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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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1112881 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
" b0 j% H) ^' BNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
5 `5 ]6 @& J% n- [+ Z& h+ Author Affiliations8 k6 G3 r; O3 X" ~9 Q

9 I% G4 X. q8 V8 ~' \- I1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
+ ^! H. t1 k# w! P2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 7 s; U6 M0 a  [5 F+ Z. ?/ o8 T6 R
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 X3 p% `+ L  H5 Z4 o% i! z, P4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ) l0 X6 V% I+ T$ t8 k
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ; P  \. w, D% y  |. G
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
+ x" {# n% h; B( X7Kinki University School of Medicine, Osaka 589-8511, Japan 2 x6 {% e( b$ M9 e  N6 V/ C
8Izumi Municipal Hospital, Osaka 594-0071, Japan , C" z( ?% u2 n7 I# d# r6 E
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan $ y9 ]) m! H+ w& y/ L# z
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
* f/ y- `9 e4 [; r, xAbstractBackground: 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. ) K2 s# N# K9 T/ Y, J9 Z. n' E$ B8 W
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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
1 o  K. @- c8 G9 u& }' j" X/ P
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato : Z& ?7 y  A& r# o
5 F  l6 Z) S# w- X+ c& j9 |3 q4 t
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  1 Q) _( P) Y7 `9 r

1 J' M4 k8 {9 A8 m$ [3 uPublished online on: Thursday, December 1, 2011 8 V1 M. E) d# i  {' ^& k' V

# B- R6 U6 G2 w* E9 ^Doi: 10.3892/ol.2011.507
2 F& e# W- ~% @2 W( I+ h
" v9 ?1 k, d; y1 D, U" A2 t2 c8 }Pages: 405-410
* u# a! ^; a8 T, C7 z) L$ e( h
- H- Y8 d% T' f# pAbstract:
. N4 `, _  h/ z" M# B* r' hS-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 G+ e& T/ K* u7 |
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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
' t6 v. O, Q) @  ?5 i3 ~7 @F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 3 l) o) e( d8 H% b6 O; q( y
+ Author Affiliations
$ m  z1 G. t# o- Q* P# B3 e1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
9 U7 o7 Y: h; Y' R2Department of Thoracic Surgery, Kyoto University, Kyoto * R+ ~6 w+ Q* n" }
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan / _( R! m5 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
; O; {) P, B( ]" P6 AReceived September 3, 2010. ( N8 F- W% z$ Y) z, x7 v
Revision received November 11, 2010. ( x5 C. f- ^5 H" X! u8 a! L  F
Accepted November 17, 2010. $ U  i9 J  E; G+ W9 ~2 D4 Z
Abstract9 Y: s: `, `$ k' B9 P0 y3 A0 l8 [
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. ) _5 O. a3 o0 N. F  u: r! r
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. 6 t* N- d) s. W1 H9 M" Q
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.
% W8 K& l5 b2 P: z9 wConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. & f# }& @% s/ E* m& @3 A
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。( D5 v* O! P% \! B
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?) B+ C  [1 J# k
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
. _5 @- y5 C/ o8 e, S8 J5 j9 Whttp://clinicaltrials.gov/ct2/show/NCT01523587* F# Y7 P' k1 w& y

' x9 E( I$ G& T7 P& XBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
1 X' [1 }& p+ }2 z$ _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
4 u3 a% \1 \3 x6 m
- X+ i* X2 j3 @2 G$ l+ W& p/ b" X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' u0 K: t$ G0 {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
0 Q; E' q# k; D/ C  X' |3 s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。
& d& G, O" R. W5 C+ y至今为止,未出 ...
) t1 F6 @$ c5 @7 @$ U
没有副作用是第一追求,效果显著是第二追求。6 \& }; t7 R; E# p0 L. I( u
不错。

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