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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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1382057 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 p9 }( ~# W) \# G
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
' x& d5 V' j" y+ Author Affiliations
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3 Z/ {) u' u9 W* l  f7 b7 m+ x1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan $ d9 M- Z+ I, P
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan & f# R1 C+ `- I/ v' {
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ' }8 G9 k% J1 y% ?% v4 X  O
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
, T8 p) O# k2 K0 O5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
/ `2 F) R% i# ^4 r! ^* l6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan + R, @; a( V* _. p0 f" A) r
7Kinki University School of Medicine, Osaka 589-8511, Japan
7 C* m9 T% r6 M1 D3 w8Izumi Municipal Hospital, Osaka 594-0071, Japan 7 K! Y0 N: P0 i1 S6 O7 R3 {& |* Z
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
8 D" D' h* E% ~# f4 Y) ?# CCorrespondence 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
2 S) @  _4 D) F" pAbstractBackground: 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
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato & N0 H" h* R2 `8 C% l
1 A  _; e$ e0 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  
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, Q  E$ M) g" c7 i3 ~0 }Published online on: Thursday, December 1, 2011
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* q4 W7 \2 D7 U9 g* GDoi: 10.3892/ol.2011.507 3 Y% k; Z4 e4 G5 {/ _

3 O: A2 I6 y& T- c" Q4 u) v: f" j. tPages: 405-410
9 M+ \2 ^: T% d; K5 ?: M  s5 r2 Q9 x9 K" [: m
Abstract:
3 n$ S: D3 H+ j5 rS-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.$ \! s- m( ~3 I- k0 b  P# r

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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& Q9 f, y. ?( P3 \6 M# p
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 + L( r; c  q- ^) p6 V& b& I
+ Author Affiliations
( c0 [/ w- K. B; p  S1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu , S. y* B  l' b, B! T! w  a. q
2Department of Thoracic Surgery, Kyoto University, Kyoto 5 @/ h2 u% a. N4 R
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
! T& C- r$ I/ c) n: t&#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 4 D9 j5 T, U, t  }
Received September 3, 2010.
& g( e  y" e! @Revision received November 11, 2010. 9 W7 t5 G9 g  X+ u' X1 x
Accepted November 17, 2010.
" a+ @7 w+ S6 \Abstract- U" P, J2 j. K8 N( b3 P
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.
4 h( I" o$ p5 }$ o5 O# r2 EPatients 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. - F3 ~; O( _% H' h0 p: J3 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. # {  V! i8 F" Z( p8 Z8 G  C% b
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. " V" r3 c; Z/ n8 `
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。
8 Q  j/ T1 A& P, {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
$ A% q. s% i. t: ?4 E; chttp://clinicaltrials.gov/ct2/show/NCT01523587* C* k+ G. z2 q' M0 S- W+ s; ?1 K

5 H" r! b. @6 u0 Z) d* B- [' ~BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
9 S1 B  K  D$ ~: Ghttp://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
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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。% U! u6 k0 Z% i; c+ c" R+ F7 F
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
( j% o7 J5 H( Z3 b+ Q: G( |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。
& n) I2 f6 ]% N) J$ g  z3 S+ J; p至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。
  u  u) x8 |  w6 ^  t不错。

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