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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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1197573 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' t) `  `/ D# o/ Q
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
8 \' A; @" d$ n7 W+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
7 r( B2 e; \/ a2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ( U) N9 M. ^5 I
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
5 K% }# z3 Q  P/ F4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan . G" g8 [2 U" g: w  P
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
$ |* P  x% w% j& f! o/ ]5 l6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
1 c* c! g- R- Q9 n" o7Kinki University School of Medicine, Osaka 589-8511, Japan
8 g; s6 D% a4 B% t2 Z8 R8Izumi Municipal Hospital, Osaka 594-0071, Japan ' f6 d) I% A8 U7 ]
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
+ D0 b1 ^" j& E' @* ?9 P) K; HCorrespondence 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
: L4 s$ j* p, z0 I6 I$ KAbstractBackground: 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. ) G4 o/ U1 d' u0 h

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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
9 b$ }7 Z! C/ g) x  j/ `6 M! I  t. O! P
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato $ q, Y4 ]: y5 D; h
7 u/ S+ W9 ?0 ?2 p7 W
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ' }$ j7 j* M3 q1 L* x* S+ Z
3 L# G2 X: D' u. N  J+ u; \1 i
Published online on: Thursday, December 1, 2011
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  _8 ]: L! k9 V- o& n" S3 rDoi: 10.3892/ol.2011.507 1 M* g* D' t; k/ H( G

( L6 O0 F4 T0 `3 N* Z1 ^Pages: 405-410 5 {/ Y! n4 ^% u5 C+ n: A5 R

7 r# z. ^: w0 r! U; nAbstract:
, X: _& _5 @% y4 a1 q' Y+ v0 u+ US-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
8 T8 i$ b# ^  ?" Y% Y6 n* @) oF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ! e2 N: ^2 |, F' j1 b4 y$ V/ J
+ Author Affiliations0 F7 h$ E5 [7 F/ C1 x: A, F
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
- |5 k' n, M( d2Department of Thoracic Surgery, Kyoto University, Kyoto 0 F: }6 a! }: L" y  L) n) \
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
& s. i- i3 R! }& ]$ f0 N&#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 7 Q- H9 Y4 `$ q3 G
Received September 3, 2010.
; k0 T5 S5 h% J# |Revision received November 11, 2010. ; w) z4 v- P1 ~! w* o
Accepted November 17, 2010.
  j* `- _% v/ l% L/ U2 d4 K/ YAbstract  j8 R: w4 {8 p: m5 d& `+ O  ~0 `5 q" }; 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.
! S, _( y4 `, L" ]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. , V9 \, o0 T  ^! y1 k1 k+ t/ v
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. # @+ z1 S: s: X% R, o) H1 ~& o
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. - L) i1 _7 m( ^2 d. [
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。, M6 }- W; e/ x  G. c
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 [; k7 }# V. B% w4 X* a9 q8 x
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) b7 c% ~. l2 `. c9 j* \# v
http://clinicaltrials.gov/ct2/show/NCT01523587
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- d$ H& K, B/ h% h1 I. M: PBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC8 j% n: j. R& D2 X
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 ! c6 v  j1 V+ h2 T5 m! ^. h1 O

7 b, l! |9 ?" y6 m8 `" G  x0 C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。
5 P% Q4 Y0 C! u7 j. h5 y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 f# S% i( |* g- F; ]: r6 R- D2 e* R* L
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。
4 h& m0 N" Q% w0 r- t. ^% Y- n至今为止,未出 ...

: A4 r" o+ ^9 n6 P4 G7 [: _没有副作用是第一追求,效果显著是第二追求。' Z) D" k8 d& U& H4 m8 `- J* e
不错。

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