JP2016080672A - Detection method of malignant lymphoma - Google Patents

Detection method of malignant lymphoma Download PDF

Info

Publication number
JP2016080672A
JP2016080672A JP2014228417A JP2014228417A JP2016080672A JP 2016080672 A JP2016080672 A JP 2016080672A JP 2014228417 A JP2014228417 A JP 2014228417A JP 2014228417 A JP2014228417 A JP 2014228417A JP 2016080672 A JP2016080672 A JP 2016080672A
Authority
JP
Japan
Prior art keywords
malignant lymphoma
pet
lymphocytes
proportion
detection method
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2014228417A
Other languages
Japanese (ja)
Inventor
勇 廣▲瀬▼
Isamu Hirose
勇 廣▲瀬▼
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to JP2014228417A priority Critical patent/JP2016080672A/en
Publication of JP2016080672A publication Critical patent/JP2016080672A/en
Pending legal-status Critical Current

Links

Landscapes

  • Investigating Or Analysing Biological Materials (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

PROBLEM TO BE SOLVED: To allow quick and easy determination of initial malignant lymphoma, by only blood test, and allow quick and easy determination when one should receive PET-CT.SOLUTION: A lymphocyte ratio in all white blood cells is calculated in blood test, and when the value is lower than a lower limit of a health range, it is determined that one may suffer from malignant lymphoma. In addition, when the value is lower than the lower limit of the health range, it is determined that one should receive PET-CT.

Description

本発明は、初期の悪性リンパ腫さえも安全安価に検出できる迅速で簡単な検出法に関するものである。  The present invention relates to a rapid and simple detection method that can detect even early malignant lymphoma safely and inexpensively.

癌は初期に発見し初期段階から治療するのが一番良いとされている。しかしながら多くの場合、癌は末期になるまで自覚症状がほとんどなく、気付いた時には極度に進行していたり転移しているなど治療が困難なケースも多い。  It is best to find cancer early and treat it from an early stage. However, in many cases, cancer has almost no subjective symptoms until the end stage, and when it is noticed, it is often difficult to treat because it is extremely advanced or metastasized.

悪性リンパ腫はリンパ球の癌で、末期になるまで自覚症状がほとんど無いという点では例外ではないうえ、悪性リンパ腫とりわけ日本人に多いびまん性大細胞型B細胞リンパ腫を、その初期段階で簡単に見つける検出法が無かったため、初期発見は困難とされてきた。  Malignant lymphoma is a cancer of lymphocytes and is no exception in that there is almost no subjective symptom until the end stage, and it is easy to find malignant lymphoma, especially diffuse large B-cell lymphoma, which is common in Japanese in its early stages. Because there was no detection method, initial discovery has been considered difficult.

一方これまで、悪性リンパ腫の検出方法としていくつかの手段が開発されている。たとえばPET−CT(陽電子放出検査)、造影剤CT、超音波検査、腫瘍マーカーであるsIL−2R(ソルブルインターロイキン2リセプター)の測定などである。  On the other hand, several means have been developed as a method for detecting malignant lymphoma. For example, PET-CT (positron emission test), contrast medium CT, ultrasonography, measurement of sIL-2R (solvable interleukin 2 receptor) which is a tumor marker, and the like.

PET−CTは癌の部分だけを特異的に検出でき、しかも比較的初期のものまで検出できるという点で極めて優れた検査法である。しかしながら、癌と認定されて専門医に掛かっている人以外は健康保険の適用を受けられず、そうでない人が受診する場合には、極めて高額な費用を自己負担しなければならない。また放射線被ばくするという問題がある。さらにまた、いつ検査を受ければよいのか分からないという問題がある。  PET-CT is an extremely excellent test method in that only the cancer part can be specifically detected, and even relatively early ones can be detected. However, other than those who are certified as cancer and have a specialist, they are not eligible for health insurance, and if those who do not have a medical examination, they must pay a very high cost. There is also the problem of radiation exposure. Furthermore, there is a problem that it is difficult to know when the examination should be performed.

この問題は特に大事である。なぜなら悪性リンパ腫には様々なタイプがあり、進行の早いものは週単位で進行するため丁度よい適切な時期に検査しなければ見逃したり手遅れになるからである。びまん性大細胞型B細胞リンパ腫は月単位で進行する中程度の進行速度の悪性リンパ腫であるが、この場合にも1年に1度といった間隔では見逃しや手遅れになる恐れがあり、これをカバーするため頻繁に受ければ高額な費用と放射線被ばくが増えるという問題があった。  This problem is particularly important. This is because there are various types of malignant lymphoma, and those that progress quickly progress weekly, so if they are not examined at the right time, they will be missed or too late. Diffuse large B-cell lymphoma is a moderately advanced malignant lymphoma that progresses on a monthly basis, but this may be overlooked or delayed at intervals of once a year. Therefore, there was a problem that the high cost and radiation exposure would increase if received frequently.

要するにPET−CTは比較的小さな初期の悪性リンパ腫さえも検出できるという点で優れた検出法ではあるが、安全安価で簡単な検出法ではない。  In short, PET-CT is an excellent detection method in that even a relatively small early malignant lymphoma can be detected, but it is not a safe, inexpensive and simple detection method.

造影剤CTの精度はPET−CTに劣らないが、悪性リンパ腫の検査法としては腫瘍部を強調して検出できるPET−CTに比べて劣るし、放射線被ばくの問題もある。  The accuracy of the contrast agent CT is not inferior to that of PET-CT, but it is inferior to PET-CT, which can detect a tumor site with emphasis, and there is a problem of radiation exposure.

超音波検査は精度の点でPET−CTや造影剤CTに劣る。  Ultrasonography is inferior to PET-CT and contrast agent CT in terms of accuracy.

腫瘍マーカーのsIL−2Rは血液検査のひとつの項目であるが、通常の健康診断や人間ドックの検査項目には無く、特別に依頼しなければならないうえ比較的高額な費用がかかる。そのうえその値は様々な疾患の影響を受け、必ずしも悪性リンパ腫の病態だけを表すものではない。  The tumor marker sIL-2R is one item of blood test, but it is not included in the normal health checkup and examination items of a medical checkup, and requires a special request and is relatively expensive. Moreover, its value is affected by various diseases and does not necessarily represent only the pathology of malignant lymphoma.

以上を要するに、各種の検出方法があるとはいえ、いずれも問題があり、初期の悪性リンパ腫さえも確実に検出できる、安全安価で迅速、簡単な検出法が求められていた。  In short, although there are various detection methods, all have problems, and there has been a need for a safe, inexpensive, quick and simple detection method that can reliably detect even early malignant lymphoma.

特表2005−508171号公法Special table 2005-508171 public law 特開2012−233889号公法Japanese Patent Laid-Open No. 2012-233889 特開2004−163121号公法Japanese Patent Laid-Open No. 2004-163121

解決しようとする課題は、自覚症状の出にくい初期の悪性リンパ腫さえも確実に検出できる安全安価で迅速、簡単な検出法がなかったという点である。  The problem to be solved is that there was no safe, inexpensive, quick and simple detection method that can reliably detect even early malignant lymphomas that are difficult to produce subjective symptoms.

またどの時点でPET−CTを受診すればよいかを判断する迅速、簡単な検出方法がなかったという点である。  Another point is that there was no quick and simple detection method for determining at which point PET-CT should be consulted.

本発明は、血液検査を行い、全白血球中に占めるリンパ球の割合が、健常時の正常な範囲の下限から外れている場合には悪性リンパ腫の疑いがあると判定することを特徴とする悪性リンパ腫の迅速、簡単な検出法である。  The present invention performs a blood test, and determines that there is a suspicion of malignant lymphoma when the proportion of lymphocytes in total white blood cells is outside the lower limit of normal normal range It is a quick and simple method for detecting lymphoma.

疑いありとされた場合にはPET−CTを受診するが、本発明はその受診時期を判定するための迅速、簡単な検出方法でもある。  If it is suspected, PET-CT is consulted, but the present invention is also a quick and simple detection method for determining the time of the visit.

本発明者は24年1月に末期のびまん性大細胞型B細胞リンパ腫になり、抗がん剤投与で寛解したものの26年5月に再発した者である。血液検査で腫瘍マーカーなどの数値に異常がないなら年1回の受診にしようと決めていて、前回受診から1年経過した26年5月にPET−CTを受診したところ偶然にも初期の悪性リンパ腫の再発が見つかった。  The present inventor is a person who became end-stage diffuse large B-cell lymphoma in January 2012 and remissioned by administration of an anticancer drug, but relapsed in May 2014. If there are no abnormalities in the tumor markers and other values in the blood test, we have decided to visit once a year, and when we visited PET-CT in May 26, one year after the previous visit, it happened to be early malignant A recurrence of lymphoma was found.

血液検査では赤血球、白血球といった成分の濃度、割合が出る。そのうち白血球は好中球、顆粒球、リンパ球などから構成されており、健常者であればその構成割合はほぼ一定に保たれている。たとえば本発明者の場合、表1のごとく全白血球に占めるリンパ球の割合は、ほぼ25ないし40パーセントの範囲にある。  Blood tests show the concentration and proportion of red blood cells and white blood cells. Among them, leukocytes are composed of neutrophils, granulocytes, lymphocytes, etc., and the proportion of the composition is kept almost constant for healthy individuals. For example, in the case of the present inventor, as shown in Table 1, the proportion of lymphocytes in the total leukocytes is in the range of approximately 25 to 40 percent.

ところが24年1、2月の最初の悪性リンパ腫の罹患時と26年5、6月の再発時には、いずれもその値が下限の25パーセントから大きく低下したのである。低下の理由は定かではないが、最初の発病と2年後の再発という2つの異なる時期で低下が見られたことから再現性については疑う余地はない。また悪性リンパ腫末期である24年1月の方が初期の26年5、6月より大きく低下している。  However, when the first malignant lymphoma was affected in January and February 24, and when it recurred in May and June 26, the value dropped significantly from the lower limit of 25 percent. The reason for the decline is not clear, but there is no doubt about the reproducibility because the decline was seen at two different times, the first onset and recurrence after 2 years. In addition, the end stage of malignant lymphoma, January 24, is significantly lower than the early May 26, 26.

全白血球に占めるリンパ球の割合の低下が悪性リンパ腫の有無や病期と関連するのかという点については、実施例1に示したように悪性リンパ腫の未罹患時、罹患初期、罹患末期における全白血球に占めるリンパ球の割合の変化と、PET−CTから見た悪性リンパ腫の病期の変化が明瞭に対応していることから、両者は間違いなく関連しているといえる。  As to whether or not the decrease in the proportion of lymphocytes in total leukocytes is related to the presence or stage of malignant lymphoma, as shown in Example 1, total leukocytes at the time of unaffected, early stage of disease, and end stage of malignant lymphoma The change in the proportion of lymphocytes in the brain and the change in the stage of malignant lymphoma as seen from PET-CT clearly correspond to each other, so it can be said that they are definitely related.

このことから、血液検査をして全白血球に占めるリンパ球の割合を算出し、それが健常時の値の範囲から下方に外れていないかを調べるだけで初期の悪性リンパ腫さえも迅速かつ簡単に判定できる。  From this, blood tests can be performed to calculate the proportion of lymphocytes in total white blood cells, and even early malignant lymphomas can be quickly and easily determined simply by checking whether they deviate downward from the normal value range. Can be judged.

またPET−CTを何時受診すべきかという判定法としても利用できる。  It can also be used as a method for determining when to receive PET-CT.

これまで悪性リンパ腫に罹ると全白血球に占めるリンパ球の割合が低下するという指摘は無かったばかりでなく、それが悪性リンパ腫の初期段階から敏感に低下し始めるということについても指摘は無かった。またこの現象を利用すれば初期の悪性リンパ腫さえも判定できるとか、PET−CTを何時受けるべきかの目安にもなるという指摘も無かったのである。  To date, there has been no indication that malignant lymphoma has a reduced proportion of lymphocytes in total white blood cells, but there has been no indication that it begins to decline sensitively from the early stages of malignant lymphoma. Moreover, there was no indication that even if this phenomenon was used, even early malignant lymphoma could be determined, and it would be a measure of when to receive PET-CT.

本発明の効果は、血液検査というごく一般の検査だけで初期の悪性リンパ腫さえも安全安価で迅速、簡単に検出できるとともに、PET−CTの適切な受診時期についても迅速、簡単に判定できることにある。  The effect of the present invention is that even an early malignant lymphoma can be detected safely, inexpensively, quickly and easily with only a general test such as a blood test, and an appropriate timing for receiving PET-CT can be quickly and easily determined. .

表、図の簡単な説明Brief description of tables and figures

[表1]表1は本発明者の14年に及ぶ血液検査、PET−CTのデーターで、リンパ球の割合、PET−CTのFDGの集積度および悪性リンパ腫の病期を検査年月日順に示したものである。

Figure 2016080672
[Table 1] Table 1 shows the data of the present inventor's 14-year blood test and PET-CT. The percentage of lymphocytes, the degree of FDG accumulation in PET-CT, and the stage of malignant lymphoma are in the order of examination date. It is shown.
Figure 2016080672

FDGの集積とは、PET−CTで使用する放射性フッソ置換したFDG(フルオロデオキシグルコース)が正常細胞よりも腫瘍細胞により多く取り込まれることを利用し、集積度を腫瘍の有無、大きさ、活性度の指標にするものである。また病期はPET−CT画像の腫瘍の広がりで判定する。  FDG accumulation is based on the fact that radioactive fluorine-substituted FDG (fluorodeoxyglucose) used in PET-CT is taken up by tumor cells more than normal cells, and the degree of accumulation is the presence, size, and activity of the tumor. It is intended to be an indicator of The stage of disease is determined by the extent of the tumor in the PET-CT image.

悪性リンパ腫を初期段階からでも捉えるための安全安価で迅速,簡単な方法を提供するという目的を、血液検査をするだけで実現した。  The purpose of providing a safe, inexpensive, quick and simple method for detecting malignant lymphoma from the early stage was realized simply by performing a blood test.

またいつPET−CTを受診すればよいかを迅速,簡単に判定する方法を提供するという目的を、血液検査をするだけで実現した。  In addition, the purpose of providing a method for quickly and easily determining when to receive PET-CT was realized simply by performing a blood test.

表1から、悪性リンパ腫に罹患していない健常な場合のリンパ球の割合は、25パーセントから39.7パーセントの間にある。罹患していない25年5月には、当然ながらFDGの集積はない。  From Table 1, the percentage of healthy lymphocytes not affected by malignant lymphoma is between 25 percent and 39.7 percent. In May 25, 2013, when there is no disease, there is no accumulation of FDG.

一方、悪性リンパ腫末期の24年1、2月のリンパ球の割合は11.6ないし13パーセントで、罹患していない場合の下限の25パーセントから大きく低下している。またFDGは強く集積している。  On the other hand, the proportion of lymphocytes at the end stage of malignant lymphoma in 1/24 and 12.4 is 11.6 to 13%, which is a significant decrease from the lower limit of 25% when not affected. In addition, FDG is strongly accumulated.

また悪性リンパ腫初期の26年5、6月の場合にもリンパ球の割合は下限の25パーセントから低下し、23ないし17パーセントである。各々の時点のFDGの集積は、各々弱く集積および集積であり、24年1月の強い集積に比べると少ない。  Also in the case of May and June 26 in the early stage of malignant lymphoma, the proportion of lymphocytes falls from the lower limit of 25 percent to 23 to 17 percent. The FDG accumulation at each point in time is weak and accumulation, and is less than the strong accumulation in January 2012.

表1に示した発明者自身のデーターから本発明に至ったもので、悪性リンパ腫の罹患、寛解、再発の経験者だからこそなしえた発明である。それだけに本発明が医療現場で悪性リンパ腫の早期発見に広く役立つことを願うものである。  The present invention is based on the inventors' own data shown in Table 1, and is an invention that can be achieved because it has experienced malignant lymphoma disease, remission, and recurrence. Therefore, I hope that the present invention is widely useful for early detection of malignant lymphoma in the medical field.

医療現場でPET−CTを受けなくとも血液検査をするだけで、悪性リンパ腫に罹患していないかを迅速、簡単に判定できる。  Whether or not a patient has malignant lymphoma can be determined quickly and easily by simply performing a blood test without undergoing PET-CT at a medical site.

また血液検査をするだけで、PET−CTをいつ受診すればよいかを迅速、簡単に判定できる。  Moreover, it is possible to quickly and easily determine when to receive a PET-CT simply by performing a blood test.

Claims (4)

血液検査で全白血球に占めるリンパ球の割合が健常時の範囲の下限未満であることを特徴とする悪性リンパ腫とりわけびまん性大細胞型B細胞リンパ腫の有無を判定する迅速で簡単な検出法  Rapid and simple detection method for determining the presence or absence of malignant lymphoma, particularly diffuse large B-cell lymphoma, characterized in that the proportion of lymphocytes in total white blood cells is less than the lower limit of the normal range in blood tests リンパ球の割合が25パーセント未満である請求項1の検出法  The method of claim 1, wherein the proportion of lymphocytes is less than 25 percent. 血液検査で全白血球に占めるリンパ球の割合が健常時の範囲の下限未満であることを特徴とするPET−CTの受診時期を判定する迅速で簡単な検出法  Rapid and simple detection method for determining the timing of PET-CT visits, characterized in that the proportion of lymphocytes in total white blood cells in blood tests is less than the lower limit of the normal range リンパ球の割合が25パーセント未満である請求項3の検出法  The method of claim 3, wherein the proportion of lymphocytes is less than 25 percent.
JP2014228417A 2014-10-17 2014-10-17 Detection method of malignant lymphoma Pending JP2016080672A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2014228417A JP2016080672A (en) 2014-10-17 2014-10-17 Detection method of malignant lymphoma

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2014228417A JP2016080672A (en) 2014-10-17 2014-10-17 Detection method of malignant lymphoma

Publications (1)

Publication Number Publication Date
JP2016080672A true JP2016080672A (en) 2016-05-16

Family

ID=55958386

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014228417A Pending JP2016080672A (en) 2014-10-17 2014-10-17 Detection method of malignant lymphoma

Country Status (1)

Country Link
JP (1) JP2016080672A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111655868A (en) * 2018-03-14 2020-09-11 深圳华大生命科学研究院 Malignant lymphoma marker and application thereof
WO2023017843A1 (en) 2021-08-12 2023-02-16 学校法人 久留米大学 Diagnosis device, information acquisition method, and program

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111655868A (en) * 2018-03-14 2020-09-11 深圳华大生命科学研究院 Malignant lymphoma marker and application thereof
WO2023017843A1 (en) 2021-08-12 2023-02-16 学校法人 久留米大学 Diagnosis device, information acquisition method, and program

Similar Documents

Publication Publication Date Title
Huang et al. The impact of T2/FLAIR evaluation per RANO criteria on response assessment of recurrent glioblastoma patients treated with bevacizumab
Lehmberg et al. Consensus recommendations for the diagnosis and management of hemophagocytic lymphohistiocytosis associated with malignancies
Pusztai et al. New strategies in breast cancer: immunotherapy
Waheed et al. Standard and novel imaging methods for multiple myeloma: correlates with prognostic laboratory variables including gene expression profiling data
Barra et al. Contrast‐enhanced mammography (CEM) for detecting residual disease after neoadjuvant chemotherapy: a comparison with breast magnetic resonance imaging (MRI)
Song et al. Cerebrospinal fluid IL-10 and IL-10/IL-6 as accurate diagnostic biomarkers for primary central nervous system large B-cell lymphoma
Aggarwal et al. Circulating tumor cells as a predictive biomarker in patients with small cell lung cancer undergoing chemotherapy
Svaton et al. Chronic inflammation as a potential predictive factor of nivolumab therapy in non-small cell lung cancer
Terai et al. Arterial blood, rather than venous blood, is a better source for circulating melanoma cells
Shen et al. Predictive and prognostic value of folate receptor-positive circulating tumor cells in small cell lung cancer patients treated with first-line chemotherapy
Rojas et al. Relapse surveillance in AFP-positive hepatoblastoma: re-evaluating the role of imaging
Inci et al. Correlation of volume, position of stone, and hydronephrosis with microhematuria in patients with solitary urolithiasis
Massard et al. RECIST response and variation of circulating tumour cells in phase 1 trials: A prospective multicentric study
WO2017077796A1 (en) Method and apparatus for testing immune state
Ma et al. A novel model to assess disease activity in Takayasu arteritis based on 18F-FDG-PET/CT: a Chinese cohort study
Kim et al. Detection of circulating tumor cells and their potential use as a biomarker for advanced renal cell carcinoma
Ueki et al. Association between sarcopenia based on psoas muscle index and the response to nivolumab in metastatic renal cell carcinoma: A retrospective study
Conteduca et al. Multimodal approach to outcome prediction in metastatic castration-resistant prostate cancer by integrating functional imaging and plasma DNA analysis
JP2016080672A (en) Detection method of malignant lymphoma
Rasmy et al. Effect of KRAS mutational status on disease behavior and treatment outcome in patients with metastatic colorectal cancer: intratumor heterogeneity and mutational status
JP7065862B2 (en) Monitoring the recurrence and progression of cancer
RU2670768C9 (en) Tumour biomarker
JP2019529959A5 (en)
Field et al. The role of early magnetic resonance imaging in predicting survival on bevacizumab for recurrent glioblastoma: results from a prospective clinical trial (CABARET)
Soman et al. Biologic effects of radiation from cardiac imaging: New insights from proteomic and genomic analyses