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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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1377133 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
$ Q6 \3 \' x! ZNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 9 z3 Q% w0 x! j8 Y: p( P
+ Author Affiliations5 P. H2 J; n1 X% a) o  i/ _

7 ?, i1 L2 S# T1 s0 h1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ! a; o  h. a. G5 i% Z
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 r0 T0 R& F7 E( W5 p- e# q9 B3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
8 @4 Z1 ^; y4 I$ t; m! i4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
. C+ C; o) Z4 U/ s& }. d4 T5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 8 N* q$ u# P% c
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
' [! o, G. p: e! A& a1 r1 n& A7Kinki University School of Medicine, Osaka 589-8511, Japan , V$ ?8 @6 P/ r& v8 L( \! ^
8Izumi Municipal Hospital, Osaka 594-0071, Japan
/ W' @3 c* }* K$ a7 _: E( b6 u9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan ' M. B1 D  @- e; K! M
Correspondence 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
! |8 F( L% ]+ c/ U8 VAbstractBackground: 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 k* F$ r5 |
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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
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9 F2 F% g6 g' G# P$ r& c5 a  X6 T$ UAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato : ~/ q# ?/ t& Z2 z, ^) c" G2 ]
& u" y& h, v& H( V0 X3 K1 `7 q
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
4 d& R8 n5 H6 z5 p; u- k+ Q2 g) ?6 m: p: U# n
Published online on: Thursday, December 1, 2011
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5 Z" q1 x9 v3 iDoi: 10.3892/ol.2011.507
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/ M, G1 P7 R8 u7 nPages: 405-410 5 Z" h4 e3 D2 d

9 B+ E. l/ {! OAbstract:! `0 @; z3 g& q; p' ]
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
2 U# j2 L! t9 @" `4 @F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ( d2 g, Q4 ^4 q- e8 ^
+ Author Affiliations
) k- i; ^. n2 P4 w3 S3 Q; n1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 0 E* i/ g/ p, |( ~
2Department of Thoracic Surgery, Kyoto University, Kyoto 8 m( M1 `1 Y- M6 F
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
# M) R( [6 }. }2 q&#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
6 t1 U9 h+ n  u$ R0 m1 [7 LReceived September 3, 2010. 2 d/ C1 h" O4 V' o0 o" D6 g$ I
Revision received November 11, 2010.
6 [: P3 u5 X  X9 XAccepted November 17, 2010.
  D0 B3 H0 j1 k1 a, j$ RAbstract% Z2 T* ^( s; e1 s
Background: 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. + l* t3 U5 ]/ Q
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. . ~$ a" i6 ]7 n$ g, ~' ^
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.
2 d, t; U7 e$ k( r# ?+ ^( ^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。
" P8 Q/ e, f4 J; 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?
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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
4 ?! ~% e7 f  L" ]  thttp://clinicaltrials.gov/ct2/show/NCT015235870 {- e' @8 W6 q" w. c1 e
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
8 M  G6 w2 o9 e2 A6 v  [http://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 ]9 d2 @% t+ S0 X+ ]6 Z# B0 a( S0 Y* q  I9 ^; v
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。
$ M% y1 x1 ?3 Z. K' A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
2 P; F" j7 q$ v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。8 t9 |8 o( W( N3 G' A- z
至今为止,未出 ...

% m+ N  y  `$ O  o' d  J' f没有副作用是第一追求,效果显著是第二追求。
& H7 d* p( n( i+ |不错。

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