherapy while no effect of immunoglobulin was found in patients treated by radiation alone. In the immunoglobulin-treated-group, the time from the beginning of therapy to the first interruption was prolonged 5 days (37.5 +/- 13.1 vs. 42.7 +/- 13.3 days), but this difference was not significant. Although prophylactic application of immunoglobulin seemed to lower the degree of radiation-induced mucositis, this effect was less significant when compared to the immunoglobulin given in a therapeutic manner.

M3 - SCORING: Zeitschriftenaufsatz

VL - 43

SP - 421

EP - 426

JO - HNO

JF - HNO

SN - 0017-6192

IS - 7

M1 - 7

ER -