Publication Name	World Journal of Clinical Oncology
Manuscript ID	53154
Country	Germany

Received	2019-12-13 08:07
Peer-Review Started	2019-12-07 20:39
To Make the First Decision
Return for Revision	2020-04-22 21:49
Revised	2020-05-18 10:09
Second Decision	2020-05-28 09:28
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2020-05-29 20:26
Articles in Press	2020-05-29 20:26
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2020-06-23 08:53
Publish the Manuscript Online	2020-06-24 10:31

ISSN	2218-4333 (online)
Open Access	This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
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Category	Oncology
Manuscript Type	Opinion Review
Article Title	Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia
Manuscript Source	Invited Manuscript
All Author List	Meinolf Suttorp, Markus Metzler and Frédéric Millot
Funding Agency and Grant Number
Corresponding Author	Meinolf Suttorp, MD, PhD, Emeritus Professor, Research Scientist, Senior Lecturer, Senior Scientist, Pediatric Hemato-Oncology, Medical Faculty, Technical University Dresden, Fetscherstr 74, Dresden D-01307, Germany. meinolf.suttorp@uniklinikum-dresden.de
Key Words	Pediatric chronic myeloid leukemia; International registry; Rare disease; Collaboration and data exchange; ;
Core Tip	Chronic myeloid leukemia (CML) in minors is a rare disease which can be effectively treated by tyrosine kinase inhibitors since the year 2000. Publications coming from the International Registry CML disseminated this useful information derived from patients who robustly participate and share information about their disease, among themselves and with their caregivers and clinicians. Patient input driving the collection of data on this rare leukemia is the basis for the considerable success of bringing new therapeutics into clinical use.
Publish Date	2020-06-24 10:31
Citation	Suttorp M, Metzler M, Millot F. Horn of plenty: Value of the international registry for pediatric chronic myeloid leukemia. World J Clin Oncol 2020; 11(6): 308-319
URL	https://www.wjgnet.com/2218-4333/full/v11/i6/308.htm
DOI	https://dx.doi.org/10.5306/wjco.v11.i6.308

Full Article (PDF)	WJCO-11-308.pdf
Full Article (Word)	WJCO-11-308.docx
Manuscript File	53154-Review.docx
Answering Reviewers	53154-Answering reviewers.pdf
Audio Core Tip	53154-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	53154-Conflict-of-interest statement.pdf
Copyright License Agreement	53154-Copyright license agreement.pdf
Non-Native Speakers of English Editing Certificate	53154-Language certificate.pdf
Peer-review Report	53154-Peer-review(s).pdf
Scientific Misconduct Check	53154-Bing-Yu XQ-1.png
Scientific Misconduct Check	53154-Bing-Yan JP-2.png
Scientific Misconduct Check	53154-Scientific misconduct check.pdf
Scientific Editor Work List	53154-Scientific editor work list.pdf