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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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1306716 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 Type1 D8 e& @9 t+ }# Y
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 " O4 Q0 o* v# m/ x5 r- P% c. }
+ Author Affiliations
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4 \; _7 v* U" n: H+ F1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
- I1 m2 o6 O6 k2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ! o7 v5 b8 n0 N
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
% e! b8 V0 _, `/ e2 M/ e4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
# j' A, e$ D8 ^, ]1 }. c2 n, n! h5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
; u! C/ j0 t% r4 y6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
# y. p' k! L& h/ \" ^5 j0 ?; Z: ]$ {7Kinki University School of Medicine, Osaka 589-8511, Japan : V4 ^, J1 E( c. E6 |$ j3 a
8Izumi Municipal Hospital, Osaka 594-0071, Japan ' o9 ~$ @/ D; i- }9 I! p1 F% r+ k, m
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
* b  K' \& c0 n1 R/ I% SCorrespondence 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 + A, U. I$ f& @  F4 |  }! Y
AbstractBackground: 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. 2 T& X. r, h. K6 Q- Q8 `
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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 - Y- A$ c' E2 E& y) O; a

: V4 ?5 e, G% VAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
7 w2 F9 m% i8 r. C: Q9 V* i) A' \# b6 |9 G( b0 A/ v
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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Published online on: Thursday, December 1, 2011 / X2 E8 U; P1 [+ q3 |; n6 P
/ [8 T2 X. `% e3 i: @- Z- _
Doi: 10.3892/ol.2011.507
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Pages: 405-410 # `4 F! l0 r5 x1 u. P2 K/ n9 k

& S  q9 @2 y5 z8 |$ d! l" t- |Abstract:' ~$ D! s6 [7 C6 A4 h" M
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! q6 C! o/ Q  \% \3 [
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
; J& p) ~1 k4 d% B+ Author Affiliations
- S3 E: q8 ^! k9 [: H1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
' o& |6 ]  O4 @- E! O2Department of Thoracic Surgery, Kyoto University, Kyoto 0 ~6 _2 z6 K$ X/ m! ]' B
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan : z2 t' \" V$ X3 A7 s
&#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 / P) |5 n/ d5 f' p" q
Received September 3, 2010. " J0 |6 M( [- V6 Q
Revision received November 11, 2010.
0 f2 W9 ^# F, H, h" sAccepted November 17, 2010.
- P! w4 h0 A! e  y/ U1 \* JAbstract
7 G9 P1 y+ b1 A- |- B  @# k9 ^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.
# J+ Y$ j  n* o. l- x7 o) Q6 P2 o9 XPatients 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.
: B3 m  y' W2 w% kResults: 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.
! k5 v% Z- V7 }& U5 ~* M9 g0 KConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ( i: M. m5 \. \! j8 R) P
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。
( x0 o6 U" Y& R" C) q* [8 Z: T* i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?+ |( E7 u( |6 d+ G& U$ Z
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* D; ]1 a  X8 I
http://clinicaltrials.gov/ct2/show/NCT01523587
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2 m8 v3 D) V/ m6 D* m8 q& o2 {BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC4 J6 l% Y. ?* W, V. F" F$ F
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 , A' v& E. o& }
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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。
" k) r4 }! k" |3 `. l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
5 z% G  F8 Y; z9 i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。- J  O9 G! x2 X, O1 Q% D
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。* q& x. S9 E( G+ ?
不错。

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