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Double‐blind placebo‐controlled multicenter phase II trial to evaluate D‐methionine in preventing/reducing oral mucositis induced by radiation and chemotherapy for head and neck cancer

Background The purpose of this study was to test if oral D‐methionine (D‐met) reduced mucositis during chemoradiotherapy. Methods We conducted a placebo‐controlled double‐blind randomized phase II trial of D‐met (100 mg/kg p.o. b.i.d.) testing the rate of severe (grades 3‐4) mucositis. Results Sixty...

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Published in:Head & neck 2018-07, Vol.40 (7), p.1375-1388
Main Authors: Hamstra, Daniel A., Lee, Kuei C., Eisbruch, Avraham, Sunkara, Prasad, Borgonha, Sudhir, Phillip, Babu, Campbell, Kathleen C. M., Ross, Brian D., Rehemtulla, Alnawaz
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cited_by cdi_FETCH-LOGICAL-c4545-73141e9ec45c12feca95ab12b53d431efd79d06ac02e50b26a7a61243043901d3
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container_issue 7
container_start_page 1375
container_title Head & neck
container_volume 40
creator Hamstra, Daniel A.
Lee, Kuei C.
Eisbruch, Avraham
Sunkara, Prasad
Borgonha, Sudhir
Phillip, Babu
Campbell, Kathleen C. M.
Ross, Brian D.
Rehemtulla, Alnawaz
description Background The purpose of this study was to test if oral D‐methionine (D‐met) reduced mucositis during chemoradiotherapy. Methods We conducted a placebo‐controlled double‐blind randomized phase II trial of D‐met (100 mg/kg p.o. b.i.d.) testing the rate of severe (grades 3‐4) mucositis. Results Sixty patients were randomized. Grade 2 + oral pain was higher with placebo (79% vs 45%; P = .0165), whereas grade 2 + body odor was greater with D‐met (3% vs 41%; P = .0015). Mucositis was decreased with D‐met by the physician (World Health Organization [WHO], P = .007; Radiation Therapy Oncology Group [RTOG], P = .009) and patient functional scales (RTOG, P = .0023). The primary end point of grades 3 to 4 mucositis on the composite scale demonstrated a decrease with D‐met (48% vs 24%; P = .058), which was borderline in significance. A planned secondary analysis of a semiquantitative scoring system noted decreased oral ulceration (2.2 vs 1.5; P = .023) and erythema (1.6 vs 1.1; P = .048) with D‐met. Conclusion Although not meeting the primary end point, results of multiple assessments suggest that D‐met decreased mucositis.
doi_str_mv 10.1002/hed.25115
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The primary end point of grades 3 to 4 mucositis on the composite scale demonstrated a decrease with D‐met (48% vs 24%; P = .058), which was borderline in significance. A planned secondary analysis of a semiquantitative scoring system noted decreased oral ulceration (2.2 vs 1.5; P = .023) and erythema (1.6 vs 1.1; P = .048) with D‐met. 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M.</creatorcontrib><creatorcontrib>Ross, Brian D.</creatorcontrib><creatorcontrib>Rehemtulla, Alnawaz</creatorcontrib><title>Double‐blind placebo‐controlled multicenter phase II trial to evaluate D‐methionine in preventing/reducing oral mucositis induced by radiation and chemotherapy for head and neck cancer</title><title>Head &amp; neck</title><addtitle>Head Neck</addtitle><description>Background The purpose of this study was to test if oral D‐methionine (D‐met) reduced mucositis during chemoradiotherapy. Methods We conducted a placebo‐controlled double‐blind randomized phase II trial of D‐met (100 mg/kg p.o. b.i.d.) testing the rate of severe (grades 3‐4) mucositis. Results Sixty patients were randomized. Grade 2 + oral pain was higher with placebo (79% vs 45%; P = .0165), whereas grade 2 + body odor was greater with D‐met (3% vs 41%; P = .0015). Mucositis was decreased with D‐met by the physician (World Health Organization [WHO], P = .007; Radiation Therapy Oncology Group [RTOG], P = .009) and patient functional scales (RTOG, P = .0023). The primary end point of grades 3 to 4 mucositis on the composite scale demonstrated a decrease with D‐met (48% vs 24%; P = .058), which was borderline in significance. A planned secondary analysis of a semiquantitative scoring system noted decreased oral ulceration (2.2 vs 1.5; P = .023) and erythema (1.6 vs 1.1; P = .048) with D‐met. Conclusion Although not meeting the primary end point, results of multiple assessments suggest that D‐met decreased mucositis.</description><subject>Cancer</subject><subject>Chemoradiotherapy</subject><subject>Chemotherapy</subject><subject>clinical trial</subject><subject>Double-blind studies</subject><subject>Erythema</subject><subject>Head &amp; neck cancer</subject><subject>Methionine</subject><subject>Mucositis</subject><subject>Odor</subject><subject>Pain</subject><subject>Radiation therapy</subject><subject>radioprotector</subject><subject>radiotherapy</subject><subject>toxicity</subject><issn>1043-3074</issn><issn>1097-0347</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kc1u1TAQhS0EoqVlwQsgS6xYpNd_ickS9RZ6pUrd0HU0sSfExbGD4xTdHY_AE_EwPAlub7vsyjPj75yxfAh5x9kZZ0xsRrRnoua8fkGOOWt1xaTSL-9rJSvJtDoib5blljEmGyVekyPRKi2F0sfk7zauvcd_v__03gVLZw8G-1h6E0NO0Xu0dFp9dgZDxkTnERakux3NyYGnOVK8A79CRrotqgnz6GJwAakLdE54V2QufN8ktKspBY2pyKbVxMVltxSqzMuOfk8TWAe5qCmUl5gRp5hHTDDv6RATHRHsw01A84MaCAbTKXk1gF_w7eN5Qm6-XHw7v6yurr_uzj9fVUbVqq605Ipji6UzXAxooK2h56KvpVWS42B1a1kDhgmsWS8a0NBwoWT5wJZxK0_Ih4PvnOLPFZfc3cY1hbKyE6xpeNs0-lOhPh4ok-KyJBy6ObkJ0r7jrLtPqitJdQ9JFfb9o-PaT2X6RD5FU4DNAfjlPO6fd-ouL7YHy_9sLaO0</recordid><startdate>201807</startdate><enddate>201807</enddate><creator>Hamstra, Daniel A.</creator><creator>Lee, Kuei C.</creator><creator>Eisbruch, Avraham</creator><creator>Sunkara, Prasad</creator><creator>Borgonha, Sudhir</creator><creator>Phillip, Babu</creator><creator>Campbell, Kathleen C. M.</creator><creator>Ross, Brian D.</creator><creator>Rehemtulla, Alnawaz</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0001-6291-3444</orcidid></search><sort><creationdate>201807</creationdate><title>Double‐blind placebo‐controlled multicenter phase II trial to evaluate D‐methionine in preventing/reducing oral mucositis induced by radiation and chemotherapy for head and neck cancer</title><author>Hamstra, Daniel A. ; Lee, Kuei C. ; Eisbruch, Avraham ; Sunkara, Prasad ; Borgonha, Sudhir ; Phillip, Babu ; Campbell, Kathleen C. 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M.</creatorcontrib><creatorcontrib>Ross, Brian D.</creatorcontrib><creatorcontrib>Rehemtulla, Alnawaz</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><jtitle>Head &amp; neck</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hamstra, Daniel A.</au><au>Lee, Kuei C.</au><au>Eisbruch, Avraham</au><au>Sunkara, Prasad</au><au>Borgonha, Sudhir</au><au>Phillip, Babu</au><au>Campbell, Kathleen C. 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Grade 2 + oral pain was higher with placebo (79% vs 45%; P = .0165), whereas grade 2 + body odor was greater with D‐met (3% vs 41%; P = .0015). Mucositis was decreased with D‐met by the physician (World Health Organization [WHO], P = .007; Radiation Therapy Oncology Group [RTOG], P = .009) and patient functional scales (RTOG, P = .0023). The primary end point of grades 3 to 4 mucositis on the composite scale demonstrated a decrease with D‐met (48% vs 24%; P = .058), which was borderline in significance. A planned secondary analysis of a semiquantitative scoring system noted decreased oral ulceration (2.2 vs 1.5; P = .023) and erythema (1.6 vs 1.1; P = .048) with D‐met. 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subjects Cancer
Chemoradiotherapy
Chemotherapy
clinical trial
Double-blind studies
Erythema
Head & neck cancer
Methionine
Mucositis
Odor
Pain
Radiation therapy
radioprotector
radiotherapy
toxicity
title Double‐blind placebo‐controlled multicenter phase II trial to evaluate D‐methionine in preventing/reducing oral mucositis induced by radiation and chemotherapy for head and neck cancer
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