Rachel Riechelmann

Dr. Rachel Riechelmann


Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2018 in Clinics
Verified
Journal Article
Open access
AFAnezka C. Rubin de Celis Ferrari
Anezka C. Rubin de Celis Ferrari
JGJoão Glasberg
João Glasberg
RRRachel Riechelmann
Rachel Riechelmann
Approximately 30-40% of patients with well-differentiated neuroendocrine tumors present with carcinoid syndrome, which is a paraneoplastic syndrome associated with the secretion of several humoral factors. Carcinoid syndrome significantly and negatively ...

8 August 2016 in ecancermedicalscience
Verified
Journal Article
Open access
JMJosé Mauricio Mota
José Mauricio Mota
LSLuana Guimarães Sousa
Luana Guimarães Sousa
RRRachel Riechelmann
Rachel Riechelmann
Ecancermedicalscience is the peer-reviewed open access cancer journal founded by the European Institute of Oncology in Milan. We consider articles on all aspects of research relating to cancer, including molecular biology, genetics, pathophysiology, epide

1 May 2017 in Cancer Treatment Reviews
Verified
Journal Article
Closed access
DGDaniel Girardi
Daniel Girardi
ASAndrea C.B. Silva
Andrea C.B. Silva
JRJuliana Florinda M. Rêgo
Juliana Florinda M. Rêgo
RCRenata A. Coudry
Renata A. Coudry
RRRachel Riechelmann
Rachel Riechelmann

2 November 2016 in Therapeutic Advances in Medical Oncology
Verified
Journal Article
Open access
RRRachel Riechelmann
Rachel Riechelmann
Allan PereiraAllan Pereira
Allan Pereira
JRJuliana F. M. Rego
Juliana F. M. Rego
FCFrederico P. Costa
Frederico P. Costa
Carcinoid syndrome (CSy) is a constellation of symptoms that may commonly present in patients with well differentiated neuroendocrine tumors (NETs), with somatostatin analogs (SSAs) being the first-line option for symptom management. However, symptomatic progression eventually occurs and in this scenario of a refractory CSy; several treatment options have been studied such as dose escalation of SSA, interferon and liver-directed therapies. Nevertheless, recent phase III trials have contributed to the understanding and management of this condition. We performed a comprehensive review of interventional studies examining refractory CSy to provide the evidence for current treatment options and propose a treatment sequence.

1 September 2017 in Clinical Colorectal Cancer
Verified
Journal Article
Closed access
AAAlexandra Khichfy Alex
Alexandra Khichfy Alex
SSSheila Siqueira
Sheila Siqueira
RCRenata Coudry
Renata Coudry
JSJuliana Santos
Juliana Santos
MAMichel Alves
Michel Alves
RRRachel Riechelmann
Rachel Riechelmann

10 November 2016 in Therapeutic Advances in Medical Oncology
Verified
Journal Article
Closed access
RRRachel Riechelmann
Rachel Riechelmann
AGAxel Grothey
Axel Grothey
Even though significant improvements in the treatment of colorectal cancer (CRC) have been made in recent years, survival rates for metastatic colorectal cancer (mCRC) are poor. Effective treatment options for metastatic colorectal cancer remain limited, and new therapeutic strategies are desperately needed. Several tyrosine kinase inhibitors (TKIs) and monoclonal antibodies (mAbs) that target angiogenesis, a critical process for facilitating tumor cell growth, invasion, and metastasis, are either approved or in clinical development for the treatment of mCRC. Many of these agents have shown efficacy in mCRC, both as single agents and in combination with standard chemotherapy regimens. However, there is a need for predictive markers of response to identify those patients most likely to benefit from antiangiogenic therapy, and, to date, no markers of this type have been validated in patients. Additionally, because antiangiogenic agents typically cause cytostatic as opposed to cytotoxic antitumor effects, it is important to determine the best strategies for evaluating therapeutic response in mCRC to ensure maximum clinical benefit. In this review, we summarize the efficacy and tolerability of approved and investigational antiangiogenic agents for the treatment of mCRC. We also discuss potential markers of response to antiangiogenic agents and how these markers, along with appropriate endpoint selection, can improve clinical trial design.