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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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1267715 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: F& L/ X1 c- J! u
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
7 }4 X4 T, v6 J7 ?8 H$ M+ Author Affiliations& T# @! r* s9 e+ d) e, p) P
0 n4 [# k: Q6 t" `6 ^) K
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
0 D7 `( f. q5 L- S2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
& K  b: ^, f. K* c  m) z, i' R4 t( L- R3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
. z7 _- ^, `2 M" Q2 y) w& q4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 2 N* I+ R$ t5 ~* v3 U3 t
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan " I3 P% W4 K8 r7 n
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
" L7 u( [8 y: s0 F+ U7Kinki University School of Medicine, Osaka 589-8511, Japan 0 B8 T; `' E- O) J
8Izumi Municipal Hospital, Osaka 594-0071, Japan 2 }( z5 M5 l& E2 k& I  f! v
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
5 B; a# A* t1 i; M8 b+ U( }4 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
  c8 Y$ f) `8 V" DAbstractBackground: 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 & P5 V  U. O+ B
9 g9 M  W- z' A) p& ]  k8 y9 |
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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5 N, Y# l# B) ]$ F1 [  s% d, ePublished online on: Thursday, December 1, 2011 0 K8 [- T1 l7 g# L( ], t3 O

8 |$ E" X  R) Y5 ?. G: F: ]6 b1 [Doi: 10.3892/ol.2011.507 6 R- w# W, x1 P6 V0 r! d

$ u$ o! u; b8 E3 v4 k# O3 {Pages: 405-410 ; i: ?& @9 F+ A

2 s+ h, V) n6 P3 w) `) sAbstract:* m- I- ^; c8 i" k( V
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.% ?7 A! j9 m: z. V2 t1 l

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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
  \3 H; d: Z, g2 }2 `& BF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
3 @$ S# F. x) n, W+ Author Affiliations
8 s, l1 J( _+ h; T1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 7 V% m2 b+ u. v& v( [* A5 p
2Department of Thoracic Surgery, Kyoto University, Kyoto 7 s( g6 w% y% b0 \3 G0 Z" ]/ n7 f3 v
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
  {& T& _* a. d, v&#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 # x8 s+ a/ l! l2 T+ M& K
Received September 3, 2010. 1 s& s5 S' n! v6 a
Revision received November 11, 2010. 3 p1 u- N( s* Z$ k4 l4 F$ c
Accepted November 17, 2010.   Z. \' Z+ i$ V
Abstract
$ @( R/ A3 \- y. r& ]5 jBackground: 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.
  U1 L0 K& M  B3 F! g$ t/ M' kPatients 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. 6 \* Z6 ^' R( `& O5 ~. L
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.
( D9 p, V" C9 d0 o4 w+ DConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 0 e# p+ B* M0 s- {# h2 W8 S  n
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 h- }+ d5 [, V/ {+ X* \1 M
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: e9 I8 |* [' ^+ N% N1 g+ S
http://clinicaltrials.gov/ct2/show/NCT01523587  K0 G% S  Z- U. N2 @' B2 c4 M

0 x! |0 N- A' |- W; n6 \+ d. H+ t9 KBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
$ }5 A  j3 ^9 A* phttp://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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# e' q" \5 C# S! _; k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。% k- v2 C7 c' r/ g8 {, e* Y3 h. J
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 - ~. Q( g5 I& e7 _7 O) l; M. P
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。
: }0 z  I  u& o: s7 @至今为止,未出 ...

/ C" q2 k+ ]2 w8 ~2 L- g没有副作用是第一追求,效果显著是第二追求。- ]( @# y( R6 i9 M
不错。

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