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      항암제 부작용에 대한 적절한 대처법 = Optimal Management of Chemotherapy-related Adverse Events

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      국문 초록 (Abstract)

      본고에서는 췌장암, 담낭 및 담도암에서 흔히 사용되는 항암치료와 관련된 골수기능억제, 오심 및 구토, 설사 및 신경병증에 대하여 설명하고 이에 대한 치료를 설명하였다. 골수기능억제는...

      본고에서는 췌장암, 담낭 및 담도암에서 흔히 사용되는 항암치료와 관련된 골수기능억제, 오심 및 구토, 설사 및 신경병증에 대하여 설명하고 이에 대한 치료를 설명하였다. 골수기능억제는 질병의 정도, 저혈압의 발생 여부, 만성 폐쇄성 폐질환의 유무, 이전에 곰팡이 감염 유무, 정맥영양 필요 여부, 호중구 감소성 발열의 발생시점과 환자의 연령에 따라 예후가 많이 달라진다. 특히 호중구 감소성 발열에서는 G-CSF의 사용을 권하며, 호중구 감소만 있는 경우에는 G-CSF를 환자의 상태에 따라 사용해야 한다. 호중구 감소가 장기간 지속되는 경우에는 pegylated G-CSF가 도움이 된다. 오심 및 구토는 급성 구토(acute emesis), 지연 구토(delayed emesis), 예측 구토(anticipatory emesis)로 NK1R antagonists, serotonin (5-HT3) receptor antagonists, glucocorticoid, metoclopramide, olanzapine, benzodiazepine 등이 사용된다. 중등도 위험군과 고위험군 항암제를 사용한 경우의 구토 예방 및 치료에서는 많은 다양한 방법들이 사용되지만 대부분 5-HT3 receptor antatonist를 단독요법으로 우선 사용해보는 것이 좋겠다. 한편, 저위험군 항암 치료 후 발생하는 구토의 경우에는 우선 스테로이드 단독요법을 사용하고, 예방치료에도 불구하고 구토가 발생한 경우에는 다음 치료일부터 중등도 위험군에 준하여 5-HT3 receptor antatonist를 단독요법으로 시행해볼 수 있다. 합병증이 동반되지 않은 1-2등급의 경한 설사의 경우에는 입원 필요 없이 장에 부담이 적은 BRAT 식단, 충분한 수분 섭취와 loperamide를 사용하는 지사요법이 도움이 되며, 합병증이 동반된 설사의 경우에는 보다 적극적으로 설사를 조절해야 한다. 암 생존자가 많아지면서 말초신경병증은 삶의 질 측면에서 심각한 영향을 미치는 부작용으로 항경련제, 항우울제, amifostine, nimodipine, vitamins, minerals, 식이보충제 등을 사용하더라도 효과가 없고, 운동 요법은 예방에서 효과가 있고, 증상완화에도 도움이 되며 duloxetine은 통증이 심한 말초신경병증에서 효과적이다.

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      다국어 초록 (Multilingual Abstract)

      This review article deals with the optimal management of chemotherapy-related adverse events which are the nausea, vomiting, diarrhea, neutropenia, peripheral polyneuropathy. Recent literatures are reviewed and pathogenetic mechanism and management of...

      This review article deals with the optimal management of chemotherapy-related adverse events which are the nausea, vomiting, diarrhea, neutropenia, peripheral polyneuropathy. Recent literatures are reviewed and pathogenetic mechanism and management of each of adverse events are summarized. It is not simple but complexed and wide. Most patients could be expected how much they feel the nausea before the chemotherapy. We could prescribe several types of antiemetic agent efficiently. When the patients suffered from the neutropenia after previous chemotherapy, we should closely monitor their blood cell count. And we could help them after giving the granulocyte colony stimulating factor. Diarrhea is one of big troublesome issue related with chemotherapy. We could control the diarrhea by reducing the dose of the chemotherapy and prescribing optimally loperamide. Cisplatin and oxaliplatin could make the patients feel paresthesia and numbness but it’s hard to reverse or prevent even though we use anticonvulsants (carbamazepine, oxcarbazepine), antidepressants (amitriptyline, venlafaxine), amifostine, nimodipine, vitamins and minerals.

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      참고문헌 (Reference)

      1 Klastersky J, "The multinational association for supportive care in cancer risk index : a multinational scoring system for identifying low-risk febrile neutropenic cancer patients" 18 : 3038-3051, 2000

      2 Cornes P, "Systematic review and meta-analysis of short-versus long-acting granulocyte colony-stimulating factors for reduction of chemotherapy-induced febrile neutropenia" 35 : 1816-1829, 2018

      3 Beck TM, "Stratified, randomized, double-blind comparison of intravenous ondansetron administered as a multiple-dose regimen versus two single-dose regimens in the prevention of cisplatin-induced nausea and vomiting" 10 : 1969-1975, 1992

      4 Gralla RJ, "Single-dose oral granisetron has equivalent antiemetic efficacy to intravenous ondansetron for highly emetogenic cisplatin-based chemotherapy" 16 : 1568-1573, 1998

      5 Benson AB 3rd, "Recommended guidelines for the treatment of cancer treatment-induced diarrhea" 22 : 2918-2926, 2004

      6 Smith TJ, "Recommendations for the use of WBC growth factors : American Society of Clinical Oncology clinical practice guideline update" 33 : 3199-3212, 2015

      7 Suzuki K, "Randomized, doubleblind, phase III trial of palonosetron versus granisetron in the triplet regimen for preventing chemotherapy-induced nausea and vomiting after highly emetogenic chemotherapy: TRIPLE study" 27 : 1601-1606, 2016

      8 Roila F, "Prevention of chemotherapy-and radiotherapy-induced emesis : results of the 2004Perugia International Antiemetic Consensus Conference" 17 : 20-28, 2006

      9 Razavi D, "Prevention of adjustment disorders and anticipatory nausea secondary to adjuvant chemotherapy:a double-blind, placebo-controlled study assessing the usefulness of alprazolam" 11 : 1384-1390, 1993

      10 Hershman DL, "Prevention and management of chemotherapy-induced peripheral neuropathy in survivors of adult cancers : American Society of Clinical Oncology clinical practice guideline" 32 : 1941-1967, 2014

      1 Klastersky J, "The multinational association for supportive care in cancer risk index : a multinational scoring system for identifying low-risk febrile neutropenic cancer patients" 18 : 3038-3051, 2000

      2 Cornes P, "Systematic review and meta-analysis of short-versus long-acting granulocyte colony-stimulating factors for reduction of chemotherapy-induced febrile neutropenia" 35 : 1816-1829, 2018

      3 Beck TM, "Stratified, randomized, double-blind comparison of intravenous ondansetron administered as a multiple-dose regimen versus two single-dose regimens in the prevention of cisplatin-induced nausea and vomiting" 10 : 1969-1975, 1992

      4 Gralla RJ, "Single-dose oral granisetron has equivalent antiemetic efficacy to intravenous ondansetron for highly emetogenic cisplatin-based chemotherapy" 16 : 1568-1573, 1998

      5 Benson AB 3rd, "Recommended guidelines for the treatment of cancer treatment-induced diarrhea" 22 : 2918-2926, 2004

      6 Smith TJ, "Recommendations for the use of WBC growth factors : American Society of Clinical Oncology clinical practice guideline update" 33 : 3199-3212, 2015

      7 Suzuki K, "Randomized, doubleblind, phase III trial of palonosetron versus granisetron in the triplet regimen for preventing chemotherapy-induced nausea and vomiting after highly emetogenic chemotherapy: TRIPLE study" 27 : 1601-1606, 2016

      8 Roila F, "Prevention of chemotherapy-and radiotherapy-induced emesis : results of the 2004Perugia International Antiemetic Consensus Conference" 17 : 20-28, 2006

      9 Razavi D, "Prevention of adjustment disorders and anticipatory nausea secondary to adjuvant chemotherapy:a double-blind, placebo-controlled study assessing the usefulness of alprazolam" 11 : 1384-1390, 1993

      10 Hershman DL, "Prevention and management of chemotherapy-induced peripheral neuropathy in survivors of adult cancers : American Society of Clinical Oncology clinical practice guideline" 32 : 1941-1967, 2014

      11 Carmona-Bayonas A, "Prediction of serious complications in patients with seemingly stable febrile neutropenia : validation of the Clinical Index of Stable Febrile Neutropenia in a prospective cohort of patients from the FINITE study" 33 : 465-471, 2015

      12 Abigerges D, "Phase I and pharmacologic studies of the camptothecin analog irinotecan administered every 3 weeks in cancer patients" 13 : 210-221, 1995

      13 Tanabe Y, "Paclitaxel-induced peripheral neuropathy in patients receiving adjuvant chemotherapy for breast cancer" 18 : 132-138, 2013

      14 Klastersky J, "Outpatient oral antibiotics for febrile neutropenic cancer patients using a score predictive for complications" 24 : 4129-4134, 2006

      15 Navari RM, "Olanzapine for the prevention of chemotherapy-induced nausea and vomiting" 375 : 134-142, 2016

      16 Sutherland A, "Olanzapine for the prevention and treatment of cancer-related nausea and vomiting in adults" 9 : CD012555-, 2018

      17 Lamberts SW, "Octreotide" 334 : 246-254, 1996

      18 dos Santos LV, "Neurokinin-1 receptor antagonists for chemotherapyinduced nausea and vomiting : a systematic review" 104 : 1280-1292, 2012

      19 Osterlund P, "Lactose intolerance associated with adjuvant 5-fluorouracil-based chemotherapy for colorectal cancer" 2 : 696-703, 2004

      20 Ikuno N, "Irinotecan(CPT-11)and characteristic mucosal changes in the mouse ileum and cecum" 87 : 1876-1883, 1995

      21 Bennett BK, "Impact of oxaliplatin-induced neuropathy : a patient perspective" 20 : 2959-2967, 2012

      22 Andreyev J, "Guidance on the management of diarrhoea during cancer chemotherapy" 15 : e447-e460, 2014

      23 Hartmann LC, "Granulocyte colony-stimulating factor in severe chemotherapy-induced afebrile neutropenia" 336 : 1776-1780, 1997

      24 del Giglio A, "Granisetron is equivalent to ondansetron for prophylaxis of chemotherapy-induced nausea and vomiting : results of a meta-analysis of randomized controlled trials" 89 : 2301-2308, 2000

      25 Reeves BN, "Further data supporting that paclitaxel-associated acute pain syndrome is associated with development of peripheral neuropathy : North Central Cancer Treatment Group trial N08C1" 118 : 5171-5178, 2012

      26 Pfeil AM, "Efficacy, effectiveness and safety of long-acting granulocyte colony-stimulating factors for prophylaxis of chemotherapy-induced neutropenia in patients with cancer: a systematic review" 23 : 525-545, 2015

      27 Boccia RV, "Efficacy and tolerability of transdermal granisetron for the control of chemotherapy-induced nausea and vomiting associated with moderately and highly emetogenic multi-day chemotherapy:a randomized, double-blind, phase III study" 19 : 1609-1617, 2011

      28 Kaizer L, "Effect of schedule and maintenance on the antiemetic efficacy of ondansetron combined with dexamethasone in acute and delayed nausea and emesis in patients receiving moderately emetogenic chemotherapy : a phase III trial by the National Cancer Institute of Canada Clinical Trials Group" 12 : 1050-1057, 1994

      29 Smith EM, "Effect of duloxetine on pain, function, and quality of life among patients with chemotherapyinduced painful peripheral neuropathy: a randomized clinical trial" 309 : 1359-1367, 2013

      30 Seynaeve C, "Comparison of the anti-emetic efficacy of different doses of ondansetron, given as either a continuous infusion or a single intravenous dose, in acute cisplatin-induced emesis. A multicentre, double-blind, randomised, parallel group study. Ondansetron Study Group" 66 : 192-197, 1992

      31 Perez EA, "Comparison of single-dose oral granisetron versus intravenous ondansetron in the prevention of nausea and vomiting induced by moderately emetogenic chemotherapy:a multicenter, double-blind, randomized parallel study" 16 : 754-760, 1998

      32 U.S. Department of Health and Human Services, "Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0" U.S. Department of Health and Human Services

      33 Nishimura J, "Combination antiemetic therapy with aprepitant/fosaprepitant in patients with colorectal cancer receiving oxaliplatin-based chemotherapy (SENRI trial): a multicentre, randomised, controlled phase 3 trial" 51 : 1274-1282, 2015

      34 Mhaskar R, "Colony-stimulating factors for chemotherapy-induced febrile neutropenia" (10) : CD003039-, 2014

      35 Freifeld AG, "Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer : 2010 update by the infectious diseases Society of America" 52 : e56-e93, 2011

      36 Mols F, "Chemotherapyinduced peripheral neuropathy and its association with quality of life : a systematic review" 22 : 2261-2269, 2014

      37 Hesketh PJ, "Antiemetics : American Society of Clinical Oncology clinical practice guideline update" 35 : 3240-3261, 2017

      38 Harman GS, "A randomized, double-blind comparison of single-dose and divided multiple-dose dolasetron for cisplatin-induced emesis" 38 : 323-328, 1996

      39 Zhang L, "A randomized phase III study evaluating the efficacy of single-dose NEPA, a fixed antiemetic combination of netupitant and palonosetron, versus an aprepitant regimen for prevention of chemotherapy-induced nausea and vomiting (CINV) in patients receiving highly emetogenic chemotherapy (HEC)" 29 : 452-458, 2018

      40 Aapro MS, "A phase III, doubleblind, randomized trial of palonosetron compared with ondansetron in preventing chemotherapy-induced nausea and vomiting following highly emetogenic chemotherapy" 17 : 1441-1449, 2006

      41 Ettinger DS, "A double-blind comparison of the efficacy of two dose regimens of oral granisetron in preventing acute emesis in patients receiving moderately emetogenic chemotherapy" 78 : 144-151, 1996

      42 Roila F, "2016 MASCC and ESMO guideline update for the prevention of chemotherapy-and radiotherapy-induced nausea and vomiting and of nausea and vomiting in advanced cancer patients" 27 (27): v119-v133, 2016

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      2024 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2019-03-14 학회명변경 한글명 : 대한췌담도학회 -> 대한췌장담도학회 KCI등재후보
      2019-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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