このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Can Cytokines Predict the Severity of Acute Mucositis and the Need for Gastrostomy Tubes (PEG)?

2007年8月9日 更新者:Hadassah Medical Organization

Can Cytokines Predict the Severity of Acute Mucositis and the Need for PEG During Chemo-Radiation Treatment to Head and Neck Cancer?

Mucositis and xerostomia are the most common complications of head and neck (H&N) irradiation, and the combination of chemotherapy and radiation therapy is associated with a significantly higher rate of complications.

Mucositis usually develops during the second or third week of a course of standard radiotherapy, and the pain it causes peaks between the third and last week of treatment. The pain then persists for at least one month following the completion of therapy, and may be so overwhelming that it prevents patients from swallowing food and fluids. The patient is therefore at a risk to develop malnutrition, and must be treated vigorously. In this respect, the use of gastrostomy tubes (PEG) has been shown to be beneficial.

Completion of the full course of irradiation, without interruption, is important for achieving best possible results in cancer of the H&N. It is therefore essential to identify and refer patients at risk to receive effective and timely nutritional intervention.

Since mucositis represents a clinical continuum which differs between patients, it is difficult to assess before-hand which patients will be at risk.

There is no simple laboratory tool available, which could predict which patients are susceptible to develop severe mucositis and dysphagia, and eventually will require a feeding gastrostomy.

The first phase of mucositis, inflammation, results in the production of pro-inflammatory cytokines such as interleukin-1 (IL-1) and tumor necrosis factor-alpha (TNF-α).

In general, the inflammatory cytokines IL-1, interleukin-6 (IL-6) and TNF-α are elevated in inflammatory conditions and are found in increased levels in blood and tissue fluid during inflammation, while anti-inflammatory cytokines are produced in a decreased manner.

The main purpose of this study is to find the best indicators and prognosticators of mucositis occurring in the healthy oral tissues of H&N cancer patients receiving treatment, and to understand the cytokines balance mechanism of action.

Assuming there is a correlation between high cytokines levels during inflammation and the severity of radiation induced mucositis, finding these prognostic factors may help us predict during the first part of the treatment the need for PEG, placing it prior to the complications associated with severe mucositis on one hand, and avoiding unnecessary procedures on the other hand.

調査の概要

状態

わからない

詳細な説明

Mucositis has a significant detrimental effect on patient's quality of life in terms of pain, ability to eat, to swallow and talk. It may be so severe that an interruption of therapy is required, consequently influencing tumor response and overall patient outcome.

The degree of mucositis varies between different patients: some patients may develop a limited condition, confined to patches of mildly sore erythematous mucosa, while others may experience diffuse areas of painful ulceration.

In the more severe cases, pain may be so overwhelming that it prevents patients from swallowing food and fluids. The patient is therefore at a risk to develop malnutrition, and must be treated vigorously. In this respect, the use of gastrostomy tubes (PEG) has been shown to be beneficial.

Another aspect of radiation induced mucositis is its health-care costs. Patients with more severe mucositis have statistically greater outpatient support costs; these include maintenance of appropriate nutritional and hydration support, such as placement of gastrostomy tubes. In the U.S, the mucositis overall medical costs are in the order of approximately $3000±$1000, per treatment.

Completion of the full course of irradiation, without interruption, is important for achieving best possible results in cancer of the H&N. It is therefore essential to identify and refer patients at risk to receive effective and timely nutritional intervention.

Since mucositis represents a clinical continuum which differs between patients, it is difficult to assess before-hand which patients will be at risk to develop severe mucositis during the course of radiotherapy. In today's practice, patients undergoing radiation therapy of the H&N will undergo feeding gastrostomy by the treating physician prior to the treatment if he will anticipate severe mucositis, based on the radiation fields, the chemotherapy used, and his prior experience. Some of these procedures were eventually unnecessary. In cases where gastrostomy was not placed a priory, the common practice is monitoring the patients during treatment. If their weight loss exceeds 10% of their initial body weight, a feeding gastrostomy is recommended (at this time point, the mucositis is usually severe, and many patients need admission for fluid administration and semi-urgent procedure).

Unfortunately, there is no simple laboratory tool available, which could predict which patients are susceptible to develop severe mucositis and dysphagia, and eventually will require a feeding gastrostomy.

Mucositis develops in four successive phases: an inflammation phase, an epithelial phase, an ulceration phase and lastly, a healing phase.

The first phase, inflammation, is also entitled "the initial tissue injury phase", and it results in the production of pro-inflammatory cytokines such as IL-1 and TNF-α .

In general, the inflammatory cytokines IL-1, IL-6 and TNF-α are elevated in inflammatory conditions and are found in increased levels in blood and tissue fluid during inflammation, while anti-inflammatory cytokines are produced in a decreased manner.

In breast cancer patients, it has been shown that changes in cytokines levels, Including IL-1β and IL-6, also correspond with the response of the malignant tissue to treatment. In this case, a good clinical response to therapy has been associated with decreases in IL-1β and IL-6 levels, versus increases in their levels which have been associated with the progression of the disease. Furthermore, tumor markers such as the cytokeratin TPS, have been shown to be sensitive in assessing the tumor's response to therapy and the patient's prognosis.

It should be emphasized though, that the findings cited above reflect the response of tumor cells to therapy, while the proposed project deals with radiation effects on both normal tissues and tumor.

The main purpose of this study is to find the best indicators and prognosticators of mucositis occurring in the healthy oral tissues of H&N cancer patients receiving treatment, and to understand the cytokines balance mechanism of action.

Assuming there is a correlation between high cytokines levels during inflammation and the severity of radiation induced mucositis, finding these prognostic factors may help us predict during the first part of the treatment the need for PEG, placing it prior to the complications associated with severe mucositis on one hand, and avoiding unnecessary procedures on the other hand. This study may also lead to a new strategy of assessing severity of mucositis by laboratory tests, a tool that can be used as an objective assessment in developing strategies that aim to reduce the mucositis. The understanding of the cytokines balance in this condition can also be translated to the use of anti-cytokine treatment for this condition, similar to other immune related diseases such as RA, Crohn's Disease and MS.

Secondary aims of this study are to measure recently available tumor markers SCC and TPS, and to correlate them with tumor response. Genetic markers will be assessed for extreme alteration in radiation reactions such as severe skin reaction, early and unexpectedly severe mucositis, and on the other hand - lack of response. The blood for these tasks will be collected prospectively, but evaluated at the end of the study.

The study will comprise of at least 14 and up to 35 patients with H&N epithelial cancer.

Patients will be clinically evaluated during the week before treatment, and during the treatment period weekly.

Blood samples will be drown for cytokines prior to treatment, at week 2, 4 and at the end of the treatment. The serum collected will be separated for the following factors:

  1. Inflammatory Cytokines: IL-1, IL-6, IL-8, IL-18 and TNF α.
  2. Anti inflammatory cytokines: IL-10 and TGF β.
  3. Tumor markers: SCC and TPS.
  4. Genetic assessment of genes that may be involved in extreme treatment reaction. At each weekly follow up, patients will be assessed for mucositis by physician using the WHO common toxicity criteria, and will answer a mucositis questionnaire (based on the RTOG/EORTC questionnaire). Patient's weight will also be recorded.

Scientific aims

The primary aims:

  1. To investigate the relationship between cytokine level and the clinically suggested PEG at the end of the H&N chemo-irradiation.
  2. To investigate whether a correlation exists between blood cytokines (inflammatory versus anti-inflammatory cytokines) levels and the severity of radiation induced mucositis in patients receiving chemo-radiotherapy for cancer of the H&N.
  3. To investigate whether blood cytokines levels could serve as a simple laboratory tool, to predict the severity of mucositis and dysphagia occurring during H&N chemo-irradiation.

The secondary aims:

  1. To study the clinical usefulness of the Tumor Markers SCC and TPS in this setting, namely, to evaluate the correlation between their blood levels and response to therapy.
  2. To compare the associated mucositis between two commonly used radiation treatment strategies - IMRT 5 field plan and classic two dimensional plan for the subgroup of patients with advanced glottic and supraglottic cancer.
  3. To assess whether cytokine levels during treatment can predict long term treatment related toxicity.

研究の種類

観察的

入学 (予想される)

35

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Jerusalem、イスラエル、91120
        • Hadassah Medical Organization

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年~85年 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Patients with H&N epithelial cancer (nasopharynx, oropharynx, oral cavity - tongue, buccal mucosae and palate, larynx and hypopharynx)
  • Treated with definitive chemo-radiation treatment and follow up
  • Male and female patients will be included, with an age ranging between 18- 85 years

Exclusion Criteria:

  • Soldiers, prisoners and pregnant women will be excluded.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Amichay Meirovitz, MD、Hadassah Medical Organization

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究の完了 (予想される)

2011年5月1日

試験登録日

最初に提出

2007年2月5日

QC基準を満たした最初の提出物

2007年2月5日

最初の投稿 (見積もり)

2007年2月6日

学習記録の更新

投稿された最後の更新 (見積もり)

2007年8月10日

QC基準を満たした最後の更新が送信されました

2007年8月9日

最終確認日

2007年2月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する