SCOPUS 정보 검색 플랫폼

Journal of Clinical Oncology

Volumn 34, Issue 18, 2016, Pages 2196-2197

The first step to integrating adapted common terminology criteria for adverse events for children

(4) De Rojas, Teresa a Bautista, Francisco José a Madero, Luis a Moreno, Lucas a

a HOSPITAL INFANTIL UNIVERSITARIO NIÑO JESÚS (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

BODY MASS; DAILY LIFE ACTIVITY; DRUG SURVEILLANCE PROGRAM; FAILURE TO THRIVE; HUMAN; LETTER; MEDICAL TERMINOLOGY; MENTAL DISEASE; PEDIATRICS; PRIORITY JOURNAL; REFERENCE VALUE; SELF REPORT; WEIGHT CHANGE; WEIGHT GAIN; ADVERSE DRUG REACTION; AGE; CHILD; CHILD BEHAVIOR; CHILD DEVELOPMENT; CLASSIFICATION; COMPLICATION; COST OF ILLNESS; INFANT; NEOPLASM; NEWBORN; NOMENCLATURE; PRESCHOOL CHILD; QUALITY OF LIFE; RADIATION INJURY; RADIOTHERAPY;

ANTINEOPLASTIC AGENT;

ACTIVITIES OF DAILY LIVING; ADVERSE DRUG REACTION REPORTING SYSTEMS; AGE FACTORS; ANTINEOPLASTIC AGENTS; CHILD; CHILD BEHAVIOR; CHILD DEVELOPMENT; CHILD, PRESCHOOL; COST OF ILLNESS; DRUG-RELATED SIDE EFFECTS AND ADVERSE REACTIONS; HUMANS; INFANT; INFANT, NEWBORN; NEOPLASMS; QUALITY OF LIFE; RADIATION INJURIES; RADIOTHERAPY; TERMINOLOGY AS TOPIC;

EID: 84973597920 PISSN: 0732183X EISSN: 15277755 Source Type: Journal
DOI: 10.1200/JCO.2016.67.7104 Document Type: Letter

Times cited : (7)

References (5)

1
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- National Cancer Institute: NCI Guidelines for Investigators, Adverse Event Reporting Requirements for DCTD (CTEP and CIP) and DCP INDs and IDEs. http://ctep.cancer.gov/protocolDevelopment/electronic-applications/docs/aeguidelines.pdf
- NCI Guidelines for Investigators, Adverse Event Reporting Requirements for DCTD (CTEP and CIP) and DCP INDs and IDEs
- National Cancer Institute¹

2
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- The first step to integrating the child's voice in adverse event reporting in oncology trials: A content validation study among pediatric oncology clinicians
- Reeve BB, Withycombe JS, Baker JN, et al: The first step to integrating the child's voice in adverse event reporting in oncology trials: A content validation study among pediatric oncology clinicians. Pediatr Blood Cancer 60:1231-1236, 2013
- (2013) Pediatr Blood Cancer , vol.60 , pp. 1231-1236
- Reeve, B.B.¹ Withycombe, J.S.² Baker, J.N.³

3
- 84965094526
- Validity and reliability of the US National Cancer Institute's Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
- Dueck AC, Mendoza TR, Mitchell SA, et al: Validity and reliability of the US National Cancer Institute's Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE). JAMA Oncol 1:1051-1059, 2015
- (2015) JAMA Oncol , vol.1 , pp. 1051-1059
- Dueck, A.C.¹ Mendoza, T.R.² Mitchell, S.A.³

4
- 84946059925
- Concept-elicitation phase for the development of the pediatric patient-reported outcome version of the Common Terminology Criteria for Adverse Events
- Weaver MS, Reeve BB, Baker JN, et al: Concept-elicitation phase for the development of the pediatric patient-reported outcome version of the Common Terminology Criteria for Adverse Events. Cancer 122:141-148, 2016
- (2016) Cancer , vol.122 , pp. 141-148
- Weaver, M.S.¹ Reeve, B.B.² Baker, J.N.³

5
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- Department of Health and Human Services, National Institutes of Health, National Cancer Institute: Common Terminology Criteria for Adverse Events v4.03. http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE-4.03-2010-06-14-QuickReference-5x7.pdf
- Common Terminology Criteria for Adverse Events V4.03
- Department of Health and Human Services¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.