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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1214247 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type! s& q  H8 l$ X, Q' W
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
& N, L& E" U8 B4 l3 T3 n6 V+ Author Affiliations& T6 e0 _- J1 i) X
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan / i- d3 j8 W+ O' M9 e) U
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ' H) I+ P/ J3 G
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
! d6 a5 u! B. o' ?4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 0 O8 r3 x; r  s2 J: S/ L
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
  Y, X  P" K( n( X6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ( Q; O. i6 f# w- o, r0 [$ W
7Kinki University School of Medicine, Osaka 589-8511, Japan
8 R9 b+ X& l& U" R  n8Izumi Municipal Hospital, Osaka 594-0071, Japan ; z5 f2 L+ A4 _" q: Y
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
! |  ^4 \& k2 q% iCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
9 Y" x* d/ u) R! YAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type 1 X2 @$ N: R4 [: {; ]
# [$ `$ ^" j! D$ ^$ @5 m& J
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
( P$ N, \( t+ z- A8 X* R( V, F: q( \0 c6 H
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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Published online on: Thursday, December 1, 2011 3 W2 _# }; W/ ]! f$ \

5 f0 c: [7 B. Y$ I0 `Doi: 10.3892/ol.2011.507 " E' c* w6 T0 K
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Pages: 405-410
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Abstract:
' y( ?  T& j' f% z. H; j& mS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population  u5 n+ O4 x$ C7 e4 ~. L# t
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
1 p4 _- y8 X' x, N/ a+ Author Affiliations5 B. L$ v0 X3 ^/ b) b1 B
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu . u. c" W+ y6 f$ c
2Department of Thoracic Surgery, Kyoto University, Kyoto
6 p2 P5 }% _% v+ x3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan / X" j  U- N6 m% {4 K& `1 q0 h7 L& L
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
1 `2 s3 ?. |9 Q- P. D& \0 eReceived September 3, 2010.
# R) u% t6 T  ~0 `# O( v& t. x9 y3 c( XRevision received November 11, 2010.
; Z# W- u  @9 ^0 K! o6 c3 FAccepted November 17, 2010. : ?) E9 R  }3 J
Abstract
4 m, p! P* H& lBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. 6 `* r- J/ [7 I2 E* \
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
* b1 ]( J* ~( C0 V1 [Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
: C; z# X' f/ o4 @Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。5 `3 K8 x1 M4 B& K
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?6 R9 m6 |6 B0 y8 n
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy4 t6 F1 _% }/ u/ {. _% H% q5 `0 h
http://clinicaltrials.gov/ct2/show/NCT01523587( X/ u2 X1 F: }. K+ \- \8 x$ f# R
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
( L+ S% ?8 p6 Xhttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 5 A- k, F  {2 F- R) P$ `# J5 W, K( i

1 }# [3 I+ N; {8 @$ @从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
! G! M) I' w; H! u1 }/ P2 i至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
% g( k/ `) l# x5 l9 |" Z从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
6 w" H8 g: W; \' B) Q5 m( m6 \至今为止,未出 ...

+ _, j: h) e* a* V" P1 A没有副作用是第一追求,效果显著是第二追求。; H3 R* Z+ R+ x0 P! e6 n
不错。

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