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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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1400802 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
6 o  J& S& X% R, e# j8 q5 H3 i& KNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
3 t1 s. }6 ^$ P) m- Q( L: @+ Author Affiliations8 m, Y) \" M4 j, ]$ F

5 M* s& O$ [. V" @5 x5 N1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan , j+ ^* j9 e. V
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
* k6 {( b( Z+ |+ Y3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; s" f# O* k6 X( W  K; P% f' x+ l
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan : r/ Q% I+ O) ^  Q+ R1 ^) p
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan % Y- V, b+ h1 R2 i- u
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 3 s. A1 j/ c' }+ L1 U& z& m
7Kinki University School of Medicine, Osaka 589-8511, Japan - ~$ c5 \  n" y  `5 c
8Izumi Municipal Hospital, Osaka 594-0071, Japan
. L5 j$ ]8 ~, Z  |; `/ I  y2 z6 ]9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
3 A) }+ O0 r2 u' E; h5 P) a, ACorrespondence 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 ( i& C: I: i/ i7 z7 ~1 ?/ ?
AbstractBackground: 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.
9 W6 ?' X+ t' Y3 j/ ?, b8 y( `2 K* e# J4 @$ ?7 [7 n" x
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 , a; N  m$ M. n$ f0 N0 I
% j" V; ]5 }) N( n+ u' j1 G' d
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
, ^+ v4 q1 Y7 }% Q0 w, l6 ~
& R8 I3 i" x( y! U5 a# K: vAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
! j4 w* p& `! x) c1 O
: L; b/ V1 t* p2 L, p9 v, h2 rPublished online on: Thursday, December 1, 2011
5 o  s# N5 [7 a$ |3 {
, F2 Y& o2 j/ L: z  s& uDoi: 10.3892/ol.2011.507
: e+ ?4 y# \; D! F
+ [' B. j( c$ Y' ZPages: 405-410 ! P9 W) Z, h# j; c) d

! L7 |7 M- U' ~* W- |9 ZAbstract:# v* g/ }1 f+ A8 y
S-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
# W) |$ ?8 H. P  U# X. V5 b, |F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
, b2 K1 f! L# i3 R5 R+ j, e% }0 l+ Author Affiliations
+ N; p7 m; g: i6 W6 t+ y1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
- x8 Q. p5 V. G& _3 G2Department of Thoracic Surgery, Kyoto University, Kyoto 2 A: P$ m2 ]7 ]6 h& V! y; h% ]
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
) Y$ J: I2 q, O5 ?9 Y&#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
5 ~, I- F+ }% C! lReceived September 3, 2010. ) f8 w; B/ V) n1 L/ l
Revision received November 11, 2010.   n$ v" y; i! u
Accepted November 17, 2010. * ^, C! i+ n2 N+ t
Abstract
5 E1 {! Z- x# |& GBackground: 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.   a3 F5 x  F2 e: {5 N# 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. 3 [7 W( f$ B' p- k
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.
/ k: X+ m# j, L! f- @Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. * r$ K7 J4 T  S
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。
" G" P7 A  ?/ J& _7 Z( B4 I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?
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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 Chemotherapy
% F! I+ G" ^/ C2 Hhttp://clinicaltrials.gov/ct2/show/NCT01523587
5 Z: }+ Q* ?& ]4 C' \2 f6 v* U6 \3 }+ H6 C9 I
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
" L- Y% G  B: zhttp://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 6 U" o. d! N5 B7 z) D. L

2 H4 U3 t/ b/ |& _, b8 Y* D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。
9 k- x8 L( w. L# V3 g: M( d% Y: v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
( M, I+ [) `, n$ j. \5 X$ I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。$ ]5 ?7 h; ~0 w4 T1 e5 ]
至今为止,未出 ...

. p0 b& x- e2 e* N" A5 ^没有副作用是第一追求,效果显著是第二追求。7 b2 f* N- P: r% {! i  W- @7 F
不错。

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