scholarly journals Combined Atezolizumab and Chemotherapy for a Patient With Double Primary Cancers

In Vivo ◽  
2019 ◽  
Vol 34 (1) ◽  
pp. 389-392
Author(s):  
SHINICHIRO OKAUCHI ◽  
YUIKA SASATANI ◽  
GEN OHARA ◽  
KATSUNORI KAGOHASHI ◽  
HIROAKI SATOH
Mutagenesis ◽  
2019 ◽  
Vol 35 (3) ◽  
pp. 207-219
Author(s):  
Hongyao Yu ◽  
Kari Hemminki

Abstract We review here data on familial risk in colorectal cancer (CRC) generated from the Swedish Family-Cancer Database, the largest resource of its kind in the world. Although the concordant familial risk for CRC (i.e. CRC risk in families of CRC patients) has been reasonably well established, the studies on discordant familial risks (i.e. CRC risk in families with any other cancers) are rare. Because different cancers could be caused by shared genetic susceptibility or shared environment, data of associations of discordant cancers may provide useful information for identifying common risk factors. In analyses between any of 33 discordant cancers relative risks (RRs) for discordant cancers were estimated in families with increasing numbers of probands with CRC; in the reverse analyses, RRs for CRC were estimated in families with increasing numbers of probands with discordant cancers. In separate analyses, hereditary non-polyposis colorectal cancer (HNPCC) families were excluded from the study, based on HNPCC related double primary cancers, to assess the residual familial RRs. We further reviewed familial risks of colon and rectal cancers separately in search for distinct discordant associations. The reviewed data suggested that colon cancer was associated with a higher familial risk for CRC compared to rectal cancer. The previous data had reported associations of CRC with melanoma, thyroid and eye cancers. Nervous system cancer was only associated with colon cancer, and lung cancer only associated with rectal cancer. The reviewed data on discordant association may provide guidance to gene identification and may help genetic counseling.


2012 ◽  
Vol 35 (2) ◽  
pp. 110
Author(s):  
Hye-Won Yun ◽  
Ki-Nam Shim ◽  
Sun-Kyung Na ◽  
Do-Kyeong Song ◽  
Jung-Wha Chung ◽  
...  

BMC Surgery ◽  
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Yan Xu ◽  
Quan-Ning Chen ◽  
Hui Wang ◽  
Nan-Bin Liu ◽  
Bao-Min Shi

Abstract Background Double primary cancers have a low incidence rate, and synchronous hepatocellular carcinoma and gallbladder adenocarcinoma are rarely reported. Here, we report such a case— the 12th case of synchronous double primary cancers featuring HCC and GC, but the first case of neuroendocrine differentiation in the gallbladder. Case presentation A 77-year-old female was admitted to the hospital complaining of weakness and inappetence for six months. Contrast-enhanced computed tomography (CT) of the abdomen indicated an 11 cm space-occupying lesion in the right lobe of the liver. Later, magnetic resonance imaging showed a high possibility of a massive hepatoma, and multiple gallstones were also seen. After transhepatic arterial chemoembolization, a repeat abdominal CT showed obvious local nodular thickening in the gallbladder wall. Finally, resection of the right lobe of the liver and cholecystectomy were performed. During an approximately 2-year follow-up, the patient recovered uneventfully without recurrence or metastasis. Conclusion The disease in this case is rare and lacked typical radiological features. More precise and advanced diagnostic techniques are needed to obtain a clear diagnosis and refine treatment strategies. The management strategy should always be curative, even in the presence of multiple malignancies.


1999 ◽  
Vol 8 (5) ◽  
pp. 823-829 ◽  
Author(s):  
A. L. Millar ◽  
T. Pal ◽  
L. Madlensky ◽  
C. Sherman ◽  
L. Temple ◽  
...  

2012 ◽  
Vol 51 (17) ◽  
pp. 2329-2335 ◽  
Author(s):  
Takaaki Murakami ◽  
Hiroki Nishikawa ◽  
Yorimitsu Koshikawa ◽  
Yoshihiro Okabe ◽  
Tomoko Wakasa ◽  
...  

1998 ◽  
Vol 35 (12) ◽  
pp. 978-984 ◽  
Author(s):  
T Pal ◽  
T Flanders ◽  
M Mitchell-Lehman ◽  
A MacMillan ◽  
J S Brunet ◽  
...  

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