AbstractChoosing the optimal therapy for a patient's cancer has long been based on whether the cancer demonstrates a predictive marker of efficacy. The U.S. Food and Drug Administration (FDA) has now approved use of a targeted therapy based solely on tumor molecular markers (pembrolizumab for tumors with deficient mismatch repair [MMR] and high microsatellite instability [MSI]) and approved another therapy based solely on a germline mutation as the predictive marker of benefit (olaparib for BRCA carriers with ovarian or breast cancer) [New Engl J Med 2017;377:1409–1412, N Engl J Med 2012;366:1382–1392, N Eng J Med 2017;377:523–533].Here, a patient is presented with a molecular diagnosis of Lynch syndrome and with breast cancer. Yet the breast cancer showed proficient expression of the same MMR gene found to be mutated in her germline testing. The case underscores the importance of tumor testing for MMR and MSI and of not assuming that the tumor is related to the Lynch syndrome rather than being sporadic. This is particularly true in patients with cancers (e.g., breast cancer) whose association with Lynch syndrome is not well established.The case presented also underscores the importance of considering next‐generation sequencing of the tumor when the therapies approved are based on a germline mutation being the predictive marker. For example, the FDA‐approved use of the PARP inhibitor olaparib is for ovarian or breast cancers in patients harboring a BRCA germline mutation [N Engl J Med 2012;366:1382–1392, N Eng J Med 2017;377:523–533]. Yet patients with tumors lacking BRCA loss of heterozygosity (LOH) or lacking other evidence of probable loss of normal BRCA gene product expression might be less likely to benefit from PARP inhibitor therapy, because the efficacy of PARP inhibitor therapy in patients with germline BRCA mutations would likely be predicated upon BRCA LOH in their tumors. The Oncologist 2018
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Σφακιανάκης Αλέξανδρος
ΩτοΡινοΛαρυγγολόγος
Αναπαύσεως 5 Άγιος Νικόλαος
Κρήτη 72100
00302841026182
00306932607174
alsfakia@gmail.com
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Δευτέρα 4 Ιουνίου 2018
The Importance of Distinguishing Sporadic Cancers from Those Related to Cancer Predisposing Germline Mutations
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- Cosmetics, Vol. 5, Pages 34: Alkenones as a Promis...
- Autophony of eyelid movement is not independent of...
- Improvement in minimal cross-sectional area and na...
- Efficiency of Tinospora crispa against Culex quinq...
- Scalable long-term extraction of photosynthetic el...
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- Simultaneous detection and determination of mercur...
- Gold nanorod embedded novel 3D graphene nanocompos...
- Wearable humidity sensor based on porous graphene ...
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- From the Literature.
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- Letter by Wang and Zhao Regarding Article, "Clinic...
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- Letter by Sniecinski et al Regarding Article, "Con...
- Response by Hyman et al to Letter Regarding Articl...
- Letter by Koh Regarding Article, "J Curve in Patie...
- Response by Kalkman et al to Letter Regarding Arti...
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- SOCS1 and SOCS3 Target IRF7 Degradation To Suppres...
- Regulation of the DNA Repair Complex during Somati...
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- Chronic Lymphocytic Leukemia-Derived IL-10 Suppres...
- The ITIM Domain-Containing NK Receptor Ly49Q Impac...
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